Phage-Resistant Bacteria Reveal a Role for Potassium in Root Colonization

ABSTRACT Bacteriophage predation is an important factor in bacterial community dynamics and evolution. Phage-bacterium interaction has mainly been studied in lab cultures, while dynamics in natural habitats, and especially in the plant root niche, are underexplored. To better understand this process...

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Autores principales: Elhanan Tzipilevich, Philip N. Benfey
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Publicado: American Society for Microbiology 2021
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spelling oai:doaj.org-article:a78d5eb2dd694dfc870a291354ab32272021-11-10T18:37:51ZPhage-Resistant Bacteria Reveal a Role for Potassium in Root Colonization10.1128/mBio.01403-212150-7511https://doaj.org/article/a78d5eb2dd694dfc870a291354ab32272021-08-01T00:00:00Zhttps://journals.asm.org/doi/10.1128/mBio.01403-21https://doaj.org/toc/2150-7511ABSTRACT Bacteriophage predation is an important factor in bacterial community dynamics and evolution. Phage-bacterium interaction has mainly been studied in lab cultures, while dynamics in natural habitats, and especially in the plant root niche, are underexplored. To better understand this process, we characterized infection of the soil bacterium Bacillus subtilis NCBI 3610 by the lytic phage SPO1 during growth in LB medium and compared it to root colonization. Resistance in vitro was primarily through modification of the phage receptor. However, this type of resistance reduced the ability to colonize the root. From a line that survived phage infection while retaining the ability to colonize the root, we identified a new phage resistance mechanism involving potassium (K+) ion influx modulation and enhanced biofilm formation. Furthermore, we show that potassium serves as a stimulator of root colonization among diverse growth-promoting bacilli species, with implications for plant health. IMPORTANCE Bacteriophage predation is an important factor in bacterial community dynamics and evolution. Phage-bacterium interaction has mainly been studied in lab cultures, while dynamics in natural habitats, and especially in the plant root niche, are underexplored. To better understand this process, we characterized infection of the soil bacterium Bacillus subtilis NCBI 3610 by the lytic phage SPO1 during growth in LB medium and compared it to root colonization. Resistance in vitro was primarily through modification of the phage receptor. However, this type of resistance reduced the ability to colonize the root. From a line that survived phage infection while retaining the ability to colonize the root, we identified a new phage resistance mechanism involving potassium (K+) ion influx modulation and enhanced biofilm formation. Furthermore, we show that potassium serves as a stimulator of root colonization among diverse growth-promoting bacilli species, with implications for plant health.Elhanan TzipilevichPhilip N. BenfeyAmerican Society for MicrobiologyarticleBacillus subtilisbacteriophage, evolutionbiofilmsplant-microbe interactionsMicrobiologyQR1-502ENmBio, Vol 12, Iss 4 (2021)
institution DOAJ
collection DOAJ
language EN
topic Bacillus subtilis
bacteriophage, evolution
biofilms
plant-microbe interactions
Microbiology
QR1-502
spellingShingle Bacillus subtilis
bacteriophage, evolution
biofilms
plant-microbe interactions
Microbiology
QR1-502
Elhanan Tzipilevich
Philip N. Benfey
Phage-Resistant Bacteria Reveal a Role for Potassium in Root Colonization
description ABSTRACT Bacteriophage predation is an important factor in bacterial community dynamics and evolution. Phage-bacterium interaction has mainly been studied in lab cultures, while dynamics in natural habitats, and especially in the plant root niche, are underexplored. To better understand this process, we characterized infection of the soil bacterium Bacillus subtilis NCBI 3610 by the lytic phage SPO1 during growth in LB medium and compared it to root colonization. Resistance in vitro was primarily through modification of the phage receptor. However, this type of resistance reduced the ability to colonize the root. From a line that survived phage infection while retaining the ability to colonize the root, we identified a new phage resistance mechanism involving potassium (K+) ion influx modulation and enhanced biofilm formation. Furthermore, we show that potassium serves as a stimulator of root colonization among diverse growth-promoting bacilli species, with implications for plant health. IMPORTANCE Bacteriophage predation is an important factor in bacterial community dynamics and evolution. Phage-bacterium interaction has mainly been studied in lab cultures, while dynamics in natural habitats, and especially in the plant root niche, are underexplored. To better understand this process, we characterized infection of the soil bacterium Bacillus subtilis NCBI 3610 by the lytic phage SPO1 during growth in LB medium and compared it to root colonization. Resistance in vitro was primarily through modification of the phage receptor. However, this type of resistance reduced the ability to colonize the root. From a line that survived phage infection while retaining the ability to colonize the root, we identified a new phage resistance mechanism involving potassium (K+) ion influx modulation and enhanced biofilm formation. Furthermore, we show that potassium serves as a stimulator of root colonization among diverse growth-promoting bacilli species, with implications for plant health.
format article
author Elhanan Tzipilevich
Philip N. Benfey
author_facet Elhanan Tzipilevich
Philip N. Benfey
author_sort Elhanan Tzipilevich
title Phage-Resistant Bacteria Reveal a Role for Potassium in Root Colonization
title_short Phage-Resistant Bacteria Reveal a Role for Potassium in Root Colonization
title_full Phage-Resistant Bacteria Reveal a Role for Potassium in Root Colonization
title_fullStr Phage-Resistant Bacteria Reveal a Role for Potassium in Root Colonization
title_full_unstemmed Phage-Resistant Bacteria Reveal a Role for Potassium in Root Colonization
title_sort phage-resistant bacteria reveal a role for potassium in root colonization
publisher American Society for Microbiology
publishDate 2021
url https://doaj.org/article/a78d5eb2dd694dfc870a291354ab3227
work_keys_str_mv AT elhanantzipilevich phageresistantbacteriarevealaroleforpotassiuminrootcolonization
AT philipnbenfey phageresistantbacteriarevealaroleforpotassiuminrootcolonization
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