TY - JOUR
T1 - Spoligotyping, phenotypic and genotypic characterization of katG, rpoB gene of M. tuberculosis isolates from Sahariya tribe of Madhya Pradesh India
AU - Gupta, Rahul
AU - Amrathlal, Rabbind Singh
AU - Prakash, Ravi
AU - Jain, Sanjay
AU - Tiwari, Pramod K.
N1 - Funding Information:
This work was supported by the Council of Scientific & Industrial Research (CSIR), Government of India, New Delhi, through a research grant (letter No. 27(0316)/16/EMR-II) to PKT. RG acknowledges financial support from Jiwaji University as fellowship. We are thankful to Mr. Rinku Mittal (Technician) RNTCP and staff of District TB Hospital, Sheopur, for their support during sampling and ZN staining and to Dr. Sachin Kumar Chandraker, Microbiologist, FIND lab, Raipur for his help in drug susceptibility test. No funding sources. None declared. Not required. Rahul Gupta: sample collection, M. tuberculosis culture, drug susceptibility testing, spoligotyping, DNA sequencing, DNA extraction, manuscript preparation & statistical analysis., Rabbind Singh: Amrathal PCR-RFLP, MAS-PCR, manuscript preparation., Ravi Prakash: biochemical identification, drug susceptibility testing., Sanjay Jain: sample collection from Sheopur region and acid fast staining., Pramod Kumar Tiwari: study design, drafting and revising the article. This study was approved by Institutional Human Ethical Committee, Jiwaji University, Gwalior (Institutional Ethical Committee no. JU/IHEC/2013-A/06).
Funding Information:
This work was supported by the Council of Scientific & Industrial Research (CSIR), Government of India, New Delhi , through a research grant (letter No. 27(0316)/16/EMR-II ) to PKT. RG acknowledges financial support from Jiwaji University as fellowship. We are thankful to Mr. Rinku Mittal (Technician) RNTCP and staff of District TB Hospital, Sheopur, for their support during sampling and ZN staining and to Dr. Sachin Kumar Chandraker, Microbiologist, FIND lab, Raipur for his help in drug susceptibility test.
Publisher Copyright:
© 2018 The Authors
PY - 2019/5/1
Y1 - 2019/5/1
N2 - Background: Sahariya, a primitive tribal group, residing in Gwalior and Sheopur districts of Madhya Pradesh, India, show high incidence and prevalence of pulmonary tuberculosis (PTB). The study was designed to understand the genetic diversity and phenotype — genotype association of drug resistant M. tuberculosis strains, infecting Sahariya tribe. Materials and methods: A total of 103 pulmonary tuberculosis patients from Sahariya tribe were recruited from Gwalior and Sheopur districts. Sputum samples were collected and cultured on LJ slants and drug sensitivity tests were carried out. Genomic DNA was extracted, followed by spoligotyping and genotyping of drug target genes, katG and rpoB, using MAS-PCR, PCR-RFLP and DNA sequencing. Result: Seventeen different spoligotypes were identified, in which, EAI3_IND/ST11 M. tuberculosis strain appeared predominant, followed by CAS1_Delhi/ST26. Results of our phenotypic drug susceptibility test identified high incidence (12.6%) of isoniazid-resistant tuberculosis, while 4.85% isolates were multi drug resistant (MDR). Further genotyping of drug target genes identified 8.7% of isoniazid-R isolates to have a mutation at katG codon 463, while 3.8% isolates showed mutations at two sites, katG codons 315 and 463. In case of MDR-TB isolates, all from CAS lineage, 3.85% had mutations on katG and rpoB genes, at codon 463 and codon 526, respectively, while 0.97% isolates were harbouring mutations at codons 315, 463 and 531. Conclusion: Our findings have revealed that EAI3_IND strain is the predominant strain infecting Sahariya. The incidence of isoniazid-R M. tuberculosis strain infection is high, with an increased propensity to evolve into MDR-TB. Therefore, the TB centres should also consider isoniazid-R status of the isolates along with CBNAAT before deciding the drug regimen for the patients.
AB - Background: Sahariya, a primitive tribal group, residing in Gwalior and Sheopur districts of Madhya Pradesh, India, show high incidence and prevalence of pulmonary tuberculosis (PTB). The study was designed to understand the genetic diversity and phenotype — genotype association of drug resistant M. tuberculosis strains, infecting Sahariya tribe. Materials and methods: A total of 103 pulmonary tuberculosis patients from Sahariya tribe were recruited from Gwalior and Sheopur districts. Sputum samples were collected and cultured on LJ slants and drug sensitivity tests were carried out. Genomic DNA was extracted, followed by spoligotyping and genotyping of drug target genes, katG and rpoB, using MAS-PCR, PCR-RFLP and DNA sequencing. Result: Seventeen different spoligotypes were identified, in which, EAI3_IND/ST11 M. tuberculosis strain appeared predominant, followed by CAS1_Delhi/ST26. Results of our phenotypic drug susceptibility test identified high incidence (12.6%) of isoniazid-resistant tuberculosis, while 4.85% isolates were multi drug resistant (MDR). Further genotyping of drug target genes identified 8.7% of isoniazid-R isolates to have a mutation at katG codon 463, while 3.8% isolates showed mutations at two sites, katG codons 315 and 463. In case of MDR-TB isolates, all from CAS lineage, 3.85% had mutations on katG and rpoB genes, at codon 463 and codon 526, respectively, while 0.97% isolates were harbouring mutations at codons 315, 463 and 531. Conclusion: Our findings have revealed that EAI3_IND strain is the predominant strain infecting Sahariya. The incidence of isoniazid-R M. tuberculosis strain infection is high, with an increased propensity to evolve into MDR-TB. Therefore, the TB centres should also consider isoniazid-R status of the isolates along with CBNAAT before deciding the drug regimen for the patients.
KW - Isoniazid resistance
KW - M. tuberculosis
KW - Multi-drug resistance
KW - Sahariya tribe
KW - Spoligotyping
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U2 - 10.1016/j.jiph.2018.12.009
DO - 10.1016/j.jiph.2018.12.009
M3 - Article
C2 - 30611735
AN - SCOPUS:85059325092
SN - 1876-0341
VL - 12
SP - 395
EP - 402
JO - Journal of Infection and Public Health
JF - Journal of Infection and Public Health
IS - 3
ER -