Babesia bigemina: Sporozoite Isolation from Boophilus microplus Nymphs and Initial Immunomolecular Characterization

: It has been hypothesized that babesial sporozoites express specific antigens that induce protective immunologic responses in cattle. However, they remain uncharacterized, partly for lack of research on the sporozoite stage of Babesia spp. This field suffers from complete knowledge of parasite deve...

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Veröffentlicht in:Annals of the New York Academy of Sciences 2004-10, Vol.1026 (1), p.222-231
Hauptverfasser: MOSQUEDA, JUAN, RAMOS, JUAN A., FALCON, ALFONSO, ALVAREZ, J ANTONIO, ARAGON, VICENTE, FIGUEROA, JULIO V.
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container_title Annals of the New York Academy of Sciences
container_volume 1026
creator MOSQUEDA, JUAN
RAMOS, JUAN A.
FALCON, ALFONSO
ALVAREZ, J ANTONIO
ARAGON, VICENTE
FIGUEROA, JULIO V.
description : It has been hypothesized that babesial sporozoites express specific antigens that induce protective immunologic responses in cattle. However, they remain uncharacterized, partly for lack of research on the sporozoite stage of Babesia spp. This field suffers from complete knowledge of parasite development in the tick salivary gland; limited amounts of sporozoites from ticks, and a lack of protocols for induction and purification of sporozoites. In this work, Boophilus microplus larvae infected with B. bigemina were fed on susceptible cattle. Nymphs were collected and macerates were separated by a Percoll density gradient. Microscopic analysis of Giemsa‐stained smears showed a larger number of sporozoites from nymphs fed for 9 days. Percoll‐purified sporozoites were observed in large numbers in groups or individually and free of tick cells. RT‐PCR analysis of total RNA extracted from purified sporozoites indicated transcription of the rhoptry associate protein 1 (rap‐1) genes: rap‐1a, rap‐b, rap‐1c, as well as the heat shock protein 20 (hsp‐20) gene. Purified sporozoites were cultured in vitro analyzed for RAP‐1a expression using an immunocytochemistry assay. Erythrocyte‐attached sporozoites reacted with a specific RAP‐1a monoclonal antibody. This is the first report of Babesia bigemina sporozoite antigens. Moreover, purified sporozoites will allow the characterization of stage‐specific antigens involved in immunologic protection.
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However, they remain uncharacterized, partly for lack of research on the sporozoite stage of Babesia spp. This field suffers from complete knowledge of parasite development in the tick salivary gland; limited amounts of sporozoites from ticks, and a lack of protocols for induction and purification of sporozoites. In this work, Boophilus microplus larvae infected with B. bigemina were fed on susceptible cattle. Nymphs were collected and macerates were separated by a Percoll density gradient. Microscopic analysis of Giemsa‐stained smears showed a larger number of sporozoites from nymphs fed for 9 days. Percoll‐purified sporozoites were observed in large numbers in groups or individually and free of tick cells. RT‐PCR analysis of total RNA extracted from purified sporozoites indicated transcription of the rhoptry associate protein 1 (rap‐1) genes: rap‐1a, rap‐b, rap‐1c, as well as the heat shock protein 20 (hsp‐20) gene. Purified sporozoites were cultured in vitro analyzed for RAP‐1a expression using an immunocytochemistry assay. Erythrocyte‐attached sporozoites reacted with a specific RAP‐1a monoclonal antibody. This is the first report of Babesia bigemina sporozoite antigens. 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However, they remain uncharacterized, partly for lack of research on the sporozoite stage of Babesia spp. This field suffers from complete knowledge of parasite development in the tick salivary gland; limited amounts of sporozoites from ticks, and a lack of protocols for induction and purification of sporozoites. In this work, Boophilus microplus larvae infected with B. bigemina were fed on susceptible cattle. Nymphs were collected and macerates were separated by a Percoll density gradient. Microscopic analysis of Giemsa‐stained smears showed a larger number of sporozoites from nymphs fed for 9 days. Percoll‐purified sporozoites were observed in large numbers in groups or individually and free of tick cells. RT‐PCR analysis of total RNA extracted from purified sporozoites indicated transcription of the rhoptry associate protein 1 (rap‐1) genes: rap‐1a, rap‐b, rap‐1c, as well as the heat shock protein 20 (hsp‐20) gene. Purified sporozoites were cultured in vitro analyzed for RAP‐1a expression using an immunocytochemistry assay. Erythrocyte‐attached sporozoites reacted with a specific RAP‐1a monoclonal antibody. This is the first report of Babesia bigemina sporozoite antigens. Moreover, purified sporozoites will allow the characterization of stage‐specific antigens involved in immunologic protection.</description><subject>Animals</subject><subject>Antigens, Protozoan - analysis</subject><subject>Babesia</subject><subject>Babesia - genetics</subject><subject>Babesia - immunology</subject><subject>Babesia - isolation &amp; purification</subject><subject>Babesia - pathogenicity</subject><subject>Babesia bigemina</subject><subject>Babesiosis - veterinary</subject><subject>Boophilus microplus</subject><subject>Cattle</subject><subject>Cattle Diseases - parasitology</subject><subject>heat shock protein 20</subject><subject>Ixodidae</subject><subject>Larva</subject><subject>nymph</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>rhoptry-associated protein 1</subject><subject>RNA</subject><subject>sporozoite</subject><subject>Ticks - parasitology</subject><issn>0077-8923</issn><issn>1749-6632</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc9v0zAYhi0EYt3gzA35xC2df9WOuW0FSsVUkAqaOFmO41KDHWd2Itb99bikguPkgy3reR99n14AXmE0x1jyS9112uc5pkjMEWVPwAwLJivOKXkKZggJUdWS0DNwnvNPhDCpmXgOzvCCI8akmIF8rRubnYaN-2GD6_RbuO1jig_RDRauc_R6cLGDuxQDvI6x3zs_ZhicSbE_vjaH0O8z1F0L150bnPZwHcLYxRC9NaPXCS73Omkz2OQe_spegGe7MrV9ebovwLcP778uP1Y3n1fr5dVNZRiSpJLaYGobxDgirWhsXT7ZwuCmlbKhUiJGWsSM2fGGYsulrTHjmJma8FaUQy_Am8nbp3g32jyo4LKx3uvOxjErLrDENSKPgljWmBdtAS8nsGyfc7I71ScXdDoojNSxEDUVoo6FqFJISbw-qccm2PY_f2qgAGwCfjtvD4_51Ob71ZaQ48jVFHN5sPf_Yjr9KmtRsVC3m5VafXmHb_mnWm3pHzn2qZs</recordid><startdate>200410</startdate><enddate>200410</enddate><creator>MOSQUEDA, JUAN</creator><creator>RAMOS, JUAN A.</creator><creator>FALCON, ALFONSO</creator><creator>ALVAREZ, J ANTONIO</creator><creator>ARAGON, VICENTE</creator><creator>FIGUEROA, JULIO V.</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</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>7T5</scope><scope>H94</scope><scope>M7N</scope><scope>7X8</scope></search><sort><creationdate>200410</creationdate><title>Babesia bigemina: Sporozoite Isolation from Boophilus microplus Nymphs and Initial Immunomolecular Characterization</title><author>MOSQUEDA, JUAN ; RAMOS, JUAN A. ; FALCON, ALFONSO ; ALVAREZ, J ANTONIO ; ARAGON, VICENTE ; FIGUEROA, JULIO V.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4092-9ac13eb04602d7be809245c1bd99b399042d04ccf6b31e69e814614c826d7d7d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Animals</topic><topic>Antigens, Protozoan - analysis</topic><topic>Babesia</topic><topic>Babesia - genetics</topic><topic>Babesia - immunology</topic><topic>Babesia - isolation &amp; purification</topic><topic>Babesia - pathogenicity</topic><topic>Babesia bigemina</topic><topic>Babesiosis - veterinary</topic><topic>Boophilus microplus</topic><topic>Cattle</topic><topic>Cattle Diseases - parasitology</topic><topic>heat shock protein 20</topic><topic>Ixodidae</topic><topic>Larva</topic><topic>nymph</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>rhoptry-associated protein 1</topic><topic>RNA</topic><topic>sporozoite</topic><topic>Ticks - parasitology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>MOSQUEDA, JUAN</creatorcontrib><creatorcontrib>RAMOS, JUAN A.</creatorcontrib><creatorcontrib>FALCON, ALFONSO</creatorcontrib><creatorcontrib>ALVAREZ, J ANTONIO</creatorcontrib><creatorcontrib>ARAGON, VICENTE</creatorcontrib><creatorcontrib>FIGUEROA, JULIO V.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>MEDLINE - Academic</collection><jtitle>Annals of the New York Academy of Sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>MOSQUEDA, JUAN</au><au>RAMOS, JUAN A.</au><au>FALCON, ALFONSO</au><au>ALVAREZ, J ANTONIO</au><au>ARAGON, VICENTE</au><au>FIGUEROA, JULIO V.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Babesia bigemina: Sporozoite Isolation from Boophilus microplus Nymphs and Initial Immunomolecular Characterization</atitle><jtitle>Annals of the New York Academy of Sciences</jtitle><addtitle>Ann N Y Acad Sci</addtitle><date>2004-10</date><risdate>2004</risdate><volume>1026</volume><issue>1</issue><spage>222</spage><epage>231</epage><pages>222-231</pages><issn>0077-8923</issn><eissn>1749-6632</eissn><abstract>: It has been hypothesized that babesial sporozoites express specific antigens that induce protective immunologic responses in cattle. However, they remain uncharacterized, partly for lack of research on the sporozoite stage of Babesia spp. This field suffers from complete knowledge of parasite development in the tick salivary gland; limited amounts of sporozoites from ticks, and a lack of protocols for induction and purification of sporozoites. In this work, Boophilus microplus larvae infected with B. bigemina were fed on susceptible cattle. Nymphs were collected and macerates were separated by a Percoll density gradient. Microscopic analysis of Giemsa‐stained smears showed a larger number of sporozoites from nymphs fed for 9 days. Percoll‐purified sporozoites were observed in large numbers in groups or individually and free of tick cells. RT‐PCR analysis of total RNA extracted from purified sporozoites indicated transcription of the rhoptry associate protein 1 (rap‐1) genes: rap‐1a, rap‐b, rap‐1c, as well as the heat shock protein 20 (hsp‐20) gene. Purified sporozoites were cultured in vitro analyzed for RAP‐1a expression using an immunocytochemistry assay. Erythrocyte‐attached sporozoites reacted with a specific RAP‐1a monoclonal antibody. This is the first report of Babesia bigemina sporozoite antigens. Moreover, purified sporozoites will allow the characterization of stage‐specific antigens involved in immunologic protection.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>15604497</pmid><doi>10.1196/annals.1307.034</doi><tpages>10</tpages></addata></record>
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subjects Animals
Antigens, Protozoan - analysis
Babesia
Babesia - genetics
Babesia - immunology
Babesia - isolation & purification
Babesia - pathogenicity
Babesia bigemina
Babesiosis - veterinary
Boophilus microplus
Cattle
Cattle Diseases - parasitology
heat shock protein 20
Ixodidae
Larva
nymph
Reverse Transcriptase Polymerase Chain Reaction
rhoptry-associated protein 1
RNA
sporozoite
Ticks - parasitology
title Babesia bigemina: Sporozoite Isolation from Boophilus microplus Nymphs and Initial Immunomolecular Characterization
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