VOLUME 19 NUMBER 1 (January to June 2026)

PSL%202021 vol14-no01-p12-28-Mikita%20and%20Padlan

SciEnggJ. 2026 19 (1) 134-139
available online: 30 March 2026
DOI: https://doi.org/10.54645/2026191XVN-65

*Corresponding author
Email Address: ibtabios2@up.edu.ph
Date received: 20 December 2025
Dates revised: 05 February 2026
Date accepted: 21 February 2026

ARTICLE

Opportunistic fecal sampling and PCR testing for canine schistosomiasis japonica surveillance in endemic settings

Hans Webster P. Labordo1, Amina C. Kunting1,2, Daria L. Manalo3, Raffy Jay C. Fornillos1,4, Juvren Romvic A. Batalon5, Efraim P. Panganiban3, Mark Joseph M. Espino3, Ian Kendrich C. Fontanilla1, Lydia R. Leonardo6, and Ian Kim B. Tabios*1,4

1Institute of Biology, College of Science, University of the Philippines Diliman, Quezon City, 1101 Philippines

2Department of Biology, School of Science and Engineering, Ateneo de Manila University, Quezon City, 1108 Philippines

3Research Institute for Tropical Medicine, Muntinlupa, 9002 Philippines

4University of the Philippines Los Baños Zoonoses Center, Laguna, 4031 Philippines

5College of Medical and Biological Sciences, University of the Immaculate Conception, Davao City, 8000 Philippines

6Office of Research Coordination, University of the East, Manila City, 1008 Philippines

KEYWORDS: Schistosoma japonicum, non-invasive sampling, fecal DNA, canine schistosomiasis, molecular diagnosis, neglected tropical disease

Among the challenges in animal surveillance for Schistosoma japonicum are the difficulty of collecting samples from free-roaming dogs and the low sensitivity of traditional diagnostics. This study evaluated opportunistic environmental fecal sampling combined with PCR as a surveillance tool for canine schistosomiasis japonica in selected endemic barangays of the northern Philippines. Dog stool samples (n = 72) were opportunistically collected in Gonzaga, Cagayan (6:00–8:00 AM) and analyzed using microscopy and PCR. All samples were examined for ova using the formalin–ether concentration technique (FECT). In parallel, DNA was extracted and screened using an internal control PCR; eligible extracts were then tested using an endpoint PCR assay targeting the S. japonicum SjR2 retrotransposon. While FECT detected no S. japonicum ova, PCR detected parasite DNA in 19.12% (13/68) of eligible samples. These findings provide proof of concept for non-invasive molecular surveillance using environmental dog fecal samples and suggest that this approach may help identify areas with canine shedding in endemic settings alongside existing One Health surveillance and control efforts.

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