Evidence map›Paper›PMID 28745309›Full record

ArticleEmerging microbes & infections2017

A quantitative and efficient approach to select MIRU-VNTR loci based on accumulation of the percentage differences of strains for discriminating divergent Mycobacterium tuberculosis sublineages.

Xin-Ling Pan, Chun-Lei Zhang, Chie Nakajima, Jin Fu, Chang-Xia Shao, Li-Na Zhao, Jia-Yi Cui, Na Jiao, Chang-Long Fan, Yasuhiko Suzuki and 3 more

Abstract read
In one paragraph

Article in Emerging microbes & infections, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

Who cites it

7 citing papers in PubMed.

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  7. Clustering and recent transmission ofInfection and drug resistance · 2018
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4 · The record

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5 · Who and what money

Authors and funding

13 authors.

Xin-Ling PanDepartment of Microbiology, Wu Lien-Teh Institute, Harbin Medical University, Heilongjiang Provincial Key Laboratory of Infection and Immunity, Key Laboratory of Pathogen Biology, Harbin 150081, China.
Chun-Lei ZhangDepartment of Clinical Laboratory, Harbin Chest Hospital, Harbin 150081, China.
Chie NakajimaDivision of Bioresources, Hokkaido University Research Center for Zoonosis Control, Sapporo 0010020, Japan.
Jin FuDepartment of Neurology, The Second Affiliated Hospital of Harbin Medical University, Harbin 150026, China.
Chang-Xia ShaoDepartment of Microbiology, Wu Lien-Teh Institute, Harbin Medical University, Heilongjiang Provincial Key Laboratory of Infection and Immunity, Key Laboratory of Pathogen Biology, Harbin 150081, China.
Li-Na ZhaoDepartment of Clinical Laboratory, Harbin Chest Hospital, Harbin 150081, China.
Jia-Yi CuiDepartment of Microbiology, Wu Lien-Teh Institute, Harbin Medical University, Heilongjiang Provincial Key Laboratory of Infection and Immunity, Key Laboratory of Pathogen Biology, Harbin 150081, China.
Na JiaoDepartment of Clinical Laboratory, Harbin Chest Hospital, Harbin 150081, China.
Chang-Long FanDepartment of Clinical Laboratory, Harbin Chest Hospital, Harbin 150081, China.
Yasuhiko SuzukiDivision of Bioresources, Hokkaido University Research Center for Zoonosis Control, Sapporo 0010020, Japan.
Toshio HattoriGraduate School of Health Science Studies, Kibi International University, Takahashi 7168508, Japan.
Di LiDepartment of Microbiology, Wu Lien-Teh Institute, Harbin Medical University, Heilongjiang Provincial Key Laboratory of Infection and Immunity, Key Laboratory of Pathogen Biology, Harbin 150081, China.
Hong LingDepartment of Microbiology, Wu Lien-Teh Institute, Harbin Medical University, Heilongjiang Provincial Key Laboratory of Infection and Immunity, Key Laboratory of Pathogen Biology, Harbin 150081, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although several optimal mycobacterial interspersed repetitive units-variable number tandem repeat (MIRU-VNTR) loci have been suggested for genotyping homogenous Mycobacterium tuberculosis, including the Beijing genotype, a more efficient and convenient selection strategy for identifying optimal VNTR loci is needed. Here 281 M. tuberculosis isolates were analyzed. Beijing genotype and non-Beijing genotypes were identified, as well as Beijing sublineages, according to single nucleotide polymorphisms. A total of 22 MIRU-VNTR loci were used for genotyping. To efficiently select optimal MIRU-VNTR loci, we established accumulations of percentage differences (APDs) between the strains among the different genotypes. In addition, we constructed a minimum spanning tree for clustering analysis of the VNTR profiles. Our findings showed that eight MIRU-VNTR loci displayed disparities in h values of ≥0.2 between the Beijing genotype and non-Beijing genotype isolates. To efficiently discriminate Beijing and non-Beijing genotypes, an optimal VNTR set was established by adding loci with APDs ranging from 87.2% to 58.8%, resulting in the construction of a nine-locus set. We also found that QUB11a is a powerful locus for separating ST10s (including ST10, STF and STCH1) and ST22s (including ST22 and ST8) strains, whereas a combination of QUB11a, QUB4156, QUB18, Mtub21 and QUB26 could efficiently discriminate Beijing sublineages. Our findings suggested that two nine-locus sets were not only efficient for distinguishing the Beijing genotype from non-Beijing genotype strains, but were also suitable for sublineage genotyping with different discriminatory powers. These results indicate that APD represents a quantitative and efficient approach for selecting MIRU-VNTR loci to discriminate between divergent M. tuberculosis sublineages.

Indexed as

Repetitive Sequences, Nucleic AcidBacterial Typing TechniquesBeijingDNA, BacterialGenetic VariationGenotypeHumansMinisatellite RepeatsMycobacterium tuberculosisPolymorphism, Single NucleotideTuberculosisDNA, Bacterial

Identifiers

PMID28745309
PMCPMC5567172

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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.