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The nose is not enough: Multi‐site sampling is best for MRSP detection in dogs and households

BACKGROUND: Following recovery from meticillin‐resistant Staphylococcus pseudintermedius (MRSP) infection of any type, dogs may continue to carry MRSP asymptomatically on skin and mucosae, contributing to the spread of this multidrug‐resistant, veterinary hospital‐associated pathogen with zoonotic p...

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Autores principales: Frosini, Sian‐Marie, Bond, Ross, King, Ruth H., Loeffler, Anette
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9804885/
https://www.ncbi.nlm.nih.gov/pubmed/36016486
http://dx.doi.org/10.1111/vde.13118
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author Frosini, Sian‐Marie
Bond, Ross
King, Ruth H.
Loeffler, Anette
author_facet Frosini, Sian‐Marie
Bond, Ross
King, Ruth H.
Loeffler, Anette
author_sort Frosini, Sian‐Marie
collection PubMed
description BACKGROUND: Following recovery from meticillin‐resistant Staphylococcus pseudintermedius (MRSP) infection of any type, dogs may continue to carry MRSP asymptomatically on skin and mucosae, contributing to the spread of this multidrug‐resistant, veterinary hospital‐associated pathogen with zoonotic potential to others and into the environment. OBJECTIVES: This study determined which canine anatomic and household environmental sites are most sensitive for sampling to identify carriage and contamination. METHODS AND MATERIALS: Fifty‐one dogs and 22 households, MRSP‐positive on at least one tested site, were sampled on 132 and 40 occasions over time, respectively. Dogs were swabbed at six sites (mouth, nose, conjunctiva, skin, prepuce/vulva, perianal area); household environments were sampled using contact plates (mannitol salt agar [MSA] and MSA + 6 mg/L oxacillin [MS+]) on five sites. MRSP was isolated after enrichment, grown on MSA/MS+ and was confirmed by PCR. Generalized estimating equations were used for calculation of sensitivity (95% confidence interval) for each site/combination. RESULTS: Each anatomical and environmental site yielded MRSP at least once. MRSP was isolated from only a single site in 27.3% of dogs, with the buccal mucosa showing the highest sensitivity (63.8%). Multi‐site sampling of a minimum of four canine anatomical or four environmental sites, respectively, was needed to achieve >95% sensitivity. CONCLUSIONS AND CLINICAL RELEVANCE: The canine buccal mucosa should be included in MRSP sampling protocols, ideally in addition to at least three other anatomical sites. Likewise, environment sampling should be of multiple household sites in cases where it is used as a part of clinical case management.
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spelling pubmed-98048852023-01-06 The nose is not enough: Multi‐site sampling is best for MRSP detection in dogs and households Frosini, Sian‐Marie Bond, Ross King, Ruth H. Loeffler, Anette Vet Dermatol Brief Communications BACKGROUND: Following recovery from meticillin‐resistant Staphylococcus pseudintermedius (MRSP) infection of any type, dogs may continue to carry MRSP asymptomatically on skin and mucosae, contributing to the spread of this multidrug‐resistant, veterinary hospital‐associated pathogen with zoonotic potential to others and into the environment. OBJECTIVES: This study determined which canine anatomic and household environmental sites are most sensitive for sampling to identify carriage and contamination. METHODS AND MATERIALS: Fifty‐one dogs and 22 households, MRSP‐positive on at least one tested site, were sampled on 132 and 40 occasions over time, respectively. Dogs were swabbed at six sites (mouth, nose, conjunctiva, skin, prepuce/vulva, perianal area); household environments were sampled using contact plates (mannitol salt agar [MSA] and MSA + 6 mg/L oxacillin [MS+]) on five sites. MRSP was isolated after enrichment, grown on MSA/MS+ and was confirmed by PCR. Generalized estimating equations were used for calculation of sensitivity (95% confidence interval) for each site/combination. RESULTS: Each anatomical and environmental site yielded MRSP at least once. MRSP was isolated from only a single site in 27.3% of dogs, with the buccal mucosa showing the highest sensitivity (63.8%). Multi‐site sampling of a minimum of four canine anatomical or four environmental sites, respectively, was needed to achieve >95% sensitivity. CONCLUSIONS AND CLINICAL RELEVANCE: The canine buccal mucosa should be included in MRSP sampling protocols, ideally in addition to at least three other anatomical sites. Likewise, environment sampling should be of multiple household sites in cases where it is used as a part of clinical case management. John Wiley and Sons Inc. 2022-08-25 2022-12 /pmc/articles/PMC9804885/ /pubmed/36016486 http://dx.doi.org/10.1111/vde.13118 Text en © 2022 The Authors. Veterinary Dermatology published by John Wiley & Sons Ltd on behalf of ESVD and ACVD. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Brief Communications
Frosini, Sian‐Marie
Bond, Ross
King, Ruth H.
Loeffler, Anette
The nose is not enough: Multi‐site sampling is best for MRSP detection in dogs and households
title The nose is not enough: Multi‐site sampling is best for MRSP detection in dogs and households
title_full The nose is not enough: Multi‐site sampling is best for MRSP detection in dogs and households
title_fullStr The nose is not enough: Multi‐site sampling is best for MRSP detection in dogs and households
title_full_unstemmed The nose is not enough: Multi‐site sampling is best for MRSP detection in dogs and households
title_short The nose is not enough: Multi‐site sampling is best for MRSP detection in dogs and households
title_sort nose is not enough: multi‐site sampling is best for mrsp detection in dogs and households
topic Brief Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9804885/
https://www.ncbi.nlm.nih.gov/pubmed/36016486
http://dx.doi.org/10.1111/vde.13118
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