Filamentous proteophosphoglycan secreted by Leishmania promastigotes forms gel-like three-dimensional networks that obstruct the digestive tract of infected sandfly vectors
Development of Leishmania parasites in the digestive tract of their sandfly vectors involves several morphological transformations from the intracellular mammalian amastigote via a succession of free and gut wall-attached promastigote stages to the infective metacyclic promastigotes. At the foregut...
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Veröffentlicht in: | European journal of cell biology 1999-10, Vol.78 (10), p.675-689 |
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creator | Stierhof, York-Dieter Bates, Paul A. Jacobson, Raymond L. Rogers, Matthew E. Schlein, Yosef Handman, Emanuela Ilg, Thomas |
description | Development of
Leishmania parasites in the digestive tract of their sandfly vectors involves several morphological transformations from the intracellular mammalian amastigote via a succession of free and gut wall-attached promastigote stages to the infective metacyclic promastigotes. At the foregut - midgut transition of
Leishmania-infected sandflies a gel-like plug of unknown origin and composition is formed, which contains high numbers of parasites, that occludes the gut lumen and which may be responsible for the often observed inability of infected sandflies to draw blood. This “blocked fly” phenotype has been linked to efficient transmission of infectious metacyclic promastigotes from the vector to the mammalian host. We show by immunofluorescence and immunoelectron microscopy on two
Leishmania/sandfly vector combinations (
Leishmania mexicana/Lutzomyia longipalpis and
L. major/Phlebotomus papatasi) that the gel-like mass is formed mainly by a parasite-derived mucin-like filamentous proteophosphoglycan (fPPG) whereas the
Leishmania polymeric secreted acid phosphatase (SAP) is not a major component of this plug. fPPG forms a dense three-dimensional network of filaments which engulf the promastigote cell bodies in a gel-like mass. We propose that the continuous secretion of fPPG by promastigotes in the sandfly gut, that causes plug formation, is an important factor for the efficient transmission to the mammalian host. |
doi_str_mv | 10.1016/S0171-9335(99)80036-3 |
format | Article |
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Leishmania parasites in the digestive tract of their sandfly vectors involves several morphological transformations from the intracellular mammalian amastigote via a succession of free and gut wall-attached promastigote stages to the infective metacyclic promastigotes. At the foregut - midgut transition of
Leishmania-infected sandflies a gel-like plug of unknown origin and composition is formed, which contains high numbers of parasites, that occludes the gut lumen and which may be responsible for the often observed inability of infected sandflies to draw blood. This “blocked fly” phenotype has been linked to efficient transmission of infectious metacyclic promastigotes from the vector to the mammalian host. We show by immunofluorescence and immunoelectron microscopy on two
Leishmania/sandfly vector combinations (
Leishmania mexicana/Lutzomyia longipalpis and
L. major/Phlebotomus papatasi) that the gel-like mass is formed mainly by a parasite-derived mucin-like filamentous proteophosphoglycan (fPPG) whereas the
Leishmania polymeric secreted acid phosphatase (SAP) is not a major component of this plug. fPPG forms a dense three-dimensional network of filaments which engulf the promastigote cell bodies in a gel-like mass. We propose that the continuous secretion of fPPG by promastigotes in the sandfly gut, that causes plug formation, is an important factor for the efficient transmission to the mammalian host.</description><identifier>ISSN: 0171-9335</identifier><identifier>EISSN: 1618-1298</identifier><identifier>DOI: 10.1016/S0171-9335(99)80036-3</identifier><identifier>PMID: 10569240</identifier><language>eng</language><publisher>Germany: Elsevier GmbH</publisher><subject>Acid Phosphatase - secretion ; Animals ; Digestive System - parasitology ; Female ; Gels ; Immunoelectron microscopy ; Insect Vectors - parasitology ; Leishmania - growth & development ; Leishmania - pathogenicity ; Leishmania - physiology ; Leishmania major - growth & development ; Leishmania major - pathogenicity ; Leishmania major - physiology ; Leishmania mexicana - growth & development ; Leishmania mexicana - pathogenicity ; Leishmania mexicana - physiology ; Microscopy, Electron, Scanning ; Microscopy, Immunoelectron ; Phlebotomus - parasitology ; Proteoglycans - chemistry ; Proteoglycans - secretion ; proteophosphoglycan ; Psychodidae - parasitology ; sandfly ; secreted acid phosphatase</subject><ispartof>European journal of cell biology, 1999-10, Vol.78 (10), p.675-689</ispartof><rights>1999 Urban & Fischer Verlag GmbH & Co. KG</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c361t-e5651a06c6adb05faf4bc5bb1499c90acf415cf470e5e19834e519efcd7724eb3</citedby><cites>FETCH-LOGICAL-c361t-e5651a06c6adb05faf4bc5bb1499c90acf415cf470e5e19834e519efcd7724eb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0171933599800363$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10569240$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Stierhof, York-Dieter</creatorcontrib><creatorcontrib>Bates, Paul A.</creatorcontrib><creatorcontrib>Jacobson, Raymond L.</creatorcontrib><creatorcontrib>Rogers, Matthew E.</creatorcontrib><creatorcontrib>Schlein, Yosef</creatorcontrib><creatorcontrib>Handman, Emanuela</creatorcontrib><creatorcontrib>Ilg, Thomas</creatorcontrib><title>Filamentous proteophosphoglycan secreted by Leishmania promastigotes forms gel-like three-dimensional networks that obstruct the digestive tract of infected sandfly vectors</title><title>European journal of cell biology</title><addtitle>Eur J Cell Biol</addtitle><description>Development of
Leishmania parasites in the digestive tract of their sandfly vectors involves several morphological transformations from the intracellular mammalian amastigote via a succession of free and gut wall-attached promastigote stages to the infective metacyclic promastigotes. At the foregut - midgut transition of
Leishmania-infected sandflies a gel-like plug of unknown origin and composition is formed, which contains high numbers of parasites, that occludes the gut lumen and which may be responsible for the often observed inability of infected sandflies to draw blood. This “blocked fly” phenotype has been linked to efficient transmission of infectious metacyclic promastigotes from the vector to the mammalian host. We show by immunofluorescence and immunoelectron microscopy on two
Leishmania/sandfly vector combinations (
Leishmania mexicana/Lutzomyia longipalpis and
L. major/Phlebotomus papatasi) that the gel-like mass is formed mainly by a parasite-derived mucin-like filamentous proteophosphoglycan (fPPG) whereas the
Leishmania polymeric secreted acid phosphatase (SAP) is not a major component of this plug. fPPG forms a dense three-dimensional network of filaments which engulf the promastigote cell bodies in a gel-like mass. We propose that the continuous secretion of fPPG by promastigotes in the sandfly gut, that causes plug formation, is an important factor for the efficient transmission to the mammalian host.</description><subject>Acid Phosphatase - secretion</subject><subject>Animals</subject><subject>Digestive System - parasitology</subject><subject>Female</subject><subject>Gels</subject><subject>Immunoelectron microscopy</subject><subject>Insect Vectors - parasitology</subject><subject>Leishmania - growth & development</subject><subject>Leishmania - pathogenicity</subject><subject>Leishmania - physiology</subject><subject>Leishmania major - growth & development</subject><subject>Leishmania major - pathogenicity</subject><subject>Leishmania major - physiology</subject><subject>Leishmania mexicana - growth & development</subject><subject>Leishmania mexicana - pathogenicity</subject><subject>Leishmania mexicana - physiology</subject><subject>Microscopy, Electron, Scanning</subject><subject>Microscopy, Immunoelectron</subject><subject>Phlebotomus - parasitology</subject><subject>Proteoglycans - chemistry</subject><subject>Proteoglycans - secretion</subject><subject>proteophosphoglycan</subject><subject>Psychodidae - parasitology</subject><subject>sandfly</subject><subject>secreted acid phosphatase</subject><issn>0171-9335</issn><issn>1618-1298</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUcGOFCEQJUbjzq5-goaT0UMrTDdMczJm464mk3hQz4SGYga3uxkpZsz8kx9pzc7GePMApOC9V9R7jL2Q4q0UUr_7KuRKNqZt1Wtj3vRCtLppH7GF1LJv5NL0j9niL-SCXSL-EEKq3pin7EIKpc2yEwv2-yaNboK55j3yXckV8m6bkdZmPHo3cwRfoELgw5GvIeF2cnNyJ-jksKYNMZDHXCbkGxibMd0Br9sC0IREupjy7EY-Q_2Vyx3Sk6s8D1jL3leqgIe0ARI6EK04usuRpzmCP_VEN4c4HvmBylzwGXsS3Yjw_OG8Yt9vPn67_tSsv9x-vv6wbnyrZW1AaSWd0F67MAgVXewGr4ZBdsZ4I5yPnVS0rQQokKZvO1DSQPRhtVp2MLRX7NVZl6b8uaff2Smhh3F0M5BPlrzre90qAqoz0JeMWCDaXUmTK0crhT3FZO9jsqcMrDH2PibbEu_lQ4P9MEH4h3XOhQDvzwCgMQ8JikWfYPYQUiEvbMjpPy3-AOBUqRw</recordid><startdate>19991001</startdate><enddate>19991001</enddate><creator>Stierhof, York-Dieter</creator><creator>Bates, Paul A.</creator><creator>Jacobson, Raymond L.</creator><creator>Rogers, Matthew E.</creator><creator>Schlein, Yosef</creator><creator>Handman, Emanuela</creator><creator>Ilg, Thomas</creator><general>Elsevier GmbH</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>7X8</scope></search><sort><creationdate>19991001</creationdate><title>Filamentous proteophosphoglycan secreted by Leishmania promastigotes forms gel-like three-dimensional networks that obstruct the digestive tract of infected sandfly vectors</title><author>Stierhof, York-Dieter ; Bates, Paul A. ; Jacobson, Raymond L. ; Rogers, Matthew E. ; Schlein, Yosef ; Handman, Emanuela ; Ilg, Thomas</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c361t-e5651a06c6adb05faf4bc5bb1499c90acf415cf470e5e19834e519efcd7724eb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Acid Phosphatase - secretion</topic><topic>Animals</topic><topic>Digestive System - parasitology</topic><topic>Female</topic><topic>Gels</topic><topic>Immunoelectron microscopy</topic><topic>Insect Vectors - parasitology</topic><topic>Leishmania - growth & development</topic><topic>Leishmania - pathogenicity</topic><topic>Leishmania - physiology</topic><topic>Leishmania major - growth & development</topic><topic>Leishmania major - pathogenicity</topic><topic>Leishmania major - physiology</topic><topic>Leishmania mexicana - growth & development</topic><topic>Leishmania mexicana - pathogenicity</topic><topic>Leishmania mexicana - physiology</topic><topic>Microscopy, Electron, Scanning</topic><topic>Microscopy, Immunoelectron</topic><topic>Phlebotomus - parasitology</topic><topic>Proteoglycans - chemistry</topic><topic>Proteoglycans - secretion</topic><topic>proteophosphoglycan</topic><topic>Psychodidae - parasitology</topic><topic>sandfly</topic><topic>secreted acid phosphatase</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Stierhof, York-Dieter</creatorcontrib><creatorcontrib>Bates, Paul A.</creatorcontrib><creatorcontrib>Jacobson, Raymond L.</creatorcontrib><creatorcontrib>Rogers, Matthew E.</creatorcontrib><creatorcontrib>Schlein, Yosef</creatorcontrib><creatorcontrib>Handman, Emanuela</creatorcontrib><creatorcontrib>Ilg, Thomas</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>European journal of cell biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stierhof, York-Dieter</au><au>Bates, Paul A.</au><au>Jacobson, Raymond L.</au><au>Rogers, Matthew E.</au><au>Schlein, Yosef</au><au>Handman, Emanuela</au><au>Ilg, Thomas</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Filamentous proteophosphoglycan secreted by Leishmania promastigotes forms gel-like three-dimensional networks that obstruct the digestive tract of infected sandfly vectors</atitle><jtitle>European journal of cell biology</jtitle><addtitle>Eur J Cell Biol</addtitle><date>1999-10-01</date><risdate>1999</risdate><volume>78</volume><issue>10</issue><spage>675</spage><epage>689</epage><pages>675-689</pages><issn>0171-9335</issn><eissn>1618-1298</eissn><abstract>Development of
Leishmania parasites in the digestive tract of their sandfly vectors involves several morphological transformations from the intracellular mammalian amastigote via a succession of free and gut wall-attached promastigote stages to the infective metacyclic promastigotes. At the foregut - midgut transition of
Leishmania-infected sandflies a gel-like plug of unknown origin and composition is formed, which contains high numbers of parasites, that occludes the gut lumen and which may be responsible for the often observed inability of infected sandflies to draw blood. This “blocked fly” phenotype has been linked to efficient transmission of infectious metacyclic promastigotes from the vector to the mammalian host. We show by immunofluorescence and immunoelectron microscopy on two
Leishmania/sandfly vector combinations (
Leishmania mexicana/Lutzomyia longipalpis and
L. major/Phlebotomus papatasi) that the gel-like mass is formed mainly by a parasite-derived mucin-like filamentous proteophosphoglycan (fPPG) whereas the
Leishmania polymeric secreted acid phosphatase (SAP) is not a major component of this plug. fPPG forms a dense three-dimensional network of filaments which engulf the promastigote cell bodies in a gel-like mass. We propose that the continuous secretion of fPPG by promastigotes in the sandfly gut, that causes plug formation, is an important factor for the efficient transmission to the mammalian host.</abstract><cop>Germany</cop><pub>Elsevier GmbH</pub><pmid>10569240</pmid><doi>10.1016/S0171-9335(99)80036-3</doi><tpages>15</tpages></addata></record> |
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subjects | Acid Phosphatase - secretion Animals Digestive System - parasitology Female Gels Immunoelectron microscopy Insect Vectors - parasitology Leishmania - growth & development Leishmania - pathogenicity Leishmania - physiology Leishmania major - growth & development Leishmania major - pathogenicity Leishmania major - physiology Leishmania mexicana - growth & development Leishmania mexicana - pathogenicity Leishmania mexicana - physiology Microscopy, Electron, Scanning Microscopy, Immunoelectron Phlebotomus - parasitology Proteoglycans - chemistry Proteoglycans - secretion proteophosphoglycan Psychodidae - parasitology sandfly secreted acid phosphatase |
title | Filamentous proteophosphoglycan secreted by Leishmania promastigotes forms gel-like three-dimensional networks that obstruct the digestive tract of infected sandfly vectors |
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