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A multistrain approach to studying the mechanisms underlying compatibility in the interaction between Biomphalaria glabrata and Schistosoma mansoni
In recent decades, numerous studies have sought to better understand the mechanisms underlying the compatibility between Biomphalaria glabrata and Schistosoma mansoni. The developments of comparative transcriptomics, comparative genomics, interactomics and more targeted approaches have enabled resea...
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Published in: | PLoS neglected tropical diseases 2017-03, Vol.11 (3), p.e0005398-e0005398 |
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creator | Galinier, Richard Roger, Emmanuel Moné, Yves Duval, David Portet, Anaïs Pinaud, Silvain Chaparro, Cristian Grunau, Christoph Genthon, Clémence Dubois, Emeric Rognon, Anne Arancibia, Nathalie Dejean, Bernard Théron, André Gourbal, Benjamin Mitta, Guillaume |
description | In recent decades, numerous studies have sought to better understand the mechanisms underlying the compatibility between Biomphalaria glabrata and Schistosoma mansoni. The developments of comparative transcriptomics, comparative genomics, interactomics and more targeted approaches have enabled researchers to identify a series of candidate genes. However, no molecular comparative work has yet been performed on multiple populations displaying different levels of compatibility. Here, we seek to fill this gap in the literature. We focused on B. glabrata FREPs and S. mansoni SmPoMucs, which were previously demonstrated to be involved in snail/schistosome compatibility. We studied the expression and polymorphisms of these factors in combinations of snail and schistosome isolates that display different levels of compatibility. We found that the polymorphism and expression levels of FREPs and SmPoMucs could be linked to the compatibility level of S. mansoni. These data and our complementary results obtained by RNA-seq of samples from various snail strains indicate that the mechanism of compatibility is much more complex than previously thought, and that it is likely to be highly variable within and between populations. This complexity must be taken into account if we hope to identify the molecular pathways that are most likely to be good targets for strategies aimed at blocking transmission of the parasite through the snail intermediate host. |
doi_str_mv | 10.1371/journal.pntd.0005398 |
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The developments of comparative transcriptomics, comparative genomics, interactomics and more targeted approaches have enabled researchers to identify a series of candidate genes. However, no molecular comparative work has yet been performed on multiple populations displaying different levels of compatibility. Here, we seek to fill this gap in the literature. We focused on B. glabrata FREPs and S. mansoni SmPoMucs, which were previously demonstrated to be involved in snail/schistosome compatibility. We studied the expression and polymorphisms of these factors in combinations of snail and schistosome isolates that display different levels of compatibility. We found that the polymorphism and expression levels of FREPs and SmPoMucs could be linked to the compatibility level of S. mansoni. These data and our complementary results obtained by RNA-seq of samples from various snail strains indicate that the mechanism of compatibility is much more complex than previously thought, and that it is likely to be highly variable within and between populations. This complexity must be taken into account if we hope to identify the molecular pathways that are most likely to be good targets for strategies aimed at blocking transmission of the parasite through the snail intermediate host.</description><identifier>ISSN: 1935-2735</identifier><identifier>ISSN: 1935-2727</identifier><identifier>EISSN: 1935-2735</identifier><identifier>DOI: 10.1371/journal.pntd.0005398</identifier><identifier>PMID: 28253264</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Animals ; Antigens, Helminth - genetics ; Antiinfectives and antibacterials ; Bioinformatics ; Biology and Life Sciences ; Biomphalaria - genetics ; Biomphalaria - parasitology ; Biomphalaria glabrata ; Blocking ; Care and treatment ; Colleges & universities ; Compatibility ; Complexity ; Computer programs ; Data acquisition ; Data processing ; Defense industry ; Defensive behavior ; Disease transmission ; Drug resistance ; Eggs ; Fibrinogen ; Galaxies ; Gene expression ; Gene Expression Profiling ; Gene polymorphism ; Genes ; Genetic aspects ; Genomics ; Hemocytes ; Host-Parasite Interactions - genetics ; Human blood fluke ; Immune system ; Immunoglobulins - genetics ; Immunological memory ; Infections ; Infectivity ; Knowledge representation ; Lists ; Malaria ; Medicine and Health Sciences ; Mollusks ; Parasites ; Parasitic diseases ; Polymorphism ; Polymorphism, Genetic ; Populations ; Praziquantel ; Proteins ; Research and Analysis Methods ; Ribonucleic acid ; Risk factors ; RNA ; Schistosoma mansoni ; Schistosoma mansoni - genetics ; Schistosoma mansoni - growth & development ; Schistosomiasis ; Sequence Analysis, DNA ; Statistical analysis ; Tropical diseases</subject><ispartof>PLoS neglected tropical diseases, 2017-03, Vol.11 (3), p.e0005398-e0005398</ispartof><rights>COPYRIGHT 2017 Public Library of Science</rights><rights>2017 Public Library of Science. 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 credited: . PLoS Negl Trop Dis 11(3): e0005398. https://doi.org/10.1371/journal.pntd.0005398</rights><rights>2017 Galinier et al 2017 Galinier et al</rights><rights>2017 Public Library of Science. 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 credited: . 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The developments of comparative transcriptomics, comparative genomics, interactomics and more targeted approaches have enabled researchers to identify a series of candidate genes. However, no molecular comparative work has yet been performed on multiple populations displaying different levels of compatibility. Here, we seek to fill this gap in the literature. We focused on B. glabrata FREPs and S. mansoni SmPoMucs, which were previously demonstrated to be involved in snail/schistosome compatibility. We studied the expression and polymorphisms of these factors in combinations of snail and schistosome isolates that display different levels of compatibility. We found that the polymorphism and expression levels of FREPs and SmPoMucs could be linked to the compatibility level of S. mansoni. These data and our complementary results obtained by RNA-seq of samples from various snail strains indicate that the mechanism of compatibility is much more complex than previously thought, and that it is likely to be highly variable within and between populations. This complexity must be taken into account if we hope to identify the molecular pathways that are most likely to be good targets for strategies aimed at blocking transmission of the parasite through the snail intermediate host.</description><subject>Animals</subject><subject>Antigens, Helminth - genetics</subject><subject>Antiinfectives and antibacterials</subject><subject>Bioinformatics</subject><subject>Biology and Life Sciences</subject><subject>Biomphalaria - genetics</subject><subject>Biomphalaria - parasitology</subject><subject>Biomphalaria glabrata</subject><subject>Blocking</subject><subject>Care and treatment</subject><subject>Colleges & universities</subject><subject>Compatibility</subject><subject>Complexity</subject><subject>Computer programs</subject><subject>Data acquisition</subject><subject>Data processing</subject><subject>Defense industry</subject><subject>Defensive behavior</subject><subject>Disease transmission</subject><subject>Drug resistance</subject><subject>Eggs</subject><subject>Fibrinogen</subject><subject>Galaxies</subject><subject>Gene expression</subject><subject>Gene Expression Profiling</subject><subject>Gene polymorphism</subject><subject>Genes</subject><subject>Genetic aspects</subject><subject>Genomics</subject><subject>Hemocytes</subject><subject>Host-Parasite Interactions - genetics</subject><subject>Human blood fluke</subject><subject>Immune system</subject><subject>Immunoglobulins - genetics</subject><subject>Immunological memory</subject><subject>Infections</subject><subject>Infectivity</subject><subject>Knowledge representation</subject><subject>Lists</subject><subject>Malaria</subject><subject>Medicine and Health Sciences</subject><subject>Mollusks</subject><subject>Parasites</subject><subject>Parasitic diseases</subject><subject>Polymorphism</subject><subject>Polymorphism, Genetic</subject><subject>Populations</subject><subject>Praziquantel</subject><subject>Proteins</subject><subject>Research and Analysis Methods</subject><subject>Ribonucleic acid</subject><subject>Risk factors</subject><subject>RNA</subject><subject>Schistosoma mansoni</subject><subject>Schistosoma mansoni - genetics</subject><subject>Schistosoma mansoni - growth & development</subject><subject>Schistosomiasis</subject><subject>Sequence Analysis, DNA</subject><subject>Statistical analysis</subject><subject>Tropical diseases</subject><issn>1935-2735</issn><issn>1935-2727</issn><issn>1935-2735</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkl9rFDEUxQdRbK1-A9GAIL7sOpNkZpMXoRb_FAo-qM_hTnJnJyWTrElG6efwC5tpt6UrZR4yJL97TnI4VfWyqdcN2zTvL8McPbj1zmezruu6ZVI8qo4bydoV3bD28b3_o-pZSpeFka1onlZHVNCW0Y4fV39PyTS7bFOOYD2B3S4G0CPJgaQ8myvrtySPSCbUI3ibpkRmbzC66xMdph1k21tn8xUp8wtqfcYIOtvgSY_5D6InH20hR3AQLZCtgz5CBgLekO96LOYhhQnIBD4Fb59XTwZwCV_s15Pq5-dPP86-ri6-fTk_O71Y6Y7yvOppjSB1z5qWNpIPtK570whGQbK-GcSm5xvUVLe9NLUQFAbAhkrJUIqBG8ZOqtc3ujsXktrnmVQjhOjajtd1Ic5vCBPgUu2inSBeqQBWXW-EuFUQs9UOlVhseGfoYJBvNAJDNEZSiloWU1q0Puzd5n5Co9GXyN2B6OGJt6Paht-qZVx2QhaBd3uBGH7NmLKabNLoHHgM83LvDeecCdkV9M1_6MOv21NbKA-wfgjFVy-i6pRLJmi9qZeU1g9Q5TM4WR08DrbsHwy8vTcwIrg8puDmpRDpEOQ3oI4hpYjDXRhNrZaO395aLR1X-46XsVf3g7wbui01-wctc_zR</recordid><startdate>20170302</startdate><enddate>20170302</enddate><creator>Galinier, Richard</creator><creator>Roger, Emmanuel</creator><creator>Moné, Yves</creator><creator>Duval, David</creator><creator>Portet, Anaïs</creator><creator>Pinaud, Silvain</creator><creator>Chaparro, Cristian</creator><creator>Grunau, Christoph</creator><creator>Genthon, Clémence</creator><creator>Dubois, Emeric</creator><creator>Rognon, Anne</creator><creator>Arancibia, Nathalie</creator><creator>Dejean, Bernard</creator><creator>Théron, André</creator><creator>Gourbal, Benjamin</creator><creator>Mitta, Guillaume</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QL</scope><scope>7SS</scope><scope>7T2</scope><scope>7T7</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8C1</scope><scope>8FD</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>F1W</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>H95</scope><scope>H97</scope><scope>K9.</scope><scope>L.G</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-4180-9303</orcidid><orcidid>https://orcid.org/0000-0002-5162-349X</orcidid><orcidid>https://orcid.org/0000-0002-6052-4178</orcidid><orcidid>https://orcid.org/0000-0001-7592-0432</orcidid><orcidid>https://orcid.org/0000-0002-9541-3611</orcidid></search><sort><creationdate>20170302</creationdate><title>A multistrain approach to studying the mechanisms underlying compatibility in the interaction between Biomphalaria glabrata and Schistosoma mansoni</title><author>Galinier, Richard ; Roger, Emmanuel ; Moné, Yves ; Duval, David ; Portet, Anaïs ; Pinaud, Silvain ; Chaparro, Cristian ; Grunau, Christoph ; Genthon, Clémence ; Dubois, Emeric ; Rognon, Anne ; Arancibia, Nathalie ; Dejean, Bernard ; Théron, André ; Gourbal, Benjamin ; Mitta, Guillaume</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c624t-b20ea9cb3152194f200bd1832a93b1f87b47ec2c5b9d0882afae12993e98f4d33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Animals</topic><topic>Antigens, Helminth - 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The developments of comparative transcriptomics, comparative genomics, interactomics and more targeted approaches have enabled researchers to identify a series of candidate genes. However, no molecular comparative work has yet been performed on multiple populations displaying different levels of compatibility. Here, we seek to fill this gap in the literature. We focused on B. glabrata FREPs and S. mansoni SmPoMucs, which were previously demonstrated to be involved in snail/schistosome compatibility. We studied the expression and polymorphisms of these factors in combinations of snail and schistosome isolates that display different levels of compatibility. We found that the polymorphism and expression levels of FREPs and SmPoMucs could be linked to the compatibility level of S. mansoni. These data and our complementary results obtained by RNA-seq of samples from various snail strains indicate that the mechanism of compatibility is much more complex than previously thought, and that it is likely to be highly variable within and between populations. This complexity must be taken into account if we hope to identify the molecular pathways that are most likely to be good targets for strategies aimed at blocking transmission of the parasite through the snail intermediate host.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>28253264</pmid><doi>10.1371/journal.pntd.0005398</doi><orcidid>https://orcid.org/0000-0002-4180-9303</orcidid><orcidid>https://orcid.org/0000-0002-5162-349X</orcidid><orcidid>https://orcid.org/0000-0002-6052-4178</orcidid><orcidid>https://orcid.org/0000-0001-7592-0432</orcidid><orcidid>https://orcid.org/0000-0002-9541-3611</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1935-2735 |
ispartof | PLoS neglected tropical diseases, 2017-03, Vol.11 (3), p.e0005398-e0005398 |
issn | 1935-2735 1935-2727 1935-2735 |
language | eng |
recordid | cdi_plos_journals_1888656400 |
source | Publicly Available Content Database; PubMed Central |
subjects | Animals Antigens, Helminth - genetics Antiinfectives and antibacterials Bioinformatics Biology and Life Sciences Biomphalaria - genetics Biomphalaria - parasitology Biomphalaria glabrata Blocking Care and treatment Colleges & universities Compatibility Complexity Computer programs Data acquisition Data processing Defense industry Defensive behavior Disease transmission Drug resistance Eggs Fibrinogen Galaxies Gene expression Gene Expression Profiling Gene polymorphism Genes Genetic aspects Genomics Hemocytes Host-Parasite Interactions - genetics Human blood fluke Immune system Immunoglobulins - genetics Immunological memory Infections Infectivity Knowledge representation Lists Malaria Medicine and Health Sciences Mollusks Parasites Parasitic diseases Polymorphism Polymorphism, Genetic Populations Praziquantel Proteins Research and Analysis Methods Ribonucleic acid Risk factors RNA Schistosoma mansoni Schistosoma mansoni - genetics Schistosoma mansoni - growth & development Schistosomiasis Sequence Analysis, DNA Statistical analysis Tropical diseases |
title | A multistrain approach to studying the mechanisms underlying compatibility in the interaction between Biomphalaria glabrata and Schistosoma mansoni |
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