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High-Throughput Analysis of Gene Function in the Bacterial Predator Bdellovibrio bacteriovorus
Bdellovibrio bacteriovorus is a bacterial predator capable of killing and replicating inside most Gram-negative bacteria, including antibiotic-resistant pathogens. Despite growing interest in this organism as a potential therapeutic, many of its genes remain uncharacterized. Here, we perform a high-...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6561027/ https://www.ncbi.nlm.nih.gov/pubmed/31186325 http://dx.doi.org/10.1128/mBio.01040-19 |
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author | Duncan, Miles C. Gillette, Rebecca K. Maglasang, Micah A. Corn, Elizabeth A. Tai, Albert K. Lazinski, David W. Shanks, Robert M. Q. Kadouri, Daniel E. Camilli, Andrew |
author_facet | Duncan, Miles C. Gillette, Rebecca K. Maglasang, Micah A. Corn, Elizabeth A. Tai, Albert K. Lazinski, David W. Shanks, Robert M. Q. Kadouri, Daniel E. Camilli, Andrew |
author_sort | Duncan, Miles C. |
collection | PubMed |
description | Bdellovibrio bacteriovorus is a bacterial predator capable of killing and replicating inside most Gram-negative bacteria, including antibiotic-resistant pathogens. Despite growing interest in this organism as a potential therapeutic, many of its genes remain uncharacterized. Here, we perform a high-throughput genetic screen with B. bacteriovorus using transposon sequencing (Tn-seq) to explore the genetic requirements of predation. Two hundred one genes were deemed essential for growth in the absence of prey, whereas over 100 genes were found to be specifically required for predative growth on the human pathogens Vibrio cholerae and Escherichia coli in both planktonic and biofilm states. To further this work, we created an ordered-knockout library in B. bacteriovorus and developed new high-throughput techniques to characterize the mutants by their stage of deficiency in the predator life cycle. Using microscopy and flow cytometry, we confirmed 10 mutants defective in prey attachment and eight mutants defective in prey rounding. The majority of these genes are hypothetical and previously uncharacterized. Finally, we propose new nomenclature to group B. bacteriovorus mutants into classes based on their stage of predation defect. These results contribute to our basic understanding of bacterial predation and may be useful for harnessing B. bacteriovorus to kill harmful pathogens in the clinical setting. |
format | Online Article Text |
id | pubmed-6561027 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-65610272019-06-14 High-Throughput Analysis of Gene Function in the Bacterial Predator Bdellovibrio bacteriovorus Duncan, Miles C. Gillette, Rebecca K. Maglasang, Micah A. Corn, Elizabeth A. Tai, Albert K. Lazinski, David W. Shanks, Robert M. Q. Kadouri, Daniel E. Camilli, Andrew mBio Research Article Bdellovibrio bacteriovorus is a bacterial predator capable of killing and replicating inside most Gram-negative bacteria, including antibiotic-resistant pathogens. Despite growing interest in this organism as a potential therapeutic, many of its genes remain uncharacterized. Here, we perform a high-throughput genetic screen with B. bacteriovorus using transposon sequencing (Tn-seq) to explore the genetic requirements of predation. Two hundred one genes were deemed essential for growth in the absence of prey, whereas over 100 genes were found to be specifically required for predative growth on the human pathogens Vibrio cholerae and Escherichia coli in both planktonic and biofilm states. To further this work, we created an ordered-knockout library in B. bacteriovorus and developed new high-throughput techniques to characterize the mutants by their stage of deficiency in the predator life cycle. Using microscopy and flow cytometry, we confirmed 10 mutants defective in prey attachment and eight mutants defective in prey rounding. The majority of these genes are hypothetical and previously uncharacterized. Finally, we propose new nomenclature to group B. bacteriovorus mutants into classes based on their stage of predation defect. These results contribute to our basic understanding of bacterial predation and may be useful for harnessing B. bacteriovorus to kill harmful pathogens in the clinical setting. American Society for Microbiology 2019-06-11 /pmc/articles/PMC6561027/ /pubmed/31186325 http://dx.doi.org/10.1128/mBio.01040-19 Text en Copyright © 2019 Duncan et al. https://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 (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Article Duncan, Miles C. Gillette, Rebecca K. Maglasang, Micah A. Corn, Elizabeth A. Tai, Albert K. Lazinski, David W. Shanks, Robert M. Q. Kadouri, Daniel E. Camilli, Andrew High-Throughput Analysis of Gene Function in the Bacterial Predator Bdellovibrio bacteriovorus |
title | High-Throughput Analysis of Gene Function in the Bacterial Predator Bdellovibrio bacteriovorus |
title_full | High-Throughput Analysis of Gene Function in the Bacterial Predator Bdellovibrio bacteriovorus |
title_fullStr | High-Throughput Analysis of Gene Function in the Bacterial Predator Bdellovibrio bacteriovorus |
title_full_unstemmed | High-Throughput Analysis of Gene Function in the Bacterial Predator Bdellovibrio bacteriovorus |
title_short | High-Throughput Analysis of Gene Function in the Bacterial Predator Bdellovibrio bacteriovorus |
title_sort | high-throughput analysis of gene function in the bacterial predator bdellovibrio bacteriovorus |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6561027/ https://www.ncbi.nlm.nih.gov/pubmed/31186325 http://dx.doi.org/10.1128/mBio.01040-19 |
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