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Biology subjects

Anani, H.

Publications and source records attributed to Anani, H..

2 recordsLinked to original sources

Benchmarking and integration of viral prediction tools to uncover viral dark matter across divergent low abundance metagenomes

While existing benchmark studies have focused on viral detection tools using highly-abundant virus-enriched, their performance in low-abundance metagenomic environments remains unexplored. We aimed to benchmark eleven viral prediction tools and assess combinations of the best-performing-tools in low-abundance metagenomes. We generated an artificial dataset simulating the low-abundant metagenomic samples including human,bacterial and viral sequences, using complete-Refseq genomes. Viral sequences were fragmented into varying lengths and subjected to increased levels of in silico mutations to evaluate recall and F1 score of eleven tools tested individually. We further evaluated complementary tool combinations to improve sensitivity and specificity, and assessed the best-performing multi-tools formulations on low-abundance viromes from human lower respiratory tract and air metagenomic samples. DeepVirfinder(DVF) and DIAMOND achieved the highest recall (median of 67% and 58%, respectively) on the RefSeq artificial contigs dataset along increased levels of induced mutations. On the artificially mutated RefSeq dataset, the highest sensitivity and F1 scores were achieved by 4 two-tools combinations : DVF+DeepMicroclass,DVF+ViraLM,DVF+geNomad and DVF+DIAMOND, combined with Kraken2X-filtering to remove false-positive contigs classified as Eukaryota,Bacteria,or Archaea. Using Kraken2X-filtering, DVF+ViraLM and DVF+DeepMicroclass achieved the best sensitivity across real human airway and air datasets. These combinations expanded the previously identified viral repertoire using gold-standard methods, increasing the number of viral contigs with functionally annotated CDSs and revealing previously undetected viral diversity. Benchmarking of the eleven most used tools for viral prediction showed that the complementary combination approach, improves the detection of viral sequences while limiting false positives. This provides a robust strategy for uncovering divergent viral dark matter.

bioinformatics↗

Geographic microevolution of Mycobacterium ulcerans sustains Buruli ulcer extension, Australia

The reason why severe cases of Buruli ulcers caused by Mycobacterium ulcerans are emerging in some South Australia counties has not been determined. In this study, we measured the diversity of M. ulcerans complex whole genome sequences (WGS) and reported a marker of this diversity. Using this marker as a probe, we compared WGS diversity in Buruli ulcer-epidemic South Australia counties versus non-epidemic Australian counties and further refined comparisons at the level of counties where severe Buruli ulcer cases have been reported. Analyzing 218 WGS (35 complete and 183 reconstructed WGS, including 174 Australian WGS) yielded 15 M. ulcerans complex genotypes, including three genotypes specific to Australia and one genotype specific to South Australia. A 1,068-bp PPE family protein gene exhibiting genotype-specific sequence variations was employed to further probe 13 minority clones hidden in sequence reads. The repartition of these clones significantly differed between South Australia and the rest of Australia. In addition, a significantly higher prevalence of 3/13 clones was observed in South Australia counties of the Mornington Peninsula, Melbourne and Bellarine Peninsula than in other South Australia counties. The data presented in this report suggest that the microevolution of three M. ulcerans complex clones drove the emergence of severe Buruli ulcer cases in some South Australia counties. Sequencing one specific PPE gene served to efficiently probe M. ulcerans complex clones. Further functional studies may balance the environmental adaptation and virulence of these clones.

evolutionary biology↗