Minor contribution of mutations at <it>iniA </it>codon 501 and <it>embC-embA </it>intergenic region in ethambutol-resistant clinical <it>Mycobacterium tuberculosis </it>isolates in Kuwait

<p>Abstract</p> <p>Background</p> <p>Ethambutol (EMB) is a first-line drug for the treatment of tuberculosis (TB). Resistance to EMB in <it>Mycobacterium tuberculosis </it>isolates is mediated by mutations in several genes involved in arabinan synthesis nota...

Full description

Bibliographic Details
Main Authors: Ahmad Suhail, Jaber Al-Anoud, Mokaddas Eiman
Format: Article
Language:English
Published: BMC 2009-01-01
Series:Annals of Clinical Microbiology and Antimicrobials
Online Access:http://www.ann-clinmicrob.com/content/8/1/2
_version_ 1811260424102871040
author Ahmad Suhail
Jaber Al-Anoud
Mokaddas Eiman
author_facet Ahmad Suhail
Jaber Al-Anoud
Mokaddas Eiman
author_sort Ahmad Suhail
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>Ethambutol (EMB) is a first-line drug for the treatment of tuberculosis (TB). Resistance to EMB in <it>Mycobacterium tuberculosis </it>isolates is mediated by mutations in several genes involved in arabinan synthesis notably three <it>emb </it>(arabinosyl transferase) and <it>iniA </it>(isoniazid-inducible) genes. Most epidemiologically unrelated EMB-resistant <it>M. tuberculosis </it>strains contain mutations at <it>embB </it>codons 306, 406 and 497, <it>embC-embA </it>intergenic region (IGR) and <it>iniA </it>codon 501 (<it>iniA501</it>).</p> <p>Objective</p> <p>To develop a more comprehensive molecular screen for EMB-resistance detectioamong epidemiologically unrelated EMB-resistant <it>M. tuberculosis </it>strains previously analyzed for <it>embB </it>codon 306, 406 and 497 mutations by including analysis of mutations at <it>iniA501 </it>and in <it>embC-embA </it>IGR.</p> <p>Methods</p> <p>Fifty consecutive and phenotypically documented EMB-resistant and 25 pansusceptible <it>M. tuberculosis </it>strains isolated from 75 different TB patients over a four-year period in Kuwait were analyzed. Mutations at <it>iniA501 </it>were detected by PCR amplification followed by restriction fragment length polymorphism (RFLP) patterns generated with <it>Hpy </it>99 I. Direct DNA sequencing was used to confirm RFLP results and for detecting mutations in <it>embC-embA </it>IGR.</p> <p>Results</p> <p>Nearly same number of EMB-resistant <it>M. tuberculosis </it>strains were resistant to EMB alone and EMB together with additional resistance to rifampicin and isoniazid (9 of 50, 18% and 11 of 50, 22%, respectively). All the 25 pansusceptible strains contained wild-type sequences at <it>iniA501 </it>and in <it>embC-embA </it>IGR. The analysis of 50 EMB-resistant <it>M. tuberculosis </it>isolates showed that only one strain contained a mutated <it>iniA501 </it>while no mutation was detected in <it>embC-embA </it>IGR in any of the isolate.</p> <p>Conclusion</p> <p>Analysis of <it>iniA501 </it>and <it>embC-embA </it>IGR in epidemiologically unrelated EMB-resistant <it>M. tuberculosis </it>isolates in Kuwait indicate that mutations at these locations occur very infrequently and their inclusion for the development of a comprehensive molecular screen will make only minor contribution towards rapid EMB resistance detection.</p>
first_indexed 2024-04-12T18:47:09Z
format Article
id doaj.art-75a3ca16929948e0bdf0b72e9a3cec5f
institution Directory Open Access Journal
issn 1476-0711
language English
last_indexed 2024-04-12T18:47:09Z
publishDate 2009-01-01
publisher BMC
record_format Article
series Annals of Clinical Microbiology and Antimicrobials
spelling doaj.art-75a3ca16929948e0bdf0b72e9a3cec5f2022-12-22T03:20:35ZengBMCAnnals of Clinical Microbiology and Antimicrobials1476-07112009-01-0181210.1186/1476-0711-8-2Minor contribution of mutations at <it>iniA </it>codon 501 and <it>embC-embA </it>intergenic region in ethambutol-resistant clinical <it>Mycobacterium tuberculosis </it>isolates in KuwaitAhmad SuhailJaber Al-AnoudMokaddas Eiman<p>Abstract</p> <p>Background</p> <p>Ethambutol (EMB) is a first-line drug for the treatment of tuberculosis (TB). Resistance to EMB in <it>Mycobacterium tuberculosis </it>isolates is mediated by mutations in several genes involved in arabinan synthesis notably three <it>emb </it>(arabinosyl transferase) and <it>iniA </it>(isoniazid-inducible) genes. Most epidemiologically unrelated EMB-resistant <it>M. tuberculosis </it>strains contain mutations at <it>embB </it>codons 306, 406 and 497, <it>embC-embA </it>intergenic region (IGR) and <it>iniA </it>codon 501 (<it>iniA501</it>).</p> <p>Objective</p> <p>To develop a more comprehensive molecular screen for EMB-resistance detectioamong epidemiologically unrelated EMB-resistant <it>M. tuberculosis </it>strains previously analyzed for <it>embB </it>codon 306, 406 and 497 mutations by including analysis of mutations at <it>iniA501 </it>and in <it>embC-embA </it>IGR.</p> <p>Methods</p> <p>Fifty consecutive and phenotypically documented EMB-resistant and 25 pansusceptible <it>M. tuberculosis </it>strains isolated from 75 different TB patients over a four-year period in Kuwait were analyzed. Mutations at <it>iniA501 </it>were detected by PCR amplification followed by restriction fragment length polymorphism (RFLP) patterns generated with <it>Hpy </it>99 I. Direct DNA sequencing was used to confirm RFLP results and for detecting mutations in <it>embC-embA </it>IGR.</p> <p>Results</p> <p>Nearly same number of EMB-resistant <it>M. tuberculosis </it>strains were resistant to EMB alone and EMB together with additional resistance to rifampicin and isoniazid (9 of 50, 18% and 11 of 50, 22%, respectively). All the 25 pansusceptible strains contained wild-type sequences at <it>iniA501 </it>and in <it>embC-embA </it>IGR. The analysis of 50 EMB-resistant <it>M. tuberculosis </it>isolates showed that only one strain contained a mutated <it>iniA501 </it>while no mutation was detected in <it>embC-embA </it>IGR in any of the isolate.</p> <p>Conclusion</p> <p>Analysis of <it>iniA501 </it>and <it>embC-embA </it>IGR in epidemiologically unrelated EMB-resistant <it>M. tuberculosis </it>isolates in Kuwait indicate that mutations at these locations occur very infrequently and their inclusion for the development of a comprehensive molecular screen will make only minor contribution towards rapid EMB resistance detection.</p>http://www.ann-clinmicrob.com/content/8/1/2
spellingShingle Ahmad Suhail
Jaber Al-Anoud
Mokaddas Eiman
Minor contribution of mutations at <it>iniA </it>codon 501 and <it>embC-embA </it>intergenic region in ethambutol-resistant clinical <it>Mycobacterium tuberculosis </it>isolates in Kuwait
Annals of Clinical Microbiology and Antimicrobials
title Minor contribution of mutations at <it>iniA </it>codon 501 and <it>embC-embA </it>intergenic region in ethambutol-resistant clinical <it>Mycobacterium tuberculosis </it>isolates in Kuwait
title_full Minor contribution of mutations at <it>iniA </it>codon 501 and <it>embC-embA </it>intergenic region in ethambutol-resistant clinical <it>Mycobacterium tuberculosis </it>isolates in Kuwait
title_fullStr Minor contribution of mutations at <it>iniA </it>codon 501 and <it>embC-embA </it>intergenic region in ethambutol-resistant clinical <it>Mycobacterium tuberculosis </it>isolates in Kuwait
title_full_unstemmed Minor contribution of mutations at <it>iniA </it>codon 501 and <it>embC-embA </it>intergenic region in ethambutol-resistant clinical <it>Mycobacterium tuberculosis </it>isolates in Kuwait
title_short Minor contribution of mutations at <it>iniA </it>codon 501 and <it>embC-embA </it>intergenic region in ethambutol-resistant clinical <it>Mycobacterium tuberculosis </it>isolates in Kuwait
title_sort minor contribution of mutations at it inia it codon 501 and it embc emba it intergenic region in ethambutol resistant clinical it mycobacterium tuberculosis it isolates in kuwait
url http://www.ann-clinmicrob.com/content/8/1/2
work_keys_str_mv AT ahmadsuhail minorcontributionofmutationsatitiniaitcodon501anditembcembaitintergenicregioninethambutolresistantclinicalitmycobacteriumtuberculosisitisolatesinkuwait
AT jaberalanoud minorcontributionofmutationsatitiniaitcodon501anditembcembaitintergenicregioninethambutolresistantclinicalitmycobacteriumtuberculosisitisolatesinkuwait
AT mokaddaseiman minorcontributionofmutationsatitiniaitcodon501anditembcembaitintergenicregioninethambutolresistantclinicalitmycobacteriumtuberculosisitisolatesinkuwait