Evidence map›Paper›PMID 28574018›Full record

ArticleThe Indian journal of medical research2017

Genetic diversity & drug sensitivity profiles of

Bharti Malhotra, Deepti Dashora, Vipin Kumar, Sumit Goyal, Bhavana Sharma, Madhu Kumar, Kailash Narayan Gupta, Vishnu Dutt Sharma, D S Chauhan, Kiran Katoch and 1 more

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Article in The Indian journal of medical research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed, 1 citations in OpenAlex.

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4 · The record

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5 · Who and what money

Authors and funding

11 authors at 1 institution in 1 country.

Bharti MalhotraDepartment of Microbiology & Immunology, SMS Medical College, Rajasthan, India.
Deepti DashoraDepartment of Microbiology & Immunology, SMS Medical College; Department of Zoology, Cell & Molecular Biology Laboratory, University of Rajasthan, Rajasthan, India.
Vipin KumarDepartment of Microbiology & Immunology, SMS Medical College, Rajasthan, India.
Sumit GoyalDepartment of Microbiology & Immunology, SMS Medical College, Rajasthan, India.
Bhavana SharmaDepartment of Microbiology & Immunology, SMS Medical College, Rajasthan, India.
Madhu KumarDepartment of Zoology, Cell & Molecular Biology Laboratory, University of Rajasthan, Rajasthan, India.
Kailash Narayan GuptaState TB Control Program Officer RNTCP, Rajasthan, India.
Vishnu Dutt SharmaDepartment of Microbiology & Molecular Biology, National JALMA Institute for Leprosy & Other Mycobacterial Diseases, Agra, India.
D S ChauhanDepartment of Microbiology & Molecular Biology, National JALMA Institute for Leprosy & Other Mycobacterial Diseases, Agra, India.
Kiran KatochDepartment of Medicine, National JALMA Institute for Leprosy & Other Mycobacterial Diseases, Agra, India.
Vishwa Mohan KatochDepartment of Microbiology & Molecular Biology, National JALMA Institute for Leprosy & Other Mycobacterial Diseases, Agra; Former Secretary, Department of Health Research & Director-General, Indian Council of Medical Research, New Delhi, India.
University of Rajasthan · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND &

objectivesSlums are considered as hotspots of tuberculosis (TB). The study of genetic diversity and drug susceptibility profile of Mycobacterium tuberculosis (MTB) will help understand the transmission dynamics and can be used for better prevention and control of the disease. The aim of this study was to determine the drug susceptibility profiles and genetic diversity using the random amplified polymorphic DNA (RAPD) and mycobacterial interspersed repetitive units-variable number of tandem repeats (MIRU VNTR) of MTB isolates from sputum samples of pulmonary TB patients residing in the two slums of Jaipur city in Rajasthan, India.

methodsSputum samples collected from pulmonary TB patients, their contacts and suspects during 2010-2012 were processed for microscopy and mycobacterial culture. Drug susceptibility testing was done by one per cent indirect proportion method on Lowenstein-Jensen medium for first-line anti-TB drugs rifampicin, isoniazid, ethambutol and streptomycin. MTB DNA was extracted by physicochemical method, and DNA fingerprinting was done by RAPD and MIRU VNTR analysis.

resultsAmong 175 sputum samples collected, 75 were positive (43.8%) for acid-fast bacilli, 83 for MTB culture and four were contaminated. Fifty two isolates (62.7%) were fully sensitive to four drugs, and five (6%) were multidrug resistant (MDR). RAPD analysis of 81 isolates revealed six clusters containing 23 (28.4%) isolates, and 58 (71.6%) were unique. MIRU VNTR analysis clustered 20 (24.7%) isolates, and 61 (75.3%) were unique. INTERPRETATION &

conclusionsAbout 62.7 per cent isolates from the sputum samples from slum areas were sensitive to four drugs; six per cent of isolates were MDR. Poly-resistance other than MDR was high (16%). About one-fourth isolates were clustered by either method. RAPD was rapid, less expensive but had low reproducibility. MIRU VNTR analysis could identify to greater extent the epidemiological link in the population studied.

Indexed as

AdolescentAdultAgedChildChild, PreschoolDrug Resistance, Multiple, BacterialFemaleGenetic VariationGenotypeHumansInterspersed Repetitive SequencesIsoniazidMaleMicrobial Sensitivity TestsMiddle AgedMinisatellite RepeatsIsoniazidRifampin

Identifiers

PMID28574018
PMCPMC5460578
OpenAlexW2617027872

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.