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- Publisher Website: 10.1128/JCM.06843-11
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- PMID: 22442318
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Article: Automated pangenomic analysis in target selection for PCR detection and identification of bacteria by use of ssGeneFinder Webserver and its application to Salmonella enterica serovar Typhi
Title | Automated pangenomic analysis in target selection for PCR detection and identification of bacteria by use of ssGeneFinder Webserver and its application to Salmonella enterica serovar Typhi | ||||||||||||||
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Authors | |||||||||||||||
Issue Date | 2012 | ||||||||||||||
Publisher | American Society for Microbiology. | ||||||||||||||
Citation | Journal of Clinical Microbiology, 2012, v. 50 n. 6, p. 1905-1911 How to Cite? | ||||||||||||||
Abstract | With the advent of high-throughput DNA sequencing, more than 4,000 bacterial genomes have been sequenced and are publicly available. We report a user-friendly web platform, ssGeneFinder Webserver (http://147.8.74.24/ssGeneFinder/), which is updated weekly for the automated pangenomic selection of specific targets for direct PCR detection and the identification of clinically important bacteria without the need of gene sequencing. To apply the ssGeneFinder Webserver for identifying specific targets for Salmonella enterica serovar Typhi, we analyzed 11 S. Typhi genomes, generated two specific targets, and validated them using 40 S. Typhi, 110 non-Typhi Salmonella serovars (serovar Paratyphi A, n = 4; Paratyphi B, n = 1; Typhimurium, n = 5; Enteritidis, n = 12; non-Paratyphi group A, n = 6; non-Paratyphi group B, n = 29; non-Paratyphi group C, n = 12; non-Typhi group D, n = 35; group E and others, n = 6), 115 Enterobacteriaceae isolates (Escherichia, n = 78; Shigella, n = 2; Klebsiella, n = 13; Enterobacter, n = 9; others, n = 13), and 66 human stool samples that were culture negative for S. Typhi. Both targets successfully detected all typical and atypical S. Typhi isolates, including an H1-j flagellin gene mutant, an aflagellated mutant which reacted with 2O Salmonella antiserum, and the Vi-negative attenuated vaccine strain Ty21a. No false positive was detected from any of the bacterial isolates and stool samples. DNA sequencing confirmed the identity of all positive amplicons. The PCR assays have detection limits as low as 100 CFU per reaction and were tested using spiked stool samples. Using a pangenomic approach, ssGeneFinder Webserver generated targets specific to S. Typhi. These and other validated targets should be applicable to the identification and direct PCR detection of bacterial pathogens from uncultured, mixed, and environmental samples. | ||||||||||||||
Persistent Identifier | http://hdl.handle.net/10722/157706 | ||||||||||||||
ISSN | 2023 Impact Factor: 6.1 2023 SCImago Journal Rankings: 1.653 | ||||||||||||||
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Funding Information: This work was partly supported by the HKSAR Research Fund for the Control of Infectious Diseases of the Health, Welfare and Food Bureau, Research Grants Council Grant, University Development Fund, Committee for Conference and Research Grant, The University of Hong Kong, and the Croucher Foundation. | ||||||||||||||
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Ho, CC | en_US |
dc.contributor.author | Wu, AKL | en_US |
dc.contributor.author | Tse, CWS | en_US |
dc.contributor.author | Yuen, KY | en_US |
dc.contributor.author | Lau, SKP | en_US |
dc.contributor.author | Woo, PCY | en_US |
dc.date.accessioned | 2012-08-08T08:52:26Z | - |
dc.date.available | 2012-08-08T08:52:26Z | - |
dc.date.issued | 2012 | en_US |
dc.identifier.citation | Journal of Clinical Microbiology, 2012, v. 50 n. 6, p. 1905-1911 | en_US |
dc.identifier.issn | 0095-1137 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/157706 | - |
dc.description.abstract | With the advent of high-throughput DNA sequencing, more than 4,000 bacterial genomes have been sequenced and are publicly available. We report a user-friendly web platform, ssGeneFinder Webserver (http://147.8.74.24/ssGeneFinder/), which is updated weekly for the automated pangenomic selection of specific targets for direct PCR detection and the identification of clinically important bacteria without the need of gene sequencing. To apply the ssGeneFinder Webserver for identifying specific targets for Salmonella enterica serovar Typhi, we analyzed 11 S. Typhi genomes, generated two specific targets, and validated them using 40 S. Typhi, 110 non-Typhi Salmonella serovars (serovar Paratyphi A, n = 4; Paratyphi B, n = 1; Typhimurium, n = 5; Enteritidis, n = 12; non-Paratyphi group A, n = 6; non-Paratyphi group B, n = 29; non-Paratyphi group C, n = 12; non-Typhi group D, n = 35; group E and others, n = 6), 115 Enterobacteriaceae isolates (Escherichia, n = 78; Shigella, n = 2; Klebsiella, n = 13; Enterobacter, n = 9; others, n = 13), and 66 human stool samples that were culture negative for S. Typhi. Both targets successfully detected all typical and atypical S. Typhi isolates, including an H1-j flagellin gene mutant, an aflagellated mutant which reacted with 2O Salmonella antiserum, and the Vi-negative attenuated vaccine strain Ty21a. No false positive was detected from any of the bacterial isolates and stool samples. DNA sequencing confirmed the identity of all positive amplicons. The PCR assays have detection limits as low as 100 CFU per reaction and were tested using spiked stool samples. Using a pangenomic approach, ssGeneFinder Webserver generated targets specific to S. Typhi. These and other validated targets should be applicable to the identification and direct PCR detection of bacterial pathogens from uncultured, mixed, and environmental samples. | en_US |
dc.language | eng | en_US |
dc.publisher | American Society for Microbiology. | - |
dc.relation.ispartof | Journal of Clinical Microbiology | en_US |
dc.rights | Journal of Clinical Microbiology. Copyright © American Society for Microbiology. | - |
dc.rights | Copyright © American Society for Microbiology, [Journal of Clinical Microbiology, 2012, v. 50 n. 6, p. 1905-1911] | - |
dc.subject.mesh | Bacteriological Techniques - methods | - |
dc.subject.mesh | Computational Biology - methods | - |
dc.subject.mesh | DNA Primers - genetics | - |
dc.subject.mesh | Molecular Diagnostic Techniques - methods | - |
dc.subject.mesh | Polymerase Chain Reaction - methods | - |
dc.title | Automated pangenomic analysis in target selection for PCR detection and identification of bacteria by use of ssGeneFinder Webserver and its application to Salmonella enterica serovar Typhi | en_US |
dc.type | Article | en_US |
dc.identifier.email | Yuen, KY: kyyuen@hkucc.hku.hk | en_US |
dc.identifier.email | Lau, SKP: skplau@hkucc.hku.hk | en_US |
dc.identifier.email | Woo, PCY: pcywoo@hkucc.hku.hk | - |
dc.identifier.authority | Lau, SKP=rp00486 | en_US |
dc.identifier.authority | Woo, PCY=rp00430 | en_US |
dc.description.nature | link_to_OA_fulltext | - |
dc.identifier.doi | 10.1128/JCM.06843-11 | en_US |
dc.identifier.pmid | 22442318 | - |
dc.identifier.pmcid | PMC3372160 | - |
dc.identifier.scopus | eid_2-s2.0-84862101373 | en_US |
dc.identifier.hkuros | 204336 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-84862101373&selection=ref&src=s&origin=recordpage | en_US |
dc.identifier.volume | 50 | en_US |
dc.identifier.issue | 6 | en_US |
dc.identifier.spage | 1905 | en_US |
dc.identifier.epage | 1911 | en_US |
dc.identifier.isi | WOS:000305119000014 | - |
dc.publisher.place | United States | en_US |
dc.identifier.scopusauthorid | Woo, PCY=7201801340 | en_US |
dc.identifier.scopusauthorid | Lau, SKP=7401596211 | en_US |
dc.identifier.scopusauthorid | Yuen, KY=55018434500 | en_US |
dc.identifier.scopusauthorid | Tse, CWS=7103295064 | en_US |
dc.identifier.scopusauthorid | Wu, AKL=55247482100 | en_US |
dc.identifier.scopusauthorid | Ho, CC=42061526500 | en_US |
dc.identifier.issnl | 0095-1137 | - |