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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Veröffentlicht in:Acta parasitologica 2021-06, Vol.66 (2), p.416-427
Hauptverfasser: Hussein, Eman M., El-Gayar, Eman K., Ismail, Ola A., Mokhtar, Amira B., Al-Abbassy, Maha M.
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container_issue 2
container_start_page 416
container_title Acta parasitologica
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creator Hussein, Eman M.
El-Gayar, Eman K.
Ismail, Ola A.
Mokhtar, Amira B.
Al-Abbassy, Maha M.
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
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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. 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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 &amp; 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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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