Ultrastructural differentiation of Toxoplasma gondii schizonts (types B to E) and gamonts in the intestines of cats fed bradyzoites
The ultrastructural characterisitics of four types of Toxoplasma gondii schizonts (types B, C, D and E) and their merozoites, microgamonts and macrogamonts were compared in cats killed at days 1, 2, 4 and 6 after feeding tissues cysts from the brains of mice. Schizonts, merozoites and gamonts contai...
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description | The ultrastructural characterisitics of four types of
Toxoplasma gondii schizonts (types B, C, D and E) and their merozoites, microgamonts and macrogamonts were compared in cats killed at days 1, 2, 4 and 6 after feeding tissues cysts from the brains of mice. Schizonts, merozoites and gamonts contained most of the ultrastructural features characteristic of the phylum Apicomplexa. All four types of schizonts developed within enterocytes or intraepithelial lymphocytes. Occasionally, type B and C schizonts developed within enterocytes that were displaced beneath the epithelium into the lamina propria. Type D and E schizonts and gamonts developed exclusively in the epithelium. Tachyzoites occurred exclusively within the lamina propria. Type B schizonts formed merozoites by endodyogeny, whereas types C to E developed by endopolygeny. The parasitophorous vacuoles surrounding type B and C schizonts consisted of a single membrane, whereas those surrounding types D and E schizonts were comprised of two to four electron-dense membranes. The parasitophorous vacuole of type B schizonts had an extensive tubulovesicular membrane network (TMN); the TMN was reduced or absent in type C schizonts and completely absent in types D and E schizonts and gamonts. Type B merozoites were ultrastructurally similar to tachyzoites, except that they were slightly larger. Type C merozoites exhibited a positive periodic acid-Schiff reaction by light microscopy and ultrastructurally contained amylopectin granules. Rhoptries were labyrinthine in type B merozoites but were electron-dense in types C–E. The development of microgamonts, macrogamont and oocysts is also described. |
doi_str_mv | 10.1016/j.ijpara.2004.11.005 |
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Toxoplasma gondii schizonts (types B, C, D and E) and their merozoites, microgamonts and macrogamonts were compared in cats killed at days 1, 2, 4 and 6 after feeding tissues cysts from the brains of mice. Schizonts, merozoites and gamonts contained most of the ultrastructural features characteristic of the phylum Apicomplexa. All four types of schizonts developed within enterocytes or intraepithelial lymphocytes. Occasionally, type B and C schizonts developed within enterocytes that were displaced beneath the epithelium into the lamina propria. Type D and E schizonts and gamonts developed exclusively in the epithelium. Tachyzoites occurred exclusively within the lamina propria. Type B schizonts formed merozoites by endodyogeny, whereas types C to E developed by endopolygeny. The parasitophorous vacuoles surrounding type B and C schizonts consisted of a single membrane, whereas those surrounding types D and E schizonts were comprised of two to four electron-dense membranes. The parasitophorous vacuole of type B schizonts had an extensive tubulovesicular membrane network (TMN); the TMN was reduced or absent in type C schizonts and completely absent in types D and E schizonts and gamonts. Type B merozoites were ultrastructurally similar to tachyzoites, except that they were slightly larger. Type C merozoites exhibited a positive periodic acid-Schiff reaction by light microscopy and ultrastructurally contained amylopectin granules. Rhoptries were labyrinthine in type B merozoites but were electron-dense in types C–E. The development of microgamonts, macrogamont and oocysts is also described.</description><identifier>ISSN: 0020-7519</identifier><identifier>EISSN: 1879-0135</identifier><identifier>DOI: 10.1016/j.ijpara.2004.11.005</identifier><identifier>PMID: 15710440</identifier><identifier>CODEN: IJPYBT</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Amylopectin - analysis ; Animals ; Apicomplexa ; Biological and medical sciences ; biological development ; bradyzoites ; Cat Diseases - parasitology ; Cats ; developmental stages ; Enterocytes - parasitology ; Enterocytes - ultrastructure ; Experimental protozoal diseases and models ; Fundamental and applied biological sciences. Psychology ; Gamonts ; infection ; Infectious diseases ; Intestinal Mucosa - parasitology ; Intestinal Mucosa - ultrastructure ; Intestine ; Intestine, Small - cytology ; Intestine, Small - parasitology ; Intestine, Small - ultrastructure ; Life Cycle Stages ; Life cycle. Host-agent relationship. Pathogenesis ; Lymphocytes - parasitology ; Lymphocytes - ultrastructure ; macrogamonts ; Medical sciences ; Membranes - ultrastructure ; Merozoites ; Mice ; microgamonts ; Microscopy, Electron - methods ; oocysts ; Oocysts - ultrastructure ; oral infection ; Parasitic diseases ; Protozoa ; Protozoal diseases ; Schizonts ; small intestine ; tachyzoites ; Toxoplasma - growth & development ; Toxoplasma - ultrastructure ; Toxoplasma gondii ; toxoplasmosis ; Toxoplasmosis, Animal - parasitology ; Types B–E ; Ultrastructure ; Vacuoles - ultrastructure</subject><ispartof>International journal for parasitology, 2005-02, Vol.35 (2), p.193-206</ispartof><rights>2004</rights><rights>2005 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c445t-714e09f33e2931ae52e45ef091d165b4afdc8daee15c0f2482f1bc89434abc043</citedby><cites>FETCH-LOGICAL-c445t-714e09f33e2931ae52e45ef091d165b4afdc8daee15c0f2482f1bc89434abc043</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.ijpara.2004.11.005$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16537068$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15710440$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Speer, C.A.</creatorcontrib><creatorcontrib>Dubey, J.P.</creatorcontrib><title>Ultrastructural differentiation of Toxoplasma gondii schizonts (types B to E) and gamonts in the intestines of cats fed bradyzoites</title><title>International journal for parasitology</title><addtitle>Int J Parasitol</addtitle><description>The ultrastructural characterisitics of four types of
Toxoplasma gondii schizonts (types B, C, D and E) and their merozoites, microgamonts and macrogamonts were compared in cats killed at days 1, 2, 4 and 6 after feeding tissues cysts from the brains of mice. Schizonts, merozoites and gamonts contained most of the ultrastructural features characteristic of the phylum Apicomplexa. All four types of schizonts developed within enterocytes or intraepithelial lymphocytes. Occasionally, type B and C schizonts developed within enterocytes that were displaced beneath the epithelium into the lamina propria. Type D and E schizonts and gamonts developed exclusively in the epithelium. Tachyzoites occurred exclusively within the lamina propria. Type B schizonts formed merozoites by endodyogeny, whereas types C to E developed by endopolygeny. The parasitophorous vacuoles surrounding type B and C schizonts consisted of a single membrane, whereas those surrounding types D and E schizonts were comprised of two to four electron-dense membranes. The parasitophorous vacuole of type B schizonts had an extensive tubulovesicular membrane network (TMN); the TMN was reduced or absent in type C schizonts and completely absent in types D and E schizonts and gamonts. Type B merozoites were ultrastructurally similar to tachyzoites, except that they were slightly larger. Type C merozoites exhibited a positive periodic acid-Schiff reaction by light microscopy and ultrastructurally contained amylopectin granules. Rhoptries were labyrinthine in type B merozoites but were electron-dense in types C–E. The development of microgamonts, macrogamont and oocysts is also described.</description><subject>Amylopectin - analysis</subject><subject>Animals</subject><subject>Apicomplexa</subject><subject>Biological and medical sciences</subject><subject>biological development</subject><subject>bradyzoites</subject><subject>Cat Diseases - parasitology</subject><subject>Cats</subject><subject>developmental stages</subject><subject>Enterocytes - parasitology</subject><subject>Enterocytes - ultrastructure</subject><subject>Experimental protozoal diseases and models</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gamonts</subject><subject>infection</subject><subject>Infectious diseases</subject><subject>Intestinal Mucosa - parasitology</subject><subject>Intestinal Mucosa - ultrastructure</subject><subject>Intestine</subject><subject>Intestine, Small - cytology</subject><subject>Intestine, Small - parasitology</subject><subject>Intestine, Small - ultrastructure</subject><subject>Life Cycle Stages</subject><subject>Life cycle. Host-agent relationship. Pathogenesis</subject><subject>Lymphocytes - parasitology</subject><subject>Lymphocytes - ultrastructure</subject><subject>macrogamonts</subject><subject>Medical sciences</subject><subject>Membranes - ultrastructure</subject><subject>Merozoites</subject><subject>Mice</subject><subject>microgamonts</subject><subject>Microscopy, Electron - methods</subject><subject>oocysts</subject><subject>Oocysts - ultrastructure</subject><subject>oral infection</subject><subject>Parasitic diseases</subject><subject>Protozoa</subject><subject>Protozoal diseases</subject><subject>Schizonts</subject><subject>small intestine</subject><subject>tachyzoites</subject><subject>Toxoplasma - growth & development</subject><subject>Toxoplasma - ultrastructure</subject><subject>Toxoplasma gondii</subject><subject>toxoplasmosis</subject><subject>Toxoplasmosis, Animal - parasitology</subject><subject>Types B–E</subject><subject>Ultrastructure</subject><subject>Vacuoles - ultrastructure</subject><issn>0020-7519</issn><issn>1879-0135</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0U1vEzEQBuAVAtFQ-AcIfAHBIWFm187uXpCgKh9SJQ40Z2tij1NHm3WwvYj0yh_HJZF6g9Mc5pnRaN6qeo6wQMDlu-3Cb_cUaVEDyAXiAkA9qGbYtf0csFEPqxlADfNWYX9WPUlpC4CqkfJxdYaqRZASZtXv1ZAjpRwnk6dIg7DeOY48Zk_Zh1EEJ67Dr7AfKO1IbMJovRfJ3PjbMOYk3uTDnpP4KHIQl28FjVZsaPe35UeRb7iUzCn7saiyy1DpOLZiHckeboMvzafVI0dD4menel6tPl1eX3yZX337_PXiw9XcSKnyvEXJ0Lum4bpvkFjVLBU76NHiUq0lOWs6S8yoDLhadrXDtel62UhaG5DNefX6uHcfw4-pHKV3PhkeBho5TEkvW9nUncL_Qmy7pgbsC5RHaGJIKbLT--h3FA8aQd-lpLf6mJK-S0kj6pJSGXtx2j-td2zvh06xFPDqBCgZGlyk0fh075aqaWHZFffy6BwFTZtYzOp7uawB6FvVt3UR74-Cy2N_eo46Gc-jYesjm6xt8P--9Q86_L04</recordid><startdate>20050201</startdate><enddate>20050201</enddate><creator>Speer, C.A.</creator><creator>Dubey, J.P.</creator><general>Elsevier Ltd</general><general>Elsevier Science</general><scope>FBQ</scope><scope>IQODW</scope><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>M7N</scope><scope>7X8</scope></search><sort><creationdate>20050201</creationdate><title>Ultrastructural differentiation of Toxoplasma gondii schizonts (types B to E) and gamonts in the intestines of cats fed bradyzoites</title><author>Speer, C.A. ; Dubey, J.P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c445t-714e09f33e2931ae52e45ef091d165b4afdc8daee15c0f2482f1bc89434abc043</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Amylopectin - analysis</topic><topic>Animals</topic><topic>Apicomplexa</topic><topic>Biological and medical sciences</topic><topic>biological development</topic><topic>bradyzoites</topic><topic>Cat Diseases - parasitology</topic><topic>Cats</topic><topic>developmental stages</topic><topic>Enterocytes - parasitology</topic><topic>Enterocytes - ultrastructure</topic><topic>Experimental protozoal diseases and models</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gamonts</topic><topic>infection</topic><topic>Infectious diseases</topic><topic>Intestinal Mucosa - parasitology</topic><topic>Intestinal Mucosa - ultrastructure</topic><topic>Intestine</topic><topic>Intestine, Small - cytology</topic><topic>Intestine, Small - parasitology</topic><topic>Intestine, Small - ultrastructure</topic><topic>Life Cycle Stages</topic><topic>Life cycle. Host-agent relationship. Pathogenesis</topic><topic>Lymphocytes - parasitology</topic><topic>Lymphocytes - ultrastructure</topic><topic>macrogamonts</topic><topic>Medical sciences</topic><topic>Membranes - ultrastructure</topic><topic>Merozoites</topic><topic>Mice</topic><topic>microgamonts</topic><topic>Microscopy, Electron - methods</topic><topic>oocysts</topic><topic>Oocysts - ultrastructure</topic><topic>oral infection</topic><topic>Parasitic diseases</topic><topic>Protozoa</topic><topic>Protozoal diseases</topic><topic>Schizonts</topic><topic>small intestine</topic><topic>tachyzoites</topic><topic>Toxoplasma - growth & development</topic><topic>Toxoplasma - ultrastructure</topic><topic>Toxoplasma gondii</topic><topic>toxoplasmosis</topic><topic>Toxoplasmosis, Animal - parasitology</topic><topic>Types B–E</topic><topic>Ultrastructure</topic><topic>Vacuoles - ultrastructure</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Speer, C.A.</creatorcontrib><creatorcontrib>Dubey, J.P.</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>MEDLINE - Academic</collection><jtitle>International journal for parasitology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Speer, C.A.</au><au>Dubey, J.P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ultrastructural differentiation of Toxoplasma gondii schizonts (types B to E) and gamonts in the intestines of cats fed bradyzoites</atitle><jtitle>International journal for parasitology</jtitle><addtitle>Int J Parasitol</addtitle><date>2005-02-01</date><risdate>2005</risdate><volume>35</volume><issue>2</issue><spage>193</spage><epage>206</epage><pages>193-206</pages><issn>0020-7519</issn><eissn>1879-0135</eissn><coden>IJPYBT</coden><abstract>The ultrastructural characterisitics of four types of
Toxoplasma gondii schizonts (types B, C, D and E) and their merozoites, microgamonts and macrogamonts were compared in cats killed at days 1, 2, 4 and 6 after feeding tissues cysts from the brains of mice. Schizonts, merozoites and gamonts contained most of the ultrastructural features characteristic of the phylum Apicomplexa. All four types of schizonts developed within enterocytes or intraepithelial lymphocytes. Occasionally, type B and C schizonts developed within enterocytes that were displaced beneath the epithelium into the lamina propria. Type D and E schizonts and gamonts developed exclusively in the epithelium. Tachyzoites occurred exclusively within the lamina propria. Type B schizonts formed merozoites by endodyogeny, whereas types C to E developed by endopolygeny. The parasitophorous vacuoles surrounding type B and C schizonts consisted of a single membrane, whereas those surrounding types D and E schizonts were comprised of two to four electron-dense membranes. The parasitophorous vacuole of type B schizonts had an extensive tubulovesicular membrane network (TMN); the TMN was reduced or absent in type C schizonts and completely absent in types D and E schizonts and gamonts. Type B merozoites were ultrastructurally similar to tachyzoites, except that they were slightly larger. Type C merozoites exhibited a positive periodic acid-Schiff reaction by light microscopy and ultrastructurally contained amylopectin granules. Rhoptries were labyrinthine in type B merozoites but were electron-dense in types C–E. The development of microgamonts, macrogamont and oocysts is also described.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><pmid>15710440</pmid><doi>10.1016/j.ijpara.2004.11.005</doi><tpages>14</tpages></addata></record> |
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subjects | Amylopectin - analysis Animals Apicomplexa Biological and medical sciences biological development bradyzoites Cat Diseases - parasitology Cats developmental stages Enterocytes - parasitology Enterocytes - ultrastructure Experimental protozoal diseases and models Fundamental and applied biological sciences. Psychology Gamonts infection Infectious diseases Intestinal Mucosa - parasitology Intestinal Mucosa - ultrastructure Intestine Intestine, Small - cytology Intestine, Small - parasitology Intestine, Small - ultrastructure Life Cycle Stages Life cycle. Host-agent relationship. Pathogenesis Lymphocytes - parasitology Lymphocytes - ultrastructure macrogamonts Medical sciences Membranes - ultrastructure Merozoites Mice microgamonts Microscopy, Electron - methods oocysts Oocysts - ultrastructure oral infection Parasitic diseases Protozoa Protozoal diseases Schizonts small intestine tachyzoites Toxoplasma - growth & development Toxoplasma - ultrastructure Toxoplasma gondii toxoplasmosis Toxoplasmosis, Animal - parasitology Types B–E Ultrastructure Vacuoles - ultrastructure |
title | Ultrastructural differentiation of Toxoplasma gondii schizonts (types B to E) and gamonts in the intestines of cats fed bradyzoites |
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