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Monitoring biodiversity constitutes a fundamental element in assessing the ecological status of sensitive and vulnerable habitats such as inland freshwater bodies. Although conventional capture-based methodologies in fish monitoring are still widely used, the development of alternative strategies is being vigorously pursued. The use of environmental DNA (eDNA) to detect species' presence is now a standard practice in aquatic ecology and is generating considerable attention within the scientific community. Here, we present the first eDNA metabarcoding study of the Israeli freshwater ecosystems, aiming to detect and compare fish assemblages of previously surveyed sites. Four riverine systems with different characteristics and known fish fauna were sampled, in parallel to the preparation of a complete 12S rRNA barcode reference library for the Israeli freshwater ichthyofauna. In total, 25 fish species belonging to 15 families were detected from 63 water samples using 12S eDNA metabarcoding. Comparisons with previous capture-based data have shown that eDNA surveys provided better species coverage, including the first documentation of two non-indigenous species and regardless of water characteristics or volume of filtered water. Lastly, we explain and discuss discrepancies in false-negative and false-positive results between the two methods.
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http://dx.doi.org/10.1007/s10661-025-14504-6 | DOI Listing |
Environ Monit Assess
August 2025
National Institute of Oceanography, Israel Oceanographic and Limnological Research, Tel Shikmona, P.O. Box 9753, Haifa, 3109701, Israel.
Monitoring biodiversity constitutes a fundamental element in assessing the ecological status of sensitive and vulnerable habitats such as inland freshwater bodies. Although conventional capture-based methodologies in fish monitoring are still widely used, the development of alternative strategies is being vigorously pursued. The use of environmental DNA (eDNA) to detect species' presence is now a standard practice in aquatic ecology and is generating considerable attention within the scientific community.
View Article and Find Full Text PDFMol Ecol
September 2025
Graduate School of Science, Kyoto University, Kyoto, Japan.
Comparative phylogeography provides crucial insights into evolutionary processes shaping biodiversity patterns by analysing spatial genetic variations across multiple species. However, conventional capture-based methods are often labour-intensive, particularly for multi-species analyses. Environmental DNA (eDNA) analysis has significant advantages in comparative phylogeography, including simplified field surveys requiring only water collection and the potential to simultaneously analyse multiple species from a single sample.
View Article and Find Full Text PDFRespir Med Case Rep
June 2025
Department of Respiratory Medicine, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan.
For patients with advanced non-small cell lung cancer (NSCLC), genetic testing is crucial to identify alterations in targetable driver genes. ROS1-tyrosine kinase inhibitors have shown efficacy against NSCLC with common fusion genes, but the impact of rare fusion partners on therapeutic outcomes is not well understood. Here, we describe a 75-year-old female with advanced lung adenocarcinoma who was treated with crizotinib after the identification of the extremely rare fusion.
View Article and Find Full Text PDFFront Immunol
July 2025
Nephrology Department, The Affiliated Xuzhou Municipal Hospital of Xuzhou Medical University, Xuzhou, China.
Introduction: Accurate human leukocyte antigen (HLA) genotyping is critical for organ transplantation to ensure donor-recipient compatibility. Conventional methods, such as sequence-based typing (SBT), often face challenges in resolving allelic ambiguities, particularly in highly polymorphic regions of HLA loci. Therefore, this study aimed to develop 6 locus multiplex primers combined with Next-generation sequencing NGS for high-resolution of long sequenceshigh-resolution sequencing, focusing on improving sequencing depth and reducing costs.
View Article and Find Full Text PDFOrphanet J Rare Dis
July 2025
Department of Gastroenterology, Children's Hospital of Fudan University, 399 Wanyuan Road, Shanghai, 201102, China.
Background: In East Asia, IL10RA is the predominant pathogenic gene in patients with very early-onset inflammatory bowel disease (VEO-IBD), frequently characterised by refractory diarrhoea and severe perianal disease, resulting in elevated death rates. IL10RA-deficient IBD, an autosomal recessive genetic disorder, has been documented to be inherited through the conventional compound heterozygous or homozygous mutation patterns from both parents. We present two cases with apparent homozygosity resulting from distinct causes, both of which seem homozygous on the genetic map.
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