2015
DOI: 10.1016/j.rvsc.2015.04.011
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Evaluation of an indirect ELISA using recombinant granule antigen GRA1, GRA7 and soluble antigens for serodiagnosis of Toxoplasma gondii infection in chickens

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Cited by 25 publications
(25 citation statements)
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“…Although there was no solid and direct comparison between these different types of ELISA tests, from literature it seems like SAG and GRA7 based indirect ELISAs are the most reliable. The sensitivity and specificity were claimed to be nearly 100% and above 96%, respectively (Lu et al, 2006 ; Sun et al, 2015 ).…”
Section: Development Of Diagnostic Approachesmentioning
confidence: 99%
“…Although there was no solid and direct comparison between these different types of ELISA tests, from literature it seems like SAG and GRA7 based indirect ELISAs are the most reliable. The sensitivity and specificity were claimed to be nearly 100% and above 96%, respectively (Lu et al, 2006 ; Sun et al, 2015 ).…”
Section: Development Of Diagnostic Approachesmentioning
confidence: 99%
“…Recently, the recombinant antigens of secretory microneme proteins (MIC3), rhoptry proteins (ROPs), rhoptry neck proteins (RONs), and dense granule antigens (GRA) were developed as an alternative method for Toxoplasma sero-diagnosis for both humans and animals, and demonstrated to be more sensitive and specifi c at detecting T. gondii antibodies in multiple animal species compared to MAT and IFAT [33][34][35][36][37][38]. Specifi cally, Sun and colleagues reported >90% agreement between recombinant GRA1, GRA7 and Toxoplasma soluble antigens (TSA) for T. gondii antibody detection in chickens, with GRA7 showed higher sensitivity and specifi city than GRA1 and TSA [40]. To establish good epidemiological data of toxoplasmosis, additional other serological tests such as ELISA or recombinant antigen based diagnostic technique, bioassays and polymerase PCR based assays was recommended.…”
Section: Discussionmentioning
confidence: 99%
“…We also modified the incubation temperature to 37°C, according to Sun et al . ( 2015 ). Plates were incubated for 1 h with serum samples and then for 45 min with the secondary antibody.…”
Section: Methodsmentioning
confidence: 99%