Molecular epidemiology of coagulase-negative

Coagulase negative Staphylococcus (CNS) Epidemiology Genetic relatedness Mastitis pathogens Phylogeny Pulse-field gel electrophoresis (PFGE)

Journal

PeerJ
ISSN: 2167-8359
Titre abrégé: PeerJ
Pays: United States
ID NLM: 101603425

Informations de publication

Date de publication:
2019
Historique:
received: 08 10 2018
accepted: 08 03 2019
entrez: 24 5 2019
pubmed: 24 5 2019
medline: 24 5 2019
Statut: epublish

Résumé

Coagulase negative A total of 604 CNS isolates were cultured from milk samples collected during a dry-cow treatment clinical trial conducted on 6 dairy herds in 4 states in the US. All the study cows were randomized to receive 1 of the 3 different intra-mammary antimicrobial infusions (Quatermaster, Spectramast DC or ToMorrow Dry Cow) at dry-off. Milk samples were collected at dry-off, calving (0-6 days in milk, DIM), post-calving (7-13 DIM) and at mastitis events within the first 100 DIM. The CNS isolates were identified to species level by partial sequencing of the The major CNS species identified were The observed association between genetic and epidemiological distributions indicated animal-adapted nature of four CNS species, suggesting possible host-adapted and environmental transmission of these species. Multi-stage isolation of the same udder quarter strain was evidence for chronic intra-mammary infection. The different CNS species and strains circulating on US dairy herds were genetically diverse. Four species identified were likely udder-adapted pathogens, 2 of which caused persistent infection. Our findings are important in guiding the design of effective mastitis control strategies.

Sections du résumé

BACKGROUND BACKGROUND
Coagulase negative
METHODOLOGY METHODS
A total of 604 CNS isolates were cultured from milk samples collected during a dry-cow treatment clinical trial conducted on 6 dairy herds in 4 states in the US. All the study cows were randomized to receive 1 of the 3 different intra-mammary antimicrobial infusions (Quatermaster, Spectramast DC or ToMorrow Dry Cow) at dry-off. Milk samples were collected at dry-off, calving (0-6 days in milk, DIM), post-calving (7-13 DIM) and at mastitis events within the first 100 DIM. The CNS isolates were identified to species level by partial sequencing of the
RESULTS RESULTS
The major CNS species identified were
DISCUSSION CONCLUSIONS
The observed association between genetic and epidemiological distributions indicated animal-adapted nature of four CNS species, suggesting possible host-adapted and environmental transmission of these species. Multi-stage isolation of the same udder quarter strain was evidence for chronic intra-mammary infection.
CONCLUSION CONCLUSIONS
The different CNS species and strains circulating on US dairy herds were genetically diverse. Four species identified were likely udder-adapted pathogens, 2 of which caused persistent infection. Our findings are important in guiding the design of effective mastitis control strategies.

Identifiants

pubmed: 31119068
doi: 10.7717/peerj.6749
pii: 6749
pmc: PMC6507897
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e6749

Déclaration de conflit d'intérêts

The authors declare there are no competing interests.

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Auteurs

Stephen N Jenkins (SN)

Veterinary Medicine Teaching and Research Center, School of Veterinary Medicine, University of California, Davis, Tulare, CA, United States of America.

Emmanuel Okello (E)

Veterinary Medicine Teaching and Research Center, School of Veterinary Medicine, University of California, Davis, Tulare, CA, United States of America.
Department of Population Health & Reproduction, School of Veterinary Medicine, University of California, Davis, CA, United States of America.

Paul V Rossitto (PV)

Veterinary Medicine Teaching and Research Center, School of Veterinary Medicine, University of California, Davis, Tulare, CA, United States of America.

Terry W Lehenbauer (TW)

Veterinary Medicine Teaching and Research Center, School of Veterinary Medicine, University of California, Davis, Tulare, CA, United States of America.
Department of Population Health & Reproduction, School of Veterinary Medicine, University of California, Davis, CA, United States of America.

John Champagne (J)

Veterinary Medicine Teaching and Research Center, School of Veterinary Medicine, University of California, Davis, Tulare, CA, United States of America.

Maria C T Penedo (MCT)

Veterinary Genetics Laboratory, University of California, Davis, CA, United States of America.

Andréia G Arruda (AG)

Department of Veterinary Preventive Medicine, College of Veterinary Medicine, The Ohio State University, Columbus, OH, United States of America.

Sandra Godden (S)

Department of Veterinary Population Medicine, University of Minnesota, Saint Paul, MN, United States of America.

Paul Rapnicki (P)

Department of Veterinary Population Medicine, University of Minnesota, Saint Paul, MN, United States of America.

Patrick J Gorden (PJ)

Veterinary Diagnostic and Production Animal Medicine, Iowa State University, Ames, IA, United States of America.

Leo L Timms (LL)

Department of Animal Science, College of Agriculture and Life Sciences, Iowa State University, Ames, IA, United States of America.

Sharif S Aly (SS)

Veterinary Medicine Teaching and Research Center, School of Veterinary Medicine, University of California, Davis, Tulare, CA, United States of America.
Department of Population Health & Reproduction, School of Veterinary Medicine, University of California, Davis, CA, United States of America.

Classifications MeSH