<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Shi H</submitter><funding>national basic research program of china</funding><funding>National Natural Science Foundation of China</funding><funding>National Key Research and Development Program of China</funding><funding>State Key Laboratory of Pathogen Biology of Livestock Diseases Open Foundation</funding><pagination>e1009767</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8354476</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>17(7)</volume><pubmed_abstract>Hypobiosis (facultative developmental arrest) is the most important life-cycle adaptation ensuring survival of parasitic nematodes under adverse conditions. Little is known about such survival mechanisms, although ascarosides (ascarylose with fatty acid-derived side chains) have been reported to mediate the formation of dauer larvae in the free-living nematode Caenorhabditis elegans. Here, we investigated the role of a key gene acox-1, in the larval development of Haemonchus contortus, one of the most important parasitic nematodes that employ hypobiosis as a routine survival mechanism. In this parasite, acox-1 encodes three proteins (ACOXs) that all show a fatty acid oxidation activity in vitro and in vivo, and interact with a peroxin PEX-5 in peroxisomes. In particular, a peroxisomal targ</pubmed_abstract><journal>PLoS pathogens</journal><pubmed_title>Acyl-CoA oxidase ACOX-1 interacts with a peroxin PEX-5 to play roles in larval development of Haemonchus contortus.</pubmed_title><pmcid>PMC8354476</pmcid><funding_grant_id>2017YFD0501200</funding_grant_id><funding_grant_id>SKLVEB2016KFKT018</funding_grant_id><funding_grant_id>32002304</funding_grant_id><funding_grant_id>31602041</funding_grant_id><funding_grant_id>2015CB150300</funding_grant_id><pubmed_authors>Du A</pubmed_authors><pubmed_authors>Yang Y</pubmed_authors><pubmed_authors>Huang X</pubmed_authors><pubmed_authors>Yao C</pubmed_authors><pubmed_authors>Chen X</pubmed_authors><pubmed_authors>Wang Z</pubmed_authors><pubmed_authors>Wu F</pubmed_authors><pubmed_authors>Shi H</pubmed_authors><pubmed_authors>Zhou J</pubmed_authors><pubmed_authors>Ma G</pubmed_authors></additional><is_claimable>false</is_claimable><name>Acyl-CoA oxidase ACOX-1 interacts with a peroxin PEX-5 to play roles in larval development of Haemonchus contortus.</name><description>Hypobiosis (facultative developmental arrest) is the most important life-cycle adaptation ensuring survival of parasitic nematodes under adverse conditions. Little is known about such survival mechanisms, although ascarosides (ascarylose with fatty acid-derived side chains) have been reported to mediate the formation of dauer larvae in the free-living nematode Caenorhabditis elegans. Here, we investigated the role of a key gene acox-1, in the larval development of Haemonchus contortus, one of the most important parasitic nematodes that employ hypobiosis as a routine survival mechanism. In this parasite, acox-1 encodes three proteins (ACOXs) that all show a fatty acid oxidation activity in vitro and in vivo, and interact with a peroxin PEX-5 in peroxisomes. In particular, a peroxisomal targ</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Jul</publication><modification>2026-05-08T00:49:09.583Z</modification><creation>2022-02-11T06:12:43.387Z</creation></dates><accession>S-EPMC8354476</accession><cross_references><pubmed>34270617</pubmed><doi>10.1371/journal.ppat.1009767</doi></cross_references></HashMap>