Pathogens (Basel, Switzerland) · 2026
Reciprocal Genome Projection Reveals Reference-Conditioned Functional Variation in Clinical Aspergillus Section Nigri Isolates.
СтатьяНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Mbamali Siphiwengesihle Kuhle Silindile, Mohlomi Nikwando, Nest Magriet van der, Mchunu Nokuthula Peace, Permaul Kugenthiren
Аннотация
Closely related Aspergillus section Nigri species are difficult to resolve taxonomically, while short-read comparisons may be influenced by reference-genome choice. We applied reciprocal genome projection to 31 whole-genome sequencing libraries representing South African clinical section-Nigri isolates, Japanese and USA A. niger-labeled isolates, and A. welwitschiae-labeled isolates. Reads were aligned independently to A. niger ATCC 1015 and A. welwitschiae Aspwel1, followed by reference-specific differential-representation and KEGG analyses. Species-level classification showed substantial overlap between A. niger and A. welwitschiae. The A. welwitschiae-South African comparison identified 44 and 59 effect-qualified features under the respective projections, including 20 reciprocal feature pairs defining a reference-robust A. welwitschiae-associated core. The clinical Japanese-South African comparison identified 116 and 127 features, with 14 concordant KEGG orthologs involving sterol modification, protein prenylation, cofactor metabolism, redox processing, cell-wall turnover and ribosome maturation. No pathway remained significant after false discovery-rate correction; nominal pathway signals were reference-sensitive. Reciprocal projection, therefore, recovered localized cohort-associated genomic differentiation while identifying reference-conditioned effects. These findings represent differential genomic-read representation and do not independently establish copy-number variation, pathway activity, virulence or antifungal resistance.