Anthrax Treatment

A special issue of Pathogens (ISSN 2076-0817).

Deadline for manuscript submissions: closed (30 September 2021) | Viewed by 11284

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Guest Editor
Department of Microbiology & Immunology, University of Texas Medical Branch, Galveston, TX 77555, USA
Interests: Bacillus anthracis; bacterial pathogenesis; aerobiology
Special Issues, Collections and Topics in MDPI journals

Special Issue Information

Dear Colleagues,

Anthrax infection, caused by the bacteria Bacillus anthracis, is a zoonotic disease that retains the attention of the scientific community due to its potential association with bioterrorism. The bacteria produces two toxins, lethal toxin and edema toxin, which promote disease progression and have a myriad of pathological/physiological effects on the host. In the case of inhalation anthrax, the mortality rate is 80% or higher if no treatment is given or if treatment is delayed.  Therapeutic treatment of anthrax infection includes the use of various antibiotics, which, if administered soon enough, are very effective; however, due to the possible emergence of antibiotic-resistant bacterial strains, there is a critical need for new antibiotics and antitoxins.  Attempts are being made to address this need through drug development and drug repurposing.  Preventative treatment of anthrax infection is currently achieved by vaccination with the FDA-approved AVA vaccine, but the requirement for multiple injections and annual boosters makes this vaccine less than ideal.  A better vaccine would require fewer injections and would convey long-lasting immunity. For this Special Issue of Pathogens, we invite you to submit research articles, review articles, and short notes, as well as communications related to anthrax treatment, including the development of new drugs, drug repurposing, vaccine development, and immunity.  We look forward to your contribution.

Asst. Prof. Dr. William S. Lawrence
Guest Editor

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Keywords

  • anthrax
  • Bacillus anthracis
  • vaccine
  • toxins
  • therapeutic
  • immunity
  • drug development

Published Papers (4 papers)

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15 pages, 2314 KiB  
Article
Physiological Responses to Multiple Low-Doses of Bacillus anthracis Spores in the Rabbit Model of Inhalation Anthrax
by Sarah C. Taft, Tonya L. Nichols, Stephanie A. Hines, Roy E. Barnewall, Gregory V. Stark and Jason E. Comer
Pathogens 2020, 9(11), 877; https://doi.org/10.3390/pathogens9110877 - 24 Oct 2020
Cited by 2 | Viewed by 1955
Abstract
Bacillus anthracis spores that are re-aerosolized from surface deposits after initial contamination present significant health risks for personnel involved in decontamination. To model repeated exposure to low dose B. anthracis spores, three groups of seven rabbits were challenged with multiple low-doses of B. [...] Read more.
Bacillus anthracis spores that are re-aerosolized from surface deposits after initial contamination present significant health risks for personnel involved in decontamination. To model repeated exposure to low dose B. anthracis spores, three groups of seven rabbits were challenged with multiple low-doses of B. anthracis spores 5 days a week for 3 weeks. Mortality, body temperature, heart and respiration rates, hematology, C-reactive protein, bacteremia, and serum protective antigen were monitored for 21 days post-exposure after the last of multiple doses. All rabbits exposed to a mean daily dose of 2.91 × 102 colony forming units (CFU) survived and showed minimal physiological changes attributable to exposure. One of seven rabbits receiving a mean daily dose of 1.22 × 103 CFU died and four of seven receiving a mean daily dose of 1.17 × 104 CFU died. The LD50 was calculated to be 8.1 × 103 CFU of accumulated dose. Rabbits that succumbed to the higher dose exhibited bacteremia and increases above baseline in heart rate, respiration rate, and body temperature. Two rabbits in the mean daily dose group of 1.17 × 104 CFU exhibited clinical signs of inhalation anthrax yet survived. This study provides a description of lethality, pathophysiology, and pathology in a controlled multiple low-dose inhalation exposure study of B. anthracis in the rabbit model. The data suggest that the accumulated dose is important in survival outcome and that a subset of rabbits may show clinical signs of disease but fully recover without therapeutic intervention Full article
(This article belongs to the Special Issue Anthrax Treatment)
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13 pages, 2723 KiB  
Article
Teixobactin Provides Protection against Inhalation Anthrax in the Rabbit Model
by William S. Lawrence, Jennifer E. Peel, Satheesh K. Sivasubramani, Wallace B. Baze, Elbert B. Whorton, David W. C. Beasley, Jason E. Comer, Dallas E. Hughes, Losee L. Ling and Johnny W. Peterson
Pathogens 2020, 9(9), 773; https://doi.org/10.3390/pathogens9090773 - 22 Sep 2020
Cited by 4 | Viewed by 3713
Abstract
The use of antibiotics is a vital means of treating infections caused by the bacteria Bacillus (B.) anthracis. Importantly, with the potential future use of multidrug-resistant strains of B. anthracis as bioweapons, new antibiotics are needed as alternative therapeutics. In this blinded [...] Read more.
The use of antibiotics is a vital means of treating infections caused by the bacteria Bacillus (B.) anthracis. Importantly, with the potential future use of multidrug-resistant strains of B. anthracis as bioweapons, new antibiotics are needed as alternative therapeutics. In this blinded study, we assessed the protective efficacy of teixobactin, a recently discovered antibiotic, against inhalation anthrax infection in the adult rabbit model. New Zealand White rabbits were infected with a lethal dose of B. anthracis Ames spores via the inhalation route, and blood samples were collected at various times to assess antigenemia, bacteremia, tissue bacterial load, and antibody production. Treatments were administered upon detection of B. anthracis protective antigen in the animals’ sera. For comparison, a fully protective dose of levofloxacin was used as a positive control. Rabbits treated with teixobactin showed 100% survival following infection, and the bacteremia was completely resolved by 24–48 h post-treatment. In addition, the bacterial/spore loads in tissues of the animals treated with teixobactin were either zero or dramatically less relative to that of the negative control animals. Moreover, microscopic evaluation of the tissues revealed decreased pathology following treatment with teixobactin. Overall, these results show that teixobactin was protective against inhalation anthrax infection in the rabbit model, and they indicate the potential of teixobactin as a therapeutic for the disease. Full article
(This article belongs to the Special Issue Anthrax Treatment)
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16 pages, 1865 KiB  
Article
Physiological Responses to a Single Low-Dose of Bacillus anthracis Spores in the Rabbit Model of Inhalational Anthrax
by Sarah C. Taft, Tonya L. Nichols, Stephanie A. Hines, Roy E. Barnewall, Gregory V. Stark and Jason E. Comer
Pathogens 2020, 9(6), 461; https://doi.org/10.3390/pathogens9060461 - 11 Jun 2020
Cited by 1 | Viewed by 2391
Abstract
Credible dose–response relationships are needed to more accurately assess the risk posed by exposure to low-level Bacillus anthracis contamination during or following a release. To begin to fill this knowledge gap, New Zealand White rabbits were implanted with D70-PCT telemetry transmitters and subsequently [...] Read more.
Credible dose–response relationships are needed to more accurately assess the risk posed by exposure to low-level Bacillus anthracis contamination during or following a release. To begin to fill this knowledge gap, New Zealand White rabbits were implanted with D70-PCT telemetry transmitters and subsequently aerosol challenged with average inhaled doses of 2.86 × 102 to 2.75 × 105 colony forming units (CFU) of B. anthracis spores. Rabbits exposed to a single inhaled dose at or above 2.54 × 104 CFU succumbed with dose-dependent time to death. Death was associated with increases above baseline in heart rate, respiration rate, and body temperature and all rabbits that died exhibited bacteremia at some point prior to death. Rabbits that inhaled doses of 2.06 × 103 CFU or lower survived to the end of the study and showed no or minimal adverse changes in the measured physiological responses in response to the challenge. Moreover, no bacteremia nor toxemia were observed in rabbits that survived to the end of the study. Overall, the data indicate that challenge doses of B. anthracis below the level sufficient to establish systemic infection do not produce observable physiological responses; however, doses that triggered a response resulted in death. Full article
(This article belongs to the Special Issue Anthrax Treatment)
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9 pages, 1761 KiB  
Case Report
Human Anthrax in Dolj County, Romania—A Series of Three Cases
by Florentina Dumitrescu, Eugen Florin Georgescu, Lucian Giubelan, Vlad Pădureanu, Andreea Cristina Stoian, Viorica Dincă, Milena Georgescu, Livia Dragonu and Daniela Marinescu
Pathogens 2021, 10(6), 644; https://doi.org/10.3390/pathogens10060644 - 23 May 2021
Cited by 1 | Viewed by 2403
Abstract
Bacillus anthracis is the causative agent of anthrax, primarily a disease of herbivorous animals, which can be accidentally transmitted to humans. Three cases of cutaneous human anthrax were recorded in August 2020 in Dolj county, Romania. These cases included livestock farmers (husband and [...] Read more.
Bacillus anthracis is the causative agent of anthrax, primarily a disease of herbivorous animals, which can be accidentally transmitted to humans. Three cases of cutaneous human anthrax were recorded in August 2020 in Dolj county, Romania. These cases included livestock farmers (husband and wife, as well as a man from their entourage). The women presented malignant edema, which required surgery for compartment syndrome; and the men presented the common form of cutaneous anthrax. According to the laboratory investigation, two cases complied with the criteria in the case definition. All cases were successfully treated with antibiotics and the women received reconstructive plastic surgery of the skin defects, restoring normal hand function. The contact with sick animals was ruled out by the health authorities concluding that it was the contamination of pre-existing skin lesions with B. anthracis spores from the soil, the anthracogenic area. Full article
(This article belongs to the Special Issue Anthrax Treatment)
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