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序列捕获可直接从宿主组织中鉴定出挑剔的壶菌。

Sequence capture identifies fastidious chytrid fungi directly from host tissue.

机构信息

Wildlife Health Ghent, Faculty of Veterinary Medicine, Ghent University, Merelbeke, Belgium; Center for Conservation Genomics, Smithsonian National Zoo and Conservation Biology Institute, Washington, DC, USA.

Department of Biology, University of Central Florida, Orlando, FL, USA.

出版信息

Fungal Genet Biol. 2024 Feb;170:103858. doi: 10.1016/j.fgb.2023.103858. Epub 2023 Dec 13.

Abstract

The chytrid fungus Batrachochytrium dendrobatidis (Bd) was discovered in 1998 as the cause of chytridiomycosis, an emerging infectious disease causing mass declines in amphibian populations worldwide. The rapid population declines of the 1970s-1990s were likely caused by the spread of a highly virulent lineage belonging to the Bd-GPL clade that was introduced to naïve susceptible populations. Multiple genetically distinct and regional lineages of Bd have since been isolated and sequenced, greatly expanding the known biological diversity within this fungal pathogen. To date, most Bd research has been restricted to the limited number of samples that could be isolated using culturing techniques, potentially causing a selection bias for strains that can grow on media and missing other unculturable or fastidious strains that are also present on amphibians. We thus attempted to characterize potentially non-culturable genetic lineages of Bd from distinct amphibian taxa using sequence capture technology on DNA extracted from host tissue and swabs. We focused our efforts on host taxa from two different regions that likely harbored distinct Bd clades: (1) wild-caught leopard frogs (Rana) from North America, and (2) a Japanese Giant Salamander (Andrias japonicus) at the Smithsonian Institution's National Zoological Park that exhibited signs of disease and tested positive for Bd using qPCR, but multiple attempts failed to isolate and culture the strain for physiological and genetic characterization. We successfully enriched for and sequenced thousands of fungal genes from both host clades, and Bd load was positively associated with number of recovered Bd sequences. Phylogenetic reconstruction placed all the Rana-derived strains in the Bd-GPL clade. In contrast, the A. japonicus strain fell within the Bd-Asia3 clade, expanding the range of this clade and generating additional genomic data to confirm its placement. The retrieved ITS locus matched public barcoding data from wild A. japonicus and Bd infections found on other amphibians in India and China, suggesting that this uncultured clade is widespread across Asia. Our study underscores the importance of recognizing and characterizing the hidden diversity of fastidious strains in order to reconstruct the spatiotemporal and evolutionary history of Bd. The success of the sequence capture approach highlights the utility of directly sequencing pathogen DNA from host tissue to characterize cryptic diversity that is missed by culture-reliant approaches.

摘要

蛙壶菌(Batrachochytrium dendrobatidis,Bd)于 1998 年被发现,是一种新兴的传染性疾病,导致全球范围内的两栖动物种群大量减少。20 世纪 70 年代至 90 年代的快速种群减少可能是由一种高度致命的谱系传播引起的,该谱系属于 Bd-GPL 进化枝,被引入到易感的原始种群中。此后,已经分离并测序了多种遗传上不同且具有地区差异的 Bd 谱系,极大地扩展了这种真菌病原体的已知生物学多样性。迄今为止,大多数 Bd 研究仅限于使用培养技术可以分离的有限数量的样本,这可能导致对可以在培养基上生长的菌株产生选择偏差,而错过其他也存在于两栖动物上的不可培养或挑剔的菌株。因此,我们试图使用从宿主组织和拭子中提取的 DNA ,使用序列捕获技术来描述来自不同两栖动物类群的潜在不可培养的 Bd 遗传谱系。我们将重点放在两个不同地区的宿主类群上,这两个地区可能存在不同的 Bd 进化枝:(1)来自北美的野生豹蛙(Rana),(2)史密森学会国家动物园的一只日本大鲵(Andrias japonicus),它表现出疾病迹象,并通过 qPCR 检测到 Bd 呈阳性,但多次尝试均未能分离和培养该菌株进行生理和遗传特征分析。我们成功地从两个宿主进化枝中富集和测序了数千个真菌基因,Bd 载量与回收的 Bd 序列数量呈正相关。系统发育重建将所有源自 Rana 的菌株置于 Bd-GPL 进化枝中。相比之下,A. japonicus 菌株属于 Bd-Asia3 进化枝,扩大了该进化枝的范围,并生成了额外的基因组数据来确认其位置。回收的 ITS 基因座与来自印度和中国的野生 A. japonicus 和 Bd 感染的公共条形码数据匹配,表明该未培养的进化枝在亚洲广泛分布。我们的研究强调了认识和描述挑剔菌株的隐藏多样性的重要性,以便重建 Bd 的时空和进化历史。序列捕获方法的成功突出了直接从宿主组织中直接测序病原体 DNA 以描述培养依赖方法错过的隐匿多样性的实用性。

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