Comparison of ELISA, nested PCR and sequencing and a novel qPCR for detection of Giardia isolates from Jordan

• Published in: Experimental parasitology Vol. 185; pp. 23 - 28
• Main Authors: Hijjawi, Nawal, Yang, Rongchang, Hatmal, Ma'mon, Yassin, Yasmeen, Mharib, Taghrid, Mukbel, Rami, Mahmoud, Sameer Alhaj, Al-Shudifat, Abdel-Ellah, Ryan, Una
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.02.2018
• Subjects: ELISA; Giardia; Glutamate dehydrogenase (gdh); Humans; Jordan; PCR; β-giardin; Humans; Glutamate dehydrogenase (gdh); β-giardin; Giardia; Jordan; PCR; ELISA
• ISSN: 0014-4894; 1090-2449
• DOI: 10.1016/j.exppara.2018.01.011

Little is known about the prevalence of Giardia duodenalis in human patients in Jordan and all previous studies have used direct microscopy, which lacks sensitivity. The present study developed a novel quantitative PCR (qPCR) assay at the β-giardin (bg) locus and evaluated its use as a frontline test for the diagnosis of giardiasis in comparison with a commercially available ELISA using nested PCR and sequencing of the glutamate dehydrogenase (gdh) locus (gdh nPCR) as the gold standard. A total of 96 human faecal samples were collected from 96 patients suffering from diarrhoea from 5 regions of Jordan and were screened using the ELISA and qPCR. The analytical specificity of the bg qPCR assay revealed no cross-reactions with other genera and detected all the Giardia isolates tested. Analytical sensitivity was 1 Giardia cyst per μl of DNA extract. The overall prevalence of Giardia was 64.6%. The clinical sensitivity and specificity of the bg qPCR was 89.9% and 82.9% respectively compared to 76.5 and 68.0% for the ELISA. This study is the first to compare three different methods (ELISA, bg qPCR, nested PCR and sequencing at the gdh locus) to diagnose Jordanian patients suffering from giardiasis and to analyze their demographic data. [Display omitted] •Development of novel qPCR for Giardia at β-giardin (bg) locus.•Validation against nested PCR and sequencing of glutamate dehydrogenase locus.•High clinical sensitivity (89.9%) and specificity (82.9%) of the bg qPCR.