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Whole-Genome Sequencing and Concordance Between Antimicrobial Susceptibility Genotypes and Phenotypes of Bacterial Isolates Associated with Bovine Respiratory Disease

Extended laboratory culture and antimicrobial susceptibility testing timelines hinder rapid species identification and susceptibility profiling of bacterial pathogens associated with bovine respiratory disease, the most prevalent cause of cattle mortality in the United States. Whole-genome sequencin...

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Autores principales: Owen, Joseph R., Noyes, Noelle, Young, Amy E., Prince, Daniel J., Blanchard, Patricia C., Lehenbauer, Terry W., Aly, Sharif S., Davis, Jessica H., O’Rourke, Sean M., Abdo, Zaid, Belk, Keith, Miller, Michael R., Morley, Paul, Van Eenennaam, Alison L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5592931/
https://www.ncbi.nlm.nih.gov/pubmed/28739600
http://dx.doi.org/10.1534/g3.117.1137
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author Owen, Joseph R.
Noyes, Noelle
Young, Amy E.
Prince, Daniel J.
Blanchard, Patricia C.
Lehenbauer, Terry W.
Aly, Sharif S.
Davis, Jessica H.
O’Rourke, Sean M.
Abdo, Zaid
Belk, Keith
Miller, Michael R.
Morley, Paul
Van Eenennaam, Alison L.
author_facet Owen, Joseph R.
Noyes, Noelle
Young, Amy E.
Prince, Daniel J.
Blanchard, Patricia C.
Lehenbauer, Terry W.
Aly, Sharif S.
Davis, Jessica H.
O’Rourke, Sean M.
Abdo, Zaid
Belk, Keith
Miller, Michael R.
Morley, Paul
Van Eenennaam, Alison L.
author_sort Owen, Joseph R.
collection PubMed
description Extended laboratory culture and antimicrobial susceptibility testing timelines hinder rapid species identification and susceptibility profiling of bacterial pathogens associated with bovine respiratory disease, the most prevalent cause of cattle mortality in the United States. Whole-genome sequencing offers a culture-independent alternative to current bacterial identification methods, but requires a library of bacterial reference genomes for comparison. To contribute new bacterial genome assemblies and evaluate genetic diversity and variation in antimicrobial resistance genotypes, whole-genome sequencing was performed on bovine respiratory disease–associated bacterial isolates (Histophilus somni, Mycoplasma bovis, Mannheimia haemolytica, and Pasteurella multocida) from dairy and beef cattle. One hundred genomically distinct assemblies were added to the NCBI database, doubling the available genomic sequences for these four species. Computer-based methods identified 11 predicted antimicrobial resistance genes in three species, with none being detected in M. bovis. While computer-based analysis can identify antibiotic resistance genes within whole-genome sequences (genotype), it may not predict the actual antimicrobial resistance observed in a living organism (phenotype). Antimicrobial susceptibility testing on 64 H. somni, M. haemolytica, and P. multocida isolates had an overall concordance rate between genotype and phenotypic resistance to the associated class of antimicrobials of 72.7% (P < 0.001), showing substantial discordance. Concordance rates varied greatly among different antimicrobial, antibiotic resistance gene, and bacterial species combinations. This suggests that antimicrobial susceptibility phenotypes are needed to complement genomically predicted antibiotic resistance gene genotypes to better understand how the presence of antibiotic resistance genes within a given bacterial species could potentially impact optimal bovine respiratory disease treatment and morbidity/mortality outcomes.
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spelling pubmed-55929312017-09-14 Whole-Genome Sequencing and Concordance Between Antimicrobial Susceptibility Genotypes and Phenotypes of Bacterial Isolates Associated with Bovine Respiratory Disease Owen, Joseph R. Noyes, Noelle Young, Amy E. Prince, Daniel J. Blanchard, Patricia C. Lehenbauer, Terry W. Aly, Sharif S. Davis, Jessica H. O’Rourke, Sean M. Abdo, Zaid Belk, Keith Miller, Michael R. Morley, Paul Van Eenennaam, Alison L. G3 (Bethesda) Investigations Extended laboratory culture and antimicrobial susceptibility testing timelines hinder rapid species identification and susceptibility profiling of bacterial pathogens associated with bovine respiratory disease, the most prevalent cause of cattle mortality in the United States. Whole-genome sequencing offers a culture-independent alternative to current bacterial identification methods, but requires a library of bacterial reference genomes for comparison. To contribute new bacterial genome assemblies and evaluate genetic diversity and variation in antimicrobial resistance genotypes, whole-genome sequencing was performed on bovine respiratory disease–associated bacterial isolates (Histophilus somni, Mycoplasma bovis, Mannheimia haemolytica, and Pasteurella multocida) from dairy and beef cattle. One hundred genomically distinct assemblies were added to the NCBI database, doubling the available genomic sequences for these four species. Computer-based methods identified 11 predicted antimicrobial resistance genes in three species, with none being detected in M. bovis. While computer-based analysis can identify antibiotic resistance genes within whole-genome sequences (genotype), it may not predict the actual antimicrobial resistance observed in a living organism (phenotype). Antimicrobial susceptibility testing on 64 H. somni, M. haemolytica, and P. multocida isolates had an overall concordance rate between genotype and phenotypic resistance to the associated class of antimicrobials of 72.7% (P < 0.001), showing substantial discordance. Concordance rates varied greatly among different antimicrobial, antibiotic resistance gene, and bacterial species combinations. This suggests that antimicrobial susceptibility phenotypes are needed to complement genomically predicted antibiotic resistance gene genotypes to better understand how the presence of antibiotic resistance genes within a given bacterial species could potentially impact optimal bovine respiratory disease treatment and morbidity/mortality outcomes. Genetics Society of America 2017-07-26 /pmc/articles/PMC5592931/ /pubmed/28739600 http://dx.doi.org/10.1534/g3.117.1137 Text en Copyright © 2017 Owen et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Investigations
Owen, Joseph R.
Noyes, Noelle
Young, Amy E.
Prince, Daniel J.
Blanchard, Patricia C.
Lehenbauer, Terry W.
Aly, Sharif S.
Davis, Jessica H.
O’Rourke, Sean M.
Abdo, Zaid
Belk, Keith
Miller, Michael R.
Morley, Paul
Van Eenennaam, Alison L.
Whole-Genome Sequencing and Concordance Between Antimicrobial Susceptibility Genotypes and Phenotypes of Bacterial Isolates Associated with Bovine Respiratory Disease
title Whole-Genome Sequencing and Concordance Between Antimicrobial Susceptibility Genotypes and Phenotypes of Bacterial Isolates Associated with Bovine Respiratory Disease
title_full Whole-Genome Sequencing and Concordance Between Antimicrobial Susceptibility Genotypes and Phenotypes of Bacterial Isolates Associated with Bovine Respiratory Disease
title_fullStr Whole-Genome Sequencing and Concordance Between Antimicrobial Susceptibility Genotypes and Phenotypes of Bacterial Isolates Associated with Bovine Respiratory Disease
title_full_unstemmed Whole-Genome Sequencing and Concordance Between Antimicrobial Susceptibility Genotypes and Phenotypes of Bacterial Isolates Associated with Bovine Respiratory Disease
title_short Whole-Genome Sequencing and Concordance Between Antimicrobial Susceptibility Genotypes and Phenotypes of Bacterial Isolates Associated with Bovine Respiratory Disease
title_sort whole-genome sequencing and concordance between antimicrobial susceptibility genotypes and phenotypes of bacterial isolates associated with bovine respiratory disease
topic Investigations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5592931/
https://www.ncbi.nlm.nih.gov/pubmed/28739600
http://dx.doi.org/10.1534/g3.117.1137
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