<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Benomar S</submitter><funding>National Institute of General Medical Sciences</funding><funding>NIGMS NIH HHS</funding><pagination>e1008134</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6952083</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>16(1)</volume><pubmed_abstract>Caenorhabditis elegans are soil-dwelling nematodes and models for understanding innate immunity and infection. Previously, we developed a novel fluorescent dye (KR35) that accumulates in the intestine of C. elegans and reports a dynamic wave in intestinal pH associated with the defecation motor program. Here, we use KR35 to show that mutations in the Ca2+-binding protein, PBO-1, abrogate the pH wave, causing the anterior intestine to be constantly acidic. Surprisingly, pbo-1 mutants were also more susceptible to infection by several bacterial pathogens. We could suppress pathogen susceptibility in pbo-1 mutants by treating the animals with pH-buffering bicarbonate, suggesting the pathogen susceptibility is a function of the acidity of the intestinal pH. Furthermore, we use KR35 to show that upon infection by pathogens, the intestinal pH becomes neutral in a wild type, but less so in pbo-1 mutants. C. elegans is known to increase production of reactive oxygen species (ROS), such as H2O2, in response to pathogens, which is an important component of pathogen defense. We show that pbo-1 mutants exhibited decreased H2O2 in response to pathogens, which could also be partially restored in pbo-1 animals treated with bicarbonate. Ultimately, our results support a model whereby PBO-1 functions during infection to facilitate pH changes in the intestine that are protective to the host.</pubmed_abstract><journal>PLoS pathogens</journal><pubmed_title>The C. elegans CHP1 homolog, pbo-1, functions in innate immunity by regulating the pH of the intestinal lumen.</pubmed_title><pmcid>PMC6952083</pmcid><funding_grant_id>P20 GM113117</funding_grant_id><funding_grant_id>P20 GM103418</funding_grant_id><funding_grant_id>P20 GM103638</funding_grant_id><funding_grant_id>R35 GM133572</funding_grant_id><funding_grant_id>K12 GM63651</funding_grant_id><funding_grant_id>K12 GM063651</funding_grant_id><pubmed_authors>Bender AM</pubmed_authors><pubmed_authors>Peterson BR</pubmed_authors><pubmed_authors>Ackley BD</pubmed_authors><pubmed_authors>Lansdon P</pubmed_authors><pubmed_authors>Benomar S</pubmed_authors><pubmed_authors>Chandler JR</pubmed_authors></additional><is_claimable>false</is_claimable><name>The C. elegans CHP1 homolog, pbo-1, functions in innate immunity by regulating the pH of the intestinal lumen.</name><description>Caenorhabditis elegans are soil-dwelling nematodes and models for understanding innate immunity and infection. Previously, we developed a novel fluorescent dye (KR35) that accumulates in the intestine of C. elegans and reports a dynamic wave in intestinal pH associated with the defecation motor program. Here, we use KR35 to show that mutations in the Ca2+-binding protein, PBO-1, abrogate the pH wave, causing the anterior intestine to be constantly acidic. Surprisingly, pbo-1 mutants were also more susceptible to infection by several bacterial pathogens. We could suppress pathogen susceptibility in pbo-1 mutants by treating the animals with pH-buffering bicarbonate, suggesting the pathogen susceptibility is a function of the acidity of the intestinal pH. Furthermore, we use KR35 to show that upon infection by pathogens, the intestinal pH becomes neutral in a wild type, but less so in pbo-1 mutants. C. elegans is known to increase production of reactive oxygen species (ROS), such as H2O2, in response to pathogens, which is an important component of pathogen defense. We show that pbo-1 mutants exhibited decreased H2O2 in response to pathogens, which could also be partially restored in pbo-1 animals treated with bicarbonate. Ultimately, our results support a model whereby PBO-1 functions during infection to facilitate pH changes in the intestine that are protective to the host.</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Jan</publication><modification>2025-04-19T10:51:07.355Z</modification><creation>2020-05-22T08:06:52Z</creation></dates><accession>S-EPMC6952083</accession><cross_references><pubmed>31917826</pubmed><doi>10.1371/journal.ppat.1008134</doi></cross_references></HashMap>