Cargando…

Orally Administered P22 Phage Tailspike Protein Reduces Salmonella Colonization in Chickens: Prospects of a Novel Therapy against Bacterial Infections

One of the major causes of morbidity and mortality in man and economically important animals is bacterial infections of the gastrointestinal (GI) tract. The emergence of difficult-to-treat infections, primarily caused by antibiotic resistant bacteria, demands for alternatives to antibiotic therapy....

Descripción completa

Detalles Bibliográficos
Autores principales: Waseh, Shakeeba, Hanifi-Moghaddam, Pejman, Coleman, Russell, Masotti, Michael, Ryan, Shannon, Foss, Mary, MacKenzie, Roger, Henry, Matthew, Szymanski, Christine M., Tanha, Jamshid
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2989905/
https://www.ncbi.nlm.nih.gov/pubmed/21124920
http://dx.doi.org/10.1371/journal.pone.0013904
_version_ 1782192403072942080
author Waseh, Shakeeba
Hanifi-Moghaddam, Pejman
Coleman, Russell
Masotti, Michael
Ryan, Shannon
Foss, Mary
MacKenzie, Roger
Henry, Matthew
Szymanski, Christine M.
Tanha, Jamshid
author_facet Waseh, Shakeeba
Hanifi-Moghaddam, Pejman
Coleman, Russell
Masotti, Michael
Ryan, Shannon
Foss, Mary
MacKenzie, Roger
Henry, Matthew
Szymanski, Christine M.
Tanha, Jamshid
author_sort Waseh, Shakeeba
collection PubMed
description One of the major causes of morbidity and mortality in man and economically important animals is bacterial infections of the gastrointestinal (GI) tract. The emergence of difficult-to-treat infections, primarily caused by antibiotic resistant bacteria, demands for alternatives to antibiotic therapy. Currently, one of the emerging therapeutic alternatives is the use of lytic bacteriophages. In an effort to exploit the target specificity and therapeutic potential of bacteriophages, we examined the utility of bacteriophage tailspike proteins (Tsps). Among the best-characterized Tsps is that from the Podoviridae P22 bacteriophage, which recognizes the lipopolysaccharides of Salmonella enterica serovar Typhimurium. In this study, we utilized a truncated, functionally equivalent version of the P22 tailspike protein, P22sTsp, as a prototype to demonstrate the therapeutic potential of Tsps in the GI tract of chickens. Bacterial agglutination assays showed that P22sTsp was capable of agglutinating S. Typhimurium at levels similar to antibodies and incubating the Tsp with chicken GI fluids showed no proteolytic activity against the Tsp. Testing P22sTsp against the three major GI proteases showed that P22sTsp was resistant to trypsin and partially to chymotrypsin, but sensitive to pepsin. However, in formulated form for oral administration, P22sTsp was resistant to all three proteases. When administered orally to chickens, P22sTsp significantly reduced Salmonella colonization in the gut and its further penetration into internal organs. In in vitro assays, P22sTsp effectively retarded Salmonella motility, a factor implicated in bacterial colonization and invasion, suggesting that the in vivo decolonization ability of P22sTsp may, at least in part, be due to its ability to interfere with motility… Our findings show promise in terms of opening novel Tsp-based oral therapeutic approaches against bacterial infections in production animals and potentially in humans.
format Text
id pubmed-2989905
institution National Center for Biotechnology Information
language English
publishDate 2010
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-29899052010-12-01 Orally Administered P22 Phage Tailspike Protein Reduces Salmonella Colonization in Chickens: Prospects of a Novel Therapy against Bacterial Infections Waseh, Shakeeba Hanifi-Moghaddam, Pejman Coleman, Russell Masotti, Michael Ryan, Shannon Foss, Mary MacKenzie, Roger Henry, Matthew Szymanski, Christine M. Tanha, Jamshid PLoS One Research Article One of the major causes of morbidity and mortality in man and economically important animals is bacterial infections of the gastrointestinal (GI) tract. The emergence of difficult-to-treat infections, primarily caused by antibiotic resistant bacteria, demands for alternatives to antibiotic therapy. Currently, one of the emerging therapeutic alternatives is the use of lytic bacteriophages. In an effort to exploit the target specificity and therapeutic potential of bacteriophages, we examined the utility of bacteriophage tailspike proteins (Tsps). Among the best-characterized Tsps is that from the Podoviridae P22 bacteriophage, which recognizes the lipopolysaccharides of Salmonella enterica serovar Typhimurium. In this study, we utilized a truncated, functionally equivalent version of the P22 tailspike protein, P22sTsp, as a prototype to demonstrate the therapeutic potential of Tsps in the GI tract of chickens. Bacterial agglutination assays showed that P22sTsp was capable of agglutinating S. Typhimurium at levels similar to antibodies and incubating the Tsp with chicken GI fluids showed no proteolytic activity against the Tsp. Testing P22sTsp against the three major GI proteases showed that P22sTsp was resistant to trypsin and partially to chymotrypsin, but sensitive to pepsin. However, in formulated form for oral administration, P22sTsp was resistant to all three proteases. When administered orally to chickens, P22sTsp significantly reduced Salmonella colonization in the gut and its further penetration into internal organs. In in vitro assays, P22sTsp effectively retarded Salmonella motility, a factor implicated in bacterial colonization and invasion, suggesting that the in vivo decolonization ability of P22sTsp may, at least in part, be due to its ability to interfere with motility… Our findings show promise in terms of opening novel Tsp-based oral therapeutic approaches against bacterial infections in production animals and potentially in humans. Public Library of Science 2010-11-22 /pmc/articles/PMC2989905/ /pubmed/21124920 http://dx.doi.org/10.1371/journal.pone.0013904 Text en Waseh et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Waseh, Shakeeba
Hanifi-Moghaddam, Pejman
Coleman, Russell
Masotti, Michael
Ryan, Shannon
Foss, Mary
MacKenzie, Roger
Henry, Matthew
Szymanski, Christine M.
Tanha, Jamshid
Orally Administered P22 Phage Tailspike Protein Reduces Salmonella Colonization in Chickens: Prospects of a Novel Therapy against Bacterial Infections
title Orally Administered P22 Phage Tailspike Protein Reduces Salmonella Colonization in Chickens: Prospects of a Novel Therapy against Bacterial Infections
title_full Orally Administered P22 Phage Tailspike Protein Reduces Salmonella Colonization in Chickens: Prospects of a Novel Therapy against Bacterial Infections
title_fullStr Orally Administered P22 Phage Tailspike Protein Reduces Salmonella Colonization in Chickens: Prospects of a Novel Therapy against Bacterial Infections
title_full_unstemmed Orally Administered P22 Phage Tailspike Protein Reduces Salmonella Colonization in Chickens: Prospects of a Novel Therapy against Bacterial Infections
title_short Orally Administered P22 Phage Tailspike Protein Reduces Salmonella Colonization in Chickens: Prospects of a Novel Therapy against Bacterial Infections
title_sort orally administered p22 phage tailspike protein reduces salmonella colonization in chickens: prospects of a novel therapy against bacterial infections
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2989905/
https://www.ncbi.nlm.nih.gov/pubmed/21124920
http://dx.doi.org/10.1371/journal.pone.0013904
work_keys_str_mv AT wasehshakeeba orallyadministeredp22phagetailspikeproteinreducessalmonellacolonizationinchickensprospectsofanoveltherapyagainstbacterialinfections
AT hanifimoghaddampejman orallyadministeredp22phagetailspikeproteinreducessalmonellacolonizationinchickensprospectsofanoveltherapyagainstbacterialinfections
AT colemanrussell orallyadministeredp22phagetailspikeproteinreducessalmonellacolonizationinchickensprospectsofanoveltherapyagainstbacterialinfections
AT masottimichael orallyadministeredp22phagetailspikeproteinreducessalmonellacolonizationinchickensprospectsofanoveltherapyagainstbacterialinfections
AT ryanshannon orallyadministeredp22phagetailspikeproteinreducessalmonellacolonizationinchickensprospectsofanoveltherapyagainstbacterialinfections
AT fossmary orallyadministeredp22phagetailspikeproteinreducessalmonellacolonizationinchickensprospectsofanoveltherapyagainstbacterialinfections
AT mackenzieroger orallyadministeredp22phagetailspikeproteinreducessalmonellacolonizationinchickensprospectsofanoveltherapyagainstbacterialinfections
AT henrymatthew orallyadministeredp22phagetailspikeproteinreducessalmonellacolonizationinchickensprospectsofanoveltherapyagainstbacterialinfections
AT szymanskichristinem orallyadministeredp22phagetailspikeproteinreducessalmonellacolonizationinchickensprospectsofanoveltherapyagainstbacterialinfections
AT tanhajamshid orallyadministeredp22phagetailspikeproteinreducessalmonellacolonizationinchickensprospectsofanoveltherapyagainstbacterialinfections