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Development of PCR for identifying Streptococcus parasuis, a close relative of Streptococcus suis
Streptococcus parasuis has recently been removed taxonomically from Streptococcus suis, a zoonotic pathogen. S. parasuis has been detected in healthy pigs and in diseased pigs, which suggests that S. parasuis is involved in the normal microbiota of pigs and has potential pathogenicity. However, the...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Japanese Society of Veterinary Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6068303/ https://www.ncbi.nlm.nih.gov/pubmed/29877313 http://dx.doi.org/10.1292/jvms.18-0083 |
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author | YAMADA, Ryoko TIEN, Le Hong Thuy ARAI, Sakura TOHYA, Mari ISHIDA-KUROKI, Kasumi NOMOTO, Ryohei KIM, Hyunjung SUZUKI, Eriko OSAWA, Ro WATANABE, Takayasu SEKIZAKI, Tsutomu |
author_facet | YAMADA, Ryoko TIEN, Le Hong Thuy ARAI, Sakura TOHYA, Mari ISHIDA-KUROKI, Kasumi NOMOTO, Ryohei KIM, Hyunjung SUZUKI, Eriko OSAWA, Ro WATANABE, Takayasu SEKIZAKI, Tsutomu |
author_sort | YAMADA, Ryoko |
collection | PubMed |
description | Streptococcus parasuis has recently been removed taxonomically from Streptococcus suis, a zoonotic pathogen. S. parasuis has been detected in healthy pigs and in diseased pigs, which suggests that S. parasuis is involved in the normal microbiota of pigs and has potential pathogenicity. However, the pathogenicity of S. parasuis in pigs is unclear because of the lack of appropriate detection methods that discriminate S. parasuis from S. suis. In this study, we developed a PCR method that is specific for S. parasuis. The detection limit of the PCR was 350 CFU per reaction. Bacteria isolated from the saliva of eight pigs were collected and examined by PCR. Sixty-four isolates positive for PCR were obtained from the samples of all pigs. Thirteen of the 64 isolates were genetically confirmed as S. parasuis, and biologically and biochemically had nearly the same features of known S. parasuis strains, which suggested that strains positive for PCR were S. parasuis. Among the 64 isolates, 28 isolates were serotypes 20, 22, or 26 in the S. suis serotyping scheme. The remaining 36 isolates were untypeable, which suggested the presence of novel serotypes or a capsule-negative form. Therefore, the PCR method described in this study is a useful tool for identifying S. parasuis, and can be used in etiological studies on this bacterium. |
format | Online Article Text |
id | pubmed-6068303 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Japanese Society of Veterinary Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-60683032018-08-06 Development of PCR for identifying Streptococcus parasuis, a close relative of Streptococcus suis YAMADA, Ryoko TIEN, Le Hong Thuy ARAI, Sakura TOHYA, Mari ISHIDA-KUROKI, Kasumi NOMOTO, Ryohei KIM, Hyunjung SUZUKI, Eriko OSAWA, Ro WATANABE, Takayasu SEKIZAKI, Tsutomu J Vet Med Sci Bacteriology Streptococcus parasuis has recently been removed taxonomically from Streptococcus suis, a zoonotic pathogen. S. parasuis has been detected in healthy pigs and in diseased pigs, which suggests that S. parasuis is involved in the normal microbiota of pigs and has potential pathogenicity. However, the pathogenicity of S. parasuis in pigs is unclear because of the lack of appropriate detection methods that discriminate S. parasuis from S. suis. In this study, we developed a PCR method that is specific for S. parasuis. The detection limit of the PCR was 350 CFU per reaction. Bacteria isolated from the saliva of eight pigs were collected and examined by PCR. Sixty-four isolates positive for PCR were obtained from the samples of all pigs. Thirteen of the 64 isolates were genetically confirmed as S. parasuis, and biologically and biochemically had nearly the same features of known S. parasuis strains, which suggested that strains positive for PCR were S. parasuis. Among the 64 isolates, 28 isolates were serotypes 20, 22, or 26 in the S. suis serotyping scheme. The remaining 36 isolates were untypeable, which suggested the presence of novel serotypes or a capsule-negative form. Therefore, the PCR method described in this study is a useful tool for identifying S. parasuis, and can be used in etiological studies on this bacterium. The Japanese Society of Veterinary Science 2018-06-06 2018-07 /pmc/articles/PMC6068303/ /pubmed/29877313 http://dx.doi.org/10.1292/jvms.18-0083 Text en ©2018 The Japanese Society of Veterinary Science This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. (CC-BY-NC-ND 4.0: https://creativecommons.org/licenses/by-nc-nd/4.0/) |
spellingShingle | Bacteriology YAMADA, Ryoko TIEN, Le Hong Thuy ARAI, Sakura TOHYA, Mari ISHIDA-KUROKI, Kasumi NOMOTO, Ryohei KIM, Hyunjung SUZUKI, Eriko OSAWA, Ro WATANABE, Takayasu SEKIZAKI, Tsutomu Development of PCR for identifying Streptococcus parasuis, a close relative of Streptococcus suis |
title | Development of PCR for identifying Streptococcus parasuis, a close relative of Streptococcus suis |
title_full | Development of PCR for identifying Streptococcus parasuis, a close relative of Streptococcus suis |
title_fullStr | Development of PCR for identifying Streptococcus parasuis, a close relative of Streptococcus suis |
title_full_unstemmed | Development of PCR for identifying Streptococcus parasuis, a close relative of Streptococcus suis |
title_short | Development of PCR for identifying Streptococcus parasuis, a close relative of Streptococcus suis |
title_sort | development of pcr for identifying streptococcus parasuis, a close relative of streptococcus suis |
topic | Bacteriology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6068303/ https://www.ncbi.nlm.nih.gov/pubmed/29877313 http://dx.doi.org/10.1292/jvms.18-0083 |
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