Literature DB >> 10846214

Streptococcus equi with truncated M-proteins isolated from outwardly healthy horses.

Neil Chanter1, Nicola C Talbot1, J Richard Newton1, Dawn Hewson1, Kristien Verheyen1.   

Abstract

The M-protein genes of Streptococcus equi isolated from 17 outwardly healthy horses after 4 strangles outbreaks had ended, including a quarantined animal, were compared with those of S. equi isolates from 167 active cases of strangles across 4 countries. The healthy horses included 16 persistent S. equi carriers, at least one from each of the four outbreaks. These carriers, despite being outwardly healthy, had empyema of the guttural pouch(es), an enlargement of the equine Eustachian tube. A persistent carrier from two of these outbreaks, the quarantined animal and a healthy animal with normal guttural pouches, from which S. equi was isolated only once, were colonized by variant S. equi with truncated M-protein genes (24% of outwardly healthy animals with S. equi). The truncated M-protein genes had in-frame deletions in slightly different positions between the signal sequence and the central repeat region, equivalent to approximately 20% of the mature expressed protein. Immunoblotting with antibody to recombinant M-protein confirmed that the variants expressed a truncated form of the M-protein. In contrast to the outwardly healthy S. equi carriers, only 1/167 of S. equi isolates from strangles cases possessed a truncated M-protein gene (<1%; Fisher's exact test, P=0.0002). Compared with isolates from healthy horses with a truncated M-protein, much more of the N terminus of the truncated M-protein was retained in the variant S. equi from a strangles case. Variant S. equi from outwardly healthy animals were more susceptible to phagocytosis by neutrophils in vitro than typical isolates. This is the first report of detection of S. equi with a truncated M-protein. The distribution of the variants between strangles cases and carriers suggests that the 80% of the M-protein retained in the variants may contribute to colonization whilst the deleted portion of the gene may be needed for full virulence.

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Year:  2000        PMID: 10846214     DOI: 10.1099/00221287-146-6-1361

Source DB:  PubMed          Journal:  Microbiology        ISSN: 1350-0872            Impact factor:   2.777


  5 in total

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2.  Comparison of nasopharyngeal and guttural pouch specimens to determine the optimal sampling site to detect Streptococcus equi subsp equi carriers by DNA amplification.

Authors:  Ashley G Boyle; Darko Stefanovski; Shelley C Rankin
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3.  The impact of a pathogenic bacterium on a social carnivore population.

Authors:  Oliver P Höner; Bettina Wachter; Katja V Goller; Heribert Hofer; Victor Runyoro; Dagmar Thierer; Robert D Fyumagwa; Thomas Müller; Marion L East
Journal:  J Anim Ecol       Date:  2011-06-01       Impact factor: 5.091

4.  Detection of Streptococcus equi subspecies equi using a triplex qPCR assay.

Authors:  Katy Webb; Colin Barker; Tihana Harrison; Zoe Heather; Karen F Steward; Carl Robinson; J Richard Newton; Andrew S Waller
Journal:  Vet J       Date:  2012-08-10       Impact factor: 2.688

5.  Decreased Clinical Severity of Strangles in Weanlings Associated with Restricted Seroconversion to Optimized Streptococcus equi ssp equi Assays.

Authors:  L Tscheschlok; M Venner; K Steward; R Böse; M Riihimäki; J Pringle
Journal:  J Vet Intern Med       Date:  2018-01       Impact factor: 3.333

  5 in total

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