Humoral immune response and spreading of Encephalitozoon cuniculi infection in experimentally infected ponies
•Infected ponies revealed no clinical signs of microsporidiosis.•Acute microsporidiosis occurred within first 3 weeks.•Microsporidia spread into most organs.•Dynamics and spreading of infection were connected with increased humoral response.•The humoral response represents useful marker for infectio...
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Veröffentlicht in: | Veterinary parasitology 2013-10, Vol.197 (1-2), p.1-6 |
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creator | Wagnerová, Pavla Sak, Bohumil Květoňová, Dana Maršálek, Miroslav Langrová, Iva Kváč, Martin |
description | •Infected ponies revealed no clinical signs of microsporidiosis.•Acute microsporidiosis occurred within first 3 weeks.•Microsporidia spread into most organs.•Dynamics and spreading of infection were connected with increased humoral response.•The humoral response represents useful marker for infection intensity evaluation.
A total of 9 (8 stallions and 1 mare) 1 year old ponies were used for the experimental infection caused by Encephalitozoon cuniculi genotype II (107 spores per animal). Subsequently, individual horses were slaughtered 7, 14, 21, 28, 35, 42, 49, 56, and 63 days post infection. Immediately after slaughter, tissues samples of stomach, duodenum, jejunum, ileum, caecum, colon, spleen, liver, kidney, bladder, heart, lungs, and brain were sampled. In addition, urine, feces and blood specimens were collected. Enzyme-linked immunosorbent assay was used for determination of humoral immune response and nested PCR targeting 16S rDNA, whole ITS, and 5.8S rDNA was used for detection of E. cuniculi in collected organs, blood, feces and urine. No clinical signs of microsporidiosis including diarrhea or colic, neurological signs and fever were observed in any horses during whole experiment. Acute microsporidiosis in ponies was characterized by the dissemination of microsporidia into almost all organs and significant increase of concentration of specific antibodies in blood was observed from 28 to 42 DPI. After this acute stage microsporidia disappeared from most organs with the exception of the kidney, which was positive up to 63 DPI when the experiment was terminated. No pathological changes were observed in any organs with exception of one mare's brain, where E. cuniculi-positive cavity measuring 5cm×3cm in diameter formed in the lobus piriformis. |
doi_str_mv | 10.1016/j.vetpar.2013.05.007 |
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A total of 9 (8 stallions and 1 mare) 1 year old ponies were used for the experimental infection caused by Encephalitozoon cuniculi genotype II (107 spores per animal). Subsequently, individual horses were slaughtered 7, 14, 21, 28, 35, 42, 49, 56, and 63 days post infection. Immediately after slaughter, tissues samples of stomach, duodenum, jejunum, ileum, caecum, colon, spleen, liver, kidney, bladder, heart, lungs, and brain were sampled. In addition, urine, feces and blood specimens were collected. Enzyme-linked immunosorbent assay was used for determination of humoral immune response and nested PCR targeting 16S rDNA, whole ITS, and 5.8S rDNA was used for detection of E. cuniculi in collected organs, blood, feces and urine. No clinical signs of microsporidiosis including diarrhea or colic, neurological signs and fever were observed in any horses during whole experiment. Acute microsporidiosis in ponies was characterized by the dissemination of microsporidia into almost all organs and significant increase of concentration of specific antibodies in blood was observed from 28 to 42 DPI. After this acute stage microsporidia disappeared from most organs with the exception of the kidney, which was positive up to 63 DPI when the experiment was terminated. No pathological changes were observed in any organs with exception of one mare's brain, where E. cuniculi-positive cavity measuring 5cm×3cm in diameter formed in the lobus piriformis.</description><identifier>ISSN: 0304-4017</identifier><identifier>EISSN: 1873-2550</identifier><identifier>DOI: 10.1016/j.vetpar.2013.05.007</identifier><identifier>PMID: 23747106</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Animals ; Antibodies ; bladder ; blood ; brain ; cecum ; colic ; colon ; diarrhea ; duodenum ; Encephalitozoon cuniculi ; Encephalitozoon cuniculi - immunology ; Encephalitozoon cuniculi genotype II ; Encephalitozoonosis - immunology ; Encephalitozoonosis - veterinary ; enzyme-linked immunosorbent assay ; Experimental infection ; feces ; Female ; fever ; genotype ; heart ; Horse Diseases - immunology ; Horse Diseases - microbiology ; Horses ; humoral immunity ; ileum ; Immunity, Humoral - physiology ; internal transcribed spacers ; jejunum ; kidneys ; liver ; lungs ; Male ; mares ; Microsporidia ; microsporidiosis ; PCR ; polymerase chain reaction ; Ponies ; ribosomal DNA ; slaughter ; spleen ; spores ; stallions ; stomach ; urine</subject><ispartof>Veterinary parasitology, 2013-10, Vol.197 (1-2), p.1-6</ispartof><rights>2013 Elsevier B.V.</rights><rights>Copyright © 2013 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c419t-866f0bfe1be0328da9bb11377ea54204f99243ec27f21d60b28419ac4d92dc7e3</citedby><cites>FETCH-LOGICAL-c419t-866f0bfe1be0328da9bb11377ea54204f99243ec27f21d60b28419ac4d92dc7e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.vetpar.2013.05.007$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23747106$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wagnerová, Pavla</creatorcontrib><creatorcontrib>Sak, Bohumil</creatorcontrib><creatorcontrib>Květoňová, Dana</creatorcontrib><creatorcontrib>Maršálek, Miroslav</creatorcontrib><creatorcontrib>Langrová, Iva</creatorcontrib><creatorcontrib>Kváč, Martin</creatorcontrib><title>Humoral immune response and spreading of Encephalitozoon cuniculi infection in experimentally infected ponies</title><title>Veterinary parasitology</title><addtitle>Vet Parasitol</addtitle><description>•Infected ponies revealed no clinical signs of microsporidiosis.•Acute microsporidiosis occurred within first 3 weeks.•Microsporidia spread into most organs.•Dynamics and spreading of infection were connected with increased humoral response.•The humoral response represents useful marker for infection intensity evaluation.
A total of 9 (8 stallions and 1 mare) 1 year old ponies were used for the experimental infection caused by Encephalitozoon cuniculi genotype II (107 spores per animal). Subsequently, individual horses were slaughtered 7, 14, 21, 28, 35, 42, 49, 56, and 63 days post infection. Immediately after slaughter, tissues samples of stomach, duodenum, jejunum, ileum, caecum, colon, spleen, liver, kidney, bladder, heart, lungs, and brain were sampled. In addition, urine, feces and blood specimens were collected. Enzyme-linked immunosorbent assay was used for determination of humoral immune response and nested PCR targeting 16S rDNA, whole ITS, and 5.8S rDNA was used for detection of E. cuniculi in collected organs, blood, feces and urine. No clinical signs of microsporidiosis including diarrhea or colic, neurological signs and fever were observed in any horses during whole experiment. Acute microsporidiosis in ponies was characterized by the dissemination of microsporidia into almost all organs and significant increase of concentration of specific antibodies in blood was observed from 28 to 42 DPI. After this acute stage microsporidia disappeared from most organs with the exception of the kidney, which was positive up to 63 DPI when the experiment was terminated. No pathological changes were observed in any organs with exception of one mare's brain, where E. cuniculi-positive cavity measuring 5cm×3cm in diameter formed in the lobus piriformis.</description><subject>Animals</subject><subject>Antibodies</subject><subject>bladder</subject><subject>blood</subject><subject>brain</subject><subject>cecum</subject><subject>colic</subject><subject>colon</subject><subject>diarrhea</subject><subject>duodenum</subject><subject>Encephalitozoon cuniculi</subject><subject>Encephalitozoon cuniculi - immunology</subject><subject>Encephalitozoon cuniculi genotype II</subject><subject>Encephalitozoonosis - immunology</subject><subject>Encephalitozoonosis - veterinary</subject><subject>enzyme-linked immunosorbent assay</subject><subject>Experimental infection</subject><subject>feces</subject><subject>Female</subject><subject>fever</subject><subject>genotype</subject><subject>heart</subject><subject>Horse Diseases - immunology</subject><subject>Horse Diseases - microbiology</subject><subject>Horses</subject><subject>humoral immunity</subject><subject>ileum</subject><subject>Immunity, Humoral - physiology</subject><subject>internal transcribed spacers</subject><subject>jejunum</subject><subject>kidneys</subject><subject>liver</subject><subject>lungs</subject><subject>Male</subject><subject>mares</subject><subject>Microsporidia</subject><subject>microsporidiosis</subject><subject>PCR</subject><subject>polymerase chain reaction</subject><subject>Ponies</subject><subject>ribosomal DNA</subject><subject>slaughter</subject><subject>spleen</subject><subject>spores</subject><subject>stallions</subject><subject>stomach</subject><subject>urine</subject><issn>0304-4017</issn><issn>1873-2550</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkVFv1SAYholxcWfTf2CUS2_afVBa2hsTs0xnssSLuWtC4evkpIUK7bL568dJz7zUKxJ43hf4HkLeMygZsOZiXz7gMutYcmBVCXUJIF-RHWtlVfC6htdkBxWIQgCTp-QspT0ACGjkG3LKKykkg2ZHput1ClGP1E3T6pFGTHPwCan2lqY5orbO39Mw0CtvcP6lR7eEPyF4albvzDo66vyAZnF5y3mKjzNGN6Ff9Dg-Hc_Q0lzqML0lJ4MeE747rufk7uvVz8vr4ubHt--XX24KI1i3FG3TDNAPyHqEirdWd33PWCUl6lpwEEPXcVGh4XLgzDbQ8zbntBG249ZIrM7Jp613juH3imlRk0sGx1F7DGtSrOZQtV3Twv9RwTvO6rqRGRUbamJIKeKg5vxVHZ8UA3VwovZqc6IOThTUKjvJsQ_HG9Z-Qvs39CIhAx83YNBB6fvokrq7zQ0iC2OskQfi80ZgHtqDw6iScZiFWBfzfJUN7t9veAYLU6or</recordid><startdate>20131018</startdate><enddate>20131018</enddate><creator>Wagnerová, Pavla</creator><creator>Sak, Bohumil</creator><creator>Květoňová, Dana</creator><creator>Maršálek, Miroslav</creator><creator>Langrová, Iva</creator><creator>Kváč, Martin</creator><general>Elsevier B.V</general><scope>FBQ</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><scope>7T5</scope><scope>H94</scope><scope>M7N</scope></search><sort><creationdate>20131018</creationdate><title>Humoral immune response and spreading of Encephalitozoon cuniculi infection in experimentally infected ponies</title><author>Wagnerová, Pavla ; Sak, Bohumil ; Květoňová, Dana ; Maršálek, Miroslav ; Langrová, Iva ; Kváč, Martin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c419t-866f0bfe1be0328da9bb11377ea54204f99243ec27f21d60b28419ac4d92dc7e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Animals</topic><topic>Antibodies</topic><topic>bladder</topic><topic>blood</topic><topic>brain</topic><topic>cecum</topic><topic>colic</topic><topic>colon</topic><topic>diarrhea</topic><topic>duodenum</topic><topic>Encephalitozoon cuniculi</topic><topic>Encephalitozoon cuniculi - immunology</topic><topic>Encephalitozoon cuniculi genotype II</topic><topic>Encephalitozoonosis - immunology</topic><topic>Encephalitozoonosis - veterinary</topic><topic>enzyme-linked immunosorbent assay</topic><topic>Experimental infection</topic><topic>feces</topic><topic>Female</topic><topic>fever</topic><topic>genotype</topic><topic>heart</topic><topic>Horse Diseases - immunology</topic><topic>Horse Diseases - microbiology</topic><topic>Horses</topic><topic>humoral immunity</topic><topic>ileum</topic><topic>Immunity, Humoral - physiology</topic><topic>internal transcribed spacers</topic><topic>jejunum</topic><topic>kidneys</topic><topic>liver</topic><topic>lungs</topic><topic>Male</topic><topic>mares</topic><topic>Microsporidia</topic><topic>microsporidiosis</topic><topic>PCR</topic><topic>polymerase chain reaction</topic><topic>Ponies</topic><topic>ribosomal DNA</topic><topic>slaughter</topic><topic>spleen</topic><topic>spores</topic><topic>stallions</topic><topic>stomach</topic><topic>urine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wagnerová, Pavla</creatorcontrib><creatorcontrib>Sak, Bohumil</creatorcontrib><creatorcontrib>Květoňová, Dana</creatorcontrib><creatorcontrib>Maršálek, Miroslav</creatorcontrib><creatorcontrib>Langrová, Iva</creatorcontrib><creatorcontrib>Kváč, Martin</creatorcontrib><collection>AGRIS</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><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><jtitle>Veterinary parasitology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wagnerová, Pavla</au><au>Sak, Bohumil</au><au>Květoňová, Dana</au><au>Maršálek, Miroslav</au><au>Langrová, Iva</au><au>Kváč, Martin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Humoral immune response and spreading of Encephalitozoon cuniculi infection in experimentally infected ponies</atitle><jtitle>Veterinary parasitology</jtitle><addtitle>Vet Parasitol</addtitle><date>2013-10-18</date><risdate>2013</risdate><volume>197</volume><issue>1-2</issue><spage>1</spage><epage>6</epage><pages>1-6</pages><issn>0304-4017</issn><eissn>1873-2550</eissn><abstract>•Infected ponies revealed no clinical signs of microsporidiosis.•Acute microsporidiosis occurred within first 3 weeks.•Microsporidia spread into most organs.•Dynamics and spreading of infection were connected with increased humoral response.•The humoral response represents useful marker for infection intensity evaluation.
A total of 9 (8 stallions and 1 mare) 1 year old ponies were used for the experimental infection caused by Encephalitozoon cuniculi genotype II (107 spores per animal). Subsequently, individual horses were slaughtered 7, 14, 21, 28, 35, 42, 49, 56, and 63 days post infection. Immediately after slaughter, tissues samples of stomach, duodenum, jejunum, ileum, caecum, colon, spleen, liver, kidney, bladder, heart, lungs, and brain were sampled. In addition, urine, feces and blood specimens were collected. Enzyme-linked immunosorbent assay was used for determination of humoral immune response and nested PCR targeting 16S rDNA, whole ITS, and 5.8S rDNA was used for detection of E. cuniculi in collected organs, blood, feces and urine. No clinical signs of microsporidiosis including diarrhea or colic, neurological signs and fever were observed in any horses during whole experiment. Acute microsporidiosis in ponies was characterized by the dissemination of microsporidia into almost all organs and significant increase of concentration of specific antibodies in blood was observed from 28 to 42 DPI. After this acute stage microsporidia disappeared from most organs with the exception of the kidney, which was positive up to 63 DPI when the experiment was terminated. No pathological changes were observed in any organs with exception of one mare's brain, where E. cuniculi-positive cavity measuring 5cm×3cm in diameter formed in the lobus piriformis.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>23747106</pmid><doi>10.1016/j.vetpar.2013.05.007</doi><tpages>6</tpages></addata></record> |
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subjects | Animals Antibodies bladder blood brain cecum colic colon diarrhea duodenum Encephalitozoon cuniculi Encephalitozoon cuniculi - immunology Encephalitozoon cuniculi genotype II Encephalitozoonosis - immunology Encephalitozoonosis - veterinary enzyme-linked immunosorbent assay Experimental infection feces Female fever genotype heart Horse Diseases - immunology Horse Diseases - microbiology Horses humoral immunity ileum Immunity, Humoral - physiology internal transcribed spacers jejunum kidneys liver lungs Male mares Microsporidia microsporidiosis PCR polymerase chain reaction Ponies ribosomal DNA slaughter spleen spores stallions stomach urine |
title | Humoral immune response and spreading of Encephalitozoon cuniculi infection in experimentally infected ponies |
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