{"title":"基于酶联免疫吸附试验的重组副猪隐孢子虫 GP15 检测牛群中隐孢子虫暴露情况","authors":"Ajayta Rialch , Opinder Krishen Raina , Partha Sarathi Banerjee , Gorakh Mal , Birbal Singh , Rinku Sharma , Gauri Jairath , Devi Gopinath , Rajendra Damu Patil , Savita Chaudhary , Rajesh Chahota , M. Sankar , Rajat Garg","doi":"10.1016/j.vetpar.2025.110467","DOIUrl":null,"url":null,"abstract":"<div><div>The serodiagnostic potential of recombinant <em>Cryptosporidium parvum</em> glycoprotein 15 (rCpGP15) was evaluated in Enzyme Linked Immunosorbent Assay (ELISA) in the detection of exposure of bovines to <em>Cryptosporidium</em> species in Himachal Pradesh and Uttarakhand states of North India. The 11.13 kDa rCpGP15 was expressed in pET-32a (+) transformed <em>E. coli</em> BL21 cells and was purified by Ni-NTA affinity chromatography as polyhistidine tagged fusion protein of ∼ 32 kDa. Its immunogenicity was checked in western blot using rabbit antisera raised to the recombinant antigen and bovine sera naturally infected with <em>Cryptosporidium</em>. Two hundred and forty-six bovines were screened for <em>Cryptosporidium</em> spp. oocysts in faecal samples by modified-Ziehl Neelson technique and their sera were used for ELISA standardization. The rCpGP15 based indirect IgG-ELISA was standardized with 83 % sensitivity, 78.3 % specificity where ELISA cut-off and accuracy were decided using ROC curve analysis. The percent accuracy was 79.19 %, with area under the Receiver Operating Characteristic (ROC) curve value 0.827 depicting the moderate accuracy of the assay. Additionally, sera from <em>Eimeria</em> (n = 3), strongyles (n = 3), <em>Babesia</em> (n = 2), <em>Theileria</em> (n = 5), <em>Trypanosoma</em> (n = 2) and <em>Anaplasma</em> (n = 5) positive animals showed no seroreactivity. The diagnostic performance of rCpGP15 protein in differentiating <em>Cryptosporidium</em> species was predicted through <em>in-silico</em> B cell epitope prediction, homology modelling and structural comparison of GP15 protein from <em>C. parvum, C. hominis, C. bovis</em> and <em>C. ryanae.</em> Four linear antigenic epitopes were predicted in CpGP15 protein sequence by SVMTrip. The overall root mean square deviation (RMSD) values during homology modelling and structural comparison of CpGP15 and <em>C. hominis, C. bovis</em> and partial <em>C. ryanae</em> GP15 were 2.093 Å, 3.759 Å and 1.152 Å, respectively. The serodiagnostic assay developed in the present study has moderate accuracy and can be applied in serosurveillance of large bovine populations. It is capable of detecting asymptomatic animals with intermittent oocyst shedding which will further be helpful for better understanding the disease dynamics and for the timely control of cryptosporidiosis.</div></div>","PeriodicalId":23716,"journal":{"name":"Veterinary parasitology","volume":"336 ","pages":"Article 110467"},"PeriodicalIF":2.0000,"publicationDate":"2025-04-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Recombinant Cryptosporidium parvum GP15 based enzyme linked immunosorbent assay for detection of exposure of bovine populations to Cryptosporidium\",\"authors\":\"Ajayta Rialch , Opinder Krishen Raina , Partha Sarathi Banerjee , Gorakh Mal , Birbal Singh , Rinku Sharma , Gauri Jairath , Devi Gopinath , Rajendra Damu Patil , Savita Chaudhary , Rajesh Chahota , M. Sankar , Rajat Garg\",\"doi\":\"10.1016/j.vetpar.2025.110467\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The serodiagnostic potential of recombinant <em>Cryptosporidium parvum</em> glycoprotein 15 (rCpGP15) was evaluated in Enzyme Linked Immunosorbent Assay (ELISA) in the detection of exposure of bovines to <em>Cryptosporidium</em> species in Himachal Pradesh and Uttarakhand states of North India. The 11.13 kDa rCpGP15 was expressed in pET-32a (+) transformed <em>E. coli</em> BL21 cells and was purified by Ni-NTA affinity chromatography as polyhistidine tagged fusion protein of ∼ 32 kDa. Its immunogenicity was checked in western blot using rabbit antisera raised to the recombinant antigen and bovine sera naturally infected with <em>Cryptosporidium</em>. Two hundred and forty-six bovines were screened for <em>Cryptosporidium</em> spp. oocysts in faecal samples by modified-Ziehl Neelson technique and their sera were used for ELISA standardization. The rCpGP15 based indirect IgG-ELISA was standardized with 83 % sensitivity, 78.3 % specificity where ELISA cut-off and accuracy were decided using ROC curve analysis. The percent accuracy was 79.19 %, with area under the Receiver Operating Characteristic (ROC) curve value 0.827 depicting the moderate accuracy of the assay. Additionally, sera from <em>Eimeria</em> (n = 3), strongyles (n = 3), <em>Babesia</em> (n = 2), <em>Theileria</em> (n = 5), <em>Trypanosoma</em> (n = 2) and <em>Anaplasma</em> (n = 5) positive animals showed no seroreactivity. The diagnostic performance of rCpGP15 protein in differentiating <em>Cryptosporidium</em> species was predicted through <em>in-silico</em> B cell epitope prediction, homology modelling and structural comparison of GP15 protein from <em>C. parvum, C. hominis, C. bovis</em> and <em>C. ryanae.</em> Four linear antigenic epitopes were predicted in CpGP15 protein sequence by SVMTrip. The overall root mean square deviation (RMSD) values during homology modelling and structural comparison of CpGP15 and <em>C. hominis, C. bovis</em> and partial <em>C. ryanae</em> GP15 were 2.093 Å, 3.759 Å and 1.152 Å, respectively. The serodiagnostic assay developed in the present study has moderate accuracy and can be applied in serosurveillance of large bovine populations. It is capable of detecting asymptomatic animals with intermittent oocyst shedding which will further be helpful for better understanding the disease dynamics and for the timely control of cryptosporidiosis.</div></div>\",\"PeriodicalId\":23716,\"journal\":{\"name\":\"Veterinary parasitology\",\"volume\":\"336 \",\"pages\":\"Article 110467\"},\"PeriodicalIF\":2.0000,\"publicationDate\":\"2025-04-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Veterinary parasitology\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0304401725000780\",\"RegionNum\":2,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"PARASITOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Veterinary parasitology","FirstCategoryId":"97","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0304401725000780","RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PARASITOLOGY","Score":null,"Total":0}
Recombinant Cryptosporidium parvum GP15 based enzyme linked immunosorbent assay for detection of exposure of bovine populations to Cryptosporidium
The serodiagnostic potential of recombinant Cryptosporidium parvum glycoprotein 15 (rCpGP15) was evaluated in Enzyme Linked Immunosorbent Assay (ELISA) in the detection of exposure of bovines to Cryptosporidium species in Himachal Pradesh and Uttarakhand states of North India. The 11.13 kDa rCpGP15 was expressed in pET-32a (+) transformed E. coli BL21 cells and was purified by Ni-NTA affinity chromatography as polyhistidine tagged fusion protein of ∼ 32 kDa. Its immunogenicity was checked in western blot using rabbit antisera raised to the recombinant antigen and bovine sera naturally infected with Cryptosporidium. Two hundred and forty-six bovines were screened for Cryptosporidium spp. oocysts in faecal samples by modified-Ziehl Neelson technique and their sera were used for ELISA standardization. The rCpGP15 based indirect IgG-ELISA was standardized with 83 % sensitivity, 78.3 % specificity where ELISA cut-off and accuracy were decided using ROC curve analysis. The percent accuracy was 79.19 %, with area under the Receiver Operating Characteristic (ROC) curve value 0.827 depicting the moderate accuracy of the assay. Additionally, sera from Eimeria (n = 3), strongyles (n = 3), Babesia (n = 2), Theileria (n = 5), Trypanosoma (n = 2) and Anaplasma (n = 5) positive animals showed no seroreactivity. The diagnostic performance of rCpGP15 protein in differentiating Cryptosporidium species was predicted through in-silico B cell epitope prediction, homology modelling and structural comparison of GP15 protein from C. parvum, C. hominis, C. bovis and C. ryanae. Four linear antigenic epitopes were predicted in CpGP15 protein sequence by SVMTrip. The overall root mean square deviation (RMSD) values during homology modelling and structural comparison of CpGP15 and C. hominis, C. bovis and partial C. ryanae GP15 were 2.093 Å, 3.759 Å and 1.152 Å, respectively. The serodiagnostic assay developed in the present study has moderate accuracy and can be applied in serosurveillance of large bovine populations. It is capable of detecting asymptomatic animals with intermittent oocyst shedding which will further be helpful for better understanding the disease dynamics and for the timely control of cryptosporidiosis.
期刊介绍:
The journal Veterinary Parasitology has an open access mirror journal,Veterinary Parasitology: X, sharing the same aims and scope, editorial team, submission system and rigorous peer review.
This journal is concerned with those aspects of helminthology, protozoology and entomology which are of interest to animal health investigators, veterinary practitioners and others with a special interest in parasitology. Papers of the highest quality dealing with all aspects of disease prevention, pathology, treatment, epidemiology, and control of parasites in all domesticated animals, fall within the scope of the journal. Papers of geographically limited (local) interest which are not of interest to an international audience will not be accepted. Authors who submit papers based on local data will need to indicate why their paper is relevant to a broader readership.
Parasitological studies on laboratory animals fall within the scope of the journal only if they provide a reasonably close model of a disease of domestic animals. Additionally the journal will consider papers relating to wildlife species where they may act as disease reservoirs to domestic animals, or as a zoonotic reservoir. Case studies considered to be unique or of specific interest to the journal, will also be considered on occasions at the Editors'' discretion. Papers dealing exclusively with the taxonomy of parasites do not fall within the scope of the journal.