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Characterization of fatty acid modifying enzyme activity in staphylococcal mastitis isolates and other bacteria

BACKGROUND: Fatty acid modifying enzyme (FAME) has been shown to modify free fatty acids to alleviate their bactericidal effect by esterifying fatty acids to cholesterol or alcohols. Although it has been shown in previous studies that FAME is required for Staphylococcus aureus survival in skin absce...

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Autores principales: Lu, Thea, Park, Joo Youn, Parnell, Kelleen, Fox, Larry K, McGuire, Mark A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3434086/
https://www.ncbi.nlm.nih.gov/pubmed/22726316
http://dx.doi.org/10.1186/1756-0500-5-323
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author Lu, Thea
Park, Joo Youn
Parnell, Kelleen
Fox, Larry K
McGuire, Mark A
author_facet Lu, Thea
Park, Joo Youn
Parnell, Kelleen
Fox, Larry K
McGuire, Mark A
author_sort Lu, Thea
collection PubMed
description BACKGROUND: Fatty acid modifying enzyme (FAME) has been shown to modify free fatty acids to alleviate their bactericidal effect by esterifying fatty acids to cholesterol or alcohols. Although it has been shown in previous studies that FAME is required for Staphylococcus aureus survival in skin abscesses, FAME is poorly studied compared to other virulence factors. FAME activity had also been detected in coagulase-negative staphylococci (CNS). However, FAME activity was only surveyed after a bacterial culture was grown for 24 h. Therefore if FAME activity was earlier in the growth phase, it would not have been detected by the assay and those strains would have been labeled as FAME negative. RESULTS: Fifty CNS bovine mastitis isolates and several S. aureus, Escherichia coli, and Streptococcus uberis strains were assayed for FAME activity over 24 h. FAME activity was detected in 54% of CNS and 80% S. aureus strains surveyed but none in E. coli or S. uberis. While some CNS strains produced FAME activity comparable to the lab strain of S. aureus, the pattern of FAME activity varied among strains and across species of staphylococci. All CNS that produced FAME activity also exhibited lipase activity. Lipase activity relative to colony forming units of these CNS decreased over the 24 h growth period. No relationship was observed between somatic cell count in the milk and FAME activity in CNS. CONCLUSIONS: Some staphylococcal species surveyed produced FAME activity, but E. coli and S. uberis strains did not. All FAME producing CNS exhibited lipase activity which may indicate that both these enzymes work in concert to alter fatty acids in the bacterial environment.
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spelling pubmed-34340862012-09-06 Characterization of fatty acid modifying enzyme activity in staphylococcal mastitis isolates and other bacteria Lu, Thea Park, Joo Youn Parnell, Kelleen Fox, Larry K McGuire, Mark A BMC Res Notes Research Article BACKGROUND: Fatty acid modifying enzyme (FAME) has been shown to modify free fatty acids to alleviate their bactericidal effect by esterifying fatty acids to cholesterol or alcohols. Although it has been shown in previous studies that FAME is required for Staphylococcus aureus survival in skin abscesses, FAME is poorly studied compared to other virulence factors. FAME activity had also been detected in coagulase-negative staphylococci (CNS). However, FAME activity was only surveyed after a bacterial culture was grown for 24 h. Therefore if FAME activity was earlier in the growth phase, it would not have been detected by the assay and those strains would have been labeled as FAME negative. RESULTS: Fifty CNS bovine mastitis isolates and several S. aureus, Escherichia coli, and Streptococcus uberis strains were assayed for FAME activity over 24 h. FAME activity was detected in 54% of CNS and 80% S. aureus strains surveyed but none in E. coli or S. uberis. While some CNS strains produced FAME activity comparable to the lab strain of S. aureus, the pattern of FAME activity varied among strains and across species of staphylococci. All CNS that produced FAME activity also exhibited lipase activity. Lipase activity relative to colony forming units of these CNS decreased over the 24 h growth period. No relationship was observed between somatic cell count in the milk and FAME activity in CNS. CONCLUSIONS: Some staphylococcal species surveyed produced FAME activity, but E. coli and S. uberis strains did not. All FAME producing CNS exhibited lipase activity which may indicate that both these enzymes work in concert to alter fatty acids in the bacterial environment. BioMed Central 2012-06-22 /pmc/articles/PMC3434086/ /pubmed/22726316 http://dx.doi.org/10.1186/1756-0500-5-323 Text en Copyright ©2012 Lu et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Lu, Thea
Park, Joo Youn
Parnell, Kelleen
Fox, Larry K
McGuire, Mark A
Characterization of fatty acid modifying enzyme activity in staphylococcal mastitis isolates and other bacteria
title Characterization of fatty acid modifying enzyme activity in staphylococcal mastitis isolates and other bacteria
title_full Characterization of fatty acid modifying enzyme activity in staphylococcal mastitis isolates and other bacteria
title_fullStr Characterization of fatty acid modifying enzyme activity in staphylococcal mastitis isolates and other bacteria
title_full_unstemmed Characterization of fatty acid modifying enzyme activity in staphylococcal mastitis isolates and other bacteria
title_short Characterization of fatty acid modifying enzyme activity in staphylococcal mastitis isolates and other bacteria
title_sort characterization of fatty acid modifying enzyme activity in staphylococcal mastitis isolates and other bacteria
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3434086/
https://www.ncbi.nlm.nih.gov/pubmed/22726316
http://dx.doi.org/10.1186/1756-0500-5-323
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