Cargando…
Distribution of common and rare drug resistance patterns in Mycobacterium tuberculosis clinical isolates revealed by GenoType MTBDRplus and MTBDRsl assay
BACKGROUND: Tuberculosis (TB) remains a significant global health emergency caused by Mycobacterium tuberculosis (Mtb). The epidemiology, transmission, genotypes, mutational patterns, and clinical consequences of TB have been extensively studied worldwide, however, there is a lack of information reg...
Autores principales: | , , , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10636455/ https://www.ncbi.nlm.nih.gov/pubmed/37969306 http://dx.doi.org/10.21037/jtd-23-138 |
_version_ | 1785146435016065024 |
---|---|
author | Khan, Zafran Zhu, Yuting Guan, Ping Peng, Jiacong Su, Biyi Ma, Shangming Ualiyeva, Daniya Jamal, Khalid Yusuf, Buhari Ding, Jie Sapkota, Sanjeep Hameed, H. M. Adnan Tan, Yaoju Lin, Yongping Hu, Jinxing Liu, Jianxiong Zhang, Tianyu |
author_facet | Khan, Zafran Zhu, Yuting Guan, Ping Peng, Jiacong Su, Biyi Ma, Shangming Ualiyeva, Daniya Jamal, Khalid Yusuf, Buhari Ding, Jie Sapkota, Sanjeep Hameed, H. M. Adnan Tan, Yaoju Lin, Yongping Hu, Jinxing Liu, Jianxiong Zhang, Tianyu |
author_sort | Khan, Zafran |
collection | PubMed |
description | BACKGROUND: Tuberculosis (TB) remains a significant global health emergency caused by Mycobacterium tuberculosis (Mtb). The epidemiology, transmission, genotypes, mutational patterns, and clinical consequences of TB have been extensively studied worldwide, however, there is a lack of information regarding the epidemiology and mutational patterns of Mtb in Pakistan, specifically concerning the prevalence of multi-drug resistant TB (MDR-TB). METHODS: This study aimed to investigate the incidence of Mtb and associated mutational patterns using the line probe assay (LPA). Previous studies have reported a high frequency of mutations in the rpoB, inhA, and katG genes, which are associated with resistance to rifampicin (RIF) and isoniazid (INH). Therefore, the current study utilized LPA to detect mutations in the rpoB, katG, and inhA genes to identify multi-drug resistant Mtb. RESULTS: LPA analysis of a large pool of Mtb isolates, including samples from 241 sputum-positive patients, revealed that 34.85% of isolates were identified as MDR-TB, consistent with reports from various regions worldwide. The most prevalent mutations observed were rpoB S531L and inhA promoter C15T, which were associated with resistance to RIF and INH, respectively. CONCLUSIONS: This study highlights the effectiveness of GenoType MTBDRplus and MTBDRsl assays as valuable tools for TB management. These assays enable rapid detection of resistance to RIF, INH, and fluoroquinolones (FQs) in Mtb clinical isolates, surpassing the limitations of solid and liquid media-based methods. The findings contribute to our understanding of MDR-TB epidemiology and provide insights into the genetic profiles of Mtb in Pakistan, which are essential for effective TB control strategies. |
format | Online Article Text |
id | pubmed-10636455 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-106364552023-11-15 Distribution of common and rare drug resistance patterns in Mycobacterium tuberculosis clinical isolates revealed by GenoType MTBDRplus and MTBDRsl assay Khan, Zafran Zhu, Yuting Guan, Ping Peng, Jiacong Su, Biyi Ma, Shangming Ualiyeva, Daniya Jamal, Khalid Yusuf, Buhari Ding, Jie Sapkota, Sanjeep Hameed, H. M. Adnan Tan, Yaoju Lin, Yongping Hu, Jinxing Liu, Jianxiong Zhang, Tianyu J Thorac Dis Original Article BACKGROUND: Tuberculosis (TB) remains a significant global health emergency caused by Mycobacterium tuberculosis (Mtb). The epidemiology, transmission, genotypes, mutational patterns, and clinical consequences of TB have been extensively studied worldwide, however, there is a lack of information regarding the epidemiology and mutational patterns of Mtb in Pakistan, specifically concerning the prevalence of multi-drug resistant TB (MDR-TB). METHODS: This study aimed to investigate the incidence of Mtb and associated mutational patterns using the line probe assay (LPA). Previous studies have reported a high frequency of mutations in the rpoB, inhA, and katG genes, which are associated with resistance to rifampicin (RIF) and isoniazid (INH). Therefore, the current study utilized LPA to detect mutations in the rpoB, katG, and inhA genes to identify multi-drug resistant Mtb. RESULTS: LPA analysis of a large pool of Mtb isolates, including samples from 241 sputum-positive patients, revealed that 34.85% of isolates were identified as MDR-TB, consistent with reports from various regions worldwide. The most prevalent mutations observed were rpoB S531L and inhA promoter C15T, which were associated with resistance to RIF and INH, respectively. CONCLUSIONS: This study highlights the effectiveness of GenoType MTBDRplus and MTBDRsl assays as valuable tools for TB management. These assays enable rapid detection of resistance to RIF, INH, and fluoroquinolones (FQs) in Mtb clinical isolates, surpassing the limitations of solid and liquid media-based methods. The findings contribute to our understanding of MDR-TB epidemiology and provide insights into the genetic profiles of Mtb in Pakistan, which are essential for effective TB control strategies. AME Publishing Company 2023-10-08 2023-10-31 /pmc/articles/PMC10636455/ /pubmed/37969306 http://dx.doi.org/10.21037/jtd-23-138 Text en 2023 Journal of Thoracic Disease. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Original Article Khan, Zafran Zhu, Yuting Guan, Ping Peng, Jiacong Su, Biyi Ma, Shangming Ualiyeva, Daniya Jamal, Khalid Yusuf, Buhari Ding, Jie Sapkota, Sanjeep Hameed, H. M. Adnan Tan, Yaoju Lin, Yongping Hu, Jinxing Liu, Jianxiong Zhang, Tianyu Distribution of common and rare drug resistance patterns in Mycobacterium tuberculosis clinical isolates revealed by GenoType MTBDRplus and MTBDRsl assay |
title | Distribution of common and rare drug resistance patterns in Mycobacterium tuberculosis clinical isolates revealed by GenoType MTBDRplus and MTBDRsl assay |
title_full | Distribution of common and rare drug resistance patterns in Mycobacterium tuberculosis clinical isolates revealed by GenoType MTBDRplus and MTBDRsl assay |
title_fullStr | Distribution of common and rare drug resistance patterns in Mycobacterium tuberculosis clinical isolates revealed by GenoType MTBDRplus and MTBDRsl assay |
title_full_unstemmed | Distribution of common and rare drug resistance patterns in Mycobacterium tuberculosis clinical isolates revealed by GenoType MTBDRplus and MTBDRsl assay |
title_short | Distribution of common and rare drug resistance patterns in Mycobacterium tuberculosis clinical isolates revealed by GenoType MTBDRplus and MTBDRsl assay |
title_sort | distribution of common and rare drug resistance patterns in mycobacterium tuberculosis clinical isolates revealed by genotype mtbdrplus and mtbdrsl assay |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10636455/ https://www.ncbi.nlm.nih.gov/pubmed/37969306 http://dx.doi.org/10.21037/jtd-23-138 |
work_keys_str_mv | AT khanzafran distributionofcommonandraredrugresistancepatternsinmycobacteriumtuberculosisclinicalisolatesrevealedbygenotypemtbdrplusandmtbdrslassay AT zhuyuting distributionofcommonandraredrugresistancepatternsinmycobacteriumtuberculosisclinicalisolatesrevealedbygenotypemtbdrplusandmtbdrslassay AT guanping distributionofcommonandraredrugresistancepatternsinmycobacteriumtuberculosisclinicalisolatesrevealedbygenotypemtbdrplusandmtbdrslassay AT pengjiacong distributionofcommonandraredrugresistancepatternsinmycobacteriumtuberculosisclinicalisolatesrevealedbygenotypemtbdrplusandmtbdrslassay AT subiyi distributionofcommonandraredrugresistancepatternsinmycobacteriumtuberculosisclinicalisolatesrevealedbygenotypemtbdrplusandmtbdrslassay AT mashangming distributionofcommonandraredrugresistancepatternsinmycobacteriumtuberculosisclinicalisolatesrevealedbygenotypemtbdrplusandmtbdrslassay AT ualiyevadaniya distributionofcommonandraredrugresistancepatternsinmycobacteriumtuberculosisclinicalisolatesrevealedbygenotypemtbdrplusandmtbdrslassay AT jamalkhalid distributionofcommonandraredrugresistancepatternsinmycobacteriumtuberculosisclinicalisolatesrevealedbygenotypemtbdrplusandmtbdrslassay AT yusufbuhari distributionofcommonandraredrugresistancepatternsinmycobacteriumtuberculosisclinicalisolatesrevealedbygenotypemtbdrplusandmtbdrslassay AT dingjie distributionofcommonandraredrugresistancepatternsinmycobacteriumtuberculosisclinicalisolatesrevealedbygenotypemtbdrplusandmtbdrslassay AT sapkotasanjeep distributionofcommonandraredrugresistancepatternsinmycobacteriumtuberculosisclinicalisolatesrevealedbygenotypemtbdrplusandmtbdrslassay AT hameedhmadnan distributionofcommonandraredrugresistancepatternsinmycobacteriumtuberculosisclinicalisolatesrevealedbygenotypemtbdrplusandmtbdrslassay AT tanyaoju distributionofcommonandraredrugresistancepatternsinmycobacteriumtuberculosisclinicalisolatesrevealedbygenotypemtbdrplusandmtbdrslassay AT linyongping distributionofcommonandraredrugresistancepatternsinmycobacteriumtuberculosisclinicalisolatesrevealedbygenotypemtbdrplusandmtbdrslassay AT hujinxing distributionofcommonandraredrugresistancepatternsinmycobacteriumtuberculosisclinicalisolatesrevealedbygenotypemtbdrplusandmtbdrslassay AT liujianxiong distributionofcommonandraredrugresistancepatternsinmycobacteriumtuberculosisclinicalisolatesrevealedbygenotypemtbdrplusandmtbdrslassay AT zhangtianyu distributionofcommonandraredrugresistancepatternsinmycobacteriumtuberculosisclinicalisolatesrevealedbygenotypemtbdrplusandmtbdrslassay |