Identification of Rhodococcus equi using the polymerase chain reaction.
- Comparative Study
- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
This research abstract outlines the selection of species-specific primer sequences for Rhodococcus equi, a pathogenic bacterium, via polymerase chain reaction (PCR) testing. The findings demonstrate the potential of this method to unequivocally identify this species in various hosts, contributing to more effective disease diagnosis and treatment.
Primer Selection and Testing
In their research, the authors selected two regions within the gene that codes for 16S rRNA in Rhodococcus equi as species-specific primer sequences. This was accomplished using the polymerase chain reaction (PCR), a commonly employed technique in molecular biology that can amplify a single or few pieces of DNA across several orders of magnitude to generate thousands to millions of copies of a particular DNA sequence.
- The selected primers were tested against 10 strains of R. equi, including the type strain, resulting in positive outcomes for all but negative for other tested species of Rhodococcus. This indicates the specified primer’s high specificity for R. equi.
- Furthermore, the primers also returned negative results when tested against the most closely related bacterial genera and a variety of other bacterial species. This affirms the primer’s high specificity and could help minimize the risk of false positives.
Potential Applications
The primary application of such a high specificity method lies in its potential to accurately identify Rhodococcus equi. This bacterium can cause infection in the lungs or other organs in a variety of animals including horses, pigs, and humans. Although the abstract does not go into detail, it can be inferred that the PCR method using specific primers can help:
- Accurately diagnose infections caused by R. equi.
- Research the bacterium’s pathogenicity and its interaction with the host.
- Aid in epidemiological investigations, as it allows definitive identification of this pathogenic species.
- Improve treatment strategies by allowing for timely and accurate identification.
The potential applications of this research could be especially significant in veterinary and human medicine, leading to better disease management and understanding of this pathogenic species.
Cite This Article
Publication
Researcher Affiliations
- Department of Biological Sciences, Napier University, Edinburgh, UK. k.bell@napier.ac.uk
MeSH Terms
- Actinomycetales Infections / diagnosis
- Animals
- Horses
- Humans
- Molecular Sequence Data
- Polymerase Chain Reaction / methods
- RNA, Ribosomal, 16S / genetics
- Rhodococcus / genetics
- Rhodococcus / isolation & purification
- Rhodococcus equi / genetics
- Rhodococcus equi / isolation & purification
- Species Specificity
- Swine
Citations
This article has been cited 9 times.- Kalinowski M, Grądzki Z, Jarosz Ł, Adaszek Ł. Molecular analysis of the chromosomal 16S rRNA gene and vapA plasmid gene of Polish field strains of R. equi.. PLoS One 2018;13(9):e0204024.
- Javed R, Taku AK, Sharma RK, Badroo GA. Molecular characterization of Rhodococcus equi isolates in equines.. Vet World 2017 Jan;10(1):6-10.
- Kalinowski M, Grądzki Z, Jarosz Ł, Kato K, Hieda Y, Kakuda T, Takai S. Plasmid Profiles of Virulent Rhodococcus equi Strains Isolated from Infected Foals in Poland.. PLoS One 2016;11(4):e0152887.
- Krewer Cda C, Spricigo DA, de Avila Botton S, da Costa MM, Schrank I, de Vargas AC. Molecular characterization of Rhodococcus equi Isolates of horse breeding farms from an endemic region in South of Brazil by multiplex PCR.. Braz J Microbiol 2008 Jan;39(1):188-93.
- de Vargas AC, Monego F, Gressler LT, de Avila Botton S, Lazzari AM, da Costa MM, Ecco R, Ribeiro MG, Lara GH, Takai S. Bronchopneumonia in wild boar (Sus scrofa) caused by Rhodococcus equi carrying the VapB type 8 plasmid.. BMC Res Notes 2013 Mar 25;6:111.
- Monego F, Maboni F, Krewer C, Vargas A, Costa M, Loreto E. Molecular characterization of Rhodococcus equi from horse-breeding farms by means of multiplex PCR for the vap gene family.. Curr Microbiol 2009 Apr;58(4):399-403.
- Rodríguez-Lázaro D, Lewis DA, Ocampo-Sosa AA, Fogarty U, Makrai L, Navas J, Scortti M, Hernández M, Vázquez-Boland JA. Internally controlled real-time PCR method for quantitative species-specific detection and vapA genotyping of Rhodococcus equi.. Appl Environ Microbiol 2006 Jun;72(6):4256-63.
- Napoleão F, Damasco PV, Camello TC, do Vale MD, de Andrade AF, Hirata R Jr, de Mattos-Guaraldi AL. Pyogenic liver abscess due to Rhodococcus equi in an immunocompetent host.. J Clin Microbiol 2005 Feb;43(2):1002-4.
- Ladrón N, Fernández M, Agüero J, González Zörn B, Vázquez-Boland JA, Navas J. Rapid identification of Rhodococcus equi by a PCR assay targeting the choE gene.. J Clin Microbiol 2003 Jul;41(7):3241-5.