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| [http://en.wikipedia.org/wiki/Tuberculosis Tuberculosis] (TB) is a potentially deadly disease caused by pathogenic bacteria, usually <i>Mycobacterium tuberculosis</i>. It has existed in humans since ancient times and had high mortality rates without adequate treatment options before the invention of [http://en.wikipedia.org/wiki/Antibiotics antibiotics] , specifically [http://en.wikipedia.org/wiki/Streptomycin streptomycin] in 1943, that were potent enough to kill the bacteria. [[#References|[6]]] In the 1960’s, following a drastic reduction in TB rates around the world, people began to predict that the disease could be completely eradicated within a century. [[#References|[5]]] However, this goal proved overly-optimistic as drug-resistant strains had begun to emerge since the first use of antibiotics to treat TB. At first this was mainly due to only using a single drug, streptomycin, to treat the infection, prompting the use of multi-drug therapy but in recent decades [http://en.wikipedia.org/wiki/Multi-drug-resistant_tuberculosis multi-drug resistant] (MDR), [http://en.wikipedia.org/wiki/Extensively_drug-resistant_tuberculosis extensively- drug resistant] (XDR), and [http://en.wikipedia.org/wiki/Totally_drug-resistant_tuberculosis totally-drug resistant] (TDR) strains of TB have emerged. [[#References|[1]]] Many of these strains are effectively incurable, especially the XDR and TDR strains, even for patients with access to an array of anti-TB drugs. [[#References|[1]]] Given their grave public health threat it is crucial to study the molecular biology of the intrinsic and acquired mechanisms of resistance in <i>M. tuberculosis</i> in order to develop new drugs that avoid these mechanisms. | | [http://en.wikipedia.org/wiki/Tuberculosis Tuberculosis] (TB) is a potentially deadly disease caused by pathogenic bacteria, usually <i>Mycobacterium tuberculosis</i>. It has existed in humans since ancient times and had high mortality rates without adequate treatment options before the invention of [http://en.wikipedia.org/wiki/Antibiotics antibiotics] , specifically [http://en.wikipedia.org/wiki/Streptomycin streptomycin] in 1943, that were potent enough to kill the bacteria. [[#References|[6]]] In the 1960’s, following a drastic reduction in TB rates around the world, people began to predict that the disease could be completely eradicated within a century. [[#References|[5]]] However, this goal proved overly-optimistic as drug-resistant strains had begun to emerge since the first use of antibiotics to treat TB. At first this was mainly due to only using a single drug, streptomycin, to treat the infection, prompting the use of multi-drug therapy but in recent decades [http://en.wikipedia.org/wiki/Multi-drug-resistant_tuberculosis multi-drug resistant] (MDR), [http://en.wikipedia.org/wiki/Extensively_drug-resistant_tuberculosis extensively- drug resistant] (XDR), and [http://en.wikipedia.org/wiki/Totally_drug-resistant_tuberculosis totally-drug resistant] (TDR) strains of TB have emerged. [[#References|[1]]] Many of these strains are effectively incurable, especially the XDR and TDR strains, even for patients with access to an array of anti-TB drugs. [[#References|[1]]] Given their grave public health threat it is crucial to study the molecular biology of the intrinsic and acquired mechanisms of resistance in <i>M. tuberculosis</i> in order to develop new drugs that avoid these mechanisms. |
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| ==Intrinsic Drug Resistance==
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| <i>M. tuberculosis</i> possess a multitude of resistance mechanisms against a wide range of antibiotics, as far as its intrinsic mechanisms (as opposed to acquired mechanisms that are brought about by chromosomal [http://en.wikipedia.org/wiki/Mutation mutations], as discussed below) they can be divided into two categories: passive and specialized resistance. [[#References|[7]]]
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| ===Passive Resistance Mechanisms===
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| The primary feature of passive resistance to antibiotics in <i>M. tuberculosis</i> is a highly impermeable cell wall. Hydrophobic chemicals are unable to enter this cell wall due to a layer of hydrophilic [http://en.wikipedia.org/wiki/Arabinogalactan arabinogalactan] [[#References|[6]]]. This layer is then wrapped in hydrophobic [http://en.wikipedia.org/wiki/Mycolic_acid mycolic acids] which severely limits the entrance of hydrophilic molecules. The mycolic acids are added to arabinogalactan in the cell wall by group of mycolyltransferase enzymes. One gene that encodes one of the mycolytransferases is the <i>Fbp</i>A gene and studies of <i>Fbp</i>A mutants have led to the conclusion that there is a strong connection between mycolic acid content and antibiotic resistance. [[#References|[6]]] Despite being considered [http://en.wikipedia.org/wiki/Gram-positive_bacteria Gram-positive], Mycobacterium cell wall layers create space that resembles the [http://en.wikipedia.org/wiki/Periplasm periplasm] of [http://en.wikipedia.org/wiki/Gram-negative_bacteria Gram-negative bacteria]. [[#References|[6]]] Another piece of evidence supporting the impermeability of the Mycobacterial cell wall is the fact that the time it takes for [http://en.wikipedia.org/wiki/%CE%92-lactam_antibiotic β-lactam antibiotics] to diffuse through the cell wall takes a hundred times longer than it does for <i>Escherichia coli</i>. [[#References|[7]]]
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| ===Specialized Resistance Mechanisms===
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| The cell wall of mycobacteria is only part of what makes this species innately resistant to such a broad range of antibiotics. Studies have shown that the mycobacterial cell envelope lets in enough hydrophilic antibiotics over time to potentially kill the cell; however, since the cell wall significantly hinders the entrance of antibiotics it is thought that it slows antibiotic accumulation enough to allow for various cellular systems to detoxify the invading drugs. [[#References|[6]]] This is especially evident in the case of β-lactams, which work by inhibiting the assembly of [http://en.wikipedia.org/wiki/Peptidoglycan peptidoglycan] and ultimately causing cell death, as peptidoglycan is a crucial part of the bacterial cell wall. [[#References|[7]]] While the mycobacterial cell wall greatly limits the rate at which β-lactams are able to accumulate in the cell, effectively protecting against certain antibiotics, such as [http://en.wikipedia.org/wiki/Carbapenem carbapenems] which are not very stable and degrade relatively quickly, they still would be able to high enough levels over time due to the slow rate at which <i>M. tuberculosis</i> undergoes cell division. [[#References|[7]]] However, <i>M. tuberculosis</i> possesses certain enzymes called β-lactamases that effectively degrade β-lactam antibiotics. Clinical evidence and <i>in vitro</i> experiments involving successful treatments of both β-lactams and β-lactamase inhibitors, as well as β-lactamase-resistant- β-lactams have strengthened the claim that β-lactamases are the most important factor in mycobacterial resistance to β-lactams. [[#References|[6]]]
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| Another mechanism of specialized intrinsic resistance in <i>M. tuberculosis</i> is the molecular mimicry of certain drug targets by proteins. For example in the case of [http://en.wikipedia.org/wiki/Quinolone fluoroquinolones] (fluoridated quinolones), which lead to cell death by preventing transcription, replication, and repair of DNA by interfering with [http://en.wikipedia.org/wiki/DNA_gyrase DNA gyrase], a certain protein, MfpA, has been found to cause intrinsic resistance to fluoroquinolones. [[#References|[6]]] It is able to bind to DNA gyrase, inhibiting its normal activity, and this is considered DNA mimicry as MfpA is similar in shape, size, and electrostatic nature to the double-helix of DNA. [[#References|[11]]]
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| A third key mechanism of intrinsic drug resistance in <i>M. tuberculosis</i> is the presence of a multitude of drug efflux pumps that are able to expel antibiotics from the cell. In general [http://en.wikipedia.org/wiki/Efflux_%28microbiology%29 efflux pumps] are membrane-spanning proteins that are involved in transporting waste, nutrients, and other molecules across the cell wall. While deportation of certain antibiotics may be due to non-specific transportation and thus not an inherent purpose of efflux pumps, the presence of regulatory systems for these pumps that are believed to have evolved to increase antibiotic resistance makes drug efflux pumps a mechanism of specialized drug resistance. [[#References|[7]]] In a study by Dinesh et al. [[#References|[4]]] they looked at intrinsic resistance of <i>M. tuberculosis</i> efflux pumps to peptidoglycan synthesis inhibitors (PSI) with their results confirming that efflux pumps played a role in resistance to certain PSI including β-lactams, vancomycin, and bacitracin. As of 2012 there were 18 different transporters that were characterized to be involved in antibiotic resistance or susceptibility of mycobacteria. [[#References|[12]]] Two examples of these are IniBAC, causing resistance to isoniazid and ethambutol, and EfpA, which is a non-specific multi-drug transporter and returning to the concept of regulatory systems that have evolved to be responsive to the presence of antibiotics, the expression of both of these proteins is negatively controlled by a transcription regulator Lsr2 which is inducible by ethambutol or isoniazid. [[#References|[7]]] A very recent study by Li et al. [[#References|[13]]] examined gene expression of efflux pumps in clinically isolated strains of <i>M. tuberculosis</i>. Their results (|<br><b>Table 1. </b>) showed both a statistically significant difference in [http://en.wikipedia.org/wiki/Minimum_inhibitory_concentration minimum inhibitory concentrations (MICs)]
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| [[Image: ploseffluxpump.png|thumb|300px|right|<br><b>Table 1.</b>]]
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| [[Image: journal.ppat.1000645.g003.png|thumb|300px|right|<br><b>Figure 3. </b> Activity Confirmation and Target Identification for N-(2-(4-methoxyphenoxy) ethyl)-3,5-dinitrobenzamide (DNB1) (A) Chemical structure of DNB1 (B)
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| [[Image:Journal.pbio.0050156.g003.png|thumb|280px|right|<br><b>Figure 2. </b> Lateral Gene Transfer in Bacteroidetes Promotes Niche Specialization(A) Proportions of genes found in each genome. Non-laterally transferred genes (blue) are proportionally more often involved in metabolism. Genes assigned “Primary metabolism” (yellow) and “Protein biosynthesis” (red), are compared. Upward-pointing arrowhead indicate gene enrichment and downward-pointing arrowhead show gene depletion . Asterisks indicate statistical significance, single asterisk (*) indicates p < 0.05; double asterisks (**) indicate p < 0.01; and triple asterisks (***) indicate p < 0.001. For B,C, and D see original publication by [http://journals.plos.org/plosbiology/article?id=10.1371/journal.pbio.0050156#pbio-0050156-st001 Xu et al., 2007][[#References|[13]]]]
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| ==Acquired Resistance==
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| While in many other types of bacteria drug resistance is gained through horizontal gene transfer by plasmids or transposons, in M. tuberculosis all strains with acquired resistance that are currently known are through chromosomal mutations due to the selective pressure of antibiotics. [[#References|[1]]] This selection of drug-resistant strains could not occur without the extensive and prolonged use of antibiotics necessary to treat the disease as those strains would have lower fitness under normal conditions. [[#References|[7]]] Additionally recent studies, such as that by Kohanski et al. [[#References|[10]]], have shown that sub-lethal doses of antibiotics can cause multi-drug resistance in E. Coli due to increased mutation rates by free radicals. This could very well apply to M. tuberculosis as well, suggesting that current TB drugs are not only selecting for drug-resistant strains but quite possibly creating them as well.
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| ==Promising New Drugs==
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| Benzothiazinones (BTZ)
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| Dinitrobenzamide derivatives (DNB)
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| In a study by Christophe et al. [[#References|[2]]] they used confocal fluorescence microscopy to conduct an assay on the phenotypic effects of various chemical compounds on M. tuberculosis. After infecting macrophages with mycobacteria that expressed [http://en.wikipedia.org/wiki/Green_fluorescent_protein Green fluorescent protein (GFP)] they monitored both amount of green fluorescent bacteria and host cell number. They used known anti-tuberculosis drug such as isoniazid and rifampin as controls and used [http://en.wikipedia.org/wiki/High-throughput_screening high-throughput screening] to test over 50,000 synthetic chemicals. Ultimately 135 were identified as potent inhibitors of mycobacteria in cells with no toxic effect on the host cells. Of these compounds dinitrobenzamide derivatives (DNB) were highly effective even against XDR strains of <i>M. tuberculosis</i>. They then studied the mechanism of inhibition of <i>M. tuberculosis</i> by DNB and claim that this will have wide therapeutic implications for finding drugs to combat XDR-TB.
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| ==Further Reading==
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| A database that contains information on known genetic mutations in <i>M. tuberculosis</i> that confer drug resistance in which you can search by drug class: https://tbdreamdb.ki.se/Data/DrugArea.aspx?AreaID=AMI
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| ==References==
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| 1. [http://www.ncbi.nlm.nih.gov/pubmed/21558086 Almeida Da Silva PE, Palomino JC. Molecular basis and mechanisms of drug resistance in mycobacterium tuberculosis: Classical and new drugs. J Antimicrob Chemother 2011 JUL;66(7):1417-30.]
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| 2. [http://journals.plos.org/plospathogens/article?id=10.1371/journal.ppat.1000645 Christophe T, Jackson M, Jeon HK, Fenistein D, Contreras-Dominguez M, Kim J, Genovesio A, Carralot J, Ewann F, Kim EH, et al. High content screening identifies decaprenyl-phosphoribose 2 ' epimerase as a target for intracellular antimycobacterial inhibitors. Plos Pathogens 2009 OCT;5(10):e1000645.]
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| 3. [http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0016869 Crellin PK, Brammananth R, Coppel RL (2011) Decaprenylphosphoryl-β-D-Ribose 2′-Epimerase, the Target of Benzothiazinones and Dinitrobenzamides, Is an Essential Enzyme in Mycobacterium smegmatis. PLoS ONE 6(2): e16869. doi:10.1371/journal.pone.0016869]
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| 4. [http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3623302/ Dinesh N, Sharma S, Balganesh M. Involvement of Efflux Pumps in the Resistance to Peptidoglycan Synthesis Inhibitors in Mycobacterium tuberculosis. Antimicrobial Agents and Chemotherapy. 2013;57(4):1941-1943. doi:10.1128/AAC.01957-12.]
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| 5. [http://www.ncbi.nlm.nih.gov/pubmed/?term=PCR-based+methodology+for+detecting+multidrug-resistant+strains+of+Mycobacterium+tuberculosis+Beijing+family+circulating+in+Russia. Mokrousov I, Otten T, Vyazovaya A, Limeschenko E, Filipenko M, Sola C, Rastogi N, Steklova L, Vyshnevskiy B, Narvskaya O. PCR-based methodology for detecting multidrug-resistant strains of mycobacterium tuberculosis beijing family circulating in russia. European Journal of Clinical Microbiology & Infectious Diseases 2003 JUN;22(6):342-8.]
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| 6. [http://www.ncbi.nlm.nih.gov/pubmed/?term=Mycobacterial+subversion+of+chemotherapeutic+reagents+and+host+defense+tactics%3A+challenges+in+tuberculosis+drug+development. Nguyen L, Pieters J. Mycobacterial subversion of chemotherapeutic reagents and host defense tactics: challenges in tuberculosis drug development. Annu Rev Pharmacol Toxicol. 2009;49:427-53. doi: 10.1146/annurev-pharmtox-061008-103123. Review. PubMed PMID: 19281311.]
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| 7. [http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3982203/#R117 Smith T, Wolff KA, Nguyen L. Molecular Biology of Drug Resistance in Mycobacterium tuberculosis. Current topics in microbiology and immunology. 2013;374:53-80. doi:10.1007/82_2012_279.]
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| 8. [http://www.ncbi.nlm.nih.gov/pubmed/25465521 Zhao L, Sun Q, Zeng C, Chen Y, Zhao B, Liu H, Xia Q, Zhao X, Jiao W, Li G, et al. Molecular characterisation of extensively drug-resistant mycobacterium tuberculosis isolates in china. Int J Antimicrob Agents 2015 FEB;45(2):137-43.]
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| 9. [http://www.ncbi.nlm.nih.gov/pubmed/25182646 Cui Z, Li Y, Cheng S, Yang H, Lu J, Hu Z, Ge B. Mutations in the embC-embA intergenic region contribute to mycobacterium tuberculosis resistance to ethambutol. Antimicrob Agents Chemother 2014 NOV;58(11):6837-43.]
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| 10. [http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2840266/ Kohanski MA, DePristo MA, Collins JJ. Sub-lethal antibiotic treatment leads to multidrug resistance via radical-induced mutagenesis. Molecular cell. 2010;37(3):311-320. doi:10.1016/j.molcel.2010.01.003.]
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| 11. [http://www.sciencemag.org/content/308/5727/1480.long Hegde SS, Vetting MW, Roderick SL, Mitchenall LA, Maxwell A, Takiff HE, Blanchard JS. 2005. A fluoroquinolone resistance protein from mycobacterium tuberculosis that mimics DNA. Science 308(5727):1480-3.]
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| 12. [http://www.ncbi.nlm.nih.gov/pubmed/21668514/ Viveiros M, Martins M, Rodrigues L, Machado D, Couto I, Ainsa J, Amaral L Inhibitors of mycobacterial efflux pumps as potential boosters for anti-tubercular drugs. Expert Rev Anti Infect Ther. 2012 Sep; 10(9):983-98.]
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| 13. [http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0119013#pone-0119013-t001 Li G, Zhang J, Guo Q, Jiang Y, Wei J, et al. (2015) Efflux Pump Gene Expression in Multidrug-Resistant Mycobacterium tuberculosis Clinical Isolates. PLoS ONE 10(2): e0119013. doi:10.1371/journal.pone.0119013]
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| Edited by (Noah Knowlton-Latkin), a student of [http://www.jsd.claremont.edu/faculty/profile.asp?FacultyID=254 Nora Sullivan] in BIOL168L (Microbiology) in [http://www.jsd.claremont.edu/ The Keck Science Department of the Claremont Colleges] Spring 2014.
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| <!--Do not edit or remove this line-->[[Category:Pages edited by students of Nora Sullivan at the Claremont Colleges]]
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