Luke C. Cadd, Bethany Crooks, Nikki J. Marks, Aaron G. Maule, Angela Mousley, Louise E. Atkinson
{"title":"圆线虫生物测定工具箱:加速线虫寄生虫功能生物学的独特机会","authors":"Luke C. Cadd, Bethany Crooks, Nikki J. Marks, Aaron G. Maule, Angela Mousley, Louise E. Atkinson","doi":"10.1016/j.molbiopara.2022.111526","DOIUrl":null,"url":null,"abstract":"<div><p><em>Caenorhabditis elegans</em> is a uniquely powerful tool to aid understanding of fundamental nematode biology. While <em>C. elegans</em> boasts an unrivalled array of functional genomics tools and phenotype bioassays the inherent differences between free-living and parasitic nematodes underscores the need to develop these approaches in tractable parasite models. Advances in functional genomics approaches, including RNA interference and CRISPR/Cas9 gene editing, in the parasitic nematodes <em>Strongyloides ratti</em> and <em>Strongyloides stercoralis</em> provide a unique and timely opportunity to probe basic parasite biology and reveal novel anthelmintic targets in species that are both experimentally and therapeutically relevant pathogens. While <em>Strongyloides</em> functional genomics tools have progressed rapidly, the complementary range of bioassays required to elucidate phenotypic outcomes post-functional genomics remain more limited in scope. To adequately support the exploitation of functional genomic pipelines for studies of gene function in <em>Strongyloides</em> a comprehensive set of species- and parasite-specific quantitative bioassays are required to assess nematode behaviours post-genetic manipulation. Here we review the scope of the current <em>Strongyloides</em> bioassay toolbox, how established <em>Strongyloides</em> bioassays have advanced knowledge of parasite biology, opportunities for <em>Strongyloides</em> bioassay development and, the need for investment in tractable model parasite platforms such as <em>Strongyloides</em> to drive the discovery of novel targets for parasite control.</p></div>","PeriodicalId":18721,"journal":{"name":"Molecular and biochemical parasitology","volume":"252 ","pages":"Article 111526"},"PeriodicalIF":1.4000,"publicationDate":"2022-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S0166685122000809/pdfft?md5=3c691bdcb264304fa7afb24077c64a1d&pid=1-s2.0-S0166685122000809-main.pdf","citationCount":"3","resultStr":"{\"title\":\"The Strongyloides bioassay toolbox: A unique opportunity to accelerate functional biology for nematode parasites\",\"authors\":\"Luke C. Cadd, Bethany Crooks, Nikki J. Marks, Aaron G. Maule, Angela Mousley, Louise E. Atkinson\",\"doi\":\"10.1016/j.molbiopara.2022.111526\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p><em>Caenorhabditis elegans</em> is a uniquely powerful tool to aid understanding of fundamental nematode biology. While <em>C. elegans</em> boasts an unrivalled array of functional genomics tools and phenotype bioassays the inherent differences between free-living and parasitic nematodes underscores the need to develop these approaches in tractable parasite models. Advances in functional genomics approaches, including RNA interference and CRISPR/Cas9 gene editing, in the parasitic nematodes <em>Strongyloides ratti</em> and <em>Strongyloides stercoralis</em> provide a unique and timely opportunity to probe basic parasite biology and reveal novel anthelmintic targets in species that are both experimentally and therapeutically relevant pathogens. While <em>Strongyloides</em> functional genomics tools have progressed rapidly, the complementary range of bioassays required to elucidate phenotypic outcomes post-functional genomics remain more limited in scope. To adequately support the exploitation of functional genomic pipelines for studies of gene function in <em>Strongyloides</em> a comprehensive set of species- and parasite-specific quantitative bioassays are required to assess nematode behaviours post-genetic manipulation. Here we review the scope of the current <em>Strongyloides</em> bioassay toolbox, how established <em>Strongyloides</em> bioassays have advanced knowledge of parasite biology, opportunities for <em>Strongyloides</em> bioassay development and, the need for investment in tractable model parasite platforms such as <em>Strongyloides</em> to drive the discovery of novel targets for parasite control.</p></div>\",\"PeriodicalId\":18721,\"journal\":{\"name\":\"Molecular and biochemical parasitology\",\"volume\":\"252 \",\"pages\":\"Article 111526\"},\"PeriodicalIF\":1.4000,\"publicationDate\":\"2022-11-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S0166685122000809/pdfft?md5=3c691bdcb264304fa7afb24077c64a1d&pid=1-s2.0-S0166685122000809-main.pdf\",\"citationCount\":\"3\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Molecular and biochemical parasitology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0166685122000809\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular and biochemical parasitology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0166685122000809","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
The Strongyloides bioassay toolbox: A unique opportunity to accelerate functional biology for nematode parasites
Caenorhabditis elegans is a uniquely powerful tool to aid understanding of fundamental nematode biology. While C. elegans boasts an unrivalled array of functional genomics tools and phenotype bioassays the inherent differences between free-living and parasitic nematodes underscores the need to develop these approaches in tractable parasite models. Advances in functional genomics approaches, including RNA interference and CRISPR/Cas9 gene editing, in the parasitic nematodes Strongyloides ratti and Strongyloides stercoralis provide a unique and timely opportunity to probe basic parasite biology and reveal novel anthelmintic targets in species that are both experimentally and therapeutically relevant pathogens. While Strongyloides functional genomics tools have progressed rapidly, the complementary range of bioassays required to elucidate phenotypic outcomes post-functional genomics remain more limited in scope. To adequately support the exploitation of functional genomic pipelines for studies of gene function in Strongyloides a comprehensive set of species- and parasite-specific quantitative bioassays are required to assess nematode behaviours post-genetic manipulation. Here we review the scope of the current Strongyloides bioassay toolbox, how established Strongyloides bioassays have advanced knowledge of parasite biology, opportunities for Strongyloides bioassay development and, the need for investment in tractable model parasite platforms such as Strongyloides to drive the discovery of novel targets for parasite control.
期刊介绍:
The journal provides a medium for rapid publication of investigations of the molecular biology and biochemistry of parasitic protozoa and helminths and their interactions with both the definitive and intermediate host. The main subject areas covered are:
• the structure, biosynthesis, degradation, properties and function of DNA, RNA, proteins, lipids, carbohydrates and small molecular-weight substances
• intermediary metabolism and bioenergetics
• drug target characterization and the mode of action of antiparasitic drugs
• molecular and biochemical aspects of membrane structure and function
• host-parasite relationships that focus on the parasite, particularly as related to specific parasite molecules.
• analysis of genes and genome structure, function and expression
• analysis of variation in parasite populations relevant to genetic exchange, pathogenesis, drug and vaccine target characterization, and drug resistance.
• parasite protein trafficking, organelle biogenesis, and cellular structure especially with reference to the roles of specific molecules
• parasite programmed cell death, development, and cell division at the molecular level.