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Comparison of an in house and a commercial real-time polymerase chain reaction targeting Toxoplasma gondii RE gene using various samples collected from patients in Turkey

Authors :
Mert Döşkaya
Hüsnü Pullukçu
Muhammet Karakavuk
Esra Atalay Şahar
Mehmet Sezai Taşbakan
Meltem Işıkgöz Taşbakan
Mümtaz Yılmaz
Hüseyin Can
Aysu Değirmenci Döşkaya
Adnan Yüksel Gürüz
Source :
BMC Infectious Diseases, Vol 19, Iss 1, Pp 1-6 (2019)
Publication Year :
2019
Publisher :
BMC, 2019.

Abstract

Abstract Background Toxoplasma gondii is an opportunistic protozoan parasite that can infect all warm-blooded animals including humans and cause serious clinical manifestations. Toxoplasmosis can be diagnosed using histological, serological, and molecular methods. In this study, we aimed to detect T. gondii RE gene in various human samples by in house and commercial real time polymerase chain reactions. Methods A total of 38 suspected cases of toxoplasmosis [peripheral blood (n:12), amnion fluid (n:11), tissue (n:9), cerebrospinal fluid (n:5), and intraocular fluid (n:1)] were included to the study. An in house and a commercial RT-PCR were applied to investigate the T. gondii RE gene in these samples. Results The compatibility rate of the two tests was 94.7% (37/38). When the commercial RT-PCR kit was taken as reference, the sensitivity and specificity of in house RT-PCR test was 87.5 and 100%. When the in house RT-PCR test was taken as reference, the commercial RT-PCR kit has 100% sensitivity and 96.8% specificity. Incompatibility was detected in only in a buffy coat sample with high protein content. Conclusions Both the commercial and in house RT-PCR tests can be used to investigate T. gondii RE gene in various clinical specimens with their high sensitivity and specificity. In house RT-PCR assay can be favorable due to cost savings compared to using the commercial test.

Details

Language :
English
ISSN :
14712334
Volume :
19
Issue :
1
Database :
Directory of Open Access Journals
Journal :
BMC Infectious Diseases
Publication Type :
Academic Journal
Accession number :
edsdoj.4abf0d56bcd47d68de49b621f9a95ce
Document Type :
article
Full Text :
https://doi.org/10.1186/s12879-019-4666-z