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Comparison of the biological characteristics of two isolates of Neospora caninum
This study compared the biological and genetic properties of a bovine (NC-SweB1) and a canine (NC-Liverpool) isolate of Neospora caninum. A mouse model for CNS infection demonstrated marked differences in pathogenicity between the isolates. NC-Liverpool induced severe clinical signs of neosporosis i...
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Published in: | Parasitology 1999-04, Vol.118 (4), p.363-370 |
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creator | ATKINSON, R. HARPER, P. A. W. RYCE, C. MORRISON, D. A. ELLIS, J. T. |
description | This study compared the biological and genetic properties of a
bovine (NC-SweB1) and a canine (NC-Liverpool) isolate
of Neospora caninum. A mouse model for CNS infection demonstrated
marked differences in pathogenicity between the
isolates. NC-Liverpool induced severe clinical signs of neosporosis in
57/58 mice including discoordinated movement,
hindlimb paralysis and coat ruffling with severe weight loss. In contrast
NC-SweB1 induced similar but less severe
symptoms in a much smaller proportion of mice over the same time-period.
Statistically significant differences were
observed between the isolates in the response (mean weight loss) of mice
through time to the different doses inoculated.
Histopathological effects on brain tissue reflected the isolate-based differences
described above. NC-Liverpool infection
resulted in intense inflammatory infiltrates and highly necrotic lesions
whereas NC-SweB1 induced a milder meningoencephalitis.
Passage in cell-culture over a period of 14 months did not affect the pathogenicity
of NC-Liverpool.
Immunoblots showed that antibodies to N. caninum appeared earlier
in mice inoculated with NC-Liverpool than with
NC-SweB1. Finally, RAPD–PCR analysis of NC-Liverpool DNA generated
profiles distinct from that observed with
DNA from NC-SweB1 or Toxoplasma gondii. In summary this study
provides evidence for significant biological and
genetic differences between 2 isolates of N. caninum. |
doi_str_mv | 10.1017/S0031182098003898 |
format | article |
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bovine (NC-SweB1) and a canine (NC-Liverpool) isolate
of Neospora caninum. A mouse model for CNS infection demonstrated
marked differences in pathogenicity between the
isolates. NC-Liverpool induced severe clinical signs of neosporosis in
57/58 mice including discoordinated movement,
hindlimb paralysis and coat ruffling with severe weight loss. In contrast
NC-SweB1 induced similar but less severe
symptoms in a much smaller proportion of mice over the same time-period.
Statistically significant differences were
observed between the isolates in the response (mean weight loss) of mice
through time to the different doses inoculated.
Histopathological effects on brain tissue reflected the isolate-based differences
described above. NC-Liverpool infection
resulted in intense inflammatory infiltrates and highly necrotic lesions
whereas NC-SweB1 induced a milder meningoencephalitis.
Passage in cell-culture over a period of 14 months did not affect the pathogenicity
of NC-Liverpool.
Immunoblots showed that antibodies to N. caninum appeared earlier
in mice inoculated with NC-Liverpool than with
NC-SweB1. Finally, RAPD–PCR analysis of NC-Liverpool DNA generated
profiles distinct from that observed with
DNA from NC-SweB1 or Toxoplasma gondii. In summary this study
provides evidence for significant biological and
genetic differences between 2 isolates of N. caninum.</description><identifier>ISSN: 0031-1820</identifier><identifier>EISSN: 1469-8161</identifier><identifier>DOI: 10.1017/S0031182098003898</identifier><identifier>PMID: 10340326</identifier><identifier>CODEN: PARAAE</identifier><language>eng</language><publisher>Cambridge: Cambridge University Press</publisher><subject>Animals ; Biological and medical sciences ; Body Weight ; Brain - parasitology ; Brain - pathology ; Cattle ; Central Nervous System Infections - immunology ; Central Nervous System Infections - parasitology ; Central Nervous System Infections - pathology ; Coccidiosis - immunology ; Coccidiosis - parasitology ; Coccidiosis - pathology ; Cross Reactions ; Disease Models, Animal ; DNA, Protozoan - analysis ; DNA, Protozoan - genetics ; Dogs ; Female ; Fundamental and applied biological sciences. Psychology ; Immunoblotting ; Life cycle. Host-agent relationship. Pathogenesis ; Meningoencephalitis - parasitology ; Meningoencephalitis - pathology ; Mice ; Mice, Inbred BALB C ; Neospora - genetics ; Neospora - immunology ; Neospora - isolation & purification ; Neospora - pathogenicity ; Neospora caninum ; pathogenicity ; Polymerase Chain Reaction - methods ; Protozoa ; Random Amplified Polymorphic DNA Technique ; RAPD–PCR</subject><ispartof>Parasitology, 1999-04, Vol.118 (4), p.363-370</ispartof><rights>1999 Cambridge University Press</rights><rights>1999 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c408t-ffe1c4f8cd6f556dd85bd6e32f81880d7d29ed94d49bedd1f3880a363ae57d333</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.cambridge.org/core/product/identifier/S0031182098003898/type/journal_article$$EHTML$$P50$$Gcambridge$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,72832</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1802041$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10340326$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>ATKINSON, R.</creatorcontrib><creatorcontrib>HARPER, P. A. W.</creatorcontrib><creatorcontrib>RYCE, C.</creatorcontrib><creatorcontrib>MORRISON, D. A.</creatorcontrib><creatorcontrib>ELLIS, J. T.</creatorcontrib><title>Comparison of the biological characteristics of two isolates of Neospora caninum</title><title>Parasitology</title><addtitle>Parasitology</addtitle><description>This study compared the biological and genetic properties of a
bovine (NC-SweB1) and a canine (NC-Liverpool) isolate
of Neospora caninum. A mouse model for CNS infection demonstrated
marked differences in pathogenicity between the
isolates. NC-Liverpool induced severe clinical signs of neosporosis in
57/58 mice including discoordinated movement,
hindlimb paralysis and coat ruffling with severe weight loss. In contrast
NC-SweB1 induced similar but less severe
symptoms in a much smaller proportion of mice over the same time-period.
Statistically significant differences were
observed between the isolates in the response (mean weight loss) of mice
through time to the different doses inoculated.
Histopathological effects on brain tissue reflected the isolate-based differences
described above. NC-Liverpool infection
resulted in intense inflammatory infiltrates and highly necrotic lesions
whereas NC-SweB1 induced a milder meningoencephalitis.
Passage in cell-culture over a period of 14 months did not affect the pathogenicity
of NC-Liverpool.
Immunoblots showed that antibodies to N. caninum appeared earlier
in mice inoculated with NC-Liverpool than with
NC-SweB1. Finally, RAPD–PCR analysis of NC-Liverpool DNA generated
profiles distinct from that observed with
DNA from NC-SweB1 or Toxoplasma gondii. In summary this study
provides evidence for significant biological and
genetic differences between 2 isolates of N. caninum.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Body Weight</subject><subject>Brain - parasitology</subject><subject>Brain - pathology</subject><subject>Cattle</subject><subject>Central Nervous System Infections - immunology</subject><subject>Central Nervous System Infections - parasitology</subject><subject>Central Nervous System Infections - pathology</subject><subject>Coccidiosis - immunology</subject><subject>Coccidiosis - parasitology</subject><subject>Coccidiosis - pathology</subject><subject>Cross Reactions</subject><subject>Disease Models, Animal</subject><subject>DNA, Protozoan - analysis</subject><subject>DNA, Protozoan - genetics</subject><subject>Dogs</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Immunoblotting</subject><subject>Life cycle. Host-agent relationship. Pathogenesis</subject><subject>Meningoencephalitis - parasitology</subject><subject>Meningoencephalitis - pathology</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Neospora - genetics</subject><subject>Neospora - immunology</subject><subject>Neospora - isolation & purification</subject><subject>Neospora - pathogenicity</subject><subject>Neospora caninum</subject><subject>pathogenicity</subject><subject>Polymerase Chain Reaction - methods</subject><subject>Protozoa</subject><subject>Random Amplified Polymorphic DNA Technique</subject><subject>RAPD–PCR</subject><issn>0031-1820</issn><issn>1469-8161</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><recordid>eNp9kM1O3DAURi0EKgPlAdigLFB3aa_jxHGW1YgOIAqtOqwtx74G0yQe7ESUt6-HGbVISKz885179ekQckzhMwVaf_kFwCgVBTQi3UQjdsiMlrzJBeV0l8zWcb7O98lBjA8AwBkvPpB9CqwEVvAZ-TH3_UoFF_2QeZuN95i1znf-zmnVZfpeBaVHTPnodHwhnnyW6E6N-PK-Rh9XPqhMq8ENU_-R7FnVRTzanofk9tvZcn6eX90sLuZfr3Jdghhza5Hq0gptuK0qboyoWsORFVZQIcDUpmjQNKUpmxaNoZalX8U4U1jVhjF2SD5t9q6Cf5wwjrJ3UWPXqQH9FCVv6prXDBJIN6AOPsaAVq6C61V4lhTkWqN8ozHNnGyXT22P5tXExlsCTreAikmUDWrQLv7nBBRQ0oTlGyz5wz__YhV-y9StriRf_JQAy8vq-_xaLhPPtl1V3wZn7lA--CkMSeQ7bf8CJz6Y8Q</recordid><startdate>19990401</startdate><enddate>19990401</enddate><creator>ATKINSON, R.</creator><creator>HARPER, P. A. W.</creator><creator>RYCE, C.</creator><creator>MORRISON, D. A.</creator><creator>ELLIS, J. T.</creator><general>Cambridge University Press</general><scope>BSCLL</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>7X8</scope></search><sort><creationdate>19990401</creationdate><title>Comparison of the biological characteristics of two isolates of Neospora caninum</title><author>ATKINSON, R. ; HARPER, P. A. W. ; RYCE, C. ; MORRISON, D. A. ; ELLIS, J. T.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c408t-ffe1c4f8cd6f556dd85bd6e32f81880d7d29ed94d49bedd1f3880a363ae57d333</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Body Weight</topic><topic>Brain - parasitology</topic><topic>Brain - pathology</topic><topic>Cattle</topic><topic>Central Nervous System Infections - immunology</topic><topic>Central Nervous System Infections - parasitology</topic><topic>Central Nervous System Infections - pathology</topic><topic>Coccidiosis - immunology</topic><topic>Coccidiosis - parasitology</topic><topic>Coccidiosis - pathology</topic><topic>Cross Reactions</topic><topic>Disease Models, Animal</topic><topic>DNA, Protozoan - analysis</topic><topic>DNA, Protozoan - genetics</topic><topic>Dogs</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Immunoblotting</topic><topic>Life cycle. Host-agent relationship. Pathogenesis</topic><topic>Meningoencephalitis - parasitology</topic><topic>Meningoencephalitis - pathology</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Neospora - genetics</topic><topic>Neospora - immunology</topic><topic>Neospora - isolation & purification</topic><topic>Neospora - pathogenicity</topic><topic>Neospora caninum</topic><topic>pathogenicity</topic><topic>Polymerase Chain Reaction - methods</topic><topic>Protozoa</topic><topic>Random Amplified Polymorphic DNA Technique</topic><topic>RAPD–PCR</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>ATKINSON, R.</creatorcontrib><creatorcontrib>HARPER, P. A. W.</creatorcontrib><creatorcontrib>RYCE, C.</creatorcontrib><creatorcontrib>MORRISON, D. A.</creatorcontrib><creatorcontrib>ELLIS, J. T.</creatorcontrib><collection>Istex</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>MEDLINE - Academic</collection><jtitle>Parasitology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>ATKINSON, R.</au><au>HARPER, P. A. W.</au><au>RYCE, C.</au><au>MORRISON, D. A.</au><au>ELLIS, J. T.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparison of the biological characteristics of two isolates of Neospora caninum</atitle><jtitle>Parasitology</jtitle><addtitle>Parasitology</addtitle><date>1999-04-01</date><risdate>1999</risdate><volume>118</volume><issue>4</issue><spage>363</spage><epage>370</epage><pages>363-370</pages><issn>0031-1820</issn><eissn>1469-8161</eissn><coden>PARAAE</coden><abstract>This study compared the biological and genetic properties of a
bovine (NC-SweB1) and a canine (NC-Liverpool) isolate
of Neospora caninum. A mouse model for CNS infection demonstrated
marked differences in pathogenicity between the
isolates. NC-Liverpool induced severe clinical signs of neosporosis in
57/58 mice including discoordinated movement,
hindlimb paralysis and coat ruffling with severe weight loss. In contrast
NC-SweB1 induced similar but less severe
symptoms in a much smaller proportion of mice over the same time-period.
Statistically significant differences were
observed between the isolates in the response (mean weight loss) of mice
through time to the different doses inoculated.
Histopathological effects on brain tissue reflected the isolate-based differences
described above. NC-Liverpool infection
resulted in intense inflammatory infiltrates and highly necrotic lesions
whereas NC-SweB1 induced a milder meningoencephalitis.
Passage in cell-culture over a period of 14 months did not affect the pathogenicity
of NC-Liverpool.
Immunoblots showed that antibodies to N. caninum appeared earlier
in mice inoculated with NC-Liverpool than with
NC-SweB1. Finally, RAPD–PCR analysis of NC-Liverpool DNA generated
profiles distinct from that observed with
DNA from NC-SweB1 or Toxoplasma gondii. In summary this study
provides evidence for significant biological and
genetic differences between 2 isolates of N. caninum.</abstract><cop>Cambridge</cop><pub>Cambridge University Press</pub><pmid>10340326</pmid><doi>10.1017/S0031182098003898</doi><tpages>8</tpages></addata></record> |
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language | eng |
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source | Cambridge University Press |
subjects | Animals Biological and medical sciences Body Weight Brain - parasitology Brain - pathology Cattle Central Nervous System Infections - immunology Central Nervous System Infections - parasitology Central Nervous System Infections - pathology Coccidiosis - immunology Coccidiosis - parasitology Coccidiosis - pathology Cross Reactions Disease Models, Animal DNA, Protozoan - analysis DNA, Protozoan - genetics Dogs Female Fundamental and applied biological sciences. Psychology Immunoblotting Life cycle. Host-agent relationship. Pathogenesis Meningoencephalitis - parasitology Meningoencephalitis - pathology Mice Mice, Inbred BALB C Neospora - genetics Neospora - immunology Neospora - isolation & purification Neospora - pathogenicity Neospora caninum pathogenicity Polymerase Chain Reaction - methods Protozoa Random Amplified Polymorphic DNA Technique RAPD–PCR |
title | Comparison of the biological characteristics of two isolates of Neospora caninum |
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