Development of a novel molecular tool for the rapid assessment of changes in biodiversity of benthic nematodes assemblages
- Subject Areas
- Biodiversity, Ecology, Marine Biology, Molecular Biology
- assessment of biodiversity changes, benthic nematodes, dT-RFLP, new molecular tool
- © 2016 Avó et al.
- This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ PrePrints) and either DOI or URL of the article must be cited.
- Cite this article
- 2016. Development of a novel molecular tool for the rapid assessment of changes in biodiversity of benthic nematodes assemblages. PeerJ PrePrints 4:e1762v1 https://doi.org/10.7287/peerj.preprints.1762v1
Nowadays molecular approaches are being used in population estimation of terrestrial nematode communities offering a more efficient and faster alternative over microscopy-based methods. A molecular profiling tool was developed using directed Terminal-Restriction Fragment Length Polymorphism (dT-RFLP) to characterize soil nematode assemblages by relative abundance of feeding guilds, and validated by comparison with traditional morphological method. Combining morphological and molecular analysis of benthic nematodes assemblages, the main aim of this study was to develop and validate the dT-RFLP tool for benthic nematodes. Estimation of population size was derived using real time PCR (qPCR). A molecular phylogenetic analysis of benthic nematodes was created based on a database of 18S rDNA sequences related to individuals identified to species level. dT-RFLP results showed that the digest strategy developed for soil nematodes was not suitable for benthic nematodes. A new dT-RFLP strategy for benthic assemblages was designed by using the sequence database coupled with cloning and sequencing the whole assemblage from five samples. Several solutions were identified by the DRAT software and tested empirically to select the optimum solution that separates the assemblages. qPCR results showed differences in gene copy number between two sampling sites, which is consistently with the results of nematode density obtained by traditional methods. The application of these high-throughput molecular approaches for benthic nematodes will improve sample throughput and their implementation more efficient and faster as an indicator of marine ecosystem health.
This is an abstract which has been accepted for the "MARES" Conference