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PCR-RFLP Detection and Genogroup Identification of Piscirickettsia salmonis in Field Samples
Piscirickettsia salmons, the causative agent of piscirickettsiosis, is genetically divided into two genomic groups, named after the reference strains as LF-89-like or EM-90-like. Phenotypic differences have been detected between the P. salmonis genogroups, including antibiotic susceptibilities, host...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7281544/ https://www.ncbi.nlm.nih.gov/pubmed/32397152 http://dx.doi.org/10.3390/pathogens9050358 |
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author | Aravena, Pamela Pulgar, Rodrigo Ortiz-Severín, Javiera Maza, Felipe Gaete, Alexis Martínez, Sebastián Serón, Ervin González, Mauricio Cambiazo, Verónica |
author_facet | Aravena, Pamela Pulgar, Rodrigo Ortiz-Severín, Javiera Maza, Felipe Gaete, Alexis Martínez, Sebastián Serón, Ervin González, Mauricio Cambiazo, Verónica |
author_sort | Aravena, Pamela |
collection | PubMed |
description | Piscirickettsia salmons, the causative agent of piscirickettsiosis, is genetically divided into two genomic groups, named after the reference strains as LF-89-like or EM-90-like. Phenotypic differences have been detected between the P. salmonis genogroups, including antibiotic susceptibilities, host specificities and pathogenicity. In this study, we aimed to develop a rapid, sensitive and cost-effective assay for the differentiation of the P. salmonis genogroups. Using an in silico analysis of the P. salmonis 16S rDNA digestion patterns, we have designed a genogroup-specific assay based on PCR-restriction fragment length polymorphism (RFLP). An experimental validation was carried out by comparing the restriction patterns of 13 P. salmonis strains and 57 field samples obtained from the tissues of dead or moribund fish. When the bacterial composition of a set of field samples, for which we detected mixtures of bacterial DNA, was analyzed by a high-throughput sequencing of the 16S rRNA gene amplicons, a diversity of taxa could be identified, including pathogenic and commensal bacteria. Despite the presence of mixtures of bacterial DNA, the characteristic digestion pattern of the P. salmonis genogroups could be detected in the field samples without the need of a microbiological culture and bacterial isolation. |
format | Online Article Text |
id | pubmed-7281544 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-72815442020-06-17 PCR-RFLP Detection and Genogroup Identification of Piscirickettsia salmonis in Field Samples Aravena, Pamela Pulgar, Rodrigo Ortiz-Severín, Javiera Maza, Felipe Gaete, Alexis Martínez, Sebastián Serón, Ervin González, Mauricio Cambiazo, Verónica Pathogens Article Piscirickettsia salmons, the causative agent of piscirickettsiosis, is genetically divided into two genomic groups, named after the reference strains as LF-89-like or EM-90-like. Phenotypic differences have been detected between the P. salmonis genogroups, including antibiotic susceptibilities, host specificities and pathogenicity. In this study, we aimed to develop a rapid, sensitive and cost-effective assay for the differentiation of the P. salmonis genogroups. Using an in silico analysis of the P. salmonis 16S rDNA digestion patterns, we have designed a genogroup-specific assay based on PCR-restriction fragment length polymorphism (RFLP). An experimental validation was carried out by comparing the restriction patterns of 13 P. salmonis strains and 57 field samples obtained from the tissues of dead or moribund fish. When the bacterial composition of a set of field samples, for which we detected mixtures of bacterial DNA, was analyzed by a high-throughput sequencing of the 16S rRNA gene amplicons, a diversity of taxa could be identified, including pathogenic and commensal bacteria. Despite the presence of mixtures of bacterial DNA, the characteristic digestion pattern of the P. salmonis genogroups could be detected in the field samples without the need of a microbiological culture and bacterial isolation. MDPI 2020-05-08 /pmc/articles/PMC7281544/ /pubmed/32397152 http://dx.doi.org/10.3390/pathogens9050358 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Aravena, Pamela Pulgar, Rodrigo Ortiz-Severín, Javiera Maza, Felipe Gaete, Alexis Martínez, Sebastián Serón, Ervin González, Mauricio Cambiazo, Verónica PCR-RFLP Detection and Genogroup Identification of Piscirickettsia salmonis in Field Samples |
title | PCR-RFLP Detection and Genogroup Identification of Piscirickettsia salmonis in Field Samples |
title_full | PCR-RFLP Detection and Genogroup Identification of Piscirickettsia salmonis in Field Samples |
title_fullStr | PCR-RFLP Detection and Genogroup Identification of Piscirickettsia salmonis in Field Samples |
title_full_unstemmed | PCR-RFLP Detection and Genogroup Identification of Piscirickettsia salmonis in Field Samples |
title_short | PCR-RFLP Detection and Genogroup Identification of Piscirickettsia salmonis in Field Samples |
title_sort | pcr-rflp detection and genogroup identification of piscirickettsia salmonis in field samples |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7281544/ https://www.ncbi.nlm.nih.gov/pubmed/32397152 http://dx.doi.org/10.3390/pathogens9050358 |
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