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Comparison of two culture techniques used to detect environmental contamination with Salmonella enterica in a large-animal hospital

Salmonellosis is a common healthcare-associated infection in large-animal hospitals, and surveillance for Salmonella is an integral part of comprehensive infection control programmes in populations at risk. The present study compares the effectiveness of two culture techniques for recovery of Salmon...

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Autores principales: Lyle, Catriona H., Annandale, Cornelius H., Gouws, Johan, Morley, Paul S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AOSIS OpenJournals 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6138090/
https://www.ncbi.nlm.nih.gov/pubmed/26304139
http://dx.doi.org/10.4102/jsava.v86i1.1292
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author Lyle, Catriona H.
Annandale, Cornelius H.
Gouws, Johan
Morley, Paul S.
author_facet Lyle, Catriona H.
Annandale, Cornelius H.
Gouws, Johan
Morley, Paul S.
author_sort Lyle, Catriona H.
collection PubMed
description Salmonellosis is a common healthcare-associated infection in large-animal hospitals, and surveillance for Salmonella is an integral part of comprehensive infection control programmes in populations at risk. The present study compares the effectiveness of two culture techniques for recovery of Salmonella from environmental samples obtained in a large-animal referral veterinary hospital during a Salmonella outbreak. Environmental samples were collected using household cleaning cloths that were incubated overnight in buffered peptone water (BPW). Aliquots of BPW were then processed using two different selective enrichment and culture techniques. In the first technique (TBG-RV-XLT4) samples were incubated at 43 °C in tetrathionate broth and then Rappaport-Vassiliadis broth before plating on XLT4 agar. The second technique (SEL-XLD) involved incubation at 37 °C in selenite broth before plating on XLD agar. Salmonella was recovered from 49.7% (73/147) of samples using the TBG-RV-XLT4 technique, but only 10.2% (15/147) of samples using the SEL-XLD method. Fourteen samples (9.5%) were culture-positive using both methods, and 73 (49.7%) were culture-negative using both techniques. There were discordant results for 60 samples, including 59 that were only culture-positive using the TBG-RV-XLT4 method, and one sample that was only culture-positive using the SEL-XLD method. Salmonella was much more likely to be recovered using the TBG-RV-XLT4 method, and there appeared to be five times more false-negative results using the SEL-XLD technique. Environmental contamination with Salmonella may be underestimated by certain culture techniques, which may impair efforts to control spread in veterinary hospitals.
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spelling pubmed-61380902018-09-26 Comparison of two culture techniques used to detect environmental contamination with Salmonella enterica in a large-animal hospital Lyle, Catriona H. Annandale, Cornelius H. Gouws, Johan Morley, Paul S. J S Afr Vet Assoc Original Research Salmonellosis is a common healthcare-associated infection in large-animal hospitals, and surveillance for Salmonella is an integral part of comprehensive infection control programmes in populations at risk. The present study compares the effectiveness of two culture techniques for recovery of Salmonella from environmental samples obtained in a large-animal referral veterinary hospital during a Salmonella outbreak. Environmental samples were collected using household cleaning cloths that were incubated overnight in buffered peptone water (BPW). Aliquots of BPW were then processed using two different selective enrichment and culture techniques. In the first technique (TBG-RV-XLT4) samples were incubated at 43 °C in tetrathionate broth and then Rappaport-Vassiliadis broth before plating on XLT4 agar. The second technique (SEL-XLD) involved incubation at 37 °C in selenite broth before plating on XLD agar. Salmonella was recovered from 49.7% (73/147) of samples using the TBG-RV-XLT4 technique, but only 10.2% (15/147) of samples using the SEL-XLD method. Fourteen samples (9.5%) were culture-positive using both methods, and 73 (49.7%) were culture-negative using both techniques. There were discordant results for 60 samples, including 59 that were only culture-positive using the TBG-RV-XLT4 method, and one sample that was only culture-positive using the SEL-XLD method. Salmonella was much more likely to be recovered using the TBG-RV-XLT4 method, and there appeared to be five times more false-negative results using the SEL-XLD technique. Environmental contamination with Salmonella may be underestimated by certain culture techniques, which may impair efforts to control spread in veterinary hospitals. AOSIS OpenJournals 2015-08-13 /pmc/articles/PMC6138090/ /pubmed/26304139 http://dx.doi.org/10.4102/jsava.v86i1.1292 Text en © 2015. The Authors http://creativecommons.org/licenses/by/2.0/ Licensee: AOSIS OpenJournals. This work is licensed under the Creative Commons Attribution License.
spellingShingle Original Research
Lyle, Catriona H.
Annandale, Cornelius H.
Gouws, Johan
Morley, Paul S.
Comparison of two culture techniques used to detect environmental contamination with Salmonella enterica in a large-animal hospital
title Comparison of two culture techniques used to detect environmental contamination with Salmonella enterica in a large-animal hospital
title_full Comparison of two culture techniques used to detect environmental contamination with Salmonella enterica in a large-animal hospital
title_fullStr Comparison of two culture techniques used to detect environmental contamination with Salmonella enterica in a large-animal hospital
title_full_unstemmed Comparison of two culture techniques used to detect environmental contamination with Salmonella enterica in a large-animal hospital
title_short Comparison of two culture techniques used to detect environmental contamination with Salmonella enterica in a large-animal hospital
title_sort comparison of two culture techniques used to detect environmental contamination with salmonella enterica in a large-animal hospital
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6138090/
https://www.ncbi.nlm.nih.gov/pubmed/26304139
http://dx.doi.org/10.4102/jsava.v86i1.1292
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