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Review

Extensively Drug-Resistant Tuberculosis: A Sign of the Times and an Impetus for Antimicrobial Discovery

by
Shelley E. Haydel
Biodesign Institute Center for Infectious Diseases and Vaccinology, School of Life Sciences, Arizona State University, Tempe, AZ, 85287-5401, USA
Pharmaceuticals 2010, 3(7), 2268-2290; https://doi.org/10.3390/ph3072268
Submission received: 15 June 2010 / Accepted: 19 July 2010 / Published: 20 July 2010
(This article belongs to the Special Issue Antibiotics)
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Abstract

:
Mycobacterium tuberculosis is an extraordinarily successful human pathogen, infecting one-third of the world’s population and causing nearly two million deaths each year. In this article, current trends in worldwide tuberculosis (TB) incidence, prevalence, and mortality are discussed along with standard TB treatment regimens, characteristics of first-line and second-line anti-tuberculosis drugs, and mechanisms of antibiotic resistance. The global TB emergency has been further exacerbated by extensively drug-resistant (XDR) TB strains that are resistant to our best antibiotics and very difficult to treat. This review also focuses on the emergence of XDR-TB strains, the global health impact, and existing treatment options and outcomes for XDR-TB disease. Finally, this review briefly describes new anti-tuberculosis drugs currently in Phase II clinical evaluations and the impetus for discovering new antibacterial compounds to target drug-resistant M. tuberculosis and improve tuberculosis therapy.

1. Introduction

Tuberculosis (TB) is believed to have been present in humans for thousands of years, as evidenced by the bones of ancient Egyptian mummies showing deformities consistent with the disease. Historically, pulmonary TB was known as the “Great White Plague” (causing about one in four deaths) of the 17th and 18th centuries in Europe, “phthisis” (a Greek term meaning to waste away), “scrofula” (swollen glands of the neck), and “consumption” (progressive wasting of the body) [1]. From 1700 to 1900, it is estimated that TB was responsible for one billion deaths and killed more people than any other disease [1,2]. Prior to the introduction of antibiotics in the 1950s, improved sanitation and living conditions significantly reduced the incidence of TB disease.
TB is transmitted via the respiratory route as a highly infectious aerosol with varying outcomes occurring from this initial Mycobacterium tuberculosis exposure. These outcomes can range from immediate organism destruction by the host’s immune system to infected individuals developing active primary TB disease within 1–3 years [3]. However, the majority of individuals infected with M. tuberculosis have a non-contagious, clinically-latent infection with an absence of clinical symptoms [4]. Latently-infected individuals have a 5–10% risk of developing reactivation TB disease during their lifetime [3], often due to immunosuppressive circumstances, with HIV infection being the greatest identified cause [5].
The discovery of the first antibiotic, streptomycin, to treat TB in 1944 was soon met with the appearance of the first antibiotic-resistant M. tuberculosis isolates [6]. A rapid succession of additional anti-TB agents was discovered in the late 1940s through the 1950s, with the last, rifampin, discovered in the 1960s [7]. To circumvent the development and emergence of drug resistance, a multidrug chemotherapeutic approach for treating TB was also introduced in the 1960s [8,9,10]. The concomitant emergence of HIV in 1980s further complicated and worsened the ongoing TB epidemic [11], and the global TB/HIV coinfection epidemic continues today with TB infecting one-third of the 33.2 million people living with HIV [12]. Continued evolution and exacerbation of the drug resistance problem has led to extensively drug-resistant TB, or XDR-TB, which is resistant to first-line and second-line TB antibiotics [13,14]. MDR and XDR forms of TB are extraordinarily difficult to treat, particularly in immunocompromised patients, and pose serious threats to global health.

2. Global Incidence, Prevalence, and Mortality of TB

Worldwide, TB is the second leading cause of death from a single infectious agent. Highlighting its success as a human pathogen, the World Health Organization (WHO) declared TB a global emergency in 1993 and warned that the disease could kill 30 million people over the next decade if effective control efforts were not implemented. While significant epidemiological, treatment, and control strategies have been employed over the past decade, the WHO estimate of nearly 30 million deaths was relatively accurate, with TB continuing to be one of the world’s major infectious diseases. Globally, one-third of the world’s population is infected with TB, with over nine million incident cases of active TB disease and an estimated 1.3 million deaths occurring per year [15]. Regionally, the majority of TB cases in 2008 existed in Asia (55%) and Africa (30%), with significantly lower proportions of cases in the Eastern Mediterranean (7%), Europe (5%), and the Americas (3%) [16]. Given the vast number of individuals who succumb to the disease each year, long-term actions to fight this public health challenge must be and are aimed at reducing global mortality and eliminating the disease [17,18].
Global control efforts over the past decade have resulted in relative stabilization of incident and prevalent cases of TB and reduction in TB deaths (Table 1) [19]. In 2004, global incidence rates peaked at 142 cases per 100,000 population, and the slow rate of decline since 2004 has been at less than 1% per year [19]. Accounting for population growth, the currently estimated 139 incident cases per 100,000 population has remained relatively stable for the past several years [16,19,20]. Prevalence is a direct indicator of the global TB burden, referring to the number of individuals with the disease at a particular time [21,22]. The overall numbers of estimated prevalent cases of TB decreased from 13.9 to 11.1 million from 2006 to 2008, corresponding to a reduction in the number of cases per capita from 210 to 164 per 100,000 population in 2006 and 2007, respectively (Table 1) [16,19]. Globally, TB treatment success rates in 2007 were 86%, thus meeting the 85% success rate target first established by the WHO in 1991 [15,16,18].
Worldwide, TB accounts for approximately one-fourth of HIV-related deaths and is the leading cause of death in HIV-infected adults in developing countries [12,16,22,23]. In 2000, nine percent of all new TB cases and 12 percent of TB cases in adults were attributable to HIV infection [22]. In 2008, the influence of the HIV pandemic on the global burden of TB continued to escalate as an estimated 1.4 million incident cases, representing 15% of the total TB incidence, occurred in HIV-positive patients [16]. While the overall number of HIV-related or HIV-attributed TB deaths has remained relatively stable over the past decade (Table 1), the interlinked TB and HIV epidemics continue to inflect serious morbidity and mortality in sub-Saharan African countries [24]. Approximately 78% of the globally estimated 1.4 million HIV-positive TB patients live in sub-Saharan Africa [12] with 30 to 40% of these HIV-infected individuals dying from TB [25].
Table
Table 1. Estimated global incidence, prevalence, and mortality of TB [16,19,22,26].
Table 1. Estimated global incidence, prevalence, and mortality of TB [16,19,22,26].
2000200620072008
Incidencea8.3 million9.24 million9.27 million9.4 million
Prevalenceb16.6 millionc13.9 million13.7 million11.1 million
Deaths (total)1.8 million1.7 million1.7 million1.8 million
HIV-negative1.6 million1.5 million1.3 million1.3 million
HIV-positive0.226 million0.231 million0.456 milliond0.52 milliond
a Incident cases refer to the estimated number of new cases reported within a given year. b Prevalent cases refer to the estimated number of cases which exist within a population within a given year [21,22]. c In 2000, the global prevalence was estimated as twice the incidence [22].d Increased numbers of HIV-positive cases result from new data from provider-initiated HIV testing, not doubling between 2006 and 2007 [16,19].

3. Recommended TB Treatment and the Current Arsenal of TB Antibiotics

The current standard chemotherapeutic regimen for treating new pulmonary TB patients consists of a multidrug combination of the first-line anti-TB drugs-isoniazid, rifampin, pyrazinamide, and ethambutol-administered for an intensive, initial period of two months. A continuation phase of treatment for an additional four months consists of administration of isoniazid and rifampin. In countries reporting high levels of isoniazid resistance occurring in new TB patients or lacking isoniazid drug susceptibility results, ethambutol is administered throughout the four-month continuation phase of treatment [27]. Upon availability of drug susceptibility profiles and confirmed sensitivity of isoniazid, administration of ethambutol may be omitted in the continuation phase [27,28].
The implementation of the Directly Observed Treatment, Short course (DOTS) strategy by the WHO in the 1990s elicited great effectiveness in TB control, achieved cure rates of nearly 80% [29], and was subsequently expanded as an internationally recommended approach for TB control [30,31]. DOTS consists of a broad TB control effort focused upon five principal elements: (i) political commitment for financing; (ii) proper case detection with appropriate microbiological laboratory support; (iii) standard chemotherapeutic treatment with patient support and supervision, which includes directly observed therapy; (iv) consistent availability of effective drugs; and (v) standard monitoring and evaluation system with impact measurements. Supervised administration of antibiotics during the intensive phase of therapy, in accordance with the recommended DOTS strategy, results in a greater than 85% cure rate of new, antibiotic-susceptible TB cases (Figure 1) [30,32]. The DOTS supervised program facilitates patient adherence to the treatment regimen and maximizes the likelihood of treatment completion [28].
First-line anti-TB antibiotics target actively replicating M. tuberculosis cells in the lung (Table 2) and significantly reduce transmission rates of M. tuberculosis to other persons within the first two months of treatment. The bactericidal antibiotics, isoniazid and rifampin, are active against dividing cells with rifampin also having activity against dormant bacteria, thus accounting for sterilizing properties during the short-course antibiotic regimen (Table 2) [33,34,35]. Pyrazinamide exhibits greatest activity against dormant organisms localized within macrophages or the acidic environment of the pulmonary caseous lesion [36]. Inclusion of ethambutol in the first-line drug regimen is recommended to prevent rifampin resistance when isoniazid resistance is suspected [28].
Second-line antibiotics are introduced into treatment regimens when resistance to primary antibiotics emerges. However, secondary antibiotics exhibit lower potency and/or greater toxicity [38]. The fluoroquinolone, aminoglycoside, and capreomycin antibiotics target DNA replication and protein synthesis and offer the greatest effectiveness of the second-line anti-TB drugs (Table 3) [39,40]. The remaining antibiotics exhibit bacteriostatic activity (Table 3) and are considerably less potent, more toxic, and more expensive [38]. Fortunately, in 2000, the WHO and its partners established the Green Light Committee Initiative which allows countries access to concessionally-priced, second-line anti-TB drugs for treating individuals with MDR-TB in accordance with WHO guidelines [18,41,42].
Therapy for treating TB has not always been mediated via chemotherapeutic agents. Prior to the availability of effective antibiotics, surgical intervention was an important form of therapy for pulmonary TB [43]. In this day and age with the emergence of MDR- and XDR-TB, surgical pulmonary resection is once again considered effective management for the treatment of patients with drug-resistant TB [43,44,45,46,47,48]. Studies have also shown that administration of antibiotics along with surgical management of pulmonary MDR-TB result in improved outcomes compared to surgical intervention alone [43].
Table
Table 2. First-line anti-TB drugs [37].
Table 2. First-line anti-TB drugs [37].
First-line antibioticsAntibiotic class/structureDelivery routeActivityMechanism of actionGenes and gene products associated with resistance
IsoniazidPyridine hydrazideOralBactericidalInhibits mycolic acid (cell wall) synthesiskatG; catalase-peroxidase
inhA; enoyl-ACP reductase
ndh; NADH dehydrogenase II
RifampinRifamycinOralBactericidalInhibits RNA synthesisrpoB; β-subunit of RNA polymerase
PyrazinamideNicotinamide analogOralBacteriostatic/ bactericidalDisrupts cell membrane energetics and inhibits membrane transportpncA; nicotinamidase/pyrazinamidase
EthambutolEthylenediamine derivativeOralBacteriostaticInhibits arabinogalactan (cell wall) synthesisembCAB; arabinosyl transferase

4. Emergence and Global Health Impact of XDR-TB

The TB global emergency is further complicated by MDR- and XDR-TB strains that are resistant to our best antibiotics, very difficult to treat, and associated with greater morbidity and mortality than antibiotic-susceptible TB (Figure 1). An individual may develop the drug resistant form of TB via inadequate therapy that enables the selection of drug-resistance (acquired resistance) or infection with a drug-resistant TB strain (primary resistance) [49]. While infection with an exogenous drug-resistant TB strain is related to infection control measures, the development of acquired M. tuberculosis resistance is multi-faceted and can be attributed to various social, political, economic, epidemiological, and pathophysiological factors [50]. Certainly, scientists investigate the cellular and molecular mechanisms to explain the development of drug-resistant TB strains, but other influences including, but not limited to, improper or poor health management practices or infrastructure, inadequate therapeutic regimens, antibiotic misuse, insufficient or unobtainable resources, poor socioeconomic conditions, individual immunocompetence, patient compliance, and complicated personal issues have also played roles in the evolution and progression of antibiotic resistance [38,50,51,52,53,54,55].
Table
Table 3. Second-line anti-TB drugs [37].
Table 3. Second-line anti-TB drugs [37].
Second-line antibioticsAntibiotic class/structureDelivery routeaActivityMechanism of actionGenes and gene products associated with resistance
StreptomycinAminoglycosideIM injectionBactericidalInhibits protein synthesisrpsL; S12 ribosomal protein
rrs ; 16S rRNA
Kanamycin/AmikacinAminoglycosideIM injectionBactericidalInhibits protein synthesisrrs; 16S rRNA
CapreomycinPolypeptideIM injectionBactericidalInhibits protein synthesisrrs; 16S rRNA
tlyA ; putative rRNA methyltransferase
LevofloxacinFluoroquinoloneOral or IVBactericidalInhibits DNA replicationgyrA; DNA gyrase subunit A
MoxifloxacinFluoroquinoloneOral or IVBactericidalInhibits DNA replicationgyrA; DNA gyrase subunit A
GatifloxacinFluoroquinoloneOral or IVBactericidalInhibits DNA replicationgyrA; DNA gyrase subunit A
EthionamideThioamideOralBacteriostaticInhibits mycolic acid (cell wall) synthesisinhA; enoyl-ACP reductase
etaA/ethA ; flavin monooxygenase
CycloserineIsoxazolidinoneOralBacteriostaticInhibits peptidoglycan (cell wall) synthesisunknown (alrA; D-alanine racemase in Mycobacterium smegmatis)
Para-aminosalicylic acidSalicyclic acidOralBacteriostaticInhibits folic acid synthesisthyA; thymidylate synthase
a IM, intramuscular; IV, intravenous.
MDR-TB strains exhibit antibiotic resistance to two of the best first-line anti-TB antibiotics, isoniazid and rifampin, while XDR-TB is defined as being resistant to isoniazid, rifampin, to any fluoroquinolone, and one or more of three injectable anti-TB antibiotics (capreomycin, kanamycin, and amikacin) [56]. Removal of the fluoroquinolones and the injectable drugs from the TB treatment arsenal means losing the most potent and least toxic second-line antibiotic treatment options. Considering that XDR-TB is resistant to powerful first-line and second-line antibiotics, patients must be treated with more expensive, less effective second-line antibiotics, resulting in a longer treatment course for a minimum of 18–24 months, lower cure rates (Figure 1), and significantly increased healthcare costs [57]. Moreover, second-line therapeutic treatment requires strict patient monitoring, supervision, counseling, and support to prevent further drug resistance that could potentially render the disease untreatable (Figure 1) [14,58].
In 2004, there were an estimated 424,000 MDR-TB cases, representing a 64% increase from the global number of nearly 273,000 MDR-TB cases estimated in 2000 [59]. For the past several years, the number of worldwide MDR-TB cases consistently remained around 450,000 per year. XDR-TB, first described in March 2006 [13], generally evolves from MDR strains. The WHO estimates 30,000 cases of XDR-TB per year, but the number of countries or territories reporting at least one case of XDR-TB has nearly tripled from 20 in 2007 to 57 in 2009, thus emphasizing its spread [16,19]. On April 1, 2009, WHO officials stated that XDR-TB is “a very deadly and devastating epidemic” that is “poised to grow much worse very quickly.” The warning signs are certainly present, and without action, we are facing a disease epidemic that will undoubtedly continue without new drugs, diagnostics, and vaccines to combat it.
Pharmaceuticals 03 02268 g001 1024
Figure 1. Antibiotic cure rates of TB based on drug resistance patterns. Estimated cure rates for antibiotic-susceptible TB, MDR-TB, and XDR-TB in HIV-negative patients are >95%, 60–80%, and 30–60%, respectively [60,61,62,63]. Although TB strains exhibiting resistance to all first-line and second-line antibiotics have not been identified, total drug-resistant (DR)-TB would be untreatable with existing chemotherapeutic agents. INH, isoniazid; RIF, rifampin; Fqs, fluoroquinolones; Am, amikacin; Km, kanamycin; Cm, capreomycin.
Figure 1. Antibiotic cure rates of TB based on drug resistance patterns. Estimated cure rates for antibiotic-susceptible TB, MDR-TB, and XDR-TB in HIV-negative patients are >95%, 60–80%, and 30–60%, respectively [60,61,62,63]. Although TB strains exhibiting resistance to all first-line and second-line antibiotics have not been identified, total drug-resistant (DR)-TB would be untreatable with existing chemotherapeutic agents. INH, isoniazid; RIF, rifampin; Fqs, fluoroquinolones; Am, amikacin; Km, kanamycin; Cm, capreomycin.
Pharmaceuticals 03 02268 g001

5. Genetic Basis of M. tuberculosis Antibiotic Resistance

Efforts to understand the molecular basis of M. tuberculosis antibiotic resistance have advanced significantly and investigations of potentially unique genetic traits in MDR- and XDR-TB strains are ongoing. Unlike other bacterial pathogens, there is no evidence that gene acquisition contributes to antibiotic resistance in M. tuberculosis [64]. The mutated genes and gene products associated with M. tuberculosis drug resistance are included in Table 2 and Table 3. Isoniazid resistance is linked to alterations in the catalase-peroxidase gene (katG), the inhA gene, which encodes an enzyme involved in mycolic acid biosynthesis, or the NADH dehydrogenase II gene (ndh) [65,66,67,68]. Genetic mutations in rpoB, which encodes the RNA polymerase β-subunit, result in rifampin resistance [69,70,71]. Mutations in pncA that eliminate pyrazinamidase/nicotinamidase activity confer pyrazinamide resistance [72,73]. Numerous genetic mutations present within the embCAB operon, which facilitates production of arabinosyl transferase, have been linked to ethambutol resistance [74,75], but other genes may also be involved [76].
Similar to the first-line TB antibiotics, genetic mutations account for all known mechanisms of resistance for the second-line TB drugs (Table 3). Streptomycin resistance is associated with mutations in the rpsL, ribosomal S12 protein, and rrs, 16S rRNA, genes [77,78,79,80]. Similar to streptomycin, kanamycin and amikacin resistance are linked to genetic mutations that occur within the rrs gene with evidence of cross-resistance occurring between kanamycin and capreomycin or viomycin in mycobacteria [81,82,83,84,85,86]. Mutagenesis of the tlyA gene, which has homology to rRNA methyltransferases, also confers capreomycin resistance [87]. Clinical resistance to the quinolone family antibiotics, levofloxacin, moxifloxacin, and gatifloxacin, is attributed to mutations occurring within the gyrA gene encoding DNA gyrase [88,89]. Ethionamide resistance is linked to inhA mutations, whereby cross-resistance occurs between isoniazid and ethionamide [66,90], and to mutations in the etaA (ethA) gene, which codes for flavin monooxygenase responsible for activation of ethionamide [91,92]. Recent evidence links para-aminosalicylic acid resistance to mutations within the thyA gene, which produces thymidylate synthase A, but mechanisms or targets independent of thymine nucleotide biosynthesis are also likely involved [93,94]. While inactivation of the alrA gene, encoding D-alanine racemase, causes increased sensitivity to cycloserine in Mycobacterium smegmatis [95] and overexpression of alrA confers mycobacterial resistance to cycloserine [96], the genetic mechanism of cycloserine resistance in M. tuberculosis is currently unknown.
While accumulation of genetic mutations associated with first-line and second-line drug resistance is implicated in TB drug resistance, efforts to delineate molecular insight into MDR- and XDR-TB-specific genetic traits are underway. Comparative computational analysis of drug-sensitive M. tuberculosis and MDR- and XDR-TB KwaZulu-Natal strains (discussed below) suggested that drug resistance may be linked to single-nucleotide variations (348 common to all KwaZulu-Natal strains) which could influence drug susceptibility patterns and protein function [97]. Whole-genome sequencing of MDR- and XDR-TB outbreak strains in HIV-infected patients from KwaZulu-Natal revealed novel mutations not previously associated with drug resistance [98]. However, the study further determined that the majority of mutations came from a common ancestor, suggesting that XDR-TB strains can evolve without fitness changes or XDR-specific mutations [98].

6. Existing Treatment Regimens and Treatment Outcomes for XDR-TB

While MDR-TB can be effectively treated with a long-term regimen of second-line antibiotics [99], XDR-TB is often considered very difficult to treat, or is even untreatable, with existing chemotherapeutic agents [100,101]. A large retrospective study revealed that XDR-TB cases have a worse clinical outcome than MDR-TB cases resistant to all first-line antibiotics (39% vs. 54% treatment success, respectively) [102]. Importantly, susceptibility to at least one first-line drug increased treatment success of MDR-TB cases (67%), indicating that the XDR-TB designation can be a strong predictor of poor treatment outcomes [102]. Sytematic review and meta-analysis of treatment outcomes of over 8,000 patients with MDR-TB (data from 33 studies in 20 countries) determined that treatment success improved substantially when patients were treated for at least 18 months with directly observed therapy occurring throughout the entire treatment period [103,104].
XDR-TB cases with resistance patterns corresponding to the WHO definition (resistance to isoniazid, rifampin, to any fluoroquinolone, and one or more of three injectable anti-TB antibiotics) are usually not identified during clinical treatment since second-line drugs are administered upon the likelihood of first-line antibiotic resistance [102]. Moreover, because of the recent classification of XDR-TB within the past five years, patients with XDR-TB are often not differentiated from individuals with MDR-TB prior to the initiation of treatment. Therefore, most existing studies focus on retrospective identification of XDR-TB isolates from patients diagnosed with MDR-TB. Although treatment successes vary among existing studies, poor treatment outcomes appear to be invariably associated with XDR-TB (Figure 1, Table 4) [102].
A startling 2006 study revealed an XDR-TB outbreak in 53 HIV-positive patients which resulted in 52 deaths occurring within 16 days of TB diagnosis (Table 4) [105]. These patients from the province of KwaZulu Natal in the Republic of South Africa, which has a high incidence of TB (940 cases per 100,000 population) and high prevalence of HIV infection (19% of the adult population), likely had severe immunosuppression, had not previously received treatment for TB, and were not known to have acquired or been treated for resistant TB disease [49,105]. From June 2005 through March 2007 in the town of Tugela Ferry, located in central KwaZulu-Natal Province, a total of 217 XDR-TB cases were identified, yielding a striking mortality rate of 84% [106]. Retrospective assessments indicated that hospital and health system failures, inefficient airborne infection control in health care facilities, and inadequate knowledge and understanding of clinicians in KwaZulu-Natal province of South Africa influenced the high mortality and high transmission rates of this XDR-TB outbreak [49,107]. Moreover, in these HIV-positive patients, exogenous reinfection with MDR- or XDR-TB strains, rather than acquired drug resistance, was implicated in the development of this outbreak [49]. Most importantly, these reports and others in non-HIV-infected patients revealed the rapid lethality of XDR-TB and alerted public health officials of the emerging epidemic and global health significance of XDR-TB strains [57,102,108,109,110,111].
While HIV coinfection will result in poor treatment outcomes for XDR-TB patients, treatment success rates in HIV-negative, XDR-TB patients are quite variable, ranging from 29–60% (Table 4) [62,112]. In a retrospective study of South Korean XDR-TB patients treated with a median number of four anti-TB drugs (range, 0–16), the treatment success rate was 29% [63]. Patients were treated with individualized regimens based on antibiotic susceptibility profiles and direct observed therapy was only implemented upon admission into a national TB hospital [63].
Table
Table 4. XDR-TB treatment outcomes.
Table 4. XDR-TB treatment outcomes.
StudyStudy locationXDR-TB patientsHIV statusTreatment success rate
Gandhi et al. [105]KwaZulu Natal, Republic of South Africa53positive2%
Migliori et al. [102]Europe (Estonia, Germany, Italy, and Russian Federation)64negative39%
Keshavjee et al. [62]Tomsk, Russia29negative48%
Chan et al. [57]United States10negative50%
Mitnick et al. [112]Peru48negative60%
Kim et al. [63]South Korea75negative29%
As reported by Keshavjee et al. [62] and Mitnick et al. [112], more aggressive chemotherapeutic treatment approaches which incorporate the use of at least five antibiotics with demonstrated isolate susceptibility have resulted in improved treatment success rates. Aggressive treatment of HIV-negative patients with XDR-TB in Tomsk, Russia resulted in successful treatment of 14/29 (48%) patients [62]. Most XDR-TB strains in the Tomsk, Russia cohort study were resistant to all first-line antibiotics and ethionamide [62]. Although all drugs were administered under direct observation and adherence rates were similar, treatment failure was more commonly associated with XDR-TB than with non-XDR-TB (31% vs. 8.5%, respectively) [62]. Using a similar, aggressive treatment approach with daily, supervised therapy of at least five antibiotics including cycloserine, an injectable drug, and a fluoroquinolone administered at the highest tolerated doses, 29/48 (60%) of HIV-negative, XDR-TB patients in Peru were successfully treated [112]. These curative rates were comparable to the 400/603 (66%) MDR-TB patients who successfully completed treatment [112]. These encouraging results demonstrate that XDR-TB patients can be cured at respectable rates and that the disease does not automatically result in a death sentence. Incorporation of a comprehensive treatment approach with an effective and well-managed TB control program, implementation of aggressive drug treatment strategies, and further development of appropriate chemotherapeutic interventions are all deemed critical for improving treatment outcomes, eliminating the spread of XDR-TB, and avoiding the prospect of total drug-resistant TB strains [112].

7. The Inherent Need for New Anti-TB Drugs

For the most part, TB therapy has remained unchanged for nearly four decades and often consists of taking more than 10 pills per day for a minimum of six months for antibiotic-susceptible disease [113]. The diagnosis of MDR-TB or XDR-TB further subjects the patients to as many as 20 pills per day, as well as antibiotic intramuscular injections, for 18 to 24 months. This lengthy treatment is not only more expensive than first-line antibiotics, but also comes with devastating, toxic side effects, emotional and social anxieties, and pyschological stresses [114,115,116,117]. With XDR-TB treatment success rates ranging from 30–60% in HIV-negative patients (Figure 1, Table 4), XDR-TB strains threaten to return TB treatment to the pre-antibiotic era, when more than 50% of TB patients succumbed to the disease [113].
The spread of XDR-TB and the poor treatment outcomes in both developing and developed countries clearly indicate that XDR-TB knows no boundaries. Therefore, its emergence and spread potentially jeopardizes our abilities to fight the disease in all people, irrespective of geographic location, thus posing an incredible global threat to public health. While preserving the effectiveness of the existing first-line and second-line antibiotics is ideal, the mere existence of XDR-TB strains suggests that we are embarking upon an ominous era whereby totally drug-resistant TB strains could evolve. In order to combat MDR- and XDR-TB and the overall spread of antibiotic resistant TB strains, the need for new anti-TB drugs is imminent.

8. Development of Novel Chemotherapeutic Anti-TB Compounds

After discovery and development of new anti-TB drugs flourished in the mid-1900s, the TB drug pipeline was reduced to a mere leaky faucet with the discovery of new classes of antibiotics being virtually nonexistent. It has been more than 40 years since the last novel TB-specific antibiotic was introduced into clinical practice. Given the challenge of treating XDR-TB, fortunately, the existing pipeline for new classes of anti-TB drugs shows promise. While there are a number of propitious candidates currently in various stages of discovery and clinical development [118,119,120], the new anti-TB compounds described herein represent drugs with novel structures and/or mechanisms of action currently in Phase II clinical evaluations (Table 5).
A novel diarylquinoline, TMC207 (also known as R207910), exhibits potent in vitro bactericidal activity against aerobically-replicating, drug-sensitive and MDR M. tuberculosis [121] as well as dormant, antibiotic-susceptible M. tuberculosis [122]. Importantly, TMC207 also demonstrates rapid mycobactericidal activity in experimentally-infected animals [121] and in patients with drug-susceptible or MDR pulmonary TB [123,124]. The diarylquinoline, TMC207, offers a new mechanism of anti-TB action by specifically inhibiting the mycobacterial ATP synthase, thus diminishing bacterial energy production in the form of ATP molecules [121].
Table
Table 5. Novel anti-TB drugs currently in Phase II clinical trials.
Table 5. Novel anti-TB drugs currently in Phase II clinical trials.
DrugClassMechanism of action
TMC207DiarylquinolineInhibits ATP synthase and energy metabolism
PA-824Nitroimidazo-oxazineInhibits mycolic acid synthesis
OPC-67683Nitrodihydro-imidazooxazoleInhibits mycolic acid synthesis
Another class of promising compounds with anti-TB activity is the nitroimidazoles, including PA-824 and OPC-67683. Although the exact mechanism of their action is not completely understood, the PA-824 prodrug requires activation by bacterial dehydrogenase and nitroreductase to inhibit mycolic acid synthesis [125,126,127]. Mycolic acids are important constituents of the mycobacterial cell wall, are involved in pathogenicity, and exhibit diverse immunological functions [128]. PA-824 displays strong bactericidal activity against replicating and non-replicating M. tuberculosis and exhibits bactericidal activity when administered orally to experimentally-infected animals [125,129,130]. Of particular significance, a regimen of PA-824, moxifloxacin, and pyrazinamide demonstrated bactericidal and sterilizing activity against TB in experimentally-infected mice, suggesting efficacy against MDR-TB [131]. Additional safety, tolerability, and pharmacokinetic studies with PA-824 in healthy human subjects are ongoing [132,133]. The OPC-67683 dihydroimidazo-oxazole also demonstrates very potent in vitro and in vivo bactericidal activity against antibiotic-sensitive and MDR M. tuberculosis [134,135,136]. While the specific bacterial target of OPC-67683 is not yet known, the compound inhibits production of cell wall mycolic acids [134], suggesting a similar mechanism of action as PA-824. Unlike metronidazole (another nitroimidazole compound), which kills dormant M. tuberculosis under anaerobic conditions [137], OPC-67683 and PA-824 are bactericidal against M. tuberculosis grown in either aerobic or anaerobic states. The ability to target both actively replicating and dormant bacteria allows OPC-67683 and PA-824 to function as double-edged swords and could potentially shorten the duration of TB treatment [126].

9. Future Perspectives Regarding the Discovery of New Anti-TB Compounds

Fortunately, there has been a resurgence in TB drug research over the past decade, and numerous compounds are progressing through the various stages of the pharmaceutical discovery and development pipeline. Efforts by the Stop TB Partnership and the TB Alliance have been instrumental in stimulating and advancing TB research and accelerating the discovery and development of new drug therapies for treating TB. For a comprehensive list of compounds and the current phase of discovery or development, see the Stop TB Partnership Working Group on New TB Drugs (http://www.stoptb.org/wg/new_drug) and the TB Alliance (http://www.tballiance.org). Although several new anti-TB drugs have advanced to preclinical development and/or clinical trials, the timeline for their potential introduction into clinical practice and the impact on TB treatment are difficult to predict.
Drug discovery and development is a very complex and expensive process with the estimated costs between $800 million and $1 billion to bring a new drug to market [138,139]. Despite this daunting process, a continuation of the basic research and discovery processes is critical to identify new families of anti-TB agents targeting novel enzymes and/or cell processes associated with viability and/or bacterial virulence [118,120]. Exploration of novel targets and mechanisms of action are necessary to discover candidate compounds with efficacy against drug-sensitive and drug-resistant TB, with activity against active and latent TB, and with the potential to shorten chemotherapeutic treatment. Ongoing and new drug discovery research initiatives, along with improvements to known classes of compounds, will ensure that the pipeline of new anti-TB compounds continues.

10. Concluding Remarks and Perspectives

Pathogenic organisms, such as M. tuberculosis, that significantly contribute to worldwide human infectious disease are also the most common antibiotic-resistant bacteria [140]. Our arsenal of antimicrobials is currently under attack by the microorganisms themselves as clinically-significant, antibiotic-resistant bacteria evolve at alarming rates [141]. The fight against antibiotic resistance is formidable, but must be endeavored in the face of treatment failures, prolonged illnesses, increased deaths, and escalated risks of infections. With increases in worldwide cases of MDR- and XDR-TB occurring on a yearly basis, the grim progression from antibiotic effectiveness to antibiotic resistance drives this global crisis.
The comfort zone of antimicrobial discovery represents a path of proven bacterial targets, such as cell wall biosynthesis, protein synthesis, and nucleic acid metabolism and replication. The development of completely new classes of drugs necessitates new avenues of basic research which incorporate identifying new antimicrobial targets and discovering unique mechanisms of action using novel approaches. However, ensuring TB drug compliance and susceptibility testing is critical, since the introduction of new antibiotics could, ironically and unfortunately, generate additional antibiotic resistance and further intensify the existing problem. Nevertheless, aggressive strategies and innovative approaches are desperately needed to fight XDR-TB or we are likely to lose our grip on TB control and witness the emergence of completely drug-resistant TB.

Acknowledgements

The author would like to thank Shaleen Korth, Vandana Malhotra, and the anonymous reviewers for critical review of the manuscript and for helpful suggestions, discussions, comments, and advice in the preparation of this paper. The author would like to dedicate this paper to the memory of her stepfather, Kevin F. Ernst (1952-2010), who recently passed away on June 15, 2010 after an illness and long hospital stay that occurred during the final preparation of this manuscript.

References

  1. Daniel, T.M.; Bates, J.H.; Downes, K.A. History of Tuberculosis. In Tuberculosis: Pathogenesis, Protection, and Control; Bloom, B.R., Ed.; American Society for Microbiology: Washington, DC, USA, 1994; pp. 13–24. [Google Scholar]
  2. Bloom, B.R.; Murray, C.J.L. Tuberculosis: commentary on a reemergent killer. Science 1992, 257, 1055–1064. [Google Scholar]
  3. Flynn, J.L.; Chan, J. Tuberculosis: latency and reactivation. Infect. Immun. 2001, 69, 4195–4201. [Google Scholar]
  4. Clark-Curtiss, J.E.; Haydel, S.E. Molecular genetics of Mycobacterium tuberculosis pathogenesis. Annu. Rev. Microbiol. 2003, 57, 517–549. [Google Scholar] [CrossRef] [PubMed]
  5. Maartens, G.; Wilkinson, R.J. Tuberculosis. Lancet 2007, 370, 2030–2043. [Google Scholar]
  6. Crofton, J.; Mitchison, D.A. Streptomycin resistance in pulmonary tuberculosis. Brit. Med. J. 1948, 2, 1009–1015. [Google Scholar]
  7. Schraufnagel, D.E. Tuberculosis treatment for the beginning of the next century. Int. J. Tuberc. Lung Dis. 1999, 3, 651–662. [Google Scholar]
  8. Corpe, R.F.; Blalock, F.A. Alternating regimens of streptomycin-pyrazinamide, isoniazid-para-aminosalicylic acid at Battey State Hospital. Amer. Rev. Resp. Dis. 1964, 90, 262–265. [Google Scholar]
  9. Corpe, R.F.; Blalock, F.A. Multi-drug therapy including ethambutol in retreatment of pulmonary tuberculosis. Ann. N Y Acad. Sci. 1966, 135, 823–830. [Google Scholar]
  10. Centres, R. The Madras Experiment. Lancet 1961, 2, 532–533. [Google Scholar]
  11. Espinal, M.A. The global situation of MDR-TB. Tuberculosis 2003, 83, 44–51. [Google Scholar]
  12. World Health Organization, TB/HIV Fact Sheet 2009; World Health Organization: Geneva, Switzerland, 2009.
  13. Centers for Disease Control and Prevention. Emergence of Mycobacterium tuberculosis with extensive resistance to second-line drugs-worldwide, 2000-2004. MMWR Recomm. Rep. 2006, 55, 301–305.
  14. Raviglione, M.C.; Smith, I. XDR tuberculosis-implications for global public health. New Engl. J. Med. 2007, 356, 656–659. [Google Scholar]
  15. World Health Organization, Tuberculosis, Fact sheet No. 104; World Health Organization: Geneva, Switzerland, 2010.
  16. World Health Organization, Global Tuberculosis Control: A Short Update to the 2009 Report; World Health Organization: Geneva, Switzerland, 2009.
  17. Raviglione, M.C.; Uplekar, M.W. WHO's new Stop TB Strategy. Lancet 2006, 367, 952–955. [Google Scholar]
  18. World Health Organization, The Global Plan to Stop TB: 2006-2015; World Health Organization: Geneva, Switzerland, 2006.
  19. World Health Organization, Global Tuberculosis Control-Epidemiology, Strategy, Financing; World Health Organization: Geneva, Switzerland, 2009.
  20. Dye, C. Global epidemiology of tuberculosis. Lancet 2006, 367, 938–940. [Google Scholar]
  21. Dye, C.; Scheele, S.; Dolin, P.; Pathania, V.; Raviglione, M.C. Global burden of tuberculosis: estimated incidence, prevalence and mortality by country. JAMA 1999, 282, 677–686. [Google Scholar]
  22. Corbett, E.L.; Watt, C.J.; Walker, N.; Maher, D.; Williams, B.G.; Raviglione, M.C.; Dye, C. The growing burden of tuberculosis: global trends and interactions with the HIV epidemic. Arch. Intern. Med. 2003, 163, 1009–1021. [Google Scholar]
  23. World Health Organization, Global Tuberculosis Control-Epidemiology, Strategy, Financing; World Health Organization: Geneva, Switzerland, 2007.
  24. Chaisson, R.E.; Martinson, N.A. Tuberculosis in Africa-Combating an HIV-driven crisis. N. Engl. J. Med. 2008, 358, 1089–1092. [Google Scholar]
  25. Ansari, N.A.; Kombe, A.H.; Kenyon, T.A.; Hone, N.M.; Tappero, J.W.; Nyirenda, S.T.; Binkin, N.J.; Lucas, S.B. Pathology and causes of death in a group of 128 predominantly HIV-positive patients in Botswana, 1997-1998. Int. J. Tuberc. Lung Dis. 2002, 6, 55–63. [Google Scholar]
  26. World Health Organization, Global Tuberculosis Control-Epidemiology, Strategy, Financing; World Health Organization: Geneva, Switzerland, 2008.
  27. World Health Organization, Treatment of Tuberculosis Guidelines, 4th ed; World Health Organization: Geneva, Switzerland, 2010.
  28. Centers for Disease Control and Prevention. Treatment of tuberculosis: American Thoracic Society, CDC, and Infectious Diseases Society of America. MMWR Recomm. Rep. 2003, 52, 1–77.
  29. Kochi, A. Tuberculosis control—is DOTS the health breakthrough of the 1990s? World Health Forum 1997, 18, 225–247. [Google Scholar] [PubMed]
  30. World Health Organization, An Expanded DOTS Framework for Effective Tuberculosis Control; WHO: Geneva, Switzerland, 2002.
  31. World Health Organization. An expanded framework for effective tuberculosis control. Int. J. Tuberc. Lung Dis. 2002, 6, 378–388. [PubMed]
  32. Dye, C.; Watt, C.J.; Bleed, D.M.; Hosseini, S.M.; Raviglione, M.C. Evolution of tuberculosis control and prospects for reducing tuberculosis incidence, prevalence, and deaths globally. JAMA 2005, 293, 2767–2775. [Google Scholar] [PubMed]
  33. Jindani, A.; Aber, V.R.; Edwards, E.A.; Mitchison, D.A. The early bactericidal activity of drugs in patients with pulmonary tuberculosis. Am. Rev. Respir. Dis. 1980, 121, 939–949. [Google Scholar]
  34. Hafner, R.; Cohn, J.A.; Wright, D.J.; Dunlap, N.E.; Egorin, M.J.; Enama, M.E.; Muth, K.; Peloquin, C.A.; Mor, N.; Heifets, L.B. Early bactericidal activity of isoniazid in pulmonary tuberculosis. Am. J. Respir. Crit. Care Med. 1997, 156, 918–923. [Google Scholar]
  35. Dickinson, J.M.; Mitchison, D.A. Experimental models to explain the high sterilizing activity of rifampin in the chemotherapy of tuberculosis. Am. J. Respir. Crit. Care Med. 1981, 159, 1580–1584. [Google Scholar]
  36. Girling, D.J. The role of pyrazinamide in primary chemotherapy for pulmonary tuberculosis. Tubercle 1984, 65, 1–4. [Google Scholar]
  37. Frieden, T.; Espinal, M. What is the Therapeutic Effect and What is the Toxicity of Antituberculosis Drugs? In Toman's Tuberculosis: Case Detection, Treatment and Monitoring: Questions and Answers, 2nd; Frieden, T., Ed.; World Health Organization: Geneva, Switzerland, 2004; pp. 110–121. [Google Scholar]
  38. Dorman, S.E.; Chaisson, R.E. From magic bullets back to the Magic Mountain: the rise of extensively drug-resistant tuberculosis. Nat. Med. 2007, 13, 295–298. [Google Scholar]
  39. Frieden, T.; Sherman, L.; Maw, K.; Fujiwara, P.; Crawford, J.; Nivin, B.; Sharp, V.; Hewlett, D.J.; Brudney, K.; Alland, D.; Kreisworth, B. A multi-institutional outbreak of highly drug-resistant tuberculosis: epidemiology and clinical outcomes. JAMA 1996, 276, 1229–1235. [Google Scholar]
  40. Mukherjee, J.S.; Rich, M.L.; Socci, A.R.; Joseph, J.K.; Virú, F.A.; Shin, S.S.; Furin, J.J.; Becerra, M.C.; Barry, D.J.; Kim, J.Y.; et al. Programmes and principles in treatment of multidrug-resistant tuberculosis. Lancet 2004, 363, 474–481. [Google Scholar] [PubMed]
  41. World Health Organization, The Global Plan to Stop TB: 2001 to 2005; World Health Organization: Geneva, Switzerland, 2001.
  42. Gupta, R.; Cegielski, J.P.; Espinal, M.A.; Henkens, M.; Kim, J.Y.; Lambregts-van Weezenbeek, S.B.; Lee, J.W.; Raviglione, M.C.; Suarez, P.G.; Varaine, F. Increasing transparency in partnerships for health-introducing the Green Light Committee. Trop. Med. Int. Health 2002, 7, 970–976. [Google Scholar]
  43. Kir, A.; Tahaoglu, K.; Okur, E.; Hatipoglu, T. Role of surgery in multi-drug-resistant tuberculosis: results of 27 cases. Eur. J. Cardio-thorac. Surg. 1997, 12, 531–534. [Google Scholar] [CrossRef]
  44. Park, S.K.; Lee, C.M.; Heu, J.P.; Song, S.D. A retrospective study for the outcome of pulmonary resection in 49 patients with multidrug-resistant tuberculosis. Int. J. Tuberc. Lung Dis. 2002, 6, 143–149. [Google Scholar]
  45. Treasure, R.L.; Seaworth, B.J. Current role of surgery in Mycobacterium tuberculosis. Ann. Thorac. Surg. 1995, 59, 1405–1409. [Google Scholar] [PubMed]
  46. Takeda, S.I.; Maeda, H.; Hayakawa, M.; Sawabata, N.; Maekura, R. Current surgical intervention for pulmonary tuberculosis. Ann. Thorac. Surg. 2005, 79, 959–963. [Google Scholar]
  47. Olcmen, A.; Gunluoglu, M.Z.; Demir, A.; Akin, H.; Kara, H.V.; Dincer, S.I. Role and outcome of surgery for pulmonary tuberculosis. Asian Cardiovasc. Thorac. Ann. 2006, 14, 363–366. [Google Scholar]
  48. Perelman, M.I.; Strelzov, V.P. Surgery for pulmonary tuberculosis. World J. Surg. 1997, 21, 457–467. [Google Scholar]
  49. Andrews, J.R.; Gandhi, N.R.; Moodley, P.; Shah, N.S.; Bohlken, L.; Moll, A.P.; Pillay, M.; Friedland, G.; Sturm, A.W. Tugela Ferry Care and Research Collaboration. Exogenous reinfection as a cause of multidrug-resistant and extensively drug-resistant tuberculosis in rural South Africa. J. Infect. Dis. 2008, 198, 1582–1589. [Google Scholar] [CrossRef] [PubMed]
  50. Kim, J.Y.; Shakow, A.; Mate, K.; Vanderwarker, C.; Gupta, R.; Farmer, P. Limited good and limited vision: multidrug-resistant tuberculosis and global health policy. Soc. Sci. Med. 2005, 61, 847–859. [Google Scholar]
  51. Espinal, M.A.; Kim, S.J.; Suarez, P.G.; Kam, K.M.; Khomenko, A.G.; Migliori, G.B.; Baéz, J.; Kochi, A.; Dye, C.; Raviglione, M.C. Standard short-course chemotherapy for drug-resistant tuberculosis. JAMA 2000, 283, 2537–2545. [Google Scholar]
  52. Furin, J.J.; Becerra, M.C.; Shin, S.S.; Kim, J.Y.; Bayona, J.; Farmer, P.E. Effect of administering short-course standardized, regimens in individuals infected with drug-resistant Mycobacterium tuberculosis strains. Eur. J. Clin. Microbiol. Infect. Dis. 2000, 19, 132–136. [Google Scholar] [CrossRef] [PubMed]
  53. Reichman, L. Timebomb: the Global Epidemic of Multi-Drug Resistant Tuberculosis; McGraw Hill: New York, NY, USA, 2001. [Google Scholar]
  54. Okeke, I.N.; Lamikanra, A.; Edelman, R. Socioeconomic and behavioral factors leading to acquired bacterial resistance to antibiotics in developing countries. Emerg. Infect. Dis. 1999, 5, 18–27. [Google Scholar]
  55. Tang, S.; Squire, S.B. What lessons can de drawn from tuberculosis (TB) control in China in the 1990s? An analysis from a health system perspective. Health Policy 2005, 72, 93–104. [Google Scholar]
  56. World Health Organization. Extensively drug-resistant tuberculosis (XDR-TB): recommendations for prevention and control. Weekly Epidemiol. Rec. 2006, 81, 430–432.
  57. Chan, E.D.; Strand, M.J.; Iseman, M.D. Treatment outcomes in extensively resistant tuberculosis. New Engl. J. Med. 2008, 359, 657–659. [Google Scholar]
  58. Hopewell, P.C.; Pai, M.; Maher, D.; Uplekar, M.; Raviglione, M.C. International standards for tuberculosis care. Lancet Infect. Dis. 2006, 6, 710–725. [Google Scholar]
  59. Zignol, M.; Hosseini, M.S.; Wright, A.; Lambregts-van Weezenbeek, C.; Nunn, P.; Watt, C.J.; Williams, B.G.; Dye, C. Global incidence of multidrug-resistant tuberculosis. J. Infect. Dis. 2006, 194, 479–485. [Google Scholar]
  60. Dye, C.; Williams, B.G. Criteria for the control of drug-resistant tuberculosis. Proc. Natl. Acad. Sci. USA 2000, 97, 8180–8185. [Google Scholar]
  61. World Health Organization, Anti-Tuberculosis Drug Resistance in the World. Report No. 4; World Health Organization: Geneva, Switzerland, 2008.
  62. Keshavjee, S.; Gelmanova, I.Y.; Farmer, P.E.; Mishustin, S.P.; Strelis, A.K.; Andreev, Y.G.; Pasechnikov, A.D.; Atwood, S.; Mukherjee, J.S.; Rich, M.L.; et al. Treatment of extensively drug-resistant tuberculosis in Tomsk, Russia: a retrospective cohort study. Lancet 2008, 372, 1403–1409. [Google Scholar] [PubMed]
  63. Kim, D.H.; Kim, H.J.; Park, S.K.; Kong, S.J.; Kim, Y.S.; Kim, T.H.; Kim, E.K.; Lee, K.M.; Lee, S.S.; Park, J.S.; Koh, W.J.; Lee, C.H.; Kim, J.Y.; Shim, T.S. Treatment outcomes and long-term survival in patients with extensively drug-resistant tuberculosis. Am. J. Respir. Crit. Care Med. 2008, 178, 1075–1082. [Google Scholar]
  64. Nachega, J.B.; Chaisson, R.E. Tuberculosis drug resistance: a global threat. Clin. Infect. Dis. 2003, 36, S24–30. [Google Scholar]
  65. Zhang, Y.; Heym, B.; Allen, B.; Young, D.; Cole, S. The catalase-peroxidase gene and isoniazid resistance of Mycobacterium tuberculosis. Nature 1992, 358, 591–593. [Google Scholar] [PubMed]
  66. Banerjee, A.; Dubnau, E.; Quemard, A.; Balasubramanian, V.; Um, K.S.; Wilson, T.; Collins, D.; de Lisle, G.; Jacobs, W.R., Jr. inhA, a gene encoding a target for isoniazid and ethionamide in Mycobacterium tuberculosis. Science 1994, 263, 227–230. [Google Scholar] [PubMed]
  67. Miesel, L.; Weisbrod, T.R.; Marcinkeviciene, J.A.; Bittman, R.; Jacobs, W.R., Jr. NADH dehydrogenase defects confer isoniazid resistance and conditional lethality in Mycobacterium smegmatis. J. Bacteriol. 1998, 180, 2459–2467. [Google Scholar] [PubMed]
  68. Lee, A.S.G.; Teo, A.S.M.; Wong, S.Y. Novel mutations in ndh in isoniazid-resistant Mycobacterium tuberculosis isolates. Antimicrob. Agents Chemother. 2001, 45, 2157–2159. [Google Scholar] [PubMed]
  69. Telenti, A.; Imboden, P.; Marchesi, F.; Lowrie, D.; Cole, S.; Colston, M.J.; Matter, L.; Schopfer, K.; Bodmer, T. Detection of rifampin-resistant mutations in Mycobacterium tuberculosis. Lancet 1993, 341, 647–650. [Google Scholar] [PubMed]
  70. Miller, L.P.; Crawford, J.T.; Shinnick, T.M. The rpoB gene of Mycobacterium tuberculosis. Antimicrob. Agents Chemother. 1994, 38, 805–811. [Google Scholar] [PubMed]
  71. Williams, D.L.; Spring, L.; Collins, L.; Miller, L.P.; Heifets, L.B.; Gangadharam, P.R.; Gillia, T.P. Contribution of rpoB mutations to development of rifamycin cross-resistance in Mycobacterium tuberculosis. Antimicrob. Agents Chemother. 1998, 42, 1853–1857. [Google Scholar] [PubMed]
  72. Scorpio, A.; Lindholm-Levy, P.; Heifets, L.; Gilman, R.; Siddiqi, S.; Cynamon, M.; Zhang, Y. Characterization of pncA mutations in pyrazinamide-resistant Mycobacterium tuberculosis. Antimicrob. Agents Chemother. 1997, 41, 540–543. [Google Scholar] [PubMed]
  73. Konno, K.; Feldmann, F.M.; McDermott, W. Pyrazinamide susceptibility and amidase activity of tubercle bacilli. Am. Rev. Respir. Dis. 1967, 95, 461–469. [Google Scholar]
  74. Sreevatsan, S.; Stockbauer, K.E.; Pan, X.; Kreiswirth, B.N.; Moghazeh, S.L.; Jacobs, W.R., Jr.; Telenti, A.; Musser, J.M. Ethambutol resistance in Mycobacterium tuberculosis: critical role of embB mutations. Antimicrob. Agents Chemother. 1997, 41, 1677–1681. [Google Scholar] [PubMed]
  75. Telenti, A.; Philipp, W.J.; Sreevatsan, S.; Bernasconi, C.; Stockbauer, K.E.; Wieles, B.; Musser, J.M.; Jacobs, W.R., Jr. The emb operon, a gene cluster of Mycobacterium tuberculosis involved in resistance to ethambutol. Nat. Med. 1997, 3, 567–570. [Google Scholar] [PubMed]
  76. Ramaswamy, S.V.; Amin, A.G.; Goksel, S.; Stager, C.E.; Dou, S.J.; El Sahly, H.; Moghazeh, S.L.; Kreiswirth, B.N.; Musser, J.M. Molecular genetic analysis of nucleotide polymorphisms associated with ethambutol resistance in human isolates of Mycobacterium tuberculosis. Antimicrob. Agents Chemother. 2000, 44, 326–336. [Google Scholar] [PubMed]
  77. Finken, M.; Kirschner, P.; Meier, A.; Wrede, A.; Böttger, E.C. Molecular basis of streptomycin resistance in Mycobacterium tuberculosis: alterations of the ribosomal protein S12 gene and point mutations within a functional 16S ribosomal RNA pseudoknot. Mol. Microbiol. 1993, 9, 1239–1246. [Google Scholar] [PubMed]
  78. Nair, J.; Rouse, D.A.; Bai, G.H.; Morris, S.L. The rpsL gene and streptomycin resistance in single and multiple drug-resistant strains of Mycobacterium tuberculosis. Mol. Microbiol. 1993, 10, 521–527. [Google Scholar] [CrossRef] [PubMed]
  79. Meier, A.; Kirschner, P.; Bange, F.C.; Vogel, U.; Böttger, E.C. Genetic alterations in streptomycin-resistant Mycobacterium tuberculosis: mapping of mutations conferring resistance. Antimicrob. Agents Chemother. 1994, 38, 228–233. [Google Scholar] [PubMed]
  80. Honore, N.; Cole, S.T. Streptomycin resistance in mycobacteria. Antimicrob. Agents Chemother. 1994, 38, 238–242. [Google Scholar]
  81. Alangaden, G.J.; Kreiswirth, B.N.; Aouad, A.; Khetarpal, M.; Igno, F.R.; Moghazeh, S.L.; Manavathu, E.K.; Lerner, S.A. Mechanism of resistance to amikacin and kanamycin in Mycobacterium tuberculosis. Antimicrob. Agents Chemother. 1998, 42, 1295–1297. [Google Scholar] [PubMed]
  82. Suzuki, Y.; Katsukawa, C.; Tamaru, A.; Abe, C.; Makino, M.; Mizuguchi, Y.; Taniguchi, H. Detection of kanamycin-resistant Mycobacterium tuberculosis by identifying mutations in the 16S rRNA gene. J. Clin. Microbiol. 1998, 36, 1220–1225. [Google Scholar] [PubMed]
  83. Taniguchi, H.; Chang, B.; Abe, C.; Nikaido, Y.; Mizuguchi, Y.; Yoshida, S.I. Molecular analysis of kanamycin and viomycin resistance in Mycobacterium smegmatis by use of the conjugation system. J. Bacteriol. 1997, 179, 4795–4801. [Google Scholar] [PubMed]
  84. McClatchy, J.K.; Kanes, W.; Davidson, P.T.; Moulding, T.S. Cross-resistance in M. tuberculosis to kanamycin, capreomycin and viomycin. Tubercle 1977, 58, 29–34. [Google Scholar] [CrossRef] [PubMed]
  85. Tsukamura, M.; Mizuno, S. Cross-resistant relationships among the aminoglucoside antibiotics in Mycobacterium tuberculosis. J. Gen. Microbiol. 1975, 88, 269–274. [Google Scholar] [PubMed]
  86. Maus, C.E.; Plikaytis, B.B.; Shinnick, T.M. Molecular analysis of cross-resistance to capreomycin, kanamycin, amikacin, and viomycin in Mycobacterium tuberculos. Antimicrob. Agents Chemother. 2005, 49, 3192–3197. [Google Scholar] [PubMed]
  87. Maus, C.E.; Plikaytis, B.B.; Shinnick, T.M. Mutation of tlyA confers capreomycin resistance in Mycobacterium tuberculosis. Antimicrob. Agents Chemother. 2005, 49, 571–577. [Google Scholar] [PubMed]
  88. Takiff, H.E.; Salazar, L.; Guerrero, C.; Philipp, W.; Huang, W.M.; Kreiswirth, B.; Cole, S.T.; Jacobs, W.R., Jr.; Telenti, A. Cloning and nucleotide sequence of Mycobacterium tuberculosis gyrA and gyrB genes and detection of quinolone resistance mutations. Antimicrob. Agents Chemother. 1994, 38, 773–780. [Google Scholar] [PubMed]
  89. Cambau, E.; Sougakoff, W.; Besson, M.; Truffot-Pernot, C.; Grosset, J.; Jarlier, V. Selection of a gyrA mutant of Mycobacterium tuberculosis resistant to fluoroquinolones during treatment with ofloxacin. J. Infect. Dis. 1994, 170, 479–483. [Google Scholar] [CrossRef] [PubMed]
  90. Morlock, G.P.; Metchock, B.; Sikes, D.; Crawford, J.T.; Cooksey, R.C. ethA, inhA, and katG loci of ethionamide-resistant clinical Mycobacterium tuberculosis isolates. Antimicrob. Agents Chemother. 2003, 47, 3799–3805. [Google Scholar] [PubMed]
  91. DeBarber, A.E.; Mdluli, K.; Bosman, M.; Bekker, L.G.; Barry, C.E., 3rd. Ethionamide activation and sensitivity in multidrug-resistant Mycobacterium tuberculosis. Proc. Natl. Acad. Sci. USA 2000, 97, 9677–9682. [Google Scholar]
  92. Baulard, A.R.; Betts, J.C.; Engohang-Ndong, J.; Quan, S.; McAdam, R.A.; Brennan, P.J.; Locht, C.; Besra, G.S. Activation of the pro-drug ethionamide is regulated in mycobacteria. J. Biol. Chem. 2000, 275, 28326–28331. [Google Scholar]
  93. Rengarajan, J.; Sassetti, C.M.; Naroditskaya, V.; Sloutsky, A.; Bloom, B.R.; Rubin, E.J. The folate pathway is a target for resistance to the drug para-aminosalicylic acid (PAS) in mycobacteria. Mol. Microbiol. 2004, 53, 275–282. [Google Scholar]
  94. Mathys, V.; Wintjens, R.; Lefevre, P.; Bertout, J.; Singhal, A.; Kiass, M.; Kurepina, N.; Wang, X.M.; Mathema, B.; Baulard, A.; Kreiswirth, B.N.; Bifani, P. Molecular genetics of para-aminosalicylic acid resistance in clinical isolates and spontaneous mutants of Mycobacterium tuberculosis. Antimicrob. Agents Chemother. 2009, 53, 2100–2109. [Google Scholar] [PubMed]
  95. Chacon, O.; Feng, Z.; Harris, N.B.; Caceres, N.E.; Adams, L.G.; Barletta, R.G. Mycobacterium smegmatis D-alanine racemase mutants are not dependent on D-alanine for growth. Antimicrob. Agents Chemother. 2002, 46, 47–54. [Google Scholar] [PubMed]
  96. Caceres, N.E.; Harris, N.B.; Wellehan, J.F.; Feng, Z.; Kapur, V.; Barletta, R.G. Overexpression of the D-alanine racemase gene confers resistance to D-cycloserine in Mycobacterium smegmatis. J. Bacteriol. 1997, 179, 5046–5055. [Google Scholar] [PubMed]
  97. Das, S.; Yennamalli, R.M.; Vishnoi, A.; Gupta, P.; Bhattacharya, A. Single-nucleotide variations associated with Mycobacterium tuberculosis KwaZulu-Natal strains. J. Biosci. 2009, 34, 397–404. [Google Scholar] [CrossRef] [PubMed]
  98. Motiwala, A.S.; Dai, Y.; Jones-López, E.C.; Hwang, S.H.; Lee, J.S.; Cho, S.N.; Via, L.E.; Barry, C.E., III.; Alland, D. Mutations in extensively drug-resistant Mycobacterium tuberculosis that do not code for known drug-resistance mechanisms. J. Infect. Dis. 2010, 201, 881–888. [Google Scholar] [PubMed]
  99. Nathanson, E.; Weezenbeek, C.L.V.; Ric, M.L.; Gupta, R.; Bayona, J.; Blöndal, K.; Caminero, J.A.; Cegielski, J.P.; Danilovits, M.; Espinal, M.A.; et al. Multidrug-resistant tuberculosis management in resource-limited settings. Emerg. Infect. Dis. 2006, 12, 1389–1397. [Google Scholar] [CrossRef] [PubMed]
  100. Raviglione, M.C. XDR-TB: entering the post-antibiotic era? Int. J. Tuberc. Lung Dis. 2006, 10, 1185–1187. [Google Scholar] [PubMed]
  101. Matteelli, A.; Migliori, G.B.; Cirillo, D.; Centis, R.; Girardi, E.; Raviglione, M. Multidrug-resistant and extensively drug-resistant Mycobacterium tuberculosis: epidemiology and control. Expert Rev. Anti. Infect. Ther. 2007, 5, 857–871. [Google Scholar] [CrossRef] [PubMed]
  102. Migliori, G.B.; Besozzi, G.; Girardi, E.; Kliiman, K.; Lange, C.; Toungoussovae, O.S.; Ferrara, G.; Cirillo, D.M.; Gori, A.; Matteelli, A.; Spanevelloe, A.; Codecasa, L.R.; Raviglione, M.C. SMIRA/TBNET Study Group. Clinical and operational value of the extensively drug-resistant tuberculosis definition. Eur. Respir. J. 2007, 30, 623–626. [Google Scholar] [PubMed]
  103. Orenstein, E.W.; Basu, S.; Shah, N.S.; Andrews, J.R.; Friedland, G.H.; Moll, A.P.; Gandhi, N.R.; Galvani, A.P. Treatment outcomes among patients with multidrug-resistant tuberculosis: systematic review and meta-analysis. Lancet Infect. Dis. 2009, 9, 153–161. [Google Scholar]
  104. Orenstein, E.W.; Galvani, A.P. Treatment outcomes among patients with multidrug-resistant tuberculosis-Authors' reply. Lancet Infect. Dis. 2010, 10, 215–216. [Google Scholar]
  105. Gandhi, N.R.; Moll, A.; Sturm, A.W.; Pawinski, R.; Govender, T.; Lalloo, U.; Zeller, K.; Andrews, J.; Friedland, G. Extensively drug-resistant tuberculosis as a cause of death in patients co-infected with tuberculosis and HIV in a rural areas of South Africa. Lancet 2006, 368, 1575–1580. [Google Scholar]
  106. Koenig, R. In South Africa, XDR TB and HIV prove a deadly combination. Science 2008, 319, 894–897. [Google Scholar]
  107. Loveday, M.; Thomson, L.; Chopra, M.; Ndlela, Z. A health systems assessment of the KwaZulu-Natal tuberculosis programme in the context of increasing drug resistance. Int. J. Tuberc. Lung Dis. 2008, 12, 1042–1047. [Google Scholar]
  108. Shah, N.S.; Wright, A.; Bai, G.H.; Barrera, L.; Boulahbal, F.; Martín-Casabona, N.; Drobniewski, F.; Gilpin, C.; Havelková, M.; Lepe, R.; et al. Worldwide emergence of extensively drug-resistant tuberculosis. Emerg. Infect. Dis. 2007, 13, 380–387. [Google Scholar] [PubMed]
  109. Masjedi, M.R.; Farnia, P.; Sorooch, S.; Pooramiri, M.V.; Mansoori, S.D.; Zarifi, A.Z.; Akbarvelayati, A.; Hoffner, S. Extensively drug-resistant tuberculosis: 2 years of surveillance in Iran. Clin. Infect. Dis. 2006, 43, 841–847. [Google Scholar]
  110. Migliori, G.B.; Ortmann, J.; Girardi, E.; Besozzi, G.; Lange, C.; Cirillo, D.M.; Ferrarese, M.; Iaco, G.D.; Gori, A.; Raviglione, M.C.; Group, S.T.S. Extensively drug-resistant tuberculosis, Italy and Germany. Emerg. Infect. Dis. 2007, 13, 780–782. [Google Scholar] [PubMed]
  111. Kim, H.R.; Hwang, S.S.; Kim, H.J.; Lee, S.M.; Yoo, C.G.; Kim, Y.W.; Han, S.K.; Shim, Y.S.; Yim, J.J. Impact of extensive drug resistance on treatment outcomes in non-HIV-infected patients with multidrug-resistant tuberculosis. Clin. Infect. Dis. 2007, 45, 1290–1295. [Google Scholar]
  112. Mitnick, C.D.; Shin, S.S.; Seung, K.J.; Rich, M.L.; Atwood, S.S.; Furin, J.J.; Fitzmaurice, G.M.; Viru, F.A.A.; Appleton, S.C.; Bayona, J.N.; et al. Comprehensive treatment of extensively drug-resistant tuberculosis. New Engl. J. Med. 2008, 359, 563–574. [Google Scholar]
  113. Hamilton, C.D.; Sterling, T.R.; Blumberg, H.M.; Leonard, M.; McAuley, J.; Schlossberg, D.; Stout, J.; Huitt, G. Extensively drug-resistant tuberculosis: are we learning from history or repeating it? Clin. Infect. Dis. 2007, 45, 338–342. [Google Scholar] [PubMed]
  114. Jakubowiak, W.M.; Bogorodskaya, E.M.; Borisov, S.E.; Danilova, I.D.; Lomakina, O.B.; Kourbatova, E.V. Impact of socio-psychological factors on treatment adherence of TB patients in Russia. Tuberculosis 2008, 88, 495–502. [Google Scholar]
  115. White, V.L.C.; Moore-Gillon, J. Resource implications of patients with multidrug resistant tuberculosis. Thorax 2000, 55, 962–963. [Google Scholar]
  116. Rajbhandary, S.S.; Marks, S.M.; Bock, N.N. Costs of patients hospitalized for multidrug-resistant tuberculosis. Int. J. Tuberc. Lung Dis. 2004, 8, 1012–1016. [Google Scholar]
  117. Iseman, M.D. Treatment of multidrug-resistant tuberculosis. New Engl. J. Med. 1993, 329, 784–791. [Google Scholar]
  118. Mdluli, K.; Spigelman, M. Novel targets for tuberculosis drug discovery. Curr. Opin. Pharmacol. 2006, 6, 459–467. [Google Scholar]
  119. Spigelman, M.; Gillespie, S. Tuberculosis drug development pipeline: progress and hope. Lancet 2006, 367, 945–947. [Google Scholar] [CrossRef] [PubMed]
  120. Zhang, Y. The magic bullets and tuberculosis drug targets. Annu. Rev. Pharmacol. Toxicol. 2005, 45, 529–564. [Google Scholar]
  121. Andries, K.; Verhasselt, P.; Guillemont, J.; Göhlmann, H.W.H.; Neefs, J.M.; Winkler, H.; Van Gestel, J.; Timmerman, P.; Zhu, M.; Lee, E.; Williams, P.; de Chaffoy, D.; Huitric, E.; Hoffner, S.; Cambau, E.; Truffot-Pernot, C.; Lounis, N.; Jarlier, V. A diarylquinoline drug active on the ATP synthase of Mycobacterium tuberculosis. Science 2005, 223–227. [Google Scholar]
  122. Koul, A.; Vranckx, L.; Dendouga, N.; Balemans, W.; Van den Wyngaert, I.; Vergauwen, K.; Göhlmann, H.W.H.; Willebrords, R.; Poncelet, A.; Guillemont, J.; Bald, D.; Andries, K. Diarylquinolines are bactericidal for dormant mycobacteria as a result of disturbed ATP homeostasis. J. Biol. Chem. 2008, 283, 25273–25280. [Google Scholar]
  123. Diacon, A.H.; Pym, A.; Grobusch, M.; Patientia, R.; Rustomjee, R.; Page-Shipp, L.; Pistorius, C.; Krause, R.; Bogoshi, M.; Churchyard, G.; et al. The diarylquinoline TMC207 for multidrug-resistant tuberculosis. New Engl. J. Med. 2009, 360, 2397–2405. [Google Scholar]
  124. Rustomjee, R.; Diacon, A.H.; Allen, J.; Venter, A.; Reddy, C.; Patientia, R.F.; Mthiyane, T.C.P.; Marez, T.D.; van Heeswijk, R.; Kerstens, R.; Koul, A.; Beule, K.D.; Donald, P.R.; McNeeley, D.F. Early bactericidal activity and pharmacokinetics of the diarylquinoline TMC207 in treatment of pulmonary tuberculosis. Antimicrob. Agents Chemother. 2008, 52, 2831–2835. [Google Scholar]
  125. Stover, C.K.; Warrener, P.; Van Devanter, D.R.; Sherman, D.R.; Arain, T.M.; Langhorne, M.H.; Anderson, S.W.; Towell, J.A.; Yuan, Y.; McMurray, D.N.; et al. A small-molecule nitroimidazopyran drug candidate for the treatment of tuberculosis. Nature 2000, 405, 962–966. [Google Scholar] [PubMed]
  126. Singh, R.; Manjunatha, U.; Boshoff, H.I.M.; Ha, Y.H.; Niyomrattanakit, P.; Ledwidge, R.; Dowd, C.S.; Lee, I.Y.; Kim, P.; Zhang, L.; et al. PA-824 kills nonreplicating Mycobacterium tuberculosis by intracellular NO release. Science 2008, 322, 1392–1395. [Google Scholar] [PubMed]
  127. Manjunatha, U.; Boshoff, H.I.; Barry, C.E., III. The mechanism of action of PA-824: novel insights from transcriptional profiling. Commun. Integr. Biol. 2009, 2, 215–218. [Google Scholar]
  128. Kremer, L.; Besra, G.S. A waxy tale, by Mycobacterium tuberculosis. In Tuberculosis and the tubercle bacillus; Cole, S.T., Eisenach, K.D., McMurray, D.N., Jacobs, W.R., Jr., Eds.; ASM Press: Washington, D.C., USA, 2005; pp. 287–305. [Google Scholar]
  129. Lenaerts, A.J.; Gruppo, V.; Marietta, K.S.; Johnson, C.M.; Driscoll, D.K.; Tompkins, N.M.; Rose, J.D.; Reynolds, R.C.; Orme, I.M. Preclinical testing of the nitroimidazopyran PA-824 for activity against Mycobacterium tuberculosis in a series of in vitro and in vivo models. Antimicrob. Agents Chemother. 2005, 49, 2294–2301. [Google Scholar] [PubMed]
  130. Tyagi, S.; Nuermberger, E.; Yoshimatsu, T.; Williams, K.; Rosenthal, I.; Lounis, N.; Bishai, W.; Grosset, J. Bactericidal activity of the nitroimidazopyran PA-824 in a murine model of tuberculosis. Antimicrob. Agents Chemother. 2005, 49, 2289–2293. [Google Scholar]
  131. Nuermberger, E.; Tyagi, S.; Tasneen, R.; Williams, K.N.; Almeida, D.; Rosenthal, I.; Grosset, J.H. Powerful bactericidal and sterilizing activity of a regimen containing PA-824, moxifloxacin, and pyrazinamide in a murine model of tuberculosis. Antimicrob. Agents Chemother. 2008, 52, 1522–1524. [Google Scholar] [PubMed]
  132. Ginsberg, A.M.; Laurenzi, M.W.; Rouse, D.J.; Whitney, K.D.; Spigelman, M.K. Safety, tolerability, and pharmacokinetics of PA-824 in healthy subjects. Antimicrob. Agents Chemother. 2009, 53, 3720–3725. [Google Scholar] [PubMed]
  133. Ginsberg, A.M.; Laurenzi, M.W.; Rouse, D.J.; Whitney, K.D.; Spigelman, M.K. Assessment of the effects of the nitroimidazo-oxazine, PA-824, on renal function in healthy subjects. Antimicrob. Agents Chemother. 2009, 53, 3726–3733. [Google Scholar] [PubMed]
  134. Matsumoto, M.; Hashizume, H.; Tomishige, T.; Kawasaki, M.; Tsubouchi, H.; Sasaki, H.; Shimokawa, Y.; Komatsu, M. OPC-67683, a nitro-dihydro-imidazooxazole derivative with promising action against tuberculosis in vitro and in mice. PLoS Med. 2006, 3, 2131–2144. [Google Scholar]
  135. Saliu, O.Y.; Crismale, C.; Schwander, S.K.; Wallis, R.S. Bactericidal activity of OPC-67683 against drug-tolerant Mycobacterium tuberculosis. J. Antimicrob. Chemother. 2007, 60, 994–998. [Google Scholar] [CrossRef] [PubMed]
  136. Sasaki, H.; Haraguchi, Y.; Itotani, M.; Kuroda, H.; Hashizume, H.; Tomishige, T.; Kawasaki, M.; Matsumoto, M.; Komatsu, M.; Tsubouchi, H. Synthesis and antituberculosis activity of a novel series of optically active 6-nitro-2,3-dihydroimidazo[2,1-b]oxazoles. J. Med. Chem. 2006, 49, 7854–7860. [Google Scholar] [PubMed]
  137. Wayne, L.G.; Sramek, H.A. Metronidazole is bactericidal to dormant cells of Mycobacterium tuberculosis. Antimicrob. Agents Chemother. 1994, 38, 2054–2058. [Google Scholar] [PubMed]
  138. Showalter, H.D.H.; Denny, W.A. A roadmap for drug discovery and its translation to small molecule agents in clinical development for tuberculosis treatment. Tuberculosis 2008, 88, S3–S17. [Google Scholar]
  139. DiMasi, J.A.; Hansen, R.W.; Grabowski, H.G. The price of innovation: new estimates of drug development costs. J. Health Econ. 2003, 22, 151–185. [Google Scholar]
  140. World Health Organization, Antimicrobial Resistance, Fact Sheet No. 194; World Health Organization: Geneva, Switzerland, 2002.
  141. Walsh, C. Molecular mechanisms that confer antibacterial drug resistance. Nature 2000, 406, 775–781. [Google Scholar]

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Haydel, S.E. Extensively Drug-Resistant Tuberculosis: A Sign of the Times and an Impetus for Antimicrobial Discovery. Pharmaceuticals 2010, 3, 2268-2290. https://doi.org/10.3390/ph3072268

AMA Style

Haydel SE. Extensively Drug-Resistant Tuberculosis: A Sign of the Times and an Impetus for Antimicrobial Discovery. Pharmaceuticals. 2010; 3(7):2268-2290. https://doi.org/10.3390/ph3072268

Chicago/Turabian Style

Haydel, Shelley E. 2010. "Extensively Drug-Resistant Tuberculosis: A Sign of the Times and an Impetus for Antimicrobial Discovery" Pharmaceuticals 3, no. 7: 2268-2290. https://doi.org/10.3390/ph3072268

APA Style

Haydel, S. E. (2010). Extensively Drug-Resistant Tuberculosis: A Sign of the Times and an Impetus for Antimicrobial Discovery. Pharmaceuticals, 3(7), 2268-2290. https://doi.org/10.3390/ph3072268

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