Mucin and Agitation Shape Predation of <i>Escherichia coli</i> by Lytic Coliphage

The ability of bacteriophage (phage), abundant within the gastrointestinal microbiome, to regulate bacterial populations within the same micro-environment offers prophylactic and therapeutic opportunities. Bacteria and phage have both been shown to interact intimately with mucin, and these interacti...

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Main Authors: Amanda Carroll-Portillo, Kellin N. Rumsey, Cody A. Braun, Derek M. Lin, Cristina N. Coffman, Joe A. Alcock, Sudha B. Singh, Henry C. Lin
Format: Article
Language:English
Published: MDPI AG 2023-02-01
Series:Microorganisms
Subjects:
Online Access:https://www.mdpi.com/2076-2607/11/2/508
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author Amanda Carroll-Portillo
Kellin N. Rumsey
Cody A. Braun
Derek M. Lin
Cristina N. Coffman
Joe A. Alcock
Sudha B. Singh
Henry C. Lin
author_facet Amanda Carroll-Portillo
Kellin N. Rumsey
Cody A. Braun
Derek M. Lin
Cristina N. Coffman
Joe A. Alcock
Sudha B. Singh
Henry C. Lin
author_sort Amanda Carroll-Portillo
collection DOAJ
description The ability of bacteriophage (phage), abundant within the gastrointestinal microbiome, to regulate bacterial populations within the same micro-environment offers prophylactic and therapeutic opportunities. Bacteria and phage have both been shown to interact intimately with mucin, and these interactions invariably effect the outcomes of phage predation within the intestine. To better understand the influence of the gastrointestinal micro-environment on phage predation, we employed enclosed, in vitro systems to investigate the roles of mucin concentration and agitation as a function of phage type and number on bacterial killing. Using two lytic coliphage, T4 and PhiX174, bacterial viability was quantified following exposure to phages at different multiplicities of infection (MOI) within increasing, physiological levels of mucin (0–4%) with and without agitation. Comparison of bacterial viability outcomes demonstrated that at low MOI, agitation in combination with higher mucin concentration (>2%) inhibited phage predation by both phages. However, when MOI was increased, PhiX predation was recovered regardless of mucin concentration or agitation. In contrast, only constant agitation of samples containing a high MOI of T4 demonstrated phage predation; briefly agitated samples remained hindered. Our results demonstrate that each phage–bacteria pairing is uniquely influenced by environmental factors, and these should be considered when determining the potential efficacy of phage predation under homeostatic or therapeutic circumstances.
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spelling doaj.art-2314d43847a0406080755662968166e82023-11-16T22:16:51ZengMDPI AGMicroorganisms2076-26072023-02-0111250810.3390/microorganisms11020508Mucin and Agitation Shape Predation of <i>Escherichia coli</i> by Lytic ColiphageAmanda Carroll-Portillo0Kellin N. Rumsey1Cody A. Braun2Derek M. Lin3Cristina N. Coffman4Joe A. Alcock5Sudha B. Singh6Henry C. Lin7Division of Gastroenterology and Hepatology, University of New Mexico, Albuquerque, NM 87131, USAStatistical Sciences, Los Alamos National Laboratory, Los Alamos, NM 87545, USABiomedical Research Institute of New Mexico, Albuquerque, NM 87108, USABiomedical Research Institute of New Mexico, Albuquerque, NM 87108, USABiomedical Research Institute of New Mexico, Albuquerque, NM 87108, USADepartment of Emergency Medicine, University of New Mexico, Albuquerque, NM 87131, USABiomedical Research Institute of New Mexico, Albuquerque, NM 87108, USADivision of Gastroenterology and Hepatology, University of New Mexico, Albuquerque, NM 87131, USAThe ability of bacteriophage (phage), abundant within the gastrointestinal microbiome, to regulate bacterial populations within the same micro-environment offers prophylactic and therapeutic opportunities. Bacteria and phage have both been shown to interact intimately with mucin, and these interactions invariably effect the outcomes of phage predation within the intestine. To better understand the influence of the gastrointestinal micro-environment on phage predation, we employed enclosed, in vitro systems to investigate the roles of mucin concentration and agitation as a function of phage type and number on bacterial killing. Using two lytic coliphage, T4 and PhiX174, bacterial viability was quantified following exposure to phages at different multiplicities of infection (MOI) within increasing, physiological levels of mucin (0–4%) with and without agitation. Comparison of bacterial viability outcomes demonstrated that at low MOI, agitation in combination with higher mucin concentration (>2%) inhibited phage predation by both phages. However, when MOI was increased, PhiX predation was recovered regardless of mucin concentration or agitation. In contrast, only constant agitation of samples containing a high MOI of T4 demonstrated phage predation; briefly agitated samples remained hindered. Our results demonstrate that each phage–bacteria pairing is uniquely influenced by environmental factors, and these should be considered when determining the potential efficacy of phage predation under homeostatic or therapeutic circumstances.https://www.mdpi.com/2076-2607/11/2/508bacteriophagelyticmucingastrointestinal tractmotility
spellingShingle Amanda Carroll-Portillo
Kellin N. Rumsey
Cody A. Braun
Derek M. Lin
Cristina N. Coffman
Joe A. Alcock
Sudha B. Singh
Henry C. Lin
Mucin and Agitation Shape Predation of <i>Escherichia coli</i> by Lytic Coliphage
Microorganisms
bacteriophage
lytic
mucin
gastrointestinal tract
motility
title Mucin and Agitation Shape Predation of <i>Escherichia coli</i> by Lytic Coliphage
title_full Mucin and Agitation Shape Predation of <i>Escherichia coli</i> by Lytic Coliphage
title_fullStr Mucin and Agitation Shape Predation of <i>Escherichia coli</i> by Lytic Coliphage
title_full_unstemmed Mucin and Agitation Shape Predation of <i>Escherichia coli</i> by Lytic Coliphage
title_short Mucin and Agitation Shape Predation of <i>Escherichia coli</i> by Lytic Coliphage
title_sort mucin and agitation shape predation of i escherichia coli i by lytic coliphage
topic bacteriophage
lytic
mucin
gastrointestinal tract
motility
url https://www.mdpi.com/2076-2607/11/2/508
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