Cargando…

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-...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2019
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
_version_ 1783426074673152000
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
work_keys_str_mv AT duncanmilesc highthroughputanalysisofgenefunctioninthebacterialpredatorbdellovibriobacteriovorus
AT gilletterebeccak highthroughputanalysisofgenefunctioninthebacterialpredatorbdellovibriobacteriovorus
AT maglasangmicaha highthroughputanalysisofgenefunctioninthebacterialpredatorbdellovibriobacteriovorus
AT cornelizabetha highthroughputanalysisofgenefunctioninthebacterialpredatorbdellovibriobacteriovorus
AT taialbertk highthroughputanalysisofgenefunctioninthebacterialpredatorbdellovibriobacteriovorus
AT lazinskidavidw highthroughputanalysisofgenefunctioninthebacterialpredatorbdellovibriobacteriovorus
AT shanksrobertmq highthroughputanalysisofgenefunctioninthebacterialpredatorbdellovibriobacteriovorus
AT kadouridaniele highthroughputanalysisofgenefunctioninthebacterialpredatorbdellovibriobacteriovorus
AT camilliandrew highthroughputanalysisofgenefunctioninthebacterialpredatorbdellovibriobacteriovorus