A new method for tracking poultry litter in the Potomac Basin headwaters of West Virginia

Aim To validate the distribution of a poultry litter‐specific marker gene in faecally contaminated environmental waters of an intensive poultry litter rearing region. Methods and Results A TaqMan®‐based qPCR assay for Brevibacterium sp. LA35 16S rRNA (LA35 gene), which was previously shown to be ass...

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Published inJournal of applied microbiology Vol. 115; no. 2; pp. 445 - 454
Main Authors Weidhaas, J., Lipscomb, E.
Format Journal Article
LanguageEnglish
Published Oxford Blackwell 01.08.2013
Oxford University Press
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Abstract Aim To validate the distribution of a poultry litter‐specific marker gene in faecally contaminated environmental waters of an intensive poultry litter rearing region. Methods and Results A TaqMan®‐based qPCR assay for Brevibacterium sp. LA35 16S rRNA (LA35 gene), which was previously shown to be associated with poultry litter and faeces, was tested on 126 nontarget faecal samples and 28 poultry litter and faecal samples. The TaqMan assay was sensitive (76%) and specific (100%) to the LA35 gene and exhibited a detection limit for poultry litter in water samples that is sufficiently low (2·5 × 10−2 mg litter l−1) to be applicable for environmental monitoring. The LA35 gene was detected in 43% of water samples (n = 30) collected in an intensive poultry rearing region of West Virginia which drains to the Chesapeake Bay. Conclusions The poultry‐specific TaqMan qPCR method for the LA35 gene is more specific than previously published methods and can be used to identify regions impacted by poultry rearing activities. Significance and Impact of the Study The LA35 gene appears to have a broad geographical distribution as it has been found in poultry litter and faeces from Delaware and West Virginia, in this study and from Arkansas, Georgia, Florida, Minnesota, Oklahoma and Utah previously.
AbstractList To validate the distribution of a poultry litter-specific marker gene in faecally contaminated environmental waters of an intensive poultry litter rearing region. A TaqMan registered -based qPCR assay for Brevibacterium sp. LA35 16S rRNA (LA35 gene), which was previously shown to be associated with poultry litter and faeces, was tested on 126 nontarget faecal samples and 28 poultry litter and faecal samples. The TaqMan assay was sensitive (76%) and specific (100%) to the LA35 gene and exhibited a detection limit for poultry litter in water samples that is sufficiently low (2.5 x 10 super(-2) mg litter l super(-1)) to be applicable for environmental monitoring. The LA35 gene was detected in 43% of water samples (n = 30) collected in an intensive poultry rearing region of West Virginia which drains to the Chesapeake Bay. The poultry-specific TaqMan qPCR method for the LA35 gene is more specific than previously published methods and can be used to identify regions impacted by poultry rearing activities. The LA35 gene appears to have a broad geographical distribution as it has been found in poultry litter and faeces from Delaware and West Virginia, in this study and from Arkansas, Georgia, Florida, Minnesota, Oklahoma and Utah previously.
Aim To validate the distribution of a poultry litter-specific marker gene in faecally contaminated environmental waters of an intensive poultry litter rearing region. Methods and Results A TaqMan-based qPCR assay for Brevibacterium sp. LA35 16S rRNA (LA35 gene), which was previously shown to be associated with poultry litter and faeces, was tested on 126 nontarget faecal samples and 28 poultry litter and faecal samples. The TaqMan assay was sensitive (76%) and specific (100%) to the LA35 gene and exhibited a detection limit for poultry litter in water samples that is sufficiently low (2·5 × 10-2 mg litter l-1) to be applicable for environmental monitoring. The LA35 gene was detected in 43% of water samples (n = 30) collected in an intensive poultry rearing region of West Virginia which drains to the Chesapeake Bay. Conclusions The poultry-specific TaqMan qPCR method for the LA35 gene is more specific than previously published methods and can be used to identify regions impacted by poultry rearing activities. Significance and Impact of the Study The LA35 gene appears to have a broad geographical distribution as it has been found in poultry litter and faeces from Delaware and West Virginia, in this study and from Arkansas, Georgia, Florida, Minnesota, Oklahoma and Utah previously. [PUBLICATION ABSTRACT]
To validate the distribution of a poultry litter-specific marker gene in faecally contaminated environmental waters of an intensive poultry litter rearing region. A TaqMan(®)-based qPCR assay for Brevibacterium sp. LA35 16S rRNA (LA35 gene), which was previously shown to be associated with poultry litter and faeces, was tested on 126 nontarget faecal samples and 28 poultry litter and faecal samples. The TaqMan assay was sensitive (76%) and specific (100%) to the LA35 gene and exhibited a detection limit for poultry litter in water samples that is sufficiently low (2.5 × 10(-2) mg litter l(-1)) to be applicable for environmental monitoring. The LA35 gene was detected in 43% of water samples (n = 30) collected in an intensive poultry rearing region of West Virginia which drains to the Chesapeake Bay. The poultry-specific TaqMan qPCR method for the LA35 gene is more specific than previously published methods and can be used to identify regions impacted by poultry rearing activities. The LA35 gene appears to have a broad geographical distribution as it has been found in poultry litter and faeces from Delaware and West Virginia, in this study and from Arkansas, Georgia, Florida, Minnesota, Oklahoma and Utah previously.
AIMTo validate the distribution of a poultry litter-specific marker gene in faecally contaminated environmental waters of an intensive poultry litter rearing region.METHODS AND RESULTSA TaqMan(®)-based qPCR assay for Brevibacterium sp. LA35 16S rRNA (LA35 gene), which was previously shown to be associated with poultry litter and faeces, was tested on 126 nontarget faecal samples and 28 poultry litter and faecal samples. The TaqMan assay was sensitive (76%) and specific (100%) to the LA35 gene and exhibited a detection limit for poultry litter in water samples that is sufficiently low (2.5 × 10(-2) mg litter l(-1)) to be applicable for environmental monitoring. The LA35 gene was detected in 43% of water samples (n = 30) collected in an intensive poultry rearing region of West Virginia which drains to the Chesapeake Bay.CONCLUSIONSThe poultry-specific TaqMan qPCR method for the LA35 gene is more specific than previously published methods and can be used to identify regions impacted by poultry rearing activities.SIGNIFICANCE AND IMPACT OF THE STUDYThe LA35 gene appears to have a broad geographical distribution as it has been found in poultry litter and faeces from Delaware and West Virginia, in this study and from Arkansas, Georgia, Florida, Minnesota, Oklahoma and Utah previously.
Aim To validate the distribution of a poultry litter‐specific marker gene in faecally contaminated environmental waters of an intensive poultry litter rearing region. Methods and Results A TaqMan®‐based qPCR assay for Brevibacterium sp. LA35 16S rRNA (LA35 gene), which was previously shown to be associated with poultry litter and faeces, was tested on 126 nontarget faecal samples and 28 poultry litter and faecal samples. The TaqMan assay was sensitive (76%) and specific (100%) to the LA35 gene and exhibited a detection limit for poultry litter in water samples that is sufficiently low (2·5 × 10−2 mg litter l−1) to be applicable for environmental monitoring. The LA35 gene was detected in 43% of water samples (n = 30) collected in an intensive poultry rearing region of West Virginia which drains to the Chesapeake Bay. Conclusions The poultry‐specific TaqMan qPCR method for the LA35 gene is more specific than previously published methods and can be used to identify regions impacted by poultry rearing activities. Significance and Impact of the Study The LA35 gene appears to have a broad geographical distribution as it has been found in poultry litter and faeces from Delaware and West Virginia, in this study and from Arkansas, Georgia, Florida, Minnesota, Oklahoma and Utah previously.
Author Lipscomb, E.
Weidhaas, J.
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Issue 2
Keywords Litter
Applied microbiology
Poultry
poultry litter
Brevibacteriaceae
Brevibacterium sp
Method
Rivers
Surveillance
Microbial source tracking
LA35
Brevibacterium
Bacteria
Actinomycetes
qPCR
Potomac River Basin
Brevibacterium sp. LA35
microbial source tracking
Language English
License CC BY 4.0
2013 The Society for Applied Microbiology.
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Snippet Aim To validate the distribution of a poultry litter‐specific marker gene in faecally contaminated environmental waters of an intensive poultry litter rearing...
To validate the distribution of a poultry litter-specific marker gene in faecally contaminated environmental waters of an intensive poultry litter rearing...
Aim To validate the distribution of a poultry litter-specific marker gene in faecally contaminated environmental waters of an intensive poultry litter rearing...
AIMTo validate the distribution of a poultry litter-specific marker gene in faecally contaminated environmental waters of an intensive poultry litter rearing...
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StartPage 445
SubjectTerms Animals
Biological and medical sciences
Brevibacterium
Brevibacterium - genetics
Brevibacterium - isolation & purification
Brevibacterium sp. LA35
Environmental Monitoring - methods
Feces - microbiology
Fundamental and applied biological sciences. Psychology
microbial source tracking
Microbiology
Polymerase Chain Reaction - methods
Potomac River Basin
Poultry - microbiology
poultry litter
qPCR
Rivers - microbiology
RNA, Ribosomal, 16S - genetics
Water Pollutants - isolation & purification
West Virginia
Title A new method for tracking poultry litter in the Potomac Basin headwaters of West Virginia
URI https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fjam.12231
https://www.ncbi.nlm.nih.gov/pubmed/23611303
https://www.proquest.com/docview/1427803908
https://search.proquest.com/docview/1406175680
https://search.proquest.com/docview/1419373290
Volume 115
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