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Comparative immunology, microbiology and infectious diseases2014; 37(3); 169-172; doi: 10.1016/j.cimid.2014.04.001

PCR based differentiation between Streptococcus dysgalactiae subsp. equisimilis strains isolated from humans and horses.

Abstract: Streptococcus dysgalactiae subsp. equisimilis (SDSE) can be severely pathogenic in humans and is increasingly isolated from horses with respiratory, reproductive or other diseases, although it is often considered a commensal bacterium. Here a PCR protocol is described for identifying SDSE recovered from humans. A multiplex PCR targeting the 16S rRNA and the streptokinase precursor gene has been optimized for differentiating between SDSE strains isolated from humans and those isolated from horses. Previously, the sequence of the streptokinase precursor gene of SDSE recovered from horses has been found in two human cases of pneumonia in Japan. Although further evaluation is required, the findings of this study suggest that SDSE strains are host-specific and this multiplex PCR protocol can be useful in further epidemiological studies and for investigating the zoonotic potential of SDSE.
Publication Date: 2014-04-26 PubMed ID: 24813401DOI: 10.1016/j.cimid.2014.04.001Google Scholar: Lookup
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  • Journal Article

Summary

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This research article discusses the creation of a PCR protocol capable of distinguishing between strains of the bacteria Streptococcus dysgalactiae subsp. equisimilis (SDSE) found in humans and those found in horses.

Introduction and Background

  • The bacterial strain Streptococcus dysgalactiae subsp. equisimilis (SDSE) is commonly found in both humans and horses and can cause severe diseases in both species.
  • However, it is often considered a commensal bacterium, meaning it usually lives harmlessly on or in the body without causing disease.
  • Despite their similarities, a recent trend of SDSE-associated diseases specifically within horse populations is being noticed, raising concerns about strain differentiation.

The PCR Protocol

  • To address the need for better differentiation, the researchers developed a multiplex PCR (polymetric chain reaction) protocol, a technique that amplifies DNA from the bacteria to help identify it.
  • This particular protocol targets two specific genes: the 16S rRNA gene, a commonly used benchmark for bacterial identification, and the streptokinase precursor gene, which is involved in the bacteria’s virulence or disease-causing capability.
  • The protocol was created to be able to separate and identify strains of SDSE originating from humans from those found in horses.

Implications and Future Work

  • This PCR protocol, however, needs further testing for validation, as so far the streptokinase precursor gene from SDSE in horses has been reported in only two human cases of pneumonia in Japan, suggesting transmission between species.
  • The findings imply the host-specific nature of different SDSE strains, which can be crucial in understanding and controlling potential zoonotic (animal-to-human) transmission scenarios.
  • The authors proposed that their PCR protocol could be highly useful in future epidemiological studies and in studying the zoonotic capacity of SDSE.

Cite This Article

APA
Preziuso S, Pinho MD, Attili AR, Melo-Cristino J, Acke E, Midwinter AC, Cuteri V, Ramirez M. (2014). PCR based differentiation between Streptococcus dysgalactiae subsp. equisimilis strains isolated from humans and horses. Comp Immunol Microbiol Infect Dis, 37(3), 169-172. https://doi.org/10.1016/j.cimid.2014.04.001

Publication

ISSN: 1878-1667
NlmUniqueID: 7808924
Country: England
Language: English
Volume: 37
Issue: 3
Pages: 169-172
PII: S0147-9571(14)00020-4

Researcher Affiliations

Preziuso, S
  • Department of Biosciences and Veterinary Medicine, University of Camerino, Via Circonvallazione 93/95, 62024 Matelica (MC), Italy. Electronic address: silvia.preziuso@unicam.it.
Pinho, M D
  • Instituto de Microbiologia, Instituto de Medicina Molecular, Faculdade de Medicina, Universidade de Lisboa, Av. Egas Moniz, Lisbon PT 1649-028, Portugal.
Attili, A R
  • Department of Biosciences and Veterinary Medicine, University of Camerino, Via Circonvallazione 93/95, 62024 Matelica (MC), Italy.
Melo-Cristino, J
  • Instituto de Microbiologia, Instituto de Medicina Molecular, Faculdade de Medicina, Universidade de Lisboa, Av. Egas Moniz, Lisbon PT 1649-028, Portugal.
Acke, E
  • Institute of Veterinary, Animal and Biomedical Sciences, Massey University, Palmerston North 4442, New Zealand.
Midwinter, A C
  • Institute of Veterinary, Animal and Biomedical Sciences, Massey University, Palmerston North 4442, New Zealand.
Cuteri, V
  • Department of Biosciences and Veterinary Medicine, University of Camerino, Via Circonvallazione 93/95, 62024 Matelica (MC), Italy.
Ramirez, M
  • Instituto de Microbiologia, Instituto de Medicina Molecular, Faculdade de Medicina, Universidade de Lisboa, Av. Egas Moniz, Lisbon PT 1649-028, Portugal.

MeSH Terms

  • Animals
  • Bacterial Typing Techniques
  • Dogs
  • Genes, Bacterial
  • Horses
  • Host Specificity
  • Humans
  • Multiplex Polymerase Chain Reaction / methods
  • RNA, Ribosomal, 16S / genetics
  • Streptococcus / classification
  • Streptococcus / genetics
  • Streptococcus / isolation & purification
  • Streptokinase / genetics

Citations

This article has been cited 8 times.
  1. Winter JC, Thieme K, Eule JC, Saliu EM, Kershaw O, Gehlen H. Photodermatitis and ocular changes in nine horses after ingestion of wild parsnip (pastinaca sativa). BMC Vet Res 2022 Feb 26;18(1):80.
    doi: 10.1186/s12917-022-03162-2pubmed: 35219345google scholar: lookup
  2. Oh SI, Kim JW, Kim J, So B, Kim B, Kim HY. Molecular subtyping and antimicrobial susceptibility of Streptococcus dysgalactiae subspecies equisimilis isolates from clinically diseased pigs. J Vet Sci 2020 Jul;21(4):e57.
    doi: 10.4142/jvs.2020.21.e57pubmed: 32735095google scholar: lookup
  3. Preziuso S, Sgorbini M, Marmorini P, Cuteri V. Equid alphaherpesvirus 1 from Italian Horses: Evaluation of the Variability of the ORF30, ORF33, ORF34 and ORF68 Genes. Viruses 2019 Sep 13;11(9).
    doi: 10.3390/v11090851pubmed: 31540321google scholar: lookup
  4. Babbar A, Itzek A, Pieper DH, Nitsche-Schmitz DP. Detection of Streptococcus pyogenes virulence genes in Streptococcus dysgalactiae subsp. equisimilis from Vellore, India. Folia Microbiol (Praha) 2018 Sep;63(5):581-586.
    doi: 10.1007/s12223-018-0595-2pubmed: 29532420google scholar: lookup
  5. Ciszewski M, Szewczyk EM. Potential Factors Enabling Human Body Colonization by Animal Streptococcus dysgalactiae subsp. equisimilis Strains. Curr Microbiol 2017 May;74(5):650-654.
    doi: 10.1007/s00284-017-1232-zpubmed: 28314902google scholar: lookup
  6. Pinho MD, Erol E, Ribeiro-Gonçalves B, Mendes CI, Carriço JA, Matos SC, Preziuso S, Luebke-Becker A, Wieler LH, Melo-Cristino J, Ramirez M. Beta-hemolytic Streptococcus dysgalactiae strains isolated from horses are a genetically distinct population within the Streptococcus dysgalactiae taxon. Sci Rep 2016 Aug 17;6:31736.
    doi: 10.1038/srep31736pubmed: 27530432google scholar: lookup
  7. Ciszewski M, Zegarski K, Szewczyk EM. Streptococcus dysgalactiae subsp. equisimilis Isolated From Infections in Dogs and Humans: Are Current Subspecies Identification Criteria accurate?. Curr Microbiol 2016 Nov;73(5):684-688.
    doi: 10.1007/s00284-016-1113-xpubmed: 27502064google scholar: lookup
  8. Xie O, Davies MR, Tong SYC. Streptococcus dysgalactiae subsp. equisimilis infection and its intersection with Streptococcus pyogenes. Clin Microbiol Rev 2024 Sep 12;37(3):e0017523.
    doi: 10.1128/cmr.00175-23pubmed: 38856686google scholar: lookup