Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2013;24(3):53-5.
doi: 10.1294/jes.24.53. Epub 2013 Sep 30.

Bacteriological and Molecular Detection of Streptococcus equi subsp. equi and Streptococcus equi subsp. zooepidemicus in Equines of Northern India

Affiliations

Bacteriological and Molecular Detection of Streptococcus equi subsp. equi and Streptococcus equi subsp. zooepidemicus in Equines of Northern India

Irfan Ahmad Mir et al. J Equine Sci. 2013.

Abstract

Present study was undertaken to study the prevalence of β-haemolytic streptococci in equine of northern temperate region of Jammu and Kashmir, India. One hundred and forty one samples were collected in duplicate from nasopharyngeal tract of diseased (53) and apparently healthy equine (88) for isolation and direct PCR. A total of 77 isolates of streptococci were recovered from 141 samples with an overall prevalence rate of 54.60%. Out of these 77 isolates, 52 were from diseased and 25 from apparently healthy animals. Of the 77 isolates, 4 were identified as Streptococcus equi subsp. equi, 56 as S. equi subsp. zooepidemicus and 17 as S. dysgalactiae subsp. equisimilis. Thus the overall prevalence of S. equi subsp. equi, S. equi subsp. zooepidemicus and S. dysgalactiae subsp. equisimilis was 2.83, 39.71 and 12.05% respectively. The sensitivity of the PCR for the detection of S. equi species was found higher when attempted from direct swab samples.

Keywords: S. dysgalactiae subsp. equisimilis; S. equi subsp. zooepidemicus; Streptococcus equi subsp. equi; equine.

PubMed Disclaimer

Figures

Fig. 1.
Fig. 1.
PCR amplified product of Sod A gene (235 bp) for S. equi species and SeM gene (679 bp) for S. equi subsp. equi. Lane M: 100 bp ladder, Lane 1–3: Positive samples of S. equi subsp. equi (679 bp); Lane 4, 6 & 7: Positive samples of S. equi species (235 bp); lane 5: negative sample.

Similar articles

Cited by

References

    1. Alber J., El-Sayed A., Lammler C., Hassan A., Weiss R., Zschock M.2004. Multiplex polymerase chain reaction for identification and differentiation of Streptococcus equi subsp. zooepidemicus and Streptococcus equi subsp. equi. J. Vet. Med. B. 51: 455–458 - PubMed
    1. Chen W.P., Kou T.T.1993. A simple and rapid method for the preparation of Gram-negative bacterial genomic DNA. Nuc. Aci. Res 21: 2260 - PMC - PubMed
    1. Halliwell R.E.W., McGorum B.C., Irving P., Dixon P.M.1993. Local and systemic antibody production in horses affected with chronic obstructive pulmonary disease. Vet. Immunol. Immunopathol. 38: 201–215 - PubMed
    1. Jannatabadi A.A., Mohammadi G.R., Rad M., Maleki M.2008. Molecular identification of Streptococcus equi subsp. equi and Streptococcus equi subsp. zooepidemicus in nasal swabs samples from horses suffering respiratory infections in Iran. Pak. J. Biol. Sci. 11: 468–471 - PubMed
    1. Laus F., Preziuso S., Spaterna A., Beribe F.2007. Clinical and epidemiological investigation of chronic upper respiratory diseases caused by beta haemolytic Streptococci in horses. Comp. Immunol. Microbiol. Infect. Dis. 12: 247–260 - PubMed

LinkOut - more resources