Transcriptomic differences noted in Glaesserella parasuis between growth in broth and on agar

Glaesserella parasuis is the cause of Glӓsser's disease in pigs and is a significant contributor to post-weaning mortality in the swine industry. Prevention of G. parasuis disease relies primarily on bacterin vaccines, which have shown good homologous protection and variable heterologous protec...

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Published inPloS one Vol. 14; no. 8; p. e0220365
Main Authors Hau, Samantha J, Mou, Kathy T, Bayles, Darrell O, Brockmeier, Susan L
Format Journal Article
LanguageEnglish
Published United States Public Library of Science 06.08.2019
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Abstract Glaesserella parasuis is the cause of Glӓsser's disease in pigs and is a significant contributor to post-weaning mortality in the swine industry. Prevention of G. parasuis disease relies primarily on bacterin vaccines, which have shown good homologous protection and variable heterologous protection. Bacterin production involves large scale growth of the bacteria and proteins produced during the proliferation phase of production become important antigens that stimulate the immune response. In order to evaluate genes activated during G. parasuis growth on different media substrates, the transcriptome of broth and agar grown G. parasuis strain 29755 were sequenced and compared. The transcription of most purported virulence genes were comparable between broth and agar grown G. parasuis; however, four virulence-associated genes, including ompA and vapD, had elevated expression under agar growth, while six virulence-associate genes had elevated expression during broth growth, including several protease genes. Additionally, there were metabolic shifts toward increased protein and lipid production and increased cellular division in broth grown G. parasuis. The results contribute to the understanding of how growth substrate alters gene transcription and protein expression, which may impact vaccine efficacy if immunogens important to the protective immune response are not produced under specific in vitro conditions. While the results of this work are unable to fully elucidate which growth medium presents a transcriptome more representative of in vivo samples or best suited for bacterin production, it forms a foundation that can be used for future comparisons and provides a better understanding of the metabolic differences in broth and agar grown bacteria.
AbstractList Glaesserella parasuis is the cause of Glӓsser's disease in pigs and is a significant contributor to post-weaning mortality in the swine industry. Prevention of G. parasuis disease relies primarily on bacterin vaccines, which have shown good homologous protection and variable heterologous protection. Bacterin production involves large scale growth of the bacteria and proteins produced during the proliferation phase of production become important antigens that stimulate the immune response. In order to evaluate genes activated during G. parasuis growth on different media substrates, the transcriptome of broth and agar grown G. parasuis strain 29755 were sequenced and compared. The transcription of most purported virulence genes were comparable between broth and agar grown G. parasuis; however, four virulence-associated genes, including ompA and vapD, had elevated expression under agar growth, while six virulence-associate genes had elevated expression during broth growth, including several protease genes. Additionally, there were metabolic shifts toward increased protein and lipid production and increased cellular division in broth grown G. parasuis. The results contribute to the understanding of how growth substrate alters gene transcription and protein expression, which may impact vaccine efficacy if immunogens important to the protective immune response are not produced under specific in vitro conditions. While the results of this work are unable to fully elucidate which growth medium presents a transcriptome more representative of in vivo samples or best suited for bacterin production, it forms a foundation that can be used for future comparisons and provides a better understanding of the metabolic differences in broth and agar grown bacteria.
Glaesserella parasuis is the cause of GlÓsser's disease in pigs and is a significant contributor to post-weaning mortality in the swine industry. Prevention of G. parasuis disease relies primarily on bacterin vaccines, which have shown good homologous protection and variable heterologous protection. Bacterin production involves large scale growth of the bacteria and proteins produced during the proliferation phase of production become important antigens that stimulate the immune response. In order to evaluate genes activated during G. parasuis growth on different media substrates, the transcriptome of broth and agar grown G. parasuis strain 29755 were sequenced and compared. The transcription of most purported virulence genes were comparable between broth and agar grown G. parasuis; however, four virulence-associated genes, including ompA and vapD, had elevated expression under agar growth, while six virulence-associate genes had elevated expression during broth growth, including several protease genes. Additionally, there were metabolic shifts toward increased protein and lipid production and increased cellular division in broth grown G. parasuis. The results contribute to the understanding of how growth substrate alters gene transcription and protein expression, which may impact vaccine efficacy if immunogens important to the protective immune response are not produced under specific in vitro conditions. While the results of this work are unable to fully elucidate which growth medium presents a transcriptome more representative of in vivo samples or best suited for bacterin production, it forms a foundation that can be used for future comparisons and provides a better understanding of the metabolic differences in broth and agar grown bacteria.
Glaesserella parasuis is the cause of Glӓsser’s disease in pigs and is a significant contributor to post-weaning mortality in the swine industry. Prevention of G . parasuis disease relies primarily on bacterin vaccines, which have shown good homologous protection and variable heterologous protection. Bacterin production involves large scale growth of the bacteria and proteins produced during the proliferation phase of production become important antigens that stimulate the immune response. In order to evaluate genes activated during G . parasuis growth on different media substrates, the transcriptome of broth and agar grown G . parasuis strain 29755 were sequenced and compared. The transcription of most purported virulence genes were comparable between broth and agar grown G . parasuis ; however, four virulence-associated genes, including ompA and vapD , had elevated expression under agar growth, while six virulence-associate genes had elevated expression during broth growth, including several protease genes. Additionally, there were metabolic shifts toward increased protein and lipid production and increased cellular division in broth grown G . parasuis . The results contribute to the understanding of how growth substrate alters gene transcription and protein expression, which may impact vaccine efficacy if immunogens important to the protective immune response are not produced under specific in vitro conditions. While the results of this work are unable to fully elucidate which growth medium presents a transcriptome more representative of in vivo samples or best suited for bacterin production, it forms a foundation that can be used for future comparisons and provides a better understanding of the metabolic differences in broth and agar grown bacteria.
Glaesserella parasuis is the cause of Gla¨sser’s disease in pigs and is a significant contributor to post-weaning mortality in the swine industry. Prevention of G. parasuis disease relies primarily on bacterin vaccines, which have shown good homologous protection and variable heterologous protection. Bacterin production involves large scale growth of the bacteria and proteins produced during the proliferation phase of production become important antigens that stimulate the immune response. In order to evaluate genes activated during G. parasuis growth on different media substrates, the transcriptome of broth and agar grown G. parasuis strain 29755 were sequenced and compared. The transcription of most purported virulence genes were comparable between broth and agar grown G. parasuis; however, four virulence-associated genes, including ompA and vapD, had elevated expression under agar growth, while six virulence-associate genes had elevated expression during broth growth, including several protease genes. Additionally, there were metabolic shifts toward increased protein and lipid production and increased cellular division in broth grown G. parasuis. The results contribute to the understanding of how growth substrate alters gene transcription and protein expression, which may impact vaccine efficacy if immunogens important to the protective immune response are not produced under specific in vitro conditions. While the results of this work are unable to fully elucidate which growth medium presents a transcriptome more representative of in vivo samples or best suited for bacterin production, it forms a foundation that can be used for future comparisons and provides a better understanding of the metabolic differences in broth and agar grown bacteria.
Audience Academic
Author Bayles, Darrell O
Hau, Samantha J
Mou, Kathy T
Brockmeier, Susan L
AuthorAffiliation 3 Infectious Bacterial Diseases Research Unit, National Animal Disease Center, ARS, USDA, Ames, Iowa, United States of America
Università degli Studi di Pavia, ITALY
1 Virus and Prion Research Unit, National Animal Disease Center, ARS, USDA, Ames, Iowa, United States of America
2 Oak Ridge Institute for Science and Education, Oak Ridge, Tennessee, United States of America
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crossref_primary_10_3389_fimmu_2021_635097
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SSID ssj0053866
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Snippet Glaesserella parasuis is the cause of Glӓsser's disease in pigs and is a significant contributor to post-weaning mortality in the swine industry. Prevention of...
Glaesserella parasuis is the cause of GlÓsser's disease in pigs and is a significant contributor to post-weaning mortality in the swine industry. Prevention of...
Glaesserella parasuis is the cause of Glӓsser’s disease in pigs and is a significant contributor to post-weaning mortality in the swine industry. Prevention of...
Glaesserella parasuis is the cause of Gla¨sser’s disease in pigs and is a significant contributor to post-weaning mortality in the swine industry. Prevention...
Glaesserella parasuis is the cause of Glӓsser’s disease in pigs and is a significant contributor to post-weaning mortality in the swine industry. Prevention of...
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SubjectTerms Agar
Agar - pharmacology
Animal diseases
Animals
Antigens
Bacteria
Bacterial Proteins
Bacterial Vaccines
BASIC BIOLOGICAL SCIENCES
Bioinformatics
biological transport
Biology and Life Sciences
Causes of
cell metabolism
Cell Proliferation - drug effects
Cellular manufacture
Culture Media - pharmacology
Deoxyribonucleic acid
DNA
DNA transcription
Gene expression
Gene Expression Profiling
Genes
Genes, Bacterial
Genetic aspects
Genomes
Genomics
Gram-negative bacteria
Growth
Haemophilus parasuis - genetics
Haemophilus parasuis - growth & development
Hemophilus infections
Hogs
Homology
Immune response
Immune system
Immunologic research
Immunotherapy
Infections
Lipids
Lipids - biosynthesis
Livestock
metabolic pathways
Pork industry
Prevention
Principal components analysis
Proteases
Protein Biosynthesis - drug effects
Proteins
Quality
Research and analysis methods
RNA sequencing
Substrates
Swine
Swine diseases
Transcription
Transcription (Genetics)
transcriptome analysis
Vaccine efficacy
Vaccines
Virulence
Virulence (Microbiology)
Virulence - genetics
Weaning
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Title Transcriptomic differences noted in Glaesserella parasuis between growth in broth and on agar
URI https://www.ncbi.nlm.nih.gov/pubmed/31386681
https://www.proquest.com/docview/2268998655/abstract/
https://search.proquest.com/docview/2269396124
https://www.osti.gov/servlets/purl/1904877
https://pubmed.ncbi.nlm.nih.gov/PMC6684057
https://doaj.org/article/7a6f4a4990174e5095deae5c458e892e
http://dx.doi.org/10.1371/journal.pone.0220365
Volume 14
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