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Detection of Isoniazid and Rifampin Resistance in Mycobacterium tuberculosis Clinical Isolates from Sputum Samples by High-Resolution Melting Analysis
The effective management of multidrug-resistant tuberculosis (MDR-TB) and the need for rapid and accurate screening of rifampin (RIF) and isoniazid (INH)-resistant Mycobacterium tuberculosis (Mtb) isolates are the most fundamental and difficult challenges facing the global TB control. The present st...
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Published in: | Current microbiology 2022-09, Vol.79 (9), p.257-257, Article 257 |
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creator | Parsa, Shadi Yaghoubi, Atieh Izadi, Nafiseh Sabet, Faezeh Nik, Leila babaei Derakhshan, Mohammad Rezaee, Seyed Abdolrahim Meshkat, Zahra Hoseini, Seyed Javad Jmehdar, Saeid Amel Kiani, Fatemeh Samiei, Amin Soleimanpour, Saman |
description | The effective management of multidrug-resistant tuberculosis (MDR-TB) and the need for rapid and accurate screening of rifampin (RIF) and isoniazid (INH)-resistant
Mycobacterium tuberculosis
(Mtb) isolates are the most fundamental and difficult challenges facing the global TB control. The present study aimed to compare the diagnostic accuracy of high-resolution melting-curve analysis (HRMA) in comparison to multiplex allele-specific PCR (MAS-PCR) and xpert MTB/RIF as well as the conventional drug-susceptibility test (DST) and gene sequencing for the detection of INH and RIF resistance in the Mtb isolates. In the present study, a total of 431
Mtb
isolates including 11 MDR (%2.55), 7 INH resistance (%1.62), two RIF resistance (%0.46), and 411 sensitive isolates were phenotypically confirmed. HRMA assay identified
katG
gene mutations and the
mabA-inhA
promoter region in 15 of 18 INH-resistant samples and
rpoB
gene mutations were successfully evaluated in 11 out of 13 RIF-resistant samples. The sensitivity and specificity of the HRMA method were 83.3% and 98.8% for INH and 84.6% and 99% for RIF, respectively. The most common mutation in RIF-resistance-determining region (RRDR) occurred at codon 531 (TCG → TTG)(84.6%) and then at codon 513 (CAA → GTA)(7.6%) and 526 (CAC → TAC) (7.6%), which resulted in the amino-acid changes. Also, 88.8% of INH-resistant samples had mutations in the
katG
gene and the
mabA-inhA
promoter region, of which the highest mutation occurred at codon 315 (AGC → ACC) of the
katG
gene. In conclusion, all these results indicated that the sensitivity and specificity of the HRM method were increased when the
katG
gene and the
mabA-inhA
promoter region were used as a target. |
doi_str_mv | 10.1007/s00284-022-02960-z |
format | article |
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Mycobacterium tuberculosis
(Mtb) isolates are the most fundamental and difficult challenges facing the global TB control. The present study aimed to compare the diagnostic accuracy of high-resolution melting-curve analysis (HRMA) in comparison to multiplex allele-specific PCR (MAS-PCR) and xpert MTB/RIF as well as the conventional drug-susceptibility test (DST) and gene sequencing for the detection of INH and RIF resistance in the Mtb isolates. In the present study, a total of 431
Mtb
isolates including 11 MDR (%2.55), 7 INH resistance (%1.62), two RIF resistance (%0.46), and 411 sensitive isolates were phenotypically confirmed. HRMA assay identified
katG
gene mutations and the
mabA-inhA
promoter region in 15 of 18 INH-resistant samples and
rpoB
gene mutations were successfully evaluated in 11 out of 13 RIF-resistant samples. The sensitivity and specificity of the HRMA method were 83.3% and 98.8% for INH and 84.6% and 99% for RIF, respectively. The most common mutation in RIF-resistance-determining region (RRDR) occurred at codon 531 (TCG → TTG)(84.6%) and then at codon 513 (CAA → GTA)(7.6%) and 526 (CAC → TAC) (7.6%), which resulted in the amino-acid changes. Also, 88.8% of INH-resistant samples had mutations in the
katG
gene and the
mabA-inhA
promoter region, of which the highest mutation occurred at codon 315 (AGC → ACC) of the
katG
gene. In conclusion, all these results indicated that the sensitivity and specificity of the HRM method were increased when the
katG
gene and the
mabA-inhA
promoter region were used as a target.</description><identifier>ISSN: 0343-8651</identifier><identifier>EISSN: 1432-0991</identifier><identifier>DOI: 10.1007/s00284-022-02960-z</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Amino acids ; Biomedical and Life Sciences ; Biotechnology ; Clinical isolates ; Gene sequencing ; Genetic analysis ; High resolution ; Isoniazid ; KatG gene ; Life Sciences ; Melting ; Microbiology ; Multidrug resistance ; Multidrug resistant organisms ; Mutation ; Mycobacterium tuberculosis ; Rifampin ; RpoB protein ; Sputum ; Tuberculosis</subject><ispartof>Current microbiology, 2022-09, Vol.79 (9), p.257-257, Article 257</ispartof><rights>The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2022</rights><rights>The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2022.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c352t-9cddbc8f98950a7d2d90a4402370f43f678896e7826bea210908a990b37050a83</citedby><cites>FETCH-LOGICAL-c352t-9cddbc8f98950a7d2d90a4402370f43f678896e7826bea210908a990b37050a83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Parsa, Shadi</creatorcontrib><creatorcontrib>Yaghoubi, Atieh</creatorcontrib><creatorcontrib>Izadi, Nafiseh</creatorcontrib><creatorcontrib>Sabet, Faezeh</creatorcontrib><creatorcontrib>Nik, Leila babaei</creatorcontrib><creatorcontrib>Derakhshan, Mohammad</creatorcontrib><creatorcontrib>Rezaee, Seyed Abdolrahim</creatorcontrib><creatorcontrib>Meshkat, Zahra</creatorcontrib><creatorcontrib>Hoseini, Seyed Javad</creatorcontrib><creatorcontrib>Jmehdar, Saeid Amel</creatorcontrib><creatorcontrib>Kiani, Fatemeh</creatorcontrib><creatorcontrib>Samiei, Amin</creatorcontrib><creatorcontrib>Soleimanpour, Saman</creatorcontrib><title>Detection of Isoniazid and Rifampin Resistance in Mycobacterium tuberculosis Clinical Isolates from Sputum Samples by High-Resolution Melting Analysis</title><title>Current microbiology</title><addtitle>Curr Microbiol</addtitle><description>The effective management of multidrug-resistant tuberculosis (MDR-TB) and the need for rapid and accurate screening of rifampin (RIF) and isoniazid (INH)-resistant
Mycobacterium tuberculosis
(Mtb) isolates are the most fundamental and difficult challenges facing the global TB control. The present study aimed to compare the diagnostic accuracy of high-resolution melting-curve analysis (HRMA) in comparison to multiplex allele-specific PCR (MAS-PCR) and xpert MTB/RIF as well as the conventional drug-susceptibility test (DST) and gene sequencing for the detection of INH and RIF resistance in the Mtb isolates. In the present study, a total of 431
Mtb
isolates including 11 MDR (%2.55), 7 INH resistance (%1.62), two RIF resistance (%0.46), and 411 sensitive isolates were phenotypically confirmed. HRMA assay identified
katG
gene mutations and the
mabA-inhA
promoter region in 15 of 18 INH-resistant samples and
rpoB
gene mutations were successfully evaluated in 11 out of 13 RIF-resistant samples. The sensitivity and specificity of the HRMA method were 83.3% and 98.8% for INH and 84.6% and 99% for RIF, respectively. The most common mutation in RIF-resistance-determining region (RRDR) occurred at codon 531 (TCG → TTG)(84.6%) and then at codon 513 (CAA → GTA)(7.6%) and 526 (CAC → TAC) (7.6%), which resulted in the amino-acid changes. Also, 88.8% of INH-resistant samples had mutations in the
katG
gene and the
mabA-inhA
promoter region, of which the highest mutation occurred at codon 315 (AGC → ACC) of the
katG
gene. In conclusion, all these results indicated that the sensitivity and specificity of the HRM method were increased when the
katG
gene and the
mabA-inhA
promoter region were used as a target.</description><subject>Amino acids</subject><subject>Biomedical and Life Sciences</subject><subject>Biotechnology</subject><subject>Clinical isolates</subject><subject>Gene sequencing</subject><subject>Genetic analysis</subject><subject>High resolution</subject><subject>Isoniazid</subject><subject>KatG gene</subject><subject>Life Sciences</subject><subject>Melting</subject><subject>Microbiology</subject><subject>Multidrug resistance</subject><subject>Multidrug resistant organisms</subject><subject>Mutation</subject><subject>Mycobacterium tuberculosis</subject><subject>Rifampin</subject><subject>RpoB protein</subject><subject>Sputum</subject><subject>Tuberculosis</subject><issn>0343-8651</issn><issn>1432-0991</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp9kU1rHSEUhqW00Nskf6AroZtupj06X7oMt00TSCgkzVocx7k1OHqrzuLeH9Lfm5NMoZBFFiJHn_dReAn5yOALA-i_ZgAumgo4xyU7qI5vyIY1NY5SsrdkA3VTV6Jr2XvyIecHAMYlsA35-80Wa4qLgcaJXuUYnD66keow0ls36XnvAr212eWig7EUp5uDiYM2xSa3zLQsg01m8RERuvUuOKP9k8jrYjOdUpzp3X4piN6hzePZcKCXbve7Qm30y_PbN9YXF3b0PGh_QNMpeTdpn-3Zv_2E3F98_7W9rK5__rjanl9Xpm55qaQZx8GISQrZgu5HPkrQTQO87mFq6qnrhZCd7QXvBqs5AwlCSwkD3mNA1Cfk8-rdp_hnsbmo2WVjvdfBxiUr3kmGDlG3iH56gT7EJeF_V6qVUvSAFF8pk2LOyU5qn9ys00ExUE9VqbUqhVWp56rUEUP1GsoIh51N_9WvpB4BTmuZNw</recordid><startdate>20220901</startdate><enddate>20220901</enddate><creator>Parsa, Shadi</creator><creator>Yaghoubi, Atieh</creator><creator>Izadi, Nafiseh</creator><creator>Sabet, Faezeh</creator><creator>Nik, Leila babaei</creator><creator>Derakhshan, 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of Isoniazid and Rifampin Resistance in Mycobacterium tuberculosis Clinical Isolates from Sputum Samples by High-Resolution Melting Analysis</title><author>Parsa, Shadi ; Yaghoubi, Atieh ; Izadi, Nafiseh ; Sabet, Faezeh ; Nik, Leila babaei ; Derakhshan, Mohammad ; Rezaee, Seyed Abdolrahim ; Meshkat, Zahra ; Hoseini, Seyed Javad ; Jmehdar, Saeid Amel ; Kiani, Fatemeh ; Samiei, Amin ; Soleimanpour, Saman</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c352t-9cddbc8f98950a7d2d90a4402370f43f678896e7826bea210908a990b37050a83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Amino acids</topic><topic>Biomedical and Life Sciences</topic><topic>Biotechnology</topic><topic>Clinical isolates</topic><topic>Gene sequencing</topic><topic>Genetic analysis</topic><topic>High resolution</topic><topic>Isoniazid</topic><topic>KatG gene</topic><topic>Life Sciences</topic><topic>Melting</topic><topic>Microbiology</topic><topic>Multidrug resistance</topic><topic>Multidrug resistant organisms</topic><topic>Mutation</topic><topic>Mycobacterium tuberculosis</topic><topic>Rifampin</topic><topic>RpoB protein</topic><topic>Sputum</topic><topic>Tuberculosis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Parsa, Shadi</creatorcontrib><creatorcontrib>Yaghoubi, Atieh</creatorcontrib><creatorcontrib>Izadi, Nafiseh</creatorcontrib><creatorcontrib>Sabet, Faezeh</creatorcontrib><creatorcontrib>Nik, Leila babaei</creatorcontrib><creatorcontrib>Derakhshan, Mohammad</creatorcontrib><creatorcontrib>Rezaee, Seyed Abdolrahim</creatorcontrib><creatorcontrib>Meshkat, Zahra</creatorcontrib><creatorcontrib>Hoseini, Seyed Javad</creatorcontrib><creatorcontrib>Jmehdar, Saeid Amel</creatorcontrib><creatorcontrib>Kiani, Fatemeh</creatorcontrib><creatorcontrib>Samiei, Amin</creatorcontrib><creatorcontrib>Soleimanpour, 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Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Parsa, Shadi</au><au>Yaghoubi, Atieh</au><au>Izadi, Nafiseh</au><au>Sabet, Faezeh</au><au>Nik, Leila babaei</au><au>Derakhshan, Mohammad</au><au>Rezaee, Seyed Abdolrahim</au><au>Meshkat, Zahra</au><au>Hoseini, Seyed Javad</au><au>Jmehdar, Saeid Amel</au><au>Kiani, Fatemeh</au><au>Samiei, Amin</au><au>Soleimanpour, Saman</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Detection of Isoniazid and Rifampin Resistance in Mycobacterium tuberculosis Clinical Isolates from Sputum Samples by High-Resolution Melting Analysis</atitle><jtitle>Current microbiology</jtitle><stitle>Curr Microbiol</stitle><date>2022-09-01</date><risdate>2022</risdate><volume>79</volume><issue>9</issue><spage>257</spage><epage>257</epage><pages>257-257</pages><artnum>257</artnum><issn>0343-8651</issn><eissn>1432-0991</eissn><abstract>The effective management of multidrug-resistant tuberculosis (MDR-TB) and the need for rapid and accurate screening of rifampin (RIF) and isoniazid (INH)-resistant
Mycobacterium tuberculosis
(Mtb) isolates are the most fundamental and difficult challenges facing the global TB control. The present study aimed to compare the diagnostic accuracy of high-resolution melting-curve analysis (HRMA) in comparison to multiplex allele-specific PCR (MAS-PCR) and xpert MTB/RIF as well as the conventional drug-susceptibility test (DST) and gene sequencing for the detection of INH and RIF resistance in the Mtb isolates. In the present study, a total of 431
Mtb
isolates including 11 MDR (%2.55), 7 INH resistance (%1.62), two RIF resistance (%0.46), and 411 sensitive isolates were phenotypically confirmed. HRMA assay identified
katG
gene mutations and the
mabA-inhA
promoter region in 15 of 18 INH-resistant samples and
rpoB
gene mutations were successfully evaluated in 11 out of 13 RIF-resistant samples. The sensitivity and specificity of the HRMA method were 83.3% and 98.8% for INH and 84.6% and 99% for RIF, respectively. The most common mutation in RIF-resistance-determining region (RRDR) occurred at codon 531 (TCG → TTG)(84.6%) and then at codon 513 (CAA → GTA)(7.6%) and 526 (CAC → TAC) (7.6%), which resulted in the amino-acid changes. Also, 88.8% of INH-resistant samples had mutations in the
katG
gene and the
mabA-inhA
promoter region, of which the highest mutation occurred at codon 315 (AGC → ACC) of the
katG
gene. In conclusion, all these results indicated that the sensitivity and specificity of the HRM method were increased when the
katG
gene and the
mabA-inhA
promoter region were used as a target.</abstract><cop>New York</cop><pub>Springer US</pub><doi>10.1007/s00284-022-02960-z</doi><tpages>1</tpages></addata></record> |
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subjects | Amino acids Biomedical and Life Sciences Biotechnology Clinical isolates Gene sequencing Genetic analysis High resolution Isoniazid KatG gene Life Sciences Melting Microbiology Multidrug resistance Multidrug resistant organisms Mutation Mycobacterium tuberculosis Rifampin RpoB protein Sputum Tuberculosis |
title | Detection of Isoniazid and Rifampin Resistance in Mycobacterium tuberculosis Clinical Isolates from Sputum Samples by High-Resolution Melting Analysis |
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