Literature DB >> 11093626

Control of strangles outbreaks by isolation of guttural pouch carriers identified using PCR and culture of Streptococcus equi.

J R Newton1, K Verheyen, N C Talbot, J F Timoney, J L Wood, K H Lakhani, N Chanter.   

Abstract

Previous use of repeated nasopharyngeal swabbing and culture of Streptococcus equi showed that healthy carriers developed in more than 50% of 'strangles' outbreaks. The guttural pouches were the only detectable site of S. equi colonisation on endoscopic examination of horses during one of these outbreaks and S. equi was sometimes not detected by culture of nasopharyngeal swabs from carriers for up to 2 or 3 months before nasal shedding resumed sporadically. A more sensitive way of detecting S. equi on swabs from established guttural pouch carriers was therefore required. Conveniently selected 'strangles' outbreaks were investigated in detail using endoscopy, in order to develop and assess a suitable polymerase chain reaction (PCR) test. We report here 3 protracted 'strangles' outbreaks on different kinds of establishments in which between 29 and 52% of sampled horses were infected as detected by culture and/or PCR. Of the infected horses, between 9 and 44% were identified as carrying S. equi after clinical signs had disappeared and the predominant site of carriage was the guttural pouch. Prolonged carriage of S. equi, which lasted up to 8 months, did not cease spontaneously before treatment was initiated to eliminate the infections. The detection and isolation of the carriers, in conjunction with strict hygiene measures, apparently resulted in the control of the outbreaks and allowed the premises to return to normal activity. Comparing PCR and culture, many more swabs were found to be positive using PCR (56 vs. 30% of 61 swabs). Similar results were obtained for guttural pouch samples from 12 established carriers (PCR 76% and culture 59%). These results from repeated samples from relatively few animals need confirming using more long-term carriers. PCR can also detect dead organisms and is, therefore, liable to yield false positive results. Despite this drawback, it is argued that PCR provides a potentially useful adjunct to culture of nasopharyngeal swabs in the detection of asymptomatic carriers of S. equi following outbreaks of 'strangles'.

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Year:  2000        PMID: 11093626     DOI: 10.2746/042516400777584721

Source DB:  PubMed          Journal:  Equine Vet J        ISSN: 0425-1644            Impact factor:   2.888


  17 in total

1.  Sequence variation of the SeM gene of Streptococcus equi allows discrimination of the source of strangles outbreaks.

Authors:  Charlotte Kelly; Maxine Bugg; Carl Robinson; Zoe Mitchell; Nick Davis-Poynter; J Richard Newton; Keith A Jolley; Martin C J Maiden; Andrew S Waller
Journal:  J Clin Microbiol       Date:  2006-02       Impact factor: 5.948

2.  Diagnostic testing patterns for Streptococcus equi subsp. equi in Ontario horses during the years 2008 to 2018.

Authors:  Gabrielle Brankston; Tanya M Rossi; Terri L O'Sullivan; Amy L Greer
Journal:  Can Vet J       Date:  2021-06       Impact factor: 1.008

3.  Detection of Streptococcus equi subsp. equi in guttural pouch lavage samples using a loop-mediated isothermal nucleic acid amplification microfluidic device.

Authors:  Ashley G Boyle; Shelley C Rankin; Kathleen O'Shea; Darko Stefanovski; Jing Peng; Jinzhao Song; Haim H Bau
Journal:  J Vet Intern Med       Date:  2021-03-17       Impact factor: 3.333

4.  Nasopharyngeal Microbiomes in Donkeys Shedding Streptococcus equi Subspecies equi in Comparison to Healthy Donkeys.

Authors:  Yiping Zhu; Shulei Chen; Ziwen Yi; Reed Holyoak; Tao Wang; Zhaoliang Ding; Jing Li
Journal:  Front Vet Sci       Date:  2021-04-22

5.  Genome specialization and decay of the strangles pathogen, Streptococcus equi, is driven by persistent infection.

Authors:  Simon R Harris; Carl Robinson; Karen F Steward; Katy S Webb; Romain Paillot; Julian Parkhill; Matthew T G Holden; Andrew S Waller
Journal:  Genome Res       Date:  2015-07-09       Impact factor: 9.043

6.  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

7.  A novel streptococcal integrative conjugative element involved in iron acquisition.

Authors:  Zoe Heather; Matthew T G Holden; Karen F Steward; Julian Parkhill; Lijiang Song; Gregory L Challis; Carl Robinson; Nicholas Davis-Poynter; Andrew S Waller
Journal:  Mol Microbiol       Date:  2008-12       Impact factor: 3.501

8.  A common theme in interaction of bacterial immunoglobulin-binding proteins with immunoglobulins illustrated in the equine system.

Authors:  Melanie J Lewis; Mary Meehan; Peter Owen; Jenny M Woof
Journal:  J Biol Chem       Date:  2008-04-14       Impact factor: 5.157

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

Authors:  Irfan Ahmad Mir; Bablu Kumar; Anil Taku; Farah Faridi; Mohd Altaf Bhat; Naseer Ahmad Baba; Tahir Maqbool
Journal:  J Equine Sci       Date:  2013-09-30

10.  Streptococcus equi Detection Polymerase Chain Reaction Assay for Equine Nasopharyngeal and Guttural Pouch Wash Samples.

Authors:  A G Boyle; S C Rankin; L Duffee; R C Boston; H Wheeler-Aceto
Journal:  J Vet Intern Med       Date:  2015-12-17       Impact factor: 3.333

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