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Genotyping of Salmonella Typhi using 8-loci multi locus VNTR analysis

BACKGROUND: Typhoid fever has caused severe epidemics in many Asian and African countries. The early detection of outbreaks and their sources may promote the prevention and control of typhoid fever, for which effective and timely molecular subtyping techniques are required. Pulsed field gel electrop...

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Autores principales: Wang, Hongxia, Diao, Baowei, Cui, Zhigang, Yan, Meiying, Kan, Biao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4819281/
https://www.ncbi.nlm.nih.gov/pubmed/27047570
http://dx.doi.org/10.1186/s13099-016-0094-4
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author Wang, Hongxia
Diao, Baowei
Cui, Zhigang
Yan, Meiying
Kan, Biao
author_facet Wang, Hongxia
Diao, Baowei
Cui, Zhigang
Yan, Meiying
Kan, Biao
author_sort Wang, Hongxia
collection PubMed
description BACKGROUND: Typhoid fever has caused severe epidemics in many Asian and African countries. The early detection of outbreaks and their sources may promote the prevention and control of typhoid fever, for which effective and timely molecular subtyping techniques are required. Pulsed field gel electrophoresis (PFGE) is routinely used as the molecular typing technique for foodborne and waterborne pathogens. However, maneuverable techniques remain necessary to expedite the experimental procedure and obtain more effective subtyping. The multilocus loci of a variable number of tandem repeats (VNTR) analysis (MLVA) is a polymerase chain reaction (PCR)-based subtyping method. METHODS: MLVA method and PFGE based on Xba I enzyme were applied to the 103 Salmonella Typhi (S. Typhi) isolated from different years and regions. Dendrograms were constructed and analyzed to help understand the data. The Simpson’s index of diversity (D value) was calculated to estimate the discriminatory power of MLVA and PFGE. In addition, a set of endogenous 3 bp DNA ladder markers were established to accurately determine the repeat copy number of the VNTR with only a 3 bp repetitive unit, using microfluidics chip-based electrophoresis to generate comparable VNTR data in the public health laboratory network. RESULTS: The established 8-loci MLVA for S. Typhi subtyping had higher discriminatory power than PFGE. In some cases, PFGE could not distinguish the strains isolated over long intervals and with different epidemic provinces. By contrast, 8-loci MLVA distinctly distinguished these strains, and the strains with the same MLVA patterns were from the same or contiguous years and the same province, showing its significance in epidemiological discrimination. The established set of endogenous 3 bp DNA ladder markers improved the accuracy and reproducibility of VNTR analysis using microfluidics chip-based electrophoresis to 100 %. CONCLUSIONS: Eight VNTRs can be used for the MLVA analysis of the 103 S. Typhi isolates. MLVA based on the 8-loci had higher discriminatory power than PFGE for S. Typhi subtyping. The 8-loci MLVA is easier for the analysis and interpretation of relationships between strains compared to PFGE. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13099-016-0094-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-48192812016-04-05 Genotyping of Salmonella Typhi using 8-loci multi locus VNTR analysis Wang, Hongxia Diao, Baowei Cui, Zhigang Yan, Meiying Kan, Biao Gut Pathog Research BACKGROUND: Typhoid fever has caused severe epidemics in many Asian and African countries. The early detection of outbreaks and their sources may promote the prevention and control of typhoid fever, for which effective and timely molecular subtyping techniques are required. Pulsed field gel electrophoresis (PFGE) is routinely used as the molecular typing technique for foodborne and waterborne pathogens. However, maneuverable techniques remain necessary to expedite the experimental procedure and obtain more effective subtyping. The multilocus loci of a variable number of tandem repeats (VNTR) analysis (MLVA) is a polymerase chain reaction (PCR)-based subtyping method. METHODS: MLVA method and PFGE based on Xba I enzyme were applied to the 103 Salmonella Typhi (S. Typhi) isolated from different years and regions. Dendrograms were constructed and analyzed to help understand the data. The Simpson’s index of diversity (D value) was calculated to estimate the discriminatory power of MLVA and PFGE. In addition, a set of endogenous 3 bp DNA ladder markers were established to accurately determine the repeat copy number of the VNTR with only a 3 bp repetitive unit, using microfluidics chip-based electrophoresis to generate comparable VNTR data in the public health laboratory network. RESULTS: The established 8-loci MLVA for S. Typhi subtyping had higher discriminatory power than PFGE. In some cases, PFGE could not distinguish the strains isolated over long intervals and with different epidemic provinces. By contrast, 8-loci MLVA distinctly distinguished these strains, and the strains with the same MLVA patterns were from the same or contiguous years and the same province, showing its significance in epidemiological discrimination. The established set of endogenous 3 bp DNA ladder markers improved the accuracy and reproducibility of VNTR analysis using microfluidics chip-based electrophoresis to 100 %. CONCLUSIONS: Eight VNTRs can be used for the MLVA analysis of the 103 S. Typhi isolates. MLVA based on the 8-loci had higher discriminatory power than PFGE for S. Typhi subtyping. The 8-loci MLVA is easier for the analysis and interpretation of relationships between strains compared to PFGE. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13099-016-0094-4) contains supplementary material, which is available to authorized users. BioMed Central 2016-04-04 /pmc/articles/PMC4819281/ /pubmed/27047570 http://dx.doi.org/10.1186/s13099-016-0094-4 Text en © Wang et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Wang, Hongxia
Diao, Baowei
Cui, Zhigang
Yan, Meiying
Kan, Biao
Genotyping of Salmonella Typhi using 8-loci multi locus VNTR analysis
title Genotyping of Salmonella Typhi using 8-loci multi locus VNTR analysis
title_full Genotyping of Salmonella Typhi using 8-loci multi locus VNTR analysis
title_fullStr Genotyping of Salmonella Typhi using 8-loci multi locus VNTR analysis
title_full_unstemmed Genotyping of Salmonella Typhi using 8-loci multi locus VNTR analysis
title_short Genotyping of Salmonella Typhi using 8-loci multi locus VNTR analysis
title_sort genotyping of salmonella typhi using 8-loci multi locus vntr analysis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4819281/
https://www.ncbi.nlm.nih.gov/pubmed/27047570
http://dx.doi.org/10.1186/s13099-016-0094-4
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