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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...

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Autores principales: Aravena, Pamela, Pulgar, Rodrigo, Ortiz-Severín, Javiera, Maza, Felipe, Gaete, Alexis, Martínez, Sebastián, Serón, Ervin, González, Mauricio, Cambiazo, Verónica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
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.
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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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