Fine Structural Aspects of Nuclear Division and Merogony of Eimeria ninakohlyakimovae in Cultured Cells

Fine structural aspects of nuclear division and development of first-generation merozoites of Eimeria ninakohlyakimovae in cultures of ovine trachea, kidney, and thyroid cells fixed 12, 15, and 21 days after inoculation of sporozoites were studied. In some apparently dividing nuclei, eccentric or ce...

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Veröffentlicht in:The Journal of parasitology 1973-12, Vol.59 (6), p.1071-1079
Hauptverfasser: Kelley, Gary L., Hammond, Datus M.
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Hammond, Datus M.
description Fine structural aspects of nuclear division and development of first-generation merozoites of Eimeria ninakohlyakimovae in cultures of ovine trachea, kidney, and thyroid cells fixed 12, 15, and 21 days after inoculation of sporozoites were studied. In some apparently dividing nuclei, eccentric or centrally located intranuclear spindles, with centrioles near their poles, were observed. Microtubules resembling astral rays were observed around some centrioles. In some schizonts, numerous invaginations or infoldings of the limiting membrane occurred, which sometimes led to the isolation of spheroidal blastophores, each having a number of nuclei and limited by a surface membrane derived from that of the schizont. In large schizonts and developing merozoites, aggregations of microtubules were seen. The first indication of merozoite formation was the appearance, just interior to the schizont membrane, of relatively electron-dense thickenings, each of which apparently represented the beginning of the inner membrane complex of the pellicle of a merozoite. Later, a conoid, micronemes, rhoptry anlagen, and subpellicular microtubules appeared in association with each thickening. A nucleus was usually seen nearby. Sites of merozoite formation were always observed in close proximity with a membrane surface of schizonts, infoldings of schizonts, or blastophores. Merozoite development proceeded by elongation of the merozoite and incorporation of certain organelles, such as the nucleus, Golgi apparatus, and mitochondria. Completely formed merozoites were separated posteriorly from the residual body by a pinching-off process. Some merozoites apparently undergoing a kind of binary fission were observed.
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In some apparently dividing nuclei, eccentric or centrally located intranuclear spindles, with centrioles near their poles, were observed. Microtubules resembling astral rays were observed around some centrioles. In some schizonts, numerous invaginations or infoldings of the limiting membrane occurred, which sometimes led to the isolation of spheroidal blastophores, each having a number of nuclei and limited by a surface membrane derived from that of the schizont. In large schizonts and developing merozoites, aggregations of microtubules were seen. The first indication of merozoite formation was the appearance, just interior to the schizont membrane, of relatively electron-dense thickenings, each of which apparently represented the beginning of the inner membrane complex of the pellicle of a merozoite. Later, a conoid, micronemes, rhoptry anlagen, and subpellicular microtubules appeared in association with each thickening. A nucleus was usually seen nearby. Sites of merozoite formation were always observed in close proximity with a membrane surface of schizonts, infoldings of schizonts, or blastophores. Merozoite development proceeded by elongation of the merozoite and incorporation of certain organelles, such as the nucleus, Golgi apparatus, and mitochondria. Completely formed merozoites were separated posteriorly from the residual body by a pinching-off process. 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In some apparently dividing nuclei, eccentric or centrally located intranuclear spindles, with centrioles near their poles, were observed. Microtubules resembling astral rays were observed around some centrioles. In some schizonts, numerous invaginations or infoldings of the limiting membrane occurred, which sometimes led to the isolation of spheroidal blastophores, each having a number of nuclei and limited by a surface membrane derived from that of the schizont. In large schizonts and developing merozoites, aggregations of microtubules were seen. The first indication of merozoite formation was the appearance, just interior to the schizont membrane, of relatively electron-dense thickenings, each of which apparently represented the beginning of the inner membrane complex of the pellicle of a merozoite. Later, a conoid, micronemes, rhoptry anlagen, and subpellicular microtubules appeared in association with each thickening. A nucleus was usually seen nearby. Sites of merozoite formation were always observed in close proximity with a membrane surface of schizonts, infoldings of schizonts, or blastophores. Merozoite development proceeded by elongation of the merozoite and incorporation of certain organelles, such as the nucleus, Golgi apparatus, and mitochondria. Completely formed merozoites were separated posteriorly from the residual body by a pinching-off process. Some merozoites apparently undergoing a kind of binary fission were observed.</description><subject>Animals</subject><subject>Cell Division</subject><subject>Cell Nucleus</subject><subject>Cells, Cultured</subject><subject>Centrioles</subject><subject>Cultured cells</subject><subject>Eimeria - cytology</subject><subject>Eimeria - growth &amp; development</subject><subject>Golgi Apparatus</subject><subject>Kidney</subject><subject>Merozoites</subject><subject>Microscopy, Electron</subject><subject>Microtubules</subject><subject>Mitochondria</subject><subject>Mitotic spindle apparatus</subject><subject>Nuclear membrane</subject><subject>P branes</subject><subject>Parasitism</subject><subject>Phosphotungstic Acid</subject><subject>Schizonts</subject><subject>Sheep</subject><subject>Sporozoites</subject><subject>Staining and Labeling</subject><subject>Thyroid Gland</subject><subject>Trachea</subject><issn>0022-3395</issn><issn>1937-2345</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1973</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kD1PwzAURS0EKqUgfgGSBwRTwB9xEo8otIBUYKB7ZCfPxW0SFzup1H9PqlZsDE93uEdHTxeha0oeGCfpI2dplsTiBI2p5GnEeCxO0ZgQxiLOpThHFyGsCCFiuBEaxZRlTPAxWs5sC_ir833Z9V7V-ClsoOwCdgZ_9GUNyuNnu7XBuhartsLv4N3Stbs9MLUNeKtwa1u1dt_1Tq1t47YKsG1x3teDESqcQ12HS3RmVB3g6pgTtJhNF_lrNP98ecuf5lHJieiilMZZmibcEM24rBLIdJYmVMjKqJSWWoMkpaFUUSk5KK7jODFGCKOhEhr4BN0dtBvvfnoIXdHYUA4PqBZcH4qMUZpkTA7g_QEsvQvBgyk23jbK7wpKiv2ixXHRgbw5KnvdQPXHHScc-ttDvwqd8_9qfgFYnHxQ</recordid><startdate>197312</startdate><enddate>197312</enddate><creator>Kelley, Gary L.</creator><creator>Hammond, Datus M.</creator><general>American Society of Parasitologists</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>197312</creationdate><title>Fine Structural Aspects of Nuclear Division and Merogony of Eimeria ninakohlyakimovae in Cultured Cells</title><author>Kelley, Gary L. ; Hammond, Datus M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c305t-71487763f0b239d6e8b876159dfa71cbbe90cf11a1993ea3b446ff55fbed5be3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1973</creationdate><topic>Animals</topic><topic>Cell Division</topic><topic>Cell Nucleus</topic><topic>Cells, Cultured</topic><topic>Centrioles</topic><topic>Cultured cells</topic><topic>Eimeria - cytology</topic><topic>Eimeria - growth &amp; development</topic><topic>Golgi Apparatus</topic><topic>Kidney</topic><topic>Merozoites</topic><topic>Microscopy, Electron</topic><topic>Microtubules</topic><topic>Mitochondria</topic><topic>Mitotic spindle apparatus</topic><topic>Nuclear membrane</topic><topic>P branes</topic><topic>Parasitism</topic><topic>Phosphotungstic Acid</topic><topic>Schizonts</topic><topic>Sheep</topic><topic>Sporozoites</topic><topic>Staining and Labeling</topic><topic>Thyroid Gland</topic><topic>Trachea</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kelley, Gary L.</creatorcontrib><creatorcontrib>Hammond, Datus M.</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>The Journal of parasitology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kelley, Gary L.</au><au>Hammond, Datus M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Fine Structural Aspects of Nuclear Division and Merogony of Eimeria ninakohlyakimovae in Cultured Cells</atitle><jtitle>The Journal of parasitology</jtitle><addtitle>J Parasitol</addtitle><date>1973-12</date><risdate>1973</risdate><volume>59</volume><issue>6</issue><spage>1071</spage><epage>1079</epage><pages>1071-1079</pages><issn>0022-3395</issn><eissn>1937-2345</eissn><abstract>Fine structural aspects of nuclear division and development of first-generation merozoites of Eimeria ninakohlyakimovae in cultures of ovine trachea, kidney, and thyroid cells fixed 12, 15, and 21 days after inoculation of sporozoites were studied. In some apparently dividing nuclei, eccentric or centrally located intranuclear spindles, with centrioles near their poles, were observed. Microtubules resembling astral rays were observed around some centrioles. In some schizonts, numerous invaginations or infoldings of the limiting membrane occurred, which sometimes led to the isolation of spheroidal blastophores, each having a number of nuclei and limited by a surface membrane derived from that of the schizont. In large schizonts and developing merozoites, aggregations of microtubules were seen. The first indication of merozoite formation was the appearance, just interior to the schizont membrane, of relatively electron-dense thickenings, each of which apparently represented the beginning of the inner membrane complex of the pellicle of a merozoite. Later, a conoid, micronemes, rhoptry anlagen, and subpellicular microtubules appeared in association with each thickening. A nucleus was usually seen nearby. Sites of merozoite formation were always observed in close proximity with a membrane surface of schizonts, infoldings of schizonts, or blastophores. Merozoite development proceeded by elongation of the merozoite and incorporation of certain organelles, such as the nucleus, Golgi apparatus, and mitochondria. Completely formed merozoites were separated posteriorly from the residual body by a pinching-off process. Some merozoites apparently undergoing a kind of binary fission were observed.</abstract><cop>United States</cop><pub>American Society of Parasitologists</pub><pmid>4128253</pmid><doi>10.2307/3278645</doi><tpages>9</tpages></addata></record>
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ispartof The Journal of parasitology, 1973-12, Vol.59 (6), p.1071-1079
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1937-2345
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source MEDLINE; JSTOR Archive Collection A-Z Listing
subjects Animals
Cell Division
Cell Nucleus
Cells, Cultured
Centrioles
Cultured cells
Eimeria - cytology
Eimeria - growth & development
Golgi Apparatus
Kidney
Merozoites
Microscopy, Electron
Microtubules
Mitochondria
Mitotic spindle apparatus
Nuclear membrane
P branes
Parasitism
Phosphotungstic Acid
Schizonts
Sheep
Sporozoites
Staining and Labeling
Thyroid Gland
Trachea
title Fine Structural Aspects of Nuclear Division and Merogony of Eimeria ninakohlyakimovae in Cultured Cells
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