Identification of a Cyclospora cayetanensis Oocyst Antigens and Their Validity in the Detection of Immunogenic Patterns of Cyclosporiasis Patients
Introduction The diagnosis of cyclosporiasis is currently based on the microscopic detection of oocysts, which may provide invalid results. The availability of simple, objective immunological screening tests would facilitate epidemiological studies of cyclosporiasis. Therefore, the present study aim...
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description | Introduction
The diagnosis of cyclosporiasis is currently based on the microscopic detection of oocysts, which may provide invalid results. The availability of simple, objective immunological screening tests would facilitate epidemiological studies of cyclosporiasis. Therefore, the present study aimed to identify the antigens of
Cyclospora cayetanensis
oocysts and their validity in serodiagnosis.
Methods
According to parasitological and molecular diagnoses, three study groups were specified. Group (G) I included 30 patients with cyclosporiasis, GII included 12 patients with other parasitic infections, and GIII included 16 healthy subjects. SDS-PAGE was used to analyse
C. cayetanensis
antigens, and the validity of western blotting and enzyme-linked immunosorbent assays (ELISAs) was then assessed amongst the sera of all study groups.
Results
The
C. cayetanensis
antigenic profile showed eight characteristic bands with molecular weights ranging from 14 to 175 kDa. Western blot analysis of sera revealed 93.3% (28/30 of GI) and 92.8% (26/28 of GII and III) sensitivity and specificity, respectively, dividing the patients in GI into four subgroups. The most frequent diagnostic bands (71.4% of GI sera) showed weights of 26–28 kDa, followed by 71 kDa (53.6%). ELISA sensitivity was 90% (27/30), and specificity was 78.6%. Validation showed perfect agreement between the PCR and western blot results, and ELISA presented substantial agreement with both the PCR and western blot results.
Conclusions
Our findings suggest the existence of high immunogenic diversity in
C. cayetanensis
and indicate that the 26–28 kDa immunogenic groups may potentially be used as a diagnostic marker of cyclosporiasis. Due to the high validity of ELISA, it might be the test of choice for the routine serodiagnosis of cyclosporiasis. |
doi_str_mv | 10.1007/s11686-020-00289-w |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2449961991</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2535301163</sourcerecordid><originalsourceid>FETCH-LOGICAL-c218w-5c8380ca749b22ef54653b331ff2f08c9655f7cec4f7f03965ccf891bf7f07ac3</originalsourceid><addsrcrecordid>eNp9kctOIzEQRVuIkYAMP8DKEhs2PfjRD3uJwmMiITELZraWU7HBqGMH21HUv8EXU5nwkFiwsqt8z3XZt6pOGP3FKO3PM2Od7GrKaU0pl6re7FWHTKquZrJl-7jngtZccnZQHeX8RGnTSSkPq5fZwobinQdTfAwkOmLIdIQh5lVMhoAZbTHBhuwzuYsw5kIuEHjADjFhQe4frU_knxn8wpeR-EDKoyWXtlh4N5wtl-sQkfBA_phSbEIW-x_XeLN1xyOPs-Sf1Q9nhmyP39ZJ9ff66n76u769u5lNL25r4Exu6hakkBRM36g559a1TdeKuRDMOe6oBNW1revBQuN6RwWWAE4qNt-WvQExqc52vqsUn9c2F730Geww4HPjOmveNEp1TCmG0tMv0qe4TgGn07wVraD4_QJVfKeCFHNO1ulV8kuTRs2o3sakdzFpjEn_j0lvEBI7KKM4PNj0af0N9QpeT5jS</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2535301163</pqid></control><display><type>article</type><title>Identification of a Cyclospora cayetanensis Oocyst Antigens and Their Validity in the Detection of Immunogenic Patterns of Cyclosporiasis Patients</title><source>SpringerLink Journals - AutoHoldings</source><creator>Hussein, Eman M. ; El-Gayar, Eman K. ; Ismail, Ola A. ; Mokhtar, Amira B. ; Al-Abbassy, Maha M.</creator><creatorcontrib>Hussein, Eman M. ; El-Gayar, Eman K. ; Ismail, Ola A. ; Mokhtar, Amira B. ; Al-Abbassy, Maha M.</creatorcontrib><description>Introduction
The diagnosis of cyclosporiasis is currently based on the microscopic detection of oocysts, which may provide invalid results. The availability of simple, objective immunological screening tests would facilitate epidemiological studies of cyclosporiasis. Therefore, the present study aimed to identify the antigens of
Cyclospora cayetanensis
oocysts and their validity in serodiagnosis.
Methods
According to parasitological and molecular diagnoses, three study groups were specified. Group (G) I included 30 patients with cyclosporiasis, GII included 12 patients with other parasitic infections, and GIII included 16 healthy subjects. SDS-PAGE was used to analyse
C. cayetanensis
antigens, and the validity of western blotting and enzyme-linked immunosorbent assays (ELISAs) was then assessed amongst the sera of all study groups.
Results
The
C. cayetanensis
antigenic profile showed eight characteristic bands with molecular weights ranging from 14 to 175 kDa. Western blot analysis of sera revealed 93.3% (28/30 of GI) and 92.8% (26/28 of GII and III) sensitivity and specificity, respectively, dividing the patients in GI into four subgroups. The most frequent diagnostic bands (71.4% of GI sera) showed weights of 26–28 kDa, followed by 71 kDa (53.6%). ELISA sensitivity was 90% (27/30), and specificity was 78.6%. Validation showed perfect agreement between the PCR and western blot results, and ELISA presented substantial agreement with both the PCR and western blot results.
Conclusions
Our findings suggest the existence of high immunogenic diversity in
C. cayetanensis
and indicate that the 26–28 kDa immunogenic groups may potentially be used as a diagnostic marker of cyclosporiasis. Due to the high validity of ELISA, it might be the test of choice for the routine serodiagnosis of cyclosporiasis.</description><identifier>ISSN: 1230-2821</identifier><identifier>EISSN: 1896-1851</identifier><identifier>DOI: 10.1007/s11686-020-00289-w</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Animal Systematics/Taxonomy/Biogeography ; Antigens ; Biomedical and Life Sciences ; Biomedicine ; Cyclospora cayetanensis ; Cyclosporiasis ; Diagnostic systems ; Ecology ; Enzyme-linked immunosorbent assay ; Epidemiology ; Gel electrophoresis ; Immunoassays ; Immunogenicity ; Immunology ; Medical Microbiology ; Microbiology ; Oocysts ; Original Paper ; Parasitic diseases ; Parasitology ; Protozoa ; Sensitivity ; Sodium lauryl sulfate ; Subgroups ; Validity ; Western blotting</subject><ispartof>Acta parasitologica, 2021-06, Vol.66 (2), p.416-427</ispartof><rights>Witold Stefański Institute of Parasitology, Polish Academy of Sciences 2020</rights><rights>Witold Stefański Institute of Parasitology, Polish Academy of Sciences 2020.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c218w-5c8380ca749b22ef54653b331ff2f08c9655f7cec4f7f03965ccf891bf7f07ac3</cites><orcidid>0000-0003-3362-2925</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s11686-020-00289-w$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11686-020-00289-w$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,777,781,27905,27906,41469,42538,51300</link.rule.ids></links><search><creatorcontrib>Hussein, Eman M.</creatorcontrib><creatorcontrib>El-Gayar, Eman K.</creatorcontrib><creatorcontrib>Ismail, Ola A.</creatorcontrib><creatorcontrib>Mokhtar, Amira B.</creatorcontrib><creatorcontrib>Al-Abbassy, Maha M.</creatorcontrib><title>Identification of a Cyclospora cayetanensis Oocyst Antigens and Their Validity in the Detection of Immunogenic Patterns of Cyclosporiasis Patients</title><title>Acta parasitologica</title><addtitle>Acta Parasit</addtitle><description>Introduction
The diagnosis of cyclosporiasis is currently based on the microscopic detection of oocysts, which may provide invalid results. The availability of simple, objective immunological screening tests would facilitate epidemiological studies of cyclosporiasis. Therefore, the present study aimed to identify the antigens of
Cyclospora cayetanensis
oocysts and their validity in serodiagnosis.
Methods
According to parasitological and molecular diagnoses, three study groups were specified. Group (G) I included 30 patients with cyclosporiasis, GII included 12 patients with other parasitic infections, and GIII included 16 healthy subjects. SDS-PAGE was used to analyse
C. cayetanensis
antigens, and the validity of western blotting and enzyme-linked immunosorbent assays (ELISAs) was then assessed amongst the sera of all study groups.
Results
The
C. cayetanensis
antigenic profile showed eight characteristic bands with molecular weights ranging from 14 to 175 kDa. Western blot analysis of sera revealed 93.3% (28/30 of GI) and 92.8% (26/28 of GII and III) sensitivity and specificity, respectively, dividing the patients in GI into four subgroups. The most frequent diagnostic bands (71.4% of GI sera) showed weights of 26–28 kDa, followed by 71 kDa (53.6%). ELISA sensitivity was 90% (27/30), and specificity was 78.6%. Validation showed perfect agreement between the PCR and western blot results, and ELISA presented substantial agreement with both the PCR and western blot results.
Conclusions
Our findings suggest the existence of high immunogenic diversity in
C. cayetanensis
and indicate that the 26–28 kDa immunogenic groups may potentially be used as a diagnostic marker of cyclosporiasis. Due to the high validity of ELISA, it might be the test of choice for the routine serodiagnosis of cyclosporiasis.</description><subject>Animal Systematics/Taxonomy/Biogeography</subject><subject>Antigens</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cyclospora cayetanensis</subject><subject>Cyclosporiasis</subject><subject>Diagnostic systems</subject><subject>Ecology</subject><subject>Enzyme-linked immunosorbent assay</subject><subject>Epidemiology</subject><subject>Gel electrophoresis</subject><subject>Immunoassays</subject><subject>Immunogenicity</subject><subject>Immunology</subject><subject>Medical Microbiology</subject><subject>Microbiology</subject><subject>Oocysts</subject><subject>Original Paper</subject><subject>Parasitic diseases</subject><subject>Parasitology</subject><subject>Protozoa</subject><subject>Sensitivity</subject><subject>Sodium lauryl sulfate</subject><subject>Subgroups</subject><subject>Validity</subject><subject>Western blotting</subject><issn>1230-2821</issn><issn>1896-1851</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp9kctOIzEQRVuIkYAMP8DKEhs2PfjRD3uJwmMiITELZraWU7HBqGMH21HUv8EXU5nwkFiwsqt8z3XZt6pOGP3FKO3PM2Od7GrKaU0pl6re7FWHTKquZrJl-7jngtZccnZQHeX8RGnTSSkPq5fZwobinQdTfAwkOmLIdIQh5lVMhoAZbTHBhuwzuYsw5kIuEHjADjFhQe4frU_knxn8wpeR-EDKoyWXtlh4N5wtl-sQkfBA_phSbEIW-x_XeLN1xyOPs-Sf1Q9nhmyP39ZJ9ff66n76u769u5lNL25r4Exu6hakkBRM36g559a1TdeKuRDMOe6oBNW1revBQuN6RwWWAE4qNt-WvQExqc52vqsUn9c2F730Geww4HPjOmveNEp1TCmG0tMv0qe4TgGn07wVraD4_QJVfKeCFHNO1ulV8kuTRs2o3sakdzFpjEn_j0lvEBI7KKM4PNj0af0N9QpeT5jS</recordid><startdate>20210601</startdate><enddate>20210601</enddate><creator>Hussein, Eman M.</creator><creator>El-Gayar, Eman K.</creator><creator>Ismail, Ola A.</creator><creator>Mokhtar, Amira B.</creator><creator>Al-Abbassy, Maha M.</creator><general>Springer International Publishing</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7QG</scope><scope>7QL</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7T7</scope><scope>7TM</scope><scope>7U7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-3362-2925</orcidid></search><sort><creationdate>20210601</creationdate><title>Identification of a Cyclospora cayetanensis Oocyst Antigens and Their Validity in the Detection of Immunogenic Patterns of Cyclosporiasis Patients</title><author>Hussein, Eman M. ; El-Gayar, Eman K. ; Ismail, Ola A. ; Mokhtar, Amira B. ; Al-Abbassy, Maha M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c218w-5c8380ca749b22ef54653b331ff2f08c9655f7cec4f7f03965ccf891bf7f07ac3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Animal Systematics/Taxonomy/Biogeography</topic><topic>Antigens</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Cyclospora cayetanensis</topic><topic>Cyclosporiasis</topic><topic>Diagnostic systems</topic><topic>Ecology</topic><topic>Enzyme-linked immunosorbent assay</topic><topic>Epidemiology</topic><topic>Gel electrophoresis</topic><topic>Immunoassays</topic><topic>Immunogenicity</topic><topic>Immunology</topic><topic>Medical Microbiology</topic><topic>Microbiology</topic><topic>Oocysts</topic><topic>Original Paper</topic><topic>Parasitic diseases</topic><topic>Parasitology</topic><topic>Protozoa</topic><topic>Sensitivity</topic><topic>Sodium lauryl sulfate</topic><topic>Subgroups</topic><topic>Validity</topic><topic>Western blotting</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hussein, Eman M.</creatorcontrib><creatorcontrib>El-Gayar, Eman K.</creatorcontrib><creatorcontrib>Ismail, Ola A.</creatorcontrib><creatorcontrib>Mokhtar, Amira B.</creatorcontrib><creatorcontrib>Al-Abbassy, Maha M.</creatorcontrib><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Nucleic Acids Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Acta parasitologica</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hussein, Eman M.</au><au>El-Gayar, Eman K.</au><au>Ismail, Ola A.</au><au>Mokhtar, Amira B.</au><au>Al-Abbassy, Maha M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Identification of a Cyclospora cayetanensis Oocyst Antigens and Their Validity in the Detection of Immunogenic Patterns of Cyclosporiasis Patients</atitle><jtitle>Acta parasitologica</jtitle><stitle>Acta Parasit</stitle><date>2021-06-01</date><risdate>2021</risdate><volume>66</volume><issue>2</issue><spage>416</spage><epage>427</epage><pages>416-427</pages><issn>1230-2821</issn><eissn>1896-1851</eissn><abstract>Introduction
The diagnosis of cyclosporiasis is currently based on the microscopic detection of oocysts, which may provide invalid results. The availability of simple, objective immunological screening tests would facilitate epidemiological studies of cyclosporiasis. Therefore, the present study aimed to identify the antigens of
Cyclospora cayetanensis
oocysts and their validity in serodiagnosis.
Methods
According to parasitological and molecular diagnoses, three study groups were specified. Group (G) I included 30 patients with cyclosporiasis, GII included 12 patients with other parasitic infections, and GIII included 16 healthy subjects. SDS-PAGE was used to analyse
C. cayetanensis
antigens, and the validity of western blotting and enzyme-linked immunosorbent assays (ELISAs) was then assessed amongst the sera of all study groups.
Results
The
C. cayetanensis
antigenic profile showed eight characteristic bands with molecular weights ranging from 14 to 175 kDa. Western blot analysis of sera revealed 93.3% (28/30 of GI) and 92.8% (26/28 of GII and III) sensitivity and specificity, respectively, dividing the patients in GI into four subgroups. The most frequent diagnostic bands (71.4% of GI sera) showed weights of 26–28 kDa, followed by 71 kDa (53.6%). ELISA sensitivity was 90% (27/30), and specificity was 78.6%. Validation showed perfect agreement between the PCR and western blot results, and ELISA presented substantial agreement with both the PCR and western blot results.
Conclusions
Our findings suggest the existence of high immunogenic diversity in
C. cayetanensis
and indicate that the 26–28 kDa immunogenic groups may potentially be used as a diagnostic marker of cyclosporiasis. Due to the high validity of ELISA, it might be the test of choice for the routine serodiagnosis of cyclosporiasis.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><doi>10.1007/s11686-020-00289-w</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0003-3362-2925</orcidid></addata></record> |
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subjects | Animal Systematics/Taxonomy/Biogeography Antigens Biomedical and Life Sciences Biomedicine Cyclospora cayetanensis Cyclosporiasis Diagnostic systems Ecology Enzyme-linked immunosorbent assay Epidemiology Gel electrophoresis Immunoassays Immunogenicity Immunology Medical Microbiology Microbiology Oocysts Original Paper Parasitic diseases Parasitology Protozoa Sensitivity Sodium lauryl sulfate Subgroups Validity Western blotting |
title | Identification of a Cyclospora cayetanensis Oocyst Antigens and Their Validity in the Detection of Immunogenic Patterns of Cyclosporiasis Patients |
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