Next Article in Journal
Evaluation of the Cytotoxicity of Ayahuasca Beverages
Next Article in Special Issue
Effects of Supplementary Blue and UV-A LED Lights on Morphology and Phytochemicals of Brassicaceae Baby-Leaves
Previous Article in Journal
Quantitative Comparison of the Marker Compounds in Different Medicinal Parts of Morus alba L. Using High-Performance Liquid Chromatography-Diode Array Detector with Chemometric Analysis
Previous Article in Special Issue
Inclusion Complexes of Concentrated Orange Oils and β-Cyclodextrin: Physicochemical and Biological Characterizations
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Promising Roles of Alternative Medicine and Plant-Based Nanotechnology as Remedies for Urinary Tract Infections

1
Department of Botany and Microbiology, Gurukula Kangri (Deemed to be University), Haridwar 249404, India
2
Department of Microbiology, Faculty of Science and Technology, Mewar University, Chittorgarh 312901, India
3
S-02, Scientist Hostel, Chauras Campus, Srinagar Garhwal, Uttarakhand 246174, India
4
Department of Biotechnology, H.N.B. Garhwal University (A Central University), Srinagar (Garhwal) 246174, Uttarakhand, India
5
Adarsh Vijendra Institute of Pharmaceutical Sciences, Shobhit University, Gangoh 247341, India
6
Federal Research Center, Russian Scientific Research Institute of Experimental Veterinary Medicine Named after K. I. Skryabin and Y. R. Kovalenko of the Russian Academy of Sciences, 109428 Moscow, Russia
7
Laboratory of Biocontrol and Antimicrobial Resistance, Orel State University, Named after I. S. Turgenev, 302026 Orel, Russia
8
Department of Medical Disciplines, Faculty of Medicine and Pharmacy, University of Oradea, 410073 Oradea, Romania
9
Department of Pharmacy, Faculty of Medicine and Pharmacy, University of Oradea, 410028 Oradea, Romania
*
Authors to whom correspondence should be addressed.
Molecules 2020, 25(23), 5593; https://doi.org/10.3390/molecules25235593
Submission received: 26 October 2020 / Revised: 24 November 2020 / Accepted: 25 November 2020 / Published: 28 November 2020

Abstract

:
Urinary tract infections (UTIs) are considered to be the most common infections worldwide, having an incidence rate of 40−60% in women. Moreover, the prevalence of this disorder in adult women is 30 times more than in men. UTIs are usually found in many hospitals and clinical practice; as disorders, they are complicated and uncomplicated; in uncomplicated cases, there is no structural or functional abnormality in the urogenital tract. However, obstruction, retention of urine flow and use of catheters increase the complexity. There are several bacteria (e.g., E. coli, Klebsiella pneumoniae, Proteus vulgaris, etc.) successfully residing in the tract. The diagnosis must not only be accurate but rapid, so early detection is an important step in the control of UTIs caused by uropathogens. The treatment of UTIs includes appropriate antimicrobial therapy to control the infection and kill the causal microbes inside the body. A long-time usage of antibiotics has resulted in multidrug resistance causing an impediment in treatment. Thus, alternative, combinatorial medication approaches have given some hope. Available treatments considered Homeopathic, Ayurvedic, Unani, and other herbal-based drugs. There are new upcoming roles of nanoparticles in combating UTIs which needs further validation. The role of medicinal plant-based nanotechnology approaches has shown promising results. Therefore, there must be active research in phyto-based therapies of UTIs, such as Ayurvedic Biology.

1. Introduction

The urinary tract of human beings is composed of the kidney, ureter, urethra, urinary bladder, and genital organs (male and female). The average urine excreted by human beings is 1.4 L per day (normal range: 0.6–2.6 L/day) [1]. The normal biochemical characteristics of urine have pH = 5.8; pale yellow color to deep amber; and absence of bilirubin, RBC, protein, and pus cells. If the biochemical characteristic of urine gets altered or changed such as urine frequency, kidney inflammation then the ureter, urethra, urinary bladder, and genital organs indicate such issues related to these organs. However, the most probable reason for the above mentioned symptomatic conditions may be the result of urinary tract infections (UTIs) caused by several bacteria viz. Escherichia coli, Klebsiella spp, Proteus spp., Pseudomonas spp., Enterococcus faecalis, Staphylococcus aureus, Citrobacter spp., Morganella sp., Providencia sp., Serratia sp., Mycoplasma sp., etc. [2]. Out of these microorganisms most frequently encountered bacterial species is E. coli followed by Klebsiella spp. Human beings, particularly females, encounter UTIs due to the anatomy of the urinary tract or reproductive organ (i.e., the female urethra is short, so there is the possibility of getting access to urinary bladder more frequently, another reason being the urethral opening near sources of bacteria from the anus) [3].
Other susceptible adults include the elderly, with these patients needing urethral catheters. The low water intake/day can moreover be one of the reasons for UTI, as the flushing action of water from the urinary tract is low. The person who takes adequate water during the daytime has less probability of getting UTI due to continuous flushing or cleaning of urinary as well as reproductive organs [4,5,6,7].
The occurrence of UTIs in the female is most common as compared to male in India, as well as other developed and underdeveloped countries. The incidences of UTIs were also reported from Uganda (East Africa), Kenya, United States, United Kingdom, etc. [8,9,10]. The possible reasons for UTIs can be unprotected sex, reduced water intake, and use of infected sanitary clothes (commonly used in small villages). Common symptoms of UTIs include severe back pain; inflammation or burning sensation while urinating; cloudy, dark, bloody, or bad-smelling urine; and fever or chill. If the infections reach the kidney, then it causes pyelonephritis (inflammation of the kidney) [3,11,12]. The modern medicine such as broad-spectrum antibiotics are prescribed for the control of uropathogens. However, due to the emergence of drug resistance in bacteria, there is a need for novel antimicrobial molecules. A large proportion of the Earth’s surface is covered by marine environment, so exploration of bioactive compounds from marine organisms may prove beneficial. The secondary metabolite or the potential bioactive compounds of endophytic actinomycetes Nocardiopsis sp. GRG1 (KT235640) from marine brown algae, possesses antibacterial activity against uropathogens [13].
The tunicate (Ascidians, sea squirts)-associated bacteria isolated from marine environments and antimicrobial activity of these isolated bacteria were tested against pathogenic bacteria and have shown promising results [14,15].
Based on the published literature data in the most well-known databases (MDPI, PubMed, Frontiers, Scopus, etc.), this review paper focuses on the promising role of alternative medicine and nanotechnology/nanoparticles as a remedy and possible alternative treatment in UTIs. Moreover, the aim of this study was also to highlighting new or less known aspects regarding both traditional and modern medicine related to their capacity to treat and/or cure this type of infection.
It is not confirmed that men are less prone to the UTI, but it was reported by several studies across the world that women are more prone to UTIs than the male because the woman undergoes different hormonal and physical changes [16]. The normal microflora of the vagina changes according to the stage of sexual development (i.e., before/in/after puberty). The chances of getting a maximum infection are before and after puberty, due to the lack of normal microflora Lactobacillus spp.; another reason is sexual activeness and multiple partners. It was estimated that 40% of women experienced UTI in their lifetime, and recurrent UTI has been reported in 40% of women [17].
The UTI prevalence in different age groups and sex of South Indian peoples was studied, and it was found that UTI was common in women who are in the puberty stage and post-menopausal stage. It was also revealed that the age group 21–30 years of a married woman are more susceptible to UTI. In the case of a male who is older than 55 years, having diabetes and prostrate are more prone to UTI. Kant et al. observed 1253 pregnant women and it was found that 33% of pregnant women encountered a UTI [18].

2. Diagnosis of UTI

The early and accurate diagnosis of UTIs is an important step in the treatment of the disease caused by uropathogens. The treatment of UTIs includes appropriate antimicrobial therapy to control infection and kill the causal organism inside the body. Different diagnosis methods are available for the diagnosis of UTI

2.1. Conventional Method of Detecting UTI

2.1.1. Urine Examination

In this method, morning midstream urine is collected in a universal sterile container and the microbiological investigation is performed, with the presence of motile bacteria, RBC, and the number of pus cells being determined. The presence of more than one bacterium per high power field is indicative of possible UTI [19,20]. The other known method is the urine culture and it can be done on selective and differential media (i.e., MacConkey Agar and Cysteine Lactose Electrolyte-Deficient (CLED) agar). After streaking plates on selective media are kept at 37 °C for 18–24 h, the plate is observed regarding the numbers and the characteristics of colonies [20,21].

2.1.2. Dip Slide Method

This method is a modified or rapid version of the culture method. In this method, there is no need to prepare MacConkey or CLED medium in a Petri plate. The dip slide is a readymade preparation available in the market or supplied by different manufacturers such as HiMedia, Oxoid etc. In this dip slide containing double-sided or triple-sided coated differential or selective media for detection of infection causing bacteria such CLED, MacConkey, and other media.

2.1.3. Nitrite Test to Detect Bacteriuria

The nitrite test is used to detect the nitrate reductase enzyme which is present in most of the uropathogens and can be detected by using this exam. As compared to other methods available, its sensitivity is less but have significant specificity. The method was developed by the Griess in 1879; he used sulphanilic acid and α-naphthylamine in dilute acid for nitrite detection. During this procedure, the urine sample collected from the patient is subjected to the addition of 2 mL of Griess reagent (representing the mixture of sulphanilic acid and α-naphthylamine); appearance of red color indicates a UTI [22].

2.1.4. Leukocyte Esterase (LE) Test for Detection of Pyuria

This test allows leucocyte (or white blood cell) detection, which releases the esterase enzyme due to inflammation of ureter, kidney, urethra, and prostate (being indicative of UTI or pyuria) [23]. The principle of LE test is that the esterase released from activated neutrophil cells reacts with indoxyl carbonic acid ester; indoxyl is released by the esterase and reacts with diazonium salt and is oxidized resulting in the formation of purple color. The formation of purple color indicates the presence of leucocyte esterase. The sensitivity of LET was reported to have 70% [24]. These above tests have been represented in Table 1.

3. Modern Approach in the Detection of UTI

Biosensor-Based Technique

Every patient desires a quick, less painful diagnosis of disease, at a very initial stage, for getting an early cure. Earlier, there was used of diagnostic techniques which were labor- and time-intensive and costly too apart from the use of expensive devices. But recently, the successful use of various electrochemical biosensors was developed and used [25] for the detection of infectious diseases. Biosensor is generally used to analyses samples, to find information about their structure, constituents, and function by converting a biological response into an electrical signal [26]. The electric signal is directly proportional to the amounts of analytes, being used to obtain a measurable response. Mach et al. detailed the use of biosensors in UTI diagnosis, identification of microbes, and testing of antimicrobial susceptibility [27].
In the 1980s, there was a sensitive test for quick testing of UTI pathogens and known as Limulus amebocytes lysate (LAL) assay. This test was helpful for endotoxin detection [28]. Potentiometer based biosensor testing was applied for detection of E. coli, whenever there is a change in pH due to ammonia released by this bacterium [29]. Another sensitive biophysical technique, surface plasmon resonance (SPR), was helpful for the detection of S. aureus and E. coli [30]. There are many difficulties also while taking this biosensor technology in the detection and diagnosis of UTIs from bench to bedside.

4. Treatments for UTI

4.1. Antibiotics Prescribed in UTI

The treatment of UTI is not complicated and the disorder can be easily treated with some specific antibiotics. The irrational use of antibiotics by humans made these diseases more complicated. The treatment of UTIs can be initially limited by the intake of excess water but in case of complication (i.e., pyelonephritis or the involvement of kidney) made this disease more severe even if not treated it can cause irreversible kidney damage. It has been well documented that in most of the kidney failure cases, the presence of a UTI is the main reason after diabetes. The choice of drug or antibiotics in UTI depends on the antibiotic sensitivity testing, in Indian scenario most of the treatment being based on empirical basis without much laboratory investigation.
Another reason for ineffectiveness of antibiotics is the self-medication, without concerning to medical professional, due to economic reasons (the subjects take an inappropriate antibiotic when the case become uncontrollable, avoiding visiting the doctor). Since the first antibiotic, Penicillin, was discovered, there is a wide range of antibiotics, some of them recently discovered, part of them being effective and part of them becoming ineffective in UTI due to the body resistance development against these drugs.
The major problem associated with the administration of a suitable antibiotic, as in the majority of cases, the patient of the Indian subcontinent visits the clinician only when his condition becomes more complicated. The clinician then advised the broad-spectrum antibiotic on empirical bases and without undergoing antibiotic sensitivity testing. The antibiotic which was effective once is not as effective as it was due to the development of resistance and in place of this specific antibiotic, new or stronger/better antibiotics are prescribed (Table 2).
If we track the course of antibiotic evolution and the recent addition of antibiotics, there is no new antibiotic discovered so far, and if all antibiotics become ineffective then there is no method of chemotherapy left which can tackle the emergence or outbreak of any bacterial infection. There is an urgent need for some strategy or process which can control the common disease such as UTI, typhoid, food poisoning, and other infections. We are very fortunate to have a wealth of literature on medical practice in which there is a tradition system of medicine that has immense potential to combat most of the ailments [37].

4.2. Alternative Traditional Therapies for UTI Treatment

The development of resistance in uropathogens is one of the major problems associated with effective treatment in UTI. The untreated UTI may cause severe complications such as pyelonephritis or even kidney failure. In modern medicine, there is a provision of antibiotic therapy in which broad-spectrum antibiotic can be given but, these days, due to increased incidence of multidrug resistant (MDR) uropathogens, these antibiotics are ineffective and need administration of an effective antibiotic; since the development of the first antibiotic, there are only a few new antibiotics added into the list. However, this class of drugs is effective in controlling the infection, but it has also some side effects [38]. Indian patients and those abroad now know this fact, and they are focusing more on alternative medicine/traditional system of medicine. The following are few examples of alternative medicine practices in India and in many other countries.

4.2.1. Homeopathic Medicine

Homeopathic medicine is one of the safest and well-known branches of alternative medicine and was developed in Germany. It is known to have no side effects, so people are taking interest in this treatment especially for small children and during pregnancy. During the gestation period, most of women encounter a UTI, and it is desirable to treat the infection, to avoid teratogenic infection. Therefore, there should be a recommendation of antibiotics, but these antibiotics may have an adverse effect on the embryo, having sometimes teratogenic effects. In such cases, there is needed of using some alternative medicine, the best alternative medicine being the homeopathic one. Nwabudike successfully treated three cases of recurrent UTI, in which the patient was given homeopathic preparations (homeopathic Phosphorus, Platinum metallicum, Collibacillinum and Causticum) [39]. De Paula Coelho et al. studied the effect of homeopathic medicine Cantharis on E. coli-induced cystitis and found that Cantharis modulates the uropathogenic E. coli (UPEC)-induced cystitis in susceptible mice [40].
Another study integrated homeopathic medicine with an antibiotic in the treatment of two cases of UTI. They used Thuja occidentalis, Lycopodium clavatum, Sepia officinalis, Pulsatilla pratensis, sulfur, Nux vomica, Hepar Sulphur, Rhus toxicodendron, Arnica Montana, Calcarea carbonica, Tuberculinum bovinum (Kent), Natrium muriaticum, Carbo vegetabilis, Cantharis vesicatoria, Staphisagria, and Berberis vulgaris along with antibiotic have good impact on the UTI [41].
The direct effect of a homeopathic drug on causal microorganism (like E. coli) was evaluated and it was reported that homeopathic drugs do not have any direct bactericidal and bacteriostatic effect. However, it is known they activate the immune system as well as the adhesion of bacteria on the urinary tract [42].

4.2.2. Unani Medicine

Among all the known traditional system of medicine, Unani system is less popular, but it is also practiced in India and other countries. In Unani medicine system, UTI is known as Warm-e-Majra-e-Baul and the symptoms of this disorder have different terminologies such as Warm-e-Masana (cystitis), Warm-e-Kulliya (pyelonephritis), and Ufoonat (sepsis) [43]. The Unani preparation which consists of numerous ingredients (mucilage of Althaea officinalis L., Sphaeranthus indicus L., Euphorbia hypericifolia L., Tribulus terrestris L., and Sharbat Anar shireen (Punica granatum), Citrullus vulgaris L. seeds, Cucumis melo L. seeds) were administered to the patients having gestational UTI. These Unani preparations were observed as being quite effective in the control of gestation UTI [44].
The Unani medicine Sat Behroza, Ral Safaid, Shora Qalmi, and Kaphoor were given to the patients in the form of powder. The administration of these drugs was given for one month and it caused significant improvement in UTI and in the urine composition [43]. Also, two Unani drugs (i.e., Safuf Mudir and Sharbat Bazuri motadil) were administered to patients who take these two drugs for 21 days; both Unani drugs had encouraging results on UTI [45]. In Unani, a system of medicine following preparation such as Habbul Aas, Mauljubn Tukhm E-Khira, Tukmm E-Kakri, Habb E Kaknaj, Sheerah Tukhm e-Khyar, annana stem water, Sheerah e-Khar e- Khasak, Sheerah Tukhm e-Khyarainin, Maaush Shaier, and Maul jubn, beneficial actions were observed in burning micturition, acidity, pyouria, and cystitis [46].

4.2.3. Herbal-Based Medicine

Plants have always proved to be of therapeutic value, and the research on active substances provided by the plants has opened new options. Naturally available isothiocyanates (ITCs), which are formed after enzymatic hydrolysis of glucosinolates (that can be found in Brassicaceae products) may be used as alternative therapy as they are antimicrobial [47]. The roots of Vitex negundo and the whole plant of Oroxylum indicum were effective against a few selected human uropathogens [48].
In the Ayurvedic medicine system, there are certain formulations and herbs which are quite effective in controlling and treating UTI and can also help to reduce the occurrence of this disorder. Cranberry extracts have been known about for ages [49]. Achyranthes aspera is another herb that promotes kidney function, ensuring the proper fluid metabolism and further protecting the kidney from microbial attack. Equisetum arvense and Tribulus terrestris are mild diuretics, opening urinary channels, and acting also as mild antimicrobials [50,51]. Holy basil or Ocimum sanctum has been long used as a urinary antibacterial agent and helps with neutralizing the acidity in the body [50].
It has been well established that most of the bacteria causing UTIs can colonize the epithelial lining of the urinary tract and multiply there to initiate infection. The adherence ability of bacteria in these regions is due to acidic conditions and the presence of adhesin or of fimbriae. The Gram-negative bacteria or member of Enterobacteriaceae get access from the perineum and vagina by means of these accessories and make way to reach the urethra [52]. In Ayurveda, the diseases associated with UTI are called Vata Dosha. In Mutravahasrota roga, the urinary tract and kidneys are affected, whereas when the bladder and urethra are affected, they are known as Mutraghata Rog. The metabolic diseases where excessive urination (polyuria) occurs are called Prameha. Diuretics are the compounds that stimulate the urine flow and regulate it, helping in treating the UTI and known as Mutravirechana.
The pathogenicity of some agents is due to the presence of virulence factors (such as exotoxin, plasmid and adhesion factors (pili and fimbriae)). The major step in the pathogenicity is the adhesion to a particular cell or tissue; that adhesion is facilitated by capsule, pili, or fimbriae, and if this stem is anyhow prevented, then there are least chances of getting an infection. Some medicinal plants are well-known as having anti-adhesion activity, as follows, Azadhirachta indica (Neem), Ocimum sanctum (Tulsi), Coriander leaf (Dhania), Juniperus spp., Punica granatum (Anaar), Vaccinium macrocarpon (Cranberry), Salvia officinalis (Salvia), Tribulus terrestris (Gokharu), Terminalia chebula (Harad), and Cinnamomum cassia (Dalchini) [53,54,55].
The herbs that protect the urinary bladder from uropathogens are Equisetum arvense, Hydrangea petiolaris, and Zea mays [56]. The plants like Boerhaavia diffusa, Eupatorium purpureum, Agropyron repens, and Berberis vulgaris are known to have nephroprotective activity [56]. The phenolic constituents present in the Aronia melanocarpa, in the form of juice, are capable of reducing the sensitivity to the pathogens [57]. Sharma et al. screened medicinal herbs against multidrug-resistant uropathogens and found that E. coli, Klebsiella pneumoniae, Pseudomonas aeruginosa, and Enterococcus faecalis can be isolated and reported that alcoholic extract of Zingiber officinale and Punica granatum inhibits the growth of E. coli [54]. The essential oil Origanum majorana, Thymus zygis, and Rosmarinus officinalis were tested against E. coli isolates and the highest inhibition was reported in the case of Thymus zygis [58].
The effectiveness of flowering plants viz. Anogeissus acuminata, Azadirachta indica, Bauhinia variegata, Boerhaavia diffusa, Punica granatum, Soymida febrifuga, Terminalia chebula, Tinospora cordifolia, and Tribulus terrestris were evaluated against eleven isolated uropathogens. Out of these 11 plants, three plants A. acuminata, P. granatum, and S. febrifuga were effective against all the tested uropathogens [59].
The different solvent extracts of leaves of Clitoria ternatea were tested against UTI caused by Proteus mirabilis and it was found that the maximum inhibition was seen in acetone fraction [60]. Similarly, a flavonoid extract of Algerian plant (Marrubium vulgare L.) possessed antibacterial potential [61]. The methanolic extract of Hibiscus sabdariffa was also reported to inhibit the growth of E. coli and Klebsiella pneumoniae [62]. All these important actions of the plants were highlighted in Table 3.
The main mechanism of action of most of the herbs is due to their antibacterial properties, taking into account the phytoconstituents present in the different parts of the plant (leaves, stem, flower, bark, and root). These phytoconstituents are represented by the phenols, alkaloids, terpenes, essential oils, saponins, and other secondary metabolites. The other mode of action is some plants can increase the pH of the body, a fact that influences the difficulty of bacteria accession to the urinary tract and flush out them from the body.

5. Bacteriophage Therapy

The world of the invisible creature was deciphered due to the invention of the microscope but the study of organisms that are smaller than the microscopic range has become possible due to the invention of the most advanced microscope (i.e., Transmission Electron Microscope and Scanning Electron Microscope). People who died because of an unknown reason now found the cause behind their disease, namely, the viruses which can easily pass through the bacteriological filters. The negative aspect of viruses was soon discovered but the positive part of discovering the viruses (i.e., the bacteriophage therapy) was known just after a long time, in the 1920s. The history of bacteriophage therapy was begun in India, when a British bacteriologist—Ernest Hankin, in 1896, observed the antibacterial properties of Ganga water against Vibrio cholera. The antibacterial properties are heat labile, but it can easily pass through a porcelain filter [66]. A similar finding was also observed by Frederick Twort while working on the vaccinia virus; he found that the transparent filtrate converts the bacterial culture into granules [67].
Two years later, Felix d’Herelle described a similar finding while working on a patient recovering from Shigellosis. He isolated the anti-shiga microbe from filtering the stool of the patient, and when the filtrate was added to the culture, the causal organism (i.e., Shigella sp.) get killed or lysed [68].
The use of bacteriophage therapy as a therapeutic agent is not practiced in India despite having the originating root of bacteriophage therapy but, in some countries, such as France and in Belgium, bacteriophage therapy is used for the treatment of patients who were not getting significant result from conventional treatments [69]. This therapy is successfully practiced and has shown great potential towards some human diseases. A study evaluated the effect of bacteriophage on patients who were suffering from UTI caused by uropathogens (Staphylococcus aureus, E. coli, Streptococcus spp. Pseudomonas aeruginosa, and Proteus mirabilis) and found that there were no adverse events that can be detected [70].
The adapted bacteriophage therapy might also be effective and safe for treating UTIs. The Pyo bacteriophage solution was tested against a patient with transurethral resection of the prostate, preventing UTI, and results shown the potential efficacy of this treatment [70,71]. The cocktail of commercially available bacteriophage (Pyo, Intesti, Ses, and Enko) along with 29 E. coli and 10 K. pneumoniae bacteriophages were tested against UTI isolates of E. coli and Klebsiella and it was reported the cocktail of bacteriophages showed lytic activity against these uropathogens [71].
The bacteriophage adheres to the receptor of specific uropathogens (such as coliphage on E. coli) and injects its genetic material inside the host. The genetic material of the host gets integrated into the genome of bacteria. The bacteria, while synthesizing their protein, start producing the bacteriophage components like the head, tail, capsid, protein coat, etc. and then finally the assembly. The production of bacteriophage in such a huge quantity causes the bacterial cell to burst and there is a release of bacteriophage after losing the bacterial cell. The most limiting factor to use the bacteriophage as therapeutic potential is the lack of many studies performed on a human [72]. Most of the research is done on mice model and, as far physiology of human and animal are considered, there is a considerable difference regarding their physiological behavior. Therefore, more animal trials are required. Another problem associated with this therapy is dose optimization. It may also possible that the immune system of the human being may resist in colonization in the gastrointestinal and urogenital organs. The basic mechanism of bacteriophage entry required attachment on the specific receptor present on the surface of bacteria, is possible that bacteria may lose their receptor and become resistant to bacteriophage [70,71]. However, regarding these issues associated with the bacteriophage, if we overcome these hurdles, bacteriophage can be the best alternative for bacterial infection.

6. Probiotics

The normal microbiome of a human being in the intestinal tract and genital organ is an important factor in disease prevention. It creates a competitive environment for foreign microorganisms to compete for limited space and food, and thus making it an unfavorable site for attachment and multiplication. However, if the balance of normal microflora gets disturbed by the antibiotic, weakening of the immune system and after the menopause stage, the chances of getting an infection are high. To prevent the UTI, it is necessary to restore the normal microbiome of the vagina in the female. The restoration of the vaginal microflora can be achieved through the administration of prebiotic or probiotic [73,74]. As per the U. S. Food and Drug Administration/World Health Organization (FDA/WHO) “live microorganisms that, when administered in adequate amounts, confer a health benefit on the host” is called Probiotics [75]. The concept of probiotic was given by Elie Metchnikoff, who suggested that consumption of friendly microorganisms would replace the harmful bacteria with useful bacteria. This concept of probiotic is now used by the researcher for the treatment of gastrointestinal infection and UTIs.
The comparative studies between the normal woman that do not encounter any episode of UTI vs. a woman who was suffering from recurrent UTI shown the variability in the vaginal microflora in the case of a normal woman and it was found that the normal microflora of the vagina was dominated with Lactobacillus crispatus, Lactobacillus senii, and Lactobacillus iners. However, in the case of a woman having recurrent UTIs, the presence of Lactobacilli species was not detected [76,77]. The presence of Lactobacilli spp. keeps the vaginal environment acidic due to the fermentation of lactose into lactic acid. In this acidic environment, most bacteria and yeast species are unable to proliferate or colonized and get killed. Bio-Kult Pro-Cyan is a commercially available probiotic containing two strains of Lactobacilli plus cranberry extracts, which was evaluated for preventing recurrent UTIs in premenopausal adult women, and it was reported that Bio-Kult Pro-Cyan was safe and effective to control UTI [78].
The high reduction in the occurrence of recurrent UTIs and the high level of colonization of Lactobacillus crispatus strain CTV-05 had been observed in the women who had received intravaginally the probiotic Lactobacillus crispatus [79]. Another study showed the intravaginal administration of S. cerevisiae affects the expression of virulence traits of Candida albicans such as aspartyl proteinases (SAPs) as well as hyphae-associated proteins (hyphal wall protein 1—HWP1 and endothelin converting enzyme—ECE1) [80]. The intraurethral administration of Lactobacillus casei strain Shirota against artificially induced E. coli in a murine model induced a significant reduction of E. coli and of the inflammation in the urinary tract [81]. The administration of Lactobacillus spp. as probiotic not only maintains the low pH of the genitourinary tract but it also produces hydrogen peroxide and inhibited the growth of E. coli. Probiotics also activate toll-like receptor-2 (TLR2), which produces interleukin-10 (IL-10) and myeloid differentiation factor 88 (MyD88) [82]. The use of probiotics in some countries was practiced, and it is working well [74] and regarded as safe by the Health Protection Agency Centre for Infection [83].
The probiotic bacteria inhibit or prevent the growth of uropathogens in various ways. When probiotic administrated to patients or any person, it will multiply and act as antagonistic on uropathogens by competing with the foreign pathogen for colonization and inhibiting the adherence of bacteria to the intestinal or urinary tract. It also acts by lowering the luminal pH and producing some antimicrobial compound or peptide, such as bacteriocin. Probiotic, in addition to inhibition of uropathogens, affects the mucosal cell–cell interaction by the enhancement of intestinal barrier (i.e., mucus secretion) [84].

7. Nanomedicine in UTI

In the last few decades, there has been burgeoning research on nanoparticles in the field of medical sciences. Nanotechnology is a newer branch of science, but it is now a well-established science worldwide. Nanotechnology is a promising field in the treatment of MDR pathogens and other medical fields. There are several reports from worldwide that show its application in the treatment of various ailments, including UTI.
The silver nanoparticles have proven to be effective against UTI, actioning versus microbes like P. aeruginosa and Enterobacter sp. [85]. The copper nanoparticles were prepared in a matrix having hydrogel (HCuNPs) and the nanoparticles displayed antibacterial activities against some selected UTI microbes; the hydrogel matrix as compared to copper nanoparticles showed less zone of inhibition against the pathogens [86]. Thus, such nanocomposites may have a role in biomedical applications. A new antibacterial agent (izohidrafural) when applied on a novel bioactive nanostructure having silica-titania sieves acted as carriers. These nanomaterials successfully inhibited the growth of a few uropathogens viz. Klebsiella pneumoniae and Proteus mirabilis [87]. The zinc oxide nanoparticles synthesized from the leaves of Berberis aristata have shown antibacterial activity against clinical isolates of UTI [88]. The uropathogens isolated from urine samples of the patient showed significant antibacterial activity when green synthesized ZnONPs from the leaf of Passiflora caerulea were tested against them [89]. The Serratia nematodiphila-assisted copper sulfide nanoparticles (CuS-NPs) were evaluated against uropathogens (i.e., Escherichia coli, Staphylococcus aureus, Proteus vulgaris, and Klebsiella pneumoniae) CuS-NPs, and it was found effective against the tested uropathogens [84]. These remarkable actions have been summarized in Table 4.
Divya et al. synthesized AgNPs from coral-associated bacteria [92]. The synthesized AgNPs MGL-D10 showed antimicrobial activity against UTI, causing clinical isolates (such as Bacillus sp., E. coli, K. pneumonia, P. aeruginosa, S. aureus, and C. albicans). The anti-biofilm effect of synthesized AgNPs MGL-D10 against S. aureus was assessed using confocal laser scanning microscopy. Catheter experiments also proved the antibiofilm and antimicrobial effect of synthesized AgNPs MGL-D10. The obtained results exhibit that the coating of synthesized AgNPs MGL-D10 on catheters effectively inhibited the growth and biofilm formation of UTI causing pathogens.
However, a hygienic lifestyle, practicing safe sex, and ingestion of adequate water can prevent the occurrence of UTIs; the route of UTI can be through the administration of contaminated catheter through the urinary tract, a fact that is essential during prostate enlargement and another ailment of the urinary tract. Another similar study was done by Yassin et al., in which they synthesized silver nanoparticle-containing self-polymerized polydopamine and it was utilized to form the coating on the surface of the catheter [5]. The developed silver nanoparticle coated catheter was reported to have antibacterial activity against uropathogens, and it was also reported to have antibiofilm and antifouling activity. The quorum sensing (QS) mediated antimicrobial agents have been suggested earlier but as per the ground, the scale is concerned the concept is not converted into product.
In most cases of the disease, there is the involvement of pathogen island or virulence factor which is controlled by the QS. If we target the QS-mediated pathogenic factors, the disease can be prevented. Qais et al. synthesized silver nanoparticles (Ag@CC-NPs) from aqueous extract of Carum copticum, based on the concept of QS mediated antimicrobial agents; it was found that there was significant reduction in the production of virulence factor and it was shown also antibiofilm activity by P. aeruginosa, S. marcescens, and C. violaceum [93]. These studied bacterial species are associated with catheter-associated UTIs. The coating of the catheter with this silver nanoparticle can be used for the management of UTI or other catheter induced infections.
Candida species are also related to UTIs and pose health risks. The iron oxide magnetic nanoparticles were attached to vancomycin and these conjugated nanoparticles then acted as the probe; the probes were used to trap Staphylococcus saprophyticus (which is a Gram-positive pathogenic bacterium) and the causal agent of UTIs in women. Moreover, such samples have been successfully used to fix S. aureus using a magnetic field from urine specimens [94,95]. Recently, silver nanoparticles made from Mentha piperita (aqueous and ethanolic extract) were used against C. albicans. The ethanol extract proved to be more effective as it is exposed on the surface [80].

8. Conclusions and Perspectives

Microbial resistance towards commonly administered antibiotics [2,96] has presented a problem to clinicians to find a permanent cure for UTIs and to lower the rate of occurrence, especially in females. There are many alternative therapies available, like home-based therapies, which are effective on case to case basis. However, other systems of medicines like Homeopathic, Unani and Ayurveda, are effective on UTIs as well. Figure 1 describes the main points and findings of this review type paper.
While finding the cure for UTIs, the focus must also be on the glycemic patients, so that the treatment being synchronous with the UTIs. These limitations have encouraged scientists to find other modern ways of treatment, with nanotechnology giving some hope, as there are reports regarding the effective use of nanoparticles against uropathogens. These findings will add further knowledge about reducing the occurrence of UTIs, thereby improving the clinical outcomes.

Author Contributions

All authors have contributed substantially and equal to the first authors to the work reported. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Rose, C.; Parker, A.H.; Jefferson, B.; Cartmell, E. The characterization of feces and urine: A review of the literature to inform advanced treatment technology. Crit. Rev. Environ. Sci. Technol. 2015, 45, 1827–1879. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  2. Zaha, D.C.; Bungau, S.; Aleya, S.; Tit, D.M.; Vesa, C.M.; Popa, A.R.; Pantis, C.; Maghiar, O.A.; Bratu, O.G.; Furau, C.; et al. What antibiotics for what pathogens? The sensitivity spectrum of isolated strains in an intensive care unit. Sci. Total. Environ. 2019, 687, 118–127. [Google Scholar] [CrossRef]
  3. Tamalli, M.; Bioprabhu, S.; Alghazal, M.A. Urinary tract infection during pregnancy at Al-khoms. Int. J. Med. Med. Sci. 2013, 3, 455–459. [Google Scholar]
  4. Siddiq, D.M.; Darouiche, R.O. New strategies to prevent catheter-associated urinary tract infections. Nat. Rev. Urol. 2012, 9, 305–314. [Google Scholar] [CrossRef]
  5. Yassin, M.A.; Elkhooly, T.A.; Elsherbiny, S.M.; Reicha, F.M.; Shokeir, A.A. Facile coating of urinary catheter with bio–inspired antibacterial coating. Heliyon 2019, 5, e02986. [Google Scholar] [CrossRef] [Green Version]
  6. Syed, M.A.; Manzoor, U.; Shah, I.; Bukhari, S.H. Antibacterial effects of Tungsten nanoparticles on the Escherichia coli strains isolated from catheterized urinary tract infection (UTI) cases and Staphylococcus aureus. New Microbiol. 2010, 33, 329–335. [Google Scholar]
  7. Syed, M.A.; Babar, S.; Bhatti, A.S.; Bokhari, H. Antibacterial effects of silver nanoparticles on the bacterial strains isolated from catheterized urinary tract infection cases. J. Biomed. Nanotechnol. 2009, 5, 209–214. [Google Scholar] [CrossRef]
  8. Odoki, M.; Aliero, A.A.; Tibyangye, J.; Maniga, J.N.; Wampande, E.; Kato, C.D.; Agwu, E.; Bazira, J. Prevalence of bacterial urinary tract infections and associated factors among patients attending hospitals in Bushenyi district, Uganda. Int. J. Microbiol. 2019, 2019, 1–8. [Google Scholar] [CrossRef]
  9. Warkulwiz, G.; Hannon, K.; Cabano, D.; Mehta, K. Urinary tract infections (UTIs) in rural Kenya: Screening challenges, treatment pathways, and technological solutions. In Proceedings of the 2017 IEEE Global Humanitarian Technology Conference (GHTC), San Jose, CA, USA, 19–22 October 2017; pp. 1–6. [Google Scholar] [CrossRef]
  10. Stamm, W.E.; Norrby, S.R. Urinary tract infections: Disease panorama and challenges. J. Infect. Dis. 2001, 183, S1–S4. [Google Scholar] [CrossRef]
  11. Siakwa, M.; John, M.E.; Kpikpitse, D.; Ankobil, A.; Hansen-Owoo, E. Pregnancy outcomes: A comparison of women with symptomatic and asymptomatic bacteriuria in Cape Coast, Ghana. Afr. J. Pregnancy Childbirth 2014, 2, 27–30. [Google Scholar]
  12. Tan, C.W.; Chlebicki, M.P. Urinary tract infections in adults. Singap. Med J. 2016, 57, 485–490. [Google Scholar] [CrossRef] [PubMed]
  13. Rajivgandhi, G.; Vijayan, R.; Kannan, M.; Santhanakrishnan, M.; Manoharan, N. Molecular characterization and antibacterial effect of endophytic actinomycetes Nocardiopsis sp. GRG1 (KT235640) from brown algae against MDR strains of uropathogens. Bioact. Mater. 2016, 1, 140–150. [Google Scholar] [CrossRef] [Green Version]
  14. Casertano, M.; Menna, M.; Imperatore, C. The ascidian-derived metabolites with antimicrobial properties. Antibiotics 2020, 9, 510. [Google Scholar] [CrossRef] [PubMed]
  15. Ayuningrum, D.; Liu, Y.; Riyanti; Sibero, M.T.; Kristiana, R.; Asagabaldan, M.A.; Wuisan, Z.G.; Trianto, A.; Radjasa, O.K.; Sabdono, A.; et al. Tunicate-associated bacteria show a great potential for the discovery of antimicrobial compounds. PLoS ONE 2019, 14, e0213797. [Google Scholar] [CrossRef]
  16. Tit, D.M.; Pallag, A.; Iovan, C.; Furău, G.; Furău, C.; Bungau, S. Somatic-vegetative symptoms evolution in postmenopausal women treated with phytoestrogens and hormone replacement therapy. Iran. J. Public Health 2017, 46, 1528–1534. [Google Scholar]
  17. Kunin, C.M. Urinary tract infections in females. Clin. Infect. Dis. 1994, 18, 1–12. [Google Scholar] [CrossRef]
  18. Kant, S.; Lohiya, A.; Kapil, A.; Gupta, S.K. Urinary tract infection among pregnant women at a secondary level hospital in Northern India. Indian J. Public Health 2017, 61, 118–123. [Google Scholar]
  19. Jenkins, R.D.; Fenn, J.P.; Matsen, J.M. Review of urine microscopy for bacteriuria. JAMA 1986, 255, 3397–3403. [Google Scholar] [CrossRef]
  20. Bjerrum, L.; Grinsted, P.; Søgaard, P. Detection of bacteriuria by microscopy and dipslide culture in general practice. Eur. J. Gen. Pr. 2001, 7, 55–58. [Google Scholar] [CrossRef]
  21. Collee, J.G.; Miles, R.S.; Watt, B. Mackie & McCartney Practical Medical Microbiology, 14th ed.; Churchill Livingstone: New York, NY, USA, 1996. [Google Scholar]
  22. Lenke, R.R.; Van Dorsten, J. The efficacy of the nitrite test and microscopic urinalysis in predicting urine culture results. Am. J. Obstet. Gynecol. 1981, 140, 427–429. [Google Scholar] [CrossRef]
  23. Chernow, B.; Zaloga, G.P.; Soldano, S.; Quinn, A.; Lyons, P.; McFadden, E.; Cook, D.; Rainey, T.G. Measurement of urinary leukocyte esterase activity: A screening test for urinary tract infections. Ann. Emerg. Med. 1984, 13, 150–154. [Google Scholar] [CrossRef]
  24. Kaçmaz, B.; Cakir, O.; Aksoy, A.; Biri, A. Evaluation of rapid urine screening tests to detect asymptomatic bacteriuria in pregnancy. Jpn. J. Infect. Dis. 2006, 59, 261–263. [Google Scholar] [PubMed]
  25. Ronkainen, N.J.; Halsall, H.B.; Heineman, W.R. Electrochemical biosensors. Chem. Soc. Rev. 2010, 39, 1747–1763. [Google Scholar] [CrossRef] [PubMed]
  26. Nikolaevna, K.A.; Svalova, T.; Malysheva, N.N.; Okhokhonin, A.V.; Vidrevich, M.B.; Brainina, K. Sensors Based on bio and biomimetic receptors in medical diagnostic, environment, and food analysis. Biosens 2018, 8, 35. [Google Scholar] [CrossRef] [Green Version]
  27. Mach, K.E.; Wong, P.K.; Liao, J.C. Biosensor diagnosis of urinary tract infections: A path to better treatment? Trends Pharmacol. Sci. 2011, 32, 330–336. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  28. Sakata, M.; Inoue, T.; Todokoro, M.; Kunitake, M. Limulus Amebocyte Lysate assay for endotoxins by an adsorption method with polycation-immobilized cellulose beads. Anal. Sci. 2010, 26, 291–296. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  29. Mehrotra, P. Biosensors and their applications—A review. J. Oral Biol. Craniofacial Res. 2016, 6, 153–159. [Google Scholar] [CrossRef] [Green Version]
  30. Sin, M.L.Y.; E Mach, K.; Wong, P.K.; Liao, J.C. Advances and challenges in biosensor-based diagnosis of infectious diseases. Expert Rev. Mol. Diagn. 2014, 14, 225–244. [Google Scholar] [CrossRef] [Green Version]
  31. Reid, G.; Bruce, A.W.; Cook, R.L.; Llano, M. Effect on urogenital flora of antibiotic therapy for urinary tract infection. Scand. J. Infect. Dis. 1990, 22, 43–47. [Google Scholar] [CrossRef]
  32. E Dyer, I.; Sankary, T.M.; A Dawson, J. Antibiotic resistance in bacterial urinary tract infections, 1991 to 1997. West. J. Med. 1998, 169, 265–268. [Google Scholar]
  33. Raz, R.; Rottensterich, E.; Leshem, Y.; Tabenkin, H. Double-blind study comparing 3-day regimens of cefixime and ofloxacin in treatment of uncomplicated urinary tract infections in women. Antimicrob. Agents Chemother. 1994, 38, 1176–1177. [Google Scholar] [CrossRef] [Green Version]
  34. Anderson, V.R.; Perry, C.M. Levofloxacin: A review of its use as a high-dose, short-course treatment for bacterial infection. Drugs 2008, 68, 535–565. [Google Scholar] [CrossRef] [PubMed]
  35. Gutiérrez-Castrellón, P.; Díaz-García, L.; De Colsa-Ranero, A.; Cuevas-Alpuche, J.; Jiménez-Escobar, I. Efficacy and safety of ciprofloxacin treatment in urinary tract infections (UTIs) in adults: A systematic review with meta-analysis. Gac. Med. Mex. 2015, 151, 225–244. [Google Scholar] [PubMed]
  36. Odongo, I.; Ssemambo, R.; Kungu, J.M. Prevalence of Escherichia Coli and its antimicrobial susceptibility profiles among patients with UTI at Mulago Hospital, Kampala, Uganda. Interdiscip. Perspect. Infect. Dis. 2020, 2020. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  37. Chandra, H.; Bishnoi, P.; Yadav, A.; Patni, B.; Mishra, A.P.; Nautiyal, A.R. Antimicrobial resistance and the alternative resources with special emphasis on plant-based antimicrobials—A Review. Plants 2017, 6, 16. [Google Scholar] [CrossRef] [PubMed]
  38. Chandra, H.; Srivastava, J.; Agarwal, R.K. Fundamental Techniques in Microbiology; John Publisher Pvt. Ltd.: New Delhi, India, 2016. [Google Scholar]
  39. Nwabudike, L.C. Classical homeopathy and bacterial urinary tract infections. Proc. Rom. Acad. 2017, 19, 93–96. [Google Scholar]
  40. Coelho, C.D.P.; Motta, P.D.; Petrillo, M.; Iovine, R.D.O.; Dalboni, L.C.; Santana, F.R.; Correia, M.S.F.; Casarin, R.C.V.; Carvalho, V.M.; Bonamin, L.V. Homeopathic medicine Cantharis modulates uropathogenic E. coli (UPEC)-induced cystitis in susceptible mice. Cytokine 2017, 92, 103–109. [Google Scholar] [CrossRef] [PubMed]
  41. Chand, K.S.; Kapoor, P. Two Case Reports of Integrated Management of Antibiotic-Resistant Urinary Tract Infection. Homeopathy 2020, 109, 097–106. [Google Scholar] [CrossRef]
  42. Kurmann, C.; Imbach, E.; Amsler, F.; Pannek-Rademacher, S.; Pannek, J. In-vitro effects of homeopathic drugs on cultured Escherichia coli. Homeopathy 2018, 107, 150–154. [Google Scholar] [CrossRef]
  43. Zubair, M.; Nayab, M.; Jameel, S.; Qadeer, A. Effect of Unani formulation on urine composition in the patients of Warm-e-Majra-e-Baul–An observational study. Int. J. Herb. 2014, 1, 47–50. [Google Scholar]
  44. Nishat, A.; Sultana, S.; Sultana, A. A comparative study of polyherbal Unani formulations in gestational Urinary tract infections. J. Exp. Integr. Med. 2017, 7, 1. [Google Scholar] [CrossRef]
  45. Ashraf, J.; Latafat, T.; Mohsin, M. Therapeutic evaluation of Safuf Mudir and Sharbat Bazuri Motadil in urinary tract infections (Tadiya Majrae-Baul). HJUM 2012, 7, 21–29. [Google Scholar]
  46. Ahmad, T.; Khan, A.B.; Latafat, T. Urinary tract infection (tadiya majar-e-baul) in the light of Unani system of medicine: An overview. J. Pharm. Sci. Innov. 2015, 4, 242–246. [Google Scholar] [CrossRef]
  47. Mutters, N.T.; Mampel, A.; Kropidlowski, R.; Biehler, K.; Günther, F.; Bălu, I.; Malek, V.; Frank, U. Treating urinary tract infections due to MDR E. coli with Isothiocyanates—A phytotherapeutic alternative to antibiotics? Fitoterapia 2018, 129, 237–240. [Google Scholar] [CrossRef]
  48. Mishra, S.; Mekap, S.K.; Patra, S.; Dhal, N.K.; Sahooa, S. Antioxidant and anti-infective potential of Oleanolic acid acetate vis-à-vis Vitex negundo Linn. and Oroxylum indicum Vent. against human pathogens causing infections of UT, GIT and skin. Orient. Pharm. Exp. Med. 2014, 15, 73–82. [Google Scholar] [CrossRef]
  49. McMurdo, M.E.T.; Argo, I.; Phillips, G.; Daly, F.; Davey, P. Cranberry or trimethoprim for the prevention of recurrent urinary tract infections? A randomized controlled trial in older women. J. Antimicrob. Chemother. 2008, 63, 389–395. [Google Scholar] [CrossRef] [Green Version]
  50. Sandhu, N.S.; Kaur, S.; Chopra, D. Equietum arvense: Pharmacology and phytochemistry—A review. Asian J. Pharm. Clin. Res. 2010, 3, 146–150. [Google Scholar]
  51. Carneiro, D.M.; Freire, R.C.; Honório, T.C.; Zoghaib, I.; Cardoso, F.F.; Tresvenzol, L.M.; de Paula, J.R.; Sousa, A.L.; Jardim, P.C.; da Cunha, L.C. Randomized, double-blind clinical trial to assess the acute diuretic effect of Equisetum arvense (Field Horsetail) in healthy volunteers. Evid. Based Complement. Altern. Med. 2014, 2014, 1–8. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  52. Dog, T.L. Urinary Tract Infection. In Women’s Health in Complementary and Integrative Medicine; Dog, T.L., Ed.; Churchill Livingstone: Saint Louis, MI, USA, 2005; pp. 293–306. [Google Scholar] [CrossRef]
  53. Pereira, R.S.; Sumita, T.C.; Furlan, M.R.; Jorge, A.O.C.; Ueno, M. Atividade antibacteriana de óleos essenciais em cepas isoladas de infecção urinária. Rev. Saúde Pública 2004, 38, 326–328. [Google Scholar] [CrossRef]
  54. Sharma, A.; Chandraker, S.; Patel, V.K.; Ramteke, P. Antibacterial activity of medicinal plants against pathogens causing complicated urinary tract infections. Indian J. Pharm. Sci. 2009, 71, 136–139. [Google Scholar] [CrossRef] [Green Version]
  55. Rafsanjany, N.; Lechtenberg, M.; Petereit, F.; Hensel, A. Antiadhesion as a functional concept for protection against uropathogenic Escherichia coli: Invitro studies with traditionally used plants with antiadhesive activity against uropathognic Escherichia coli. J. Ethnopharmacol. 2013, 145, 591–597. [Google Scholar] [CrossRef]
  56. Bag, A.; Bhattacharyya, S.K.; Chattopadhyay, R.R. Medicinal plants and urinary tract infections: An update. Pharm. Rev. 2008, 2, 277–284. [Google Scholar]
  57. Handeland, M.; Grude, N.; Torp, T.; Slimestad, R. Black chokeberry juice (Aronia melanocarpa) reduces incidences of urinary tract infection among nursing home residents in the long term—A pilot study. Nutr. Res. 2014, 34, 518–525. [Google Scholar] [CrossRef]
  58. Lagha, R.; Ben Abdallah, F.; Al-Sarhan, B.O.; Al-Sodany, Y.M. Antibacterial and biofilm inhibitory activity of medicinal plant essential oils against Escherichia coli isolated from UTI patients. Molecules 2019, 24, 1161. [Google Scholar] [CrossRef] [Green Version]
  59. Mishra, M.P.; Rath, S.; Swain, S.S.; Ghosh, G.; Das, D.; Padhy, R.N. In-vitro antibacterial activity of crude extracts of 9 selected medicinal plants against UTI causing MDR bacteria. J. King Saud Univ. Sci. 2017, 29, 84–95. [Google Scholar] [CrossRef] [Green Version]
  60. Dhanasekaran, S.; Rajesh, A.; Mathimani, T.; Samuel, S.M.; Shanmuganathan, R.; Brindhadevi, K.; Samuel, M.S. Efficacy of crude extracts of Clitoria ternatea for antibacterial activity against gram negative bacterium (Proteus mirabilis). Biocatal. Agric. Biotechnol. 2019, 21, 101328. [Google Scholar] [CrossRef]
  61. Bouterfas, K.; Mehdadi, Z.; Elaoufi, M.M.; Aouad, L.; Latreche, A.; Benchiha, W. Invitro antibacterial activity of flavonoids extracts from three Algerian horehound (Marrubium vulgare L.) leaves. Orient. Pharm. Exp. Med. 2017, 18, 59–66. [Google Scholar] [CrossRef]
  62. Alshami, I.; Alharbi, A.E. Antimicrobial activity of Hibiscus sabdariffa extract against uropathogenic strains isolated from recurrent urinary tract infections. Asian Pac. J. Trop. Dis. 2014, 4, 317–322. [Google Scholar] [CrossRef]
  63. Njobdi, S.; Gambo, M.; Ishaku, G.A. Antibacterial activity of Zingiber officinale on Escherichia coli and Staphylococcus aureus. J. Adv. Biol. Biotechnol. 2018, 19, 1–8. [Google Scholar] [CrossRef]
  64. Tariq, A.L.; Reyaz, A.L. Terminalia chebula: A treatment against pathogenic proteus vulgaris strains associated with urinary tract infection. Int. J. Res. Ayurveda Pharm. 2013, 4, 560–563. [Google Scholar] [CrossRef]
  65. Vineeth, T.; Deepak, M.; Shree, A.B.; Vaidya, A. Antibacterial effect of Boerhavia diffusa and Punarnavasavam on urinary tract infection (Uti) causing pathogens. World J. Pharm. Res. 2014, 3, 423–437. [Google Scholar]
  66. Hankin, M.E. The bactericidal action of the waters of the Jamuna and Ganges rivers on Cholera microbes. Ann. Inst. Pasteur 10:511–523 (1896). Bacteriophage 2011, 1, 117–126. [Google Scholar] [CrossRef]
  67. Twort, F. An investigation on the nature of ultra-microscopic viruses. Lancet 1915, 186, 1241–1243. [Google Scholar] [CrossRef] [Green Version]
  68. Ackermann, H.W. On an invisible microbe antagonistic to dysentery bacilli. Note by M. F. d’Herelle, presented by M. Roux. Comptes Rendus Academie des Sciences 1917; 165:373–5. Bacteriophage 2011, 1, 3–5. [Google Scholar] [CrossRef] [Green Version]
  69. Patey, O.; McCallin, S.; Mazure, H.; Liddle, M.; Smithyman, A.; Dublanchet, A. Clinical indications and compassionate use of phage therapy: Personal experience and literature review with a focus on osteoarticular infections. Viruses 2018, 11, 18. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  70. Ujmajuridze, A.; Chanishvili, N.; Goderdzishvili, M.; Leitner, L.; Mehnert, U.; Chkhotua, A.; Kessler, T.M.; Sybesma, W. Adapted bacteriophages for treating urinary tract infections. Front. Microbiol. 2018, 9, 1832. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  71. Sybesma, W.; Zbinden, R.; Chanishvili, N.; Kutateladze, M.; Chkhotua, A.; Ujmajuridze, A.; Mehnert, U.; Kessler, T.M. Bacteriophages as potential treatment for urinary tract infections. Front. Microbiol. 2016, 7, 465. [Google Scholar] [CrossRef]
  72. Sulakvelidze, A.; Alavidze, Z.; Morris, J.G. Bacteriophage Therapy. Antimicrob. Agents Chemother. 2001, 45, 649–659. [Google Scholar] [CrossRef] [Green Version]
  73. Reid, G.; Beuerman, D.; Heinemann, C.; Bruce, A.W. Probiotic Lactobacillus dose required to restore and maintain a normal vaginal flora. FEMS Immunol. Med Microbiol. 2001, 32, 37–41. [Google Scholar] [CrossRef] [Green Version]
  74. Borchert, D.H.; Sheridan, L.; Papatsoris, A.; Faruquz, Z.; Barua, J.M.; Junaid, I.; Pati, Y.; Chinegwundoh, F.; Buchholz, N. Prevention and treatment of urinary tract infection with probiotics: Review and research perspective. Indian J. Urol. 2008, 24, 139–144. [Google Scholar] [CrossRef]
  75. Mack, D.R. Probiotics-mixed messages. Can. Fam. Physician 2005, 51, 1455–1457. [Google Scholar] [PubMed]
  76. Reid, G.; Bruce, A.W. Probiotics to prevent urinary tract infections: The rationale and evidence. World J. Urol. 2006, 24, 28–32. [Google Scholar] [CrossRef]
  77. Butler, D.S.C.; Silvestroni, A.; Stapleton, A.E. Cytoprotective effect of Lactobacillus crispatus CTV-05 against uropathogenic E. coli. Pathogens 2016, 5, 27. [Google Scholar] [CrossRef] [Green Version]
  78. Koradia, P.; Kapadia, S.; Trivedi, Y.; Chanchu, G.; Harper, A. Probiotic and cranberry supplementation for preventing recurrent uncomplicated urinary tract infections in premenopausal women: A controlled pilot study. Expert Rev. Anti-Infect. Ther. 2019, 17, 733–740. [Google Scholar] [CrossRef] [Green Version]
  79. Stapleton, A.E.; Au-Yeung, M.; Hooton, T.M.; Fredricks, D.N.; Roberts, P.L.; Czaja, C.A.; Yarova-Yarovaya, Y.; Fiedler, T.; Cox, M.; Stamm, W.E. Randomized, placebo-controlled phase 2 trial of a Lactobacillus crispatus probiotic given intravaginally for prevention of recurrent urinary tract infection. Clin. Infect. Dis. 2011, 52, 1212–1217. [Google Scholar] [CrossRef] [PubMed]
  80. Robles-Martínez, M.; Patiño-Herrera, R.; Pérez-Vázquez, F.J.; Montejano-Carrizales, J.M.; González, J.F.C.; Pérez, E. Mentha piperita as a natural support for silver nanoparticles: A new Anti-candida albicans treatment. Colloid Interface Sci. Commun. 2020, 35, 100253. [Google Scholar] [CrossRef]
  81. Asahara, T.; Nomoto, K.; Watanuki, M.; Yokokura, T. Antimicrobial activity of intraurethrally administered probiotic Lactobacillus casei in a murine model of Escherichia coli urinary tract infection. Antimicrob. Agents Chemother. 2001, 45, 1751–1760. [Google Scholar] [CrossRef] [Green Version]
  82. Amdekar, S.; Singh, V.; Singh, D.D. Probiotic therapy: Immunomodulating approach toward urinary tract infection. Curr. Microbiol. 2011, 63, 484–490. [Google Scholar] [CrossRef]
  83. Borriello, S.P.; Hammes, W.P.; Holzapfel, W.; Marteau, P.; Schrezenmeir, J.; Vaara, M.; Valtonen, V. Safety of probiotics that contain Lactobacilli or Bifidobacteria. Clin. Infect. Dis. 2003, 36, 775–780. [Google Scholar] [CrossRef]
  84. Ng, S.C.; Hart, A.L.; Kamm, M.A.; Stagg, A.J.; Knight, S.C. Mechanisms of action of probiotics: Recent advances. Inflamm. Bowel Dis. 2009, 15, 300–310. [Google Scholar] [CrossRef]
  85. Inbaneson, S.J.; Sundaram, R.; Manikandan, N. Antibacterial potential of silver nanoparticles against isolated urinary tract infectious bacterial pathogens. Appl. Nanosci. 2011, 1, 231–236. [Google Scholar] [CrossRef] [Green Version]
  86. Al-Enizi, A.M.; Ahamad, T.; Al-Hajji, A.B.; Ahmed, J.; Chaudhary, A.A.; AlShehri, S.M. Cellulose gum and copper nanoparticles based hydrogel as antimicrobial agents against urinary tract infection (UTI) pathogens. Int. J. Biol. Macromol. 2018, 109, 803–809. [Google Scholar] [CrossRef] [PubMed]
  87. Al Tameemi, M.B.M.; Stan, R.; Prisacari, V.; Voicu, G.; Popa, M.; Chifiriuc, M.C.; Ott, C.; Marton, G.; Meghea, A. Antimicrobial performance of nanostructured silica–titania sieves loaded with izohidrafural against microbial strains isolated from urinary tract infections. Comptes Rendus Chim. 2017, 20, 475–483. [Google Scholar] [CrossRef]
  88. Chandra, H.; Patel, D.; Kumari, P.; Jangwan, J.; Yadav, S. Phyto-mediated synthesis of zinc oxide nanoparticles of Berberis aristata: Characterization, antioxidant activity and antibacterial activity with special reference to urinary tract pathogens. Mater. Sci. Eng. C 2019, 102, 212–220. [Google Scholar] [CrossRef]
  89. Santhoshkumar, J.; Kumar, S.V.; RajeshKumar, S. Synthesis of zinc oxide nanoparticles using plant leaf extract against urinary tract infection pathogen. Resour. Technol. 2017, 3, 459–465. [Google Scholar] [CrossRef]
  90. Malarkodi, C.; RajeshKumar, S. Invitro bactericidal activity of biosynthesized CuS nanoparticles against UTI-causing pathogens. Inorg. Nano-Metal Chem. 2017, 47, 1290–1297. [Google Scholar] [CrossRef]
  91. Mishra, M.P.; Padhy, R.N. Antibacterial activity of green silver nanoparticles synthesized from Anogeissus acuminata against multidrug resistant urinary tract infecting bacteria invitro and host-toxicity testing. J. Appl. Biomed. 2018, 16, 120–125. [Google Scholar] [CrossRef]
  92. Divya, M.; Kiran, G.S.; Hassan, S.; Selvin, J. Biogenic synthesis and effect of silver nanoparticles (AgNPs) to combat catheter-related urinary tract infections. Biocatal. Agric. Biotechnol. 2019, 18, 101037. [Google Scholar] [CrossRef]
  93. Qais, F.A.; Shafiqab, A.; Ahmada, I.; Husain, F.M.; Khan, R.A.; Hassane, I.; Ahmad, I.; Khan, R.A. Green synthesis of silver nanoparticles using Carum copticum: Assessment of its quorum sensing and biofilm inhibitory potential against gram negative bacterial pathogens. Microb. Pathog. 2020, 144, 104172. [Google Scholar] [CrossRef]
  94. Tallury, P.; Malhotra, A.; Byrne, L.M.; Santra, S. Nanobioimaging and sensing of infectious diseases. Adv. Drug Deliv. Rev. 2010, 62, 424–437. [Google Scholar] [CrossRef]
  95. Lin, Y.-S.; Tsai, P.-J.; Weng, M.-F.; Chen, Y.-C. Affinity capture using vancomycin-bound magnetic nanoparticles for the MALDI-MS analysis of bacteria. Anal. Chem. 2005, 77, 1753–1760. [Google Scholar] [CrossRef] [PubMed]
  96. Zaha, D.C.; Bungau, S.; Uivarosan, D.; Tit, D.M.; Maghiar, T.A.; Maghiar, O.; Pantis, C.; Fratila, O.; Rus, M.; Vesa, C.M. Antibiotic consumption and microbiological epidemiology in surgery departments: Results from a single study center. Antibiotics 2020, 9, 81. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Figure 1. Representation of UTI, prevalence, diagnosis, and treatments.
Figure 1. Representation of UTI, prevalence, diagnosis, and treatments.
Molecules 25 05593 g001
Table 1. Colony characteristics of uropathogens on selective media.
Table 1. Colony characteristics of uropathogens on selective media.
Culture MediaColony Characteristic/ColorProbable Bacterium
CLEDBlue greenE. faecalis
Pink colony with pink haloE. coli
Golden yellowS. aureus
Orange yellow/GreenishPr. mirabilis
MacConkey AgarLactose fermenting pink colonyE. coli
Lactose fermenting mucoid pink colonyKlebsiella sp.
CHROM Agar orientation (CHROM agar company, France)PinkE. coli
Turquoise blueEnterococci
Metallic blueKlebsiella pneumoniae
Metallic blueEnterobacter spp.
Gave golden, opaque small whiteS. aureus
CPS ID2 medium (bioMe’rieux)PinkE. coli
Blue GreenEnterococcus
Brown colorPtoteus mirabilis
Table 2. Antibiotics prescribed for the treatment of E. coli UTI.
Table 2. Antibiotics prescribed for the treatment of E. coli UTI.
AntibioticsYearRef.
Amoxicillin or bacampicillin1990[31]
Nitrofurantoin and trimethoprim-sulfamethoxazole (TMP/SMX)1991–1997[32]
Cefixime and Ofloxacin1994[33]
Levofloxacin2008[34]
Ciprofloxacin2015[35]
Cephalexin and Cefuroxime2016[12]
Cefotaxime/clavulanic acid2020[36]
Table 3. Plants active against uropathogens.
Table 3. Plants active against uropathogens.
PlantInhibitFractionRef
Zingiber officinaleE. coliEthanol, n-Hexane[54,63]
Punica granatumE. coli, K. pneumoniae, K. oxytoca, Proteus mirabilis, P. vulgaris, Pseudomonas aeruginosaEthanol, methanol[50,54,55,59]
Terminalia chebulaK. pneumoniae, Proteus vulgarisEthanol[54,64]
Ocimum sanctumK. pneumoniae, Enterococcus faecalisEthanol[54]
Cinnamomum cassiaPs. aeruginosaEthanol[54]
Azadirachta indicaE. faecalisEthanol[54]
Thymus zygisE. coliEssential oil[58]
Clitoria ternatea Marrubium vulgare LPr. Mirabilis E. coli, B. cereus, Pr. mirabilisAcetone Methanol[60,61]
Hibiscus sabdariffaE. coli, K. pneumoniaeMethanol[62]
Boerhavia diffusaKlebsiella sp., Pseudomonas sp., Enterococcus sp., Escherichia coli and Proteus sp.Ethanol[65]
Vitex negundo LinnE. coli, S. flexneriMethanol:dichloromethane (1:1)[48]
Oroxylum indicumE. coli, S. flexneriMethanol:dichloromethane (1:1)[48]
Table 4. Few metallic nanoparticles and their effectiveness against UTI pathogens.
Table 4. Few metallic nanoparticles and their effectiveness against UTI pathogens.
Metal NPSourceEffective AgainstRef.
ZnO-NPBeberis aristataEscherichia coli,Staphylococcus aureus,Klebsiella pneumoniae,Bacillus subtilis,Bacillus cereus,Serratia marcescens[88]
ZnO-NPPassiflora caeruleaE. coli and Enterococcus[89]
CuS-NPsSerratia nematodiphilaE. coli, S. aureus, Pr vulgaris, and K. pneumoniae[90]
AgNPChemical methodE. coli, Pseudomonas aeruginosa, Klebsiella pneumoniae, Enterobacter sp., Proteus morganii and Staphylococcus aureus[85]
AgNPAnogeissus acuminateS. aureus, Enterococcus faecalis, A. baumannii, Citrobacter freundii, Enterobacter aerogenes, Escherichia coli, Klebsiella oxytoca, K. pneumoniae, Proteus mirabilis, P. vulgaris and Pseudomonas aeruginosa[91]
AgNPChemical methodE. coli, Staphylococcus[7]
W-NPsChemical methodE, coli, Staphylococcus[6]
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Chandra, H.; Singh, C.; Kumari, P.; Yadav, S.; Mishra, A.P.; Laishevtcev, A.; Brisc, C.; Brisc, M.C.; Munteanu, M.A.; Bungau, S. Promising Roles of Alternative Medicine and Plant-Based Nanotechnology as Remedies for Urinary Tract Infections. Molecules 2020, 25, 5593. https://doi.org/10.3390/molecules25235593

AMA Style

Chandra H, Singh C, Kumari P, Yadav S, Mishra AP, Laishevtcev A, Brisc C, Brisc MC, Munteanu MA, Bungau S. Promising Roles of Alternative Medicine and Plant-Based Nanotechnology as Remedies for Urinary Tract Infections. Molecules. 2020; 25(23):5593. https://doi.org/10.3390/molecules25235593

Chicago/Turabian Style

Chandra, Harish, Chanchal Singh, Pragati Kumari, Saurabh Yadav, Abhay P. Mishra, Aleksey Laishevtcev, Ciprian Brisc, Mihaela Cristina Brisc, Mihai Alexandru Munteanu, and Simona Bungau. 2020. "Promising Roles of Alternative Medicine and Plant-Based Nanotechnology as Remedies for Urinary Tract Infections" Molecules 25, no. 23: 5593. https://doi.org/10.3390/molecules25235593

Article Metrics

Back to TopTop