Analyze Diet
Letters in applied microbiology1996; 23(2); 72-74; doi: 10.1111/j.1472-765x.1996.tb00033.x

Identification of Rhodococcus equi using the polymerase chain reaction.

Abstract: Two regions in the gene coding for 16S rRNA in Rhodococcus equi were selected as species-specific primer sequences for the polymerase chain reaction (PCR). PCR using these primers was tested against 10 strains of R. equi (including the type strain) and gave positive results for all but was negative for all other tested species of Rhodococcus; representatives of the most closely related genera and a number of other bacterial species. This method could therefore be used to identify this species which can infect the lungs or other organs of horses, pigs, humans and other animals.
Publication Date: 1996-08-01 PubMed ID: 8987445DOI: 10.1111/j.1472-765x.1996.tb00033.xGoogle Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
  • Comparative Study
  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

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

APA
Bell KS, Philp JC, Christofi N, Aw DW. (1996). Identification of Rhodococcus equi using the polymerase chain reaction. Lett Appl Microbiol, 23(2), 72-74. https://doi.org/10.1111/j.1472-765x.1996.tb00033.x

Publication

ISSN: 0266-8254
NlmUniqueID: 8510094
Country: England
Language: English
Volume: 23
Issue: 2
Pages: 72-74

Researcher Affiliations

Bell, K S
  • Department of Biological Sciences, Napier University, Edinburgh, UK. k.bell@napier.ac.uk
Philp, J C
    Christofi, N
      Aw, D W

        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.
        1. 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.
          doi: 10.1371/journal.pone.0204024pubmed: 30252885google scholar: lookup
        2. Javed R, Taku AK, Sharma RK, Badroo GA. Molecular characterization of Rhodococcus equi isolates in equines.. Vet World 2017 Jan;10(1):6-10.
          doi: 10.14202/vetworld.2017.6-10pubmed: 28246441google scholar: lookup
        3. 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.
          doi: 10.1371/journal.pone.0152887pubmed: 27074033google scholar: lookup
        4. 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.
        5. 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.
          doi: 10.1186/1756-0500-6-111pubmed: 23531380google scholar: lookup
        6. 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.
          doi: 10.1007/s00284-009-9370-6pubmed: 19205798google scholar: lookup
        7. 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.
          doi: 10.1128/AEM.02706-05pubmed: 16751540google scholar: lookup
        8. 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.
        9. 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.