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
Hauptverfasser: Wagnerová, Pavla, Sak, Bohumil, Květoňová, Dana, Maršálek, Miroslav, Langrová, Iva, Kváč, Martin
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container_end_page 6
container_issue 1-2
container_start_page 1
container_title Veterinary parasitology
container_volume 197
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. 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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><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 ; 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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.</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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