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Nucleic acid amplification techniques for the detection of Schistosoma mansoni infection in humans and the intermediate snail host: a structured review and meta-analysis of diagnostic accuracy

Journal

INTERNATIONAL JOURNAL OF INFECTIOUS DISEASES
Volume 112, Issue -, Pages 152-164

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.ijid.2021.08.061

Keywords

Schistosomiasis; Schistosoma mansoni; Human diagnosis; Snail diagnosis; Nucleic acid amplification technique; PCR-ELISA; qPCR; LAMP; PCR; nPCR

Funding

  1. Chinese National Center Programme of Tropical Diseases Research [131031104000160004]

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This review assessed the nucleic acid amplification techniques for diagnosing S. mansoni infections in humans, intermediate host snails, and rodent reservoirs. The results showed high sensitivity and specificity in human samples, with different performance in snail and rodent samples. Overall, nucleic acid amplification techniques had high diagnostic potential for identifying S. mansoni infections in humans.
Background: Schistosomiasis is a parasitic disease caused by hematodes of genus Schistosoma. This review evaluated the available nucleic acid amplification techniques for diagnosing S. mansoni infections in humans, intermediate host snails, and presumed rodent reservoirs. Methods: Sensitivity, specificity, diagnostic odds ratio (DOR), and 95% CI were calculated based on available literature. The potential of PCR, nPCR, PCR-ELISA, qPCR, and LAMP was compared for diagnosing S. mansoni infections. Results: A total of 546 published records were identified. Quality assessment by QUADAS-2 revealed an uncertain risk in most studies, and 21 references were included in the final. For human samples, the four nucleic acid amplification techniques showed an overall sensitivity of 89.79% (95% CI: 83.92%-93.67%), specificity of 87.70% (95% CI: 72.60%-95.05%), and DOR of 37.73 (95% CI: 21.79-65.33). LAMP showed the highest sensitivity, followed by PCR-ELISA, PCR, and qPCR, while this order was almost reversed for specificity; qPCR had the highest AUC. For rodent samples, qPCR showed modest sensitivity (68.75%, 95% CI: 43.32%-86.36%) and high specificity (92.45%, 95% CI: 19.94%-99.83%). For snail samples, PCR and nPCR assays showed high sensitivity of 90.06% (95% CI: 84.39%-93.82%) and specificity of 85.51% (95% CI: 54.39%96.69%). Conclusion: Nucleic acid amplification techniques had high diagnostic potential for identifying S. mansoni infections in humans. (c) 2021 The Authors. Published by Elsevier Ltd on behalf of International Society for Infectious Diseases. This is an open access article under the CC BY-NC-ND license ( http://creativecommons.org/licenses/by-nc-nd/4.0/ )

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