Deciphering the sequential events during in vivo acquisition of drug resistance in Mycobacterium tuberculosis
Abstract Tuberculosis (TB) is caused by Mycobacterium tuberculosis (MTB) and the disease has remained a major health problem in most of the developing countries, particularly after the emergence of multidrug-resistant TB (MDR-TB). The MDR-TB is an intriguing subject and very little is known about th...
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Published in | International journal of mycobacteriology Vol. 3; no. 1; pp. 36 - 40 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Netherlands
Wolters Kluwer Medknow Publications
2014
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Online Access | Get full text |
ISSN | 2212-5531 2212-554X 2212-554X |
DOI | 10.1016/j.ijmyco.2013.10.006 |
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Abstract | Abstract Tuberculosis (TB) is caused by Mycobacterium tuberculosis (MTB) and the disease has remained a major health problem in most of the developing countries, particularly after the emergence of multidrug-resistant TB (MDR-TB). The MDR-TB is an intriguing subject and very little is known about the in vivo processes which take place during the acquisition of MDR. This study describes a unique case of pulmonary TB (PTB) from which four sequential isolates of MTB could be isolated while the patient was on anti-tubercular treatment. The first baseline isolate was sensitive to all drugs, but the subsequent three isolates acquired resistance to multiple drugs and finally the patient died after 27 months post-diagnosis when his fourth isolate became resistant to isoniazid, rifampicin, ethambutol and kanamycin. All sequential cultures were identified as MTB using conventional and molecular methods, including 16s RNA sequencing and the spoligotyping. Spoligotyping followed by comparison with SITVITWEB database revealed that all the isolates belonged to the family of the Central Asian Strain Delhi (CAS1_Delhi, ST26) genotype, and no cross or mixed infections were observed. The drug resistance was further characterized at the molecular level by sequencing the target genes ( katG , inhA , rpoB , embB , eis promoter region and rrs ). The results revealed mutated alleles associated with resistance to the respective drugs. This unique case indicates that it is possible to isolate MTB during treatment if the strain is acquiring resistance. The data presented from four sequential isolates provides an insight into what sequential genetic and proteomic changes occur in the bacteria during the in vivo acquisition of MDR. |
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AbstractList | Abstract Tuberculosis (TB) is caused by Mycobacterium tuberculosis (MTB) and the disease has remained a major health problem in most of the developing countries, particularly after the emergence of multidrug-resistant TB (MDR-TB). The MDR-TB is an intriguing subject and very little is known about the in vivo processes which take place during the acquisition of MDR. This study describes a unique case of pulmonary TB (PTB) from which four sequential isolates of MTB could be isolated while the patient was on anti-tubercular treatment. The first baseline isolate was sensitive to all drugs, but the subsequent three isolates acquired resistance to multiple drugs and finally the patient died after 27 months post-diagnosis when his fourth isolate became resistant to isoniazid, rifampicin, ethambutol and kanamycin. All sequential cultures were identified as MTB using conventional and molecular methods, including 16s RNA sequencing and the spoligotyping. Spoligotyping followed by comparison with SITVITWEB database revealed that all the isolates belonged to the family of the Central Asian Strain Delhi (CAS1_Delhi, ST26) genotype, and no cross or mixed infections were observed. The drug resistance was further characterized at the molecular level by sequencing the target genes ( katG , inhA , rpoB , embB , eis promoter region and rrs ). The results revealed mutated alleles associated with resistance to the respective drugs. This unique case indicates that it is possible to isolate MTB during treatment if the strain is acquiring resistance. The data presented from four sequential isolates provides an insight into what sequential genetic and proteomic changes occur in the bacteria during the in vivo acquisition of MDR. Tuberculosis (TB) is caused by Mycobacterium tuberculosis (MTB) and the disease has remained a major health problem in most of the developing countries, particularly after the emergence of multidrug-resistant TB (MDR-TB). The MDR-TB is an intriguing subject and very little is known about the in vivo processes which take place during the acquisition of MDR. This study describes a unique case of pulmonary TB (PTB) from which four sequential isolates of MTB could be isolated while the patient was on anti-tubercular treatment. The first baseline isolate was sensitive to all drugs, but the subsequent three isolates acquired resistance to multiple drugs and finally the patient died after 27months post-diagnosis when his fourth isolate became resistant to isoniazid, rifampicin, ethambutol and kanamycin. All sequential cultures were identified as MTB using conventional and molecular methods, including 16s RNA sequencing and the spoligotyping. Spoligotyping followed by comparison with SITVITWEB database revealed that all the isolates belonged to the family of the Central Asian Strain Delhi (CAS1_Delhi, ST26) genotype, and no cross or mixed infections were observed. The drug resistance was further characterized at the molecular level by sequencing the target genes (katG, inhA, rpoB, embB, eis promoter region and rrs). The results revealed mutated alleles associated with resistance to the respective drugs. This unique case indicates that it is possible to isolate MTB during treatment if the strain is acquiring resistance. The data presented from four sequential isolates provides an insight into what sequential genetic and proteomic changes occur in the bacteria during the in vivo acquisition of MDR.Tuberculosis (TB) is caused by Mycobacterium tuberculosis (MTB) and the disease has remained a major health problem in most of the developing countries, particularly after the emergence of multidrug-resistant TB (MDR-TB). The MDR-TB is an intriguing subject and very little is known about the in vivo processes which take place during the acquisition of MDR. This study describes a unique case of pulmonary TB (PTB) from which four sequential isolates of MTB could be isolated while the patient was on anti-tubercular treatment. The first baseline isolate was sensitive to all drugs, but the subsequent three isolates acquired resistance to multiple drugs and finally the patient died after 27months post-diagnosis when his fourth isolate became resistant to isoniazid, rifampicin, ethambutol and kanamycin. All sequential cultures were identified as MTB using conventional and molecular methods, including 16s RNA sequencing and the spoligotyping. Spoligotyping followed by comparison with SITVITWEB database revealed that all the isolates belonged to the family of the Central Asian Strain Delhi (CAS1_Delhi, ST26) genotype, and no cross or mixed infections were observed. The drug resistance was further characterized at the molecular level by sequencing the target genes (katG, inhA, rpoB, embB, eis promoter region and rrs). The results revealed mutated alleles associated with resistance to the respective drugs. This unique case indicates that it is possible to isolate MTB during treatment if the strain is acquiring resistance. The data presented from four sequential isolates provides an insight into what sequential genetic and proteomic changes occur in the bacteria during the in vivo acquisition of MDR. Tuberculosis (TB) is caused by Mycobacterium tuberculosis (MTB) and the disease has remained a major health problem in most of the developing countries, particularly after the emergence of multidrug-resistant TB (MDR-TB). The MDR-TB is an intriguing subject and very little is known about the in vivo processes which take place during the acquisition of MDR. This study describes a unique case of pulmonary TB (PTB) from which four sequential isolates of MTB could be isolated while the patient was on anti-tubercular treatment. The first baseline isolate was sensitive to all drugs, but the subsequent three isolates acquired resistance to multiple drugs and finally the patient died after 27 months post-diagnosis when his fourth isolate became resistant to isoniazid, rifampicin, ethambutol and kanamycin. All sequential cultures were identified as MTB using conventional and molecular methods, including 16s RNA sequencing and the spoligotyping. Spoligotyping followed by comparison with SITVITWEB database revealed that all the isolates belonged to the family of the Central Asian Strain Delhi (CAS1_Delhi, ST26) genotype, and no cross or mixed infections were observed. The drug resistance was further characterized at the molecular level by sequencing the target genes (katG, inhA, rpoB, embB, eis promoter region and rrs). The results revealed mutated alleles associated with resistance to the respective drugs. This unique case indicates that it is possible to isolate MTB during treatment if the strain is acquiring resistance. The data presented from four sequential isolates provides an insight into what sequential genetic and proteomic changes occur in the bacteria during the in vivo acquisition of MDR. Tuberculosis (TB) is caused by Mycobacterium tuberculosis (MTB) and the disease has remained a major health problem in most of the developing countries, particularly after the emergence of multidrug-resistant TB (MDR-TB). The MDR-TB is an intriguing subject and very little is known about the in vivo processes which take place during the acquisition of MDR. This study describes a unique case of pulmonary TB (PTB) from which four sequential isolates of MTB could be isolated while the patient was on anti-tubercular treatment. The first baseline isolate was sensitive to all drugs, but the subsequent three isolates acquired resistance to multiple drugs and finally the patient died after 27months post-diagnosis when his fourth isolate became resistant to isoniazid, rifampicin, ethambutol and kanamycin. All sequential cultures were identified as MTB using conventional and molecular methods, including 16s RNA sequencing and the spoligotyping. Spoligotyping followed by comparison with SITVITWEB database revealed that all the isolates belonged to the family of the Central Asian Strain Delhi (CAS1_Delhi, ST26) genotype, and no cross or mixed infections were observed. The drug resistance was further characterized at the molecular level by sequencing the target genes (katG, inhA, rpoB, embB, eis promoter region and rrs). The results revealed mutated alleles associated with resistance to the respective drugs. This unique case indicates that it is possible to isolate MTB during treatment if the strain is acquiring resistance. The data presented from four sequential isolates provides an insight into what sequential genetic and proteomic changes occur in the bacteria during the in vivo acquisition of MDR. |
Author | Gopinath, Krishnamoorthy Singh, Amit Singh, Sarman Singh, Niti |
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Cites_doi | 10.1128/AAC.00851-09 10.1016/j.jinf.2011.01.003 10.1371/journal.pone.0004540 10.1128/JCM.31.2.406-409.1993 10.1002/jcla.20264 10.1016/j.meegid.2012.02.004 10.3201/10.3201/eid0703.0107304 10.1128/AAC.41.10.2270 10.1093/infdis/jis601 10.1128/JCM.40.12.4435-4438.2002 10.1186/1477-5956-10-14 10.1016/j.resmic.2005.01.005 10.1128/JCM.01392-06 10.1186/1477-5956-8-59 10.1016/j.pupt.2013.01.003 10.1073/pnas.0907925106 10.1111/j.1365-2672.2009.04218.x 10.1054/tube.2002.0332 10.1097/QCO.0b013e3283210020 10.1186/1471-2180-6-23 |
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References | Demay (10.1016/j.ijmyco.2013.10.006_b0065) 2012; 12 Saunders (10.1016/j.ijmyco.2013.10.006_b0105) 2011; 62 Singhal (10.1016/j.ijmyco.2013.10.006_b0100) 2012; 10 Jugheli (10.1016/j.ijmyco.2013.10.006_b0085) 2009; 53 Alcaide (10.1016/j.ijmyco.2013.10.006_b0080) 1997; 41 Singh (10.1016/j.ijmyco.2013.10.006_b0040) 2008; 22 Cavusoglu (10.1016/j.ijmyco.2013.10.006_b0075) 2002; 40 Sun (10.1016/j.ijmyco.2013.10.006_b0110) 2012; 206 Gopinath (10.1016/j.ijmyco.2013.10.006_b0035) 2009; 107 Zaunbrecher (10.1016/j.ijmyco.2013.10.006_b0090) 2009; 106 Sola (10.1016/j.ijmyco.2013.10.006_b0025) 2001; 7 Brudey (10.1016/j.ijmyco.2013.10.006_b0060) 2006; 6 Supply (10.1016/j.ijmyco.2013.10.006_b0070) 2006; 44 Shenoi (10.1016/j.ijmyco.2013.10.006_b0010) 2009; 22 Kulkarni (10.1016/j.ijmyco.2013.10.006_b0020) 2005; 156 10.1016/j.ijmyco.2013.10.006_b0005 Vijaya-Bhanu (10.1016/j.ijmyco.2013.10.006_b0115) 2002; 82 Kumar (10.1016/j.ijmyco.2013.10.006_b0050) 2013; 26 van Embden (10.1016/j.ijmyco.2013.10.006_b0055) 1993; 31 Stavrum (10.1016/j.ijmyco.2013.10.006_b0030) 2009; 4 Sharma (10.1016/j.ijmyco.2013.10.006_b0095) 2010; 8 Kent (10.1016/j.ijmyco.2013.10.006_b0045) 1985 |
References_xml | – volume: 53 start-page: 5064 year: 2009 ident: 10.1016/j.ijmyco.2013.10.006_b0085 article-title: High level of cross-resistance between kanamycin, amikacin, and capreomycin among Mycobacterium tuberculosis isolates from Georgia and a close relation with mutations in the rrs gene publication-title: Antimicrob. Agents Chemother. doi: 10.1128/AAC.00851-09 – volume: 62 start-page: 212 year: 2011 ident: 10.1016/j.ijmyco.2013.10.006_b0105 article-title: Deep re-sequencing of serial sputum isolates of Mycobacterium tuberculosis during therapeutic failure due to poor compliance reveals stepwise mutation of key resistance genes on an otherwise stable genetic background publication-title: J. Infect. doi: 10.1016/j.jinf.2011.01.003 – volume: 4 start-page: e4540 year: 2009 ident: 10.1016/j.ijmyco.2013.10.006_b0030 article-title: In-depth molecular characterization of Mycobacterium tuberculosis from New Delhi – predominance of drug resistant isolates of the “Modern” (TbD12) Type publication-title: PLoS ONE doi: 10.1371/journal.pone.0004540 – volume: 31 start-page: 406 year: 1993 ident: 10.1016/j.ijmyco.2013.10.006_b0055 article-title: Strain identification of Mycobacterium tuberculosis by DNA fingerprinting: recommendations for a standardized methodology publication-title: J. Clin. Microbiol. doi: 10.1128/JCM.31.2.406-409.1993 – volume: 22 start-page: 367 year: 2008 ident: 10.1016/j.ijmyco.2013.10.006_b0040 article-title: Comparative evaluation of Fast-Plaque assay with PCR and other conventional in-vitro diagnostic methods for the early detection of Pulmonary Tuberculosis publication-title: J. Clin. Lab. Analys. doi: 10.1002/jcla.20264 – volume: 12 start-page: 755 year: 2012 ident: 10.1016/j.ijmyco.2013.10.006_b0065 article-title: SITVITWEB a publicly available international multimarker database for studying Mycobacterium tuberculosis genetic diversity and molecular epidemiology publication-title: Infect. Genet. Evol. doi: 10.1016/j.meegid.2012.02.004 – volume: 7 start-page: 390 year: 2001 ident: 10.1016/j.ijmyco.2013.10.006_b0025 article-title: Spoligotype database of Mycobacterium tuberculosis: biogeographical distribution of shared types and epidemiological and phylogenetic perspectives publication-title: Emerg. Inf. Dis. doi: 10.3201/10.3201/eid0703.0107304 – volume: 41 start-page: 2270 year: 1997 ident: 10.1016/j.ijmyco.2013.10.006_b0080 article-title: Role of embB in natural and acquired resistance to ethambutol in mycobacteria publication-title: Antimicrob. Agents Chemother. doi: 10.1128/AAC.41.10.2270 – volume: 206 start-page: 1724 year: 2012 ident: 10.1016/j.ijmyco.2013.10.006_b0110 article-title: Dynamic population changes in Mycobacterium tuberculosis during acquisition and fixation of drug resistance in patients publication-title: J. Infect. Dis. doi: 10.1093/infdis/jis601 – volume: 40 start-page: 4435 year: 2002 ident: 10.1016/j.ijmyco.2013.10.006_b0075 article-title: Characterization of rpoB mutations in rifampin-resistant clinical isolates of Mycobacterium tuberculosis from Turkey by DNA sequencing and line probe assay publication-title: J Clin. Microbiol. doi: 10.1128/JCM.40.12.4435-4438.2002 – volume: 10 start-page: 14 year: 2012 ident: 10.1016/j.ijmyco.2013.10.006_b0100 article-title: Analysis of intracellular expressed proteins of Mycobacterium tuberculosis clinical isolates publication-title: Proteome Sci. doi: 10.1186/1477-5956-10-14 – volume: 156 start-page: 588 year: 2005 ident: 10.1016/j.ijmyco.2013.10.006_b0020 article-title: Spoligotyping of Mycobacterium tuberculosis isolates from patients with pulmonary tuberculosis in Mumbai, India publication-title: Res. Microbiol. doi: 10.1016/j.resmic.2005.01.005 – volume: 44 start-page: 4498 year: 2006 ident: 10.1016/j.ijmyco.2013.10.006_b0070 article-title: Proposal for standardization of optimized mycobacterial interspersed repetitive unit-variable-number tandem repeat typing of Mycobacterium tuberculosis publication-title: J. Clin. Microbiol. doi: 10.1128/JCM.01392-06 – volume: 8 start-page: 59 year: 2010 ident: 10.1016/j.ijmyco.2013.10.006_b0095 article-title: Proteomic analysis of streptomycin resistant and sensitive clinical isolates of Mycobacterium tuberculosis publication-title: Proteome Sci. doi: 10.1186/1477-5956-8-59 – volume: 26 start-page: 332 year: 2013 ident: 10.1016/j.ijmyco.2013.10.006_b0050 article-title: Anti-mycobacterial activity of plumericin and isoplumericin against MDR Mycobacterium tuberculosis publication-title: Pulm. Pharmacol. Ther. doi: 10.1016/j.pupt.2013.01.003 – volume: 106 start-page: 20004 year: 2009 ident: 10.1016/j.ijmyco.2013.10.006_b0090 article-title: Overexpression of the chromosomally encoded aminoglycoside acetyltransferase eis confers kanamycin resistance in Mycobacterium tuberculosis publication-title: Proc. Natl. Acad. Sci. USA doi: 10.1073/pnas.0907925106 – volume: 107 start-page: 425 year: 2009 ident: 10.1016/j.ijmyco.2013.10.006_b0035 article-title: Multiplex PCR assay for simultaneous detection and differentiation of Mycobacterium tuberculosis, M. avium complexes, and other mycobacterial species directly from clinical specimen publication-title: J. Appl. Microbiol. doi: 10.1111/j.1365-2672.2009.04218.x – volume: 82 start-page: 105 year: 2002 ident: 10.1016/j.ijmyco.2013.10.006_b0115 article-title: Predominance of a novel Mycobacterium tuberculosis genotype in the Delhi region of India publication-title: Tuberculosis doi: 10.1054/tube.2002.0332 – year: 1985 ident: 10.1016/j.ijmyco.2013.10.006_b0045 – ident: 10.1016/j.ijmyco.2013.10.006_b0005 – volume: 22 start-page: 11 year: 2009 ident: 10.1016/j.ijmyco.2013.10.006_b0010 article-title: Multidrug-resistant and extensively drug-resistant tuberculosis: consequences for the global HIV community publication-title: Curr. Opin. Infect. Dis. doi: 10.1097/QCO.0b013e3283210020 – volume: 6 start-page: 23 year: 2006 ident: 10.1016/j.ijmyco.2013.10.006_b0060 article-title: Mycobacterium tuberculosis complex genetic diversity: mining the fourth international spoligotyping database (SpolDB4) for classification, population genetics and epidemiology publication-title: BMC Microbiol. doi: 10.1186/1471-2180-6-23 |
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Snippet | Abstract Tuberculosis (TB) is caused by Mycobacterium tuberculosis (MTB) and the disease has remained a major health problem in most of the developing... Tuberculosis (TB) is caused by Mycobacterium tuberculosis (MTB) and the disease has remained a major health problem in most of the developing countries,... |
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Title | Deciphering the sequential events during in vivo acquisition of drug resistance in Mycobacterium tuberculosis |
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