Environmental DNA metabarcoding of freshwater fish in Malaysian tropical rivers using short-read nanopore sequencing as a potential biomonitoring tool

• Main Authors: Munian, Kaviarasu, Ramli, Farah Farhana, Othman, Nursyuhada, Mahyudin, Nur Aina Amira, Sariyati, Nur Hartini, Abdullah-Fauzi, Nurfatiha Akmal Fawwazah, Haris, Hidayah, Ilham-Norhakim, Mohd Lokman, Abdul-Latiff, Muhammad Abu Bakar
• Format: Article
• Language: English
• Published: Wiley 2024
• Subjects: QH Natural history
• Online Access: http://eprints.uthm.edu.my/11985/1/J17625_63b7a8f72b27f3662866a4fdd9b7ab24.pdf; http://eprints.uthm.edu.my/11985/; https://doi.org/10.1111/1755-0998.13936

The approach of combining cost-effective nanopore sequencing and emerging environmental DNA (eDNA) metabarcoding could prove to be a promising tool for biodiversity documentation, especially in Malaysia. Given the substantial funding constraints in recent years, especially in relation to the country's biodiversity, manyresearchers have been limited to conduct restricted research without extended monitoring periods, potentially hindering comprehensive surveys and could compromise the conservation efforts. Therefore, the present study aimed to evaluate the application of eDNA metabarcoding on freshwater fish using short reads generated through nanopore sequencing. This assessment focused on species detection in three selected rivers within the Endau Rompin Landscape in Malaysia. Additionally, the study compared levels of species detection between eDNA metabarcoding and conventional sampling methods, examined the effectiveness of primer choice, and applied both metabarcoding and shotgun sequencing to the eDNA approach. We successfully identified a total of 22 and 71 species with an identification threshold of >97% and >90%, respectively, through the MinION platform. The eDNA metabarcoding approach detected over 13% more freshwater fish species than when the conventional method was used. Notably, the distinction in freshwater fish detection between eDNA primers for 12S rRNA and cytochrome oxidase I was insignificant. The cost for eDNA metabarcoding proved to be more effective compared to conventional sampling with cost reduction at 33.4%. With favourable cost-effectiveness and increased species detection, eDNA metabarcoding could complement existing methods, enhance holistic diversity documentation for targeted habitats and facilitate effective conservation planning.