通过序列捕获直接从宿主组织中鉴定快活糜烂真菌

IF 2.4 3区 生物学 Q3 GENETICS & HEREDITY Fungal Genetics and Biology Pub Date : 2023-12-13 DOI:10.1016/j.fgb.2023.103858
Kevin P. Mulder , Anna E. Savage , Brian Gratwicke , Joyce E. Longcore , Ed Bronikowski , Matthew Evans , Ana V. Longo , Naoko P. Kurata , Tim Walsh , Frank Pasmans , Nancy McInerney , Suzan Murray , An Martel , Robert C. Fleischer
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引用次数: 0

摘要

糜烂真菌 Batrachochytrium dendrobatidis(Bd)于 1998 年被发现是糜烂真菌病的病原体,这种新出现的传染病导致全球两栖动物种群数量大量减少。20 世纪 70-90 年代种群数量的迅速减少很可能是由于属于 Bd-GPL 支系的高致病性品系传播到了幼稚的易感种群中。从那时起,人们分离并测序了多个不同基因的区域性 Bd 系,大大扩展了这种真菌病原体的已知生物多样性。迄今为止,大多数 Bd 研究仅限于利用培养技术分离出的数量有限的样本,这可能会造成对可在培养基上生长的菌株的选择偏差,而遗漏了两栖动物身上存在的其他不可培养或难以培养的菌株。因此,我们尝试利用序列捕获技术,对从宿主组织和拭子中提取的 DNA 进行分析,以确定不同两栖动物类群中潜在的不可培养的 Bd 遗传系的特征。我们将工作重点放在两个不同地区的宿主类群上,这些宿主类群可能蕴藏着不同的 Bd 支系:(1) 北美洲野生捕获的豹纹蛙(Rana);(2) 史密森学会国家动物园的日本大鲵(Andrias japonicus),该大鲵表现出疾病症状,使用 qPCR 对 Bd 检测呈阳性,但多次尝试都未能分离和培养出菌株,以进行生理和遗传特征鉴定。我们成功地从两个宿主支系中富集了数千个真菌基因并进行了测序,Bd 负荷与恢复的 Bd 序列数量呈正相关。系统发育重建将所有蕉属菌株归入 Bd-GPL 支系。相比之下,日本蛙菌株属于 Bd-Asia3 支系,扩大了该支系的范围,并产生了更多的基因组数据来确认其位置。检索到的 ITS 位点与来自野生日本蛙的公共条形码数据以及在印度和中国其他两栖动物身上发现的 Bd 感染相匹配,这表明这个未培养的支系广泛分布于亚洲各地。我们的研究强调了认识和描述快速菌株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显了直接对宿主组织中的病原体DNA进行测序的实用性,以描述依赖培养方法所遗漏的隐蔽多样性。
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Sequence capture identifies fastidious chytrid fungi directly from host tissue

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.

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来源期刊
Fungal Genetics and Biology
Fungal Genetics and Biology 生物-遗传学
CiteScore
6.20
自引率
3.30%
发文量
66
审稿时长
85 days
期刊介绍: Fungal Genetics and Biology, formerly known as Experimental Mycology, publishes experimental investigations of fungi and their traditional allies that relate structure and function to growth, reproduction, morphogenesis, and differentiation. This journal especially welcomes studies of gene organization and expression and of developmental processes at the cellular, subcellular, and molecular levels. The journal also includes suitable experimental inquiries into fungal cytology, biochemistry, physiology, genetics, and phylogeny. Fungal Genetics and Biology publishes basic research conducted by mycologists, cell biologists, biochemists, geneticists, and molecular biologists. Research Areas include: • Biochemistry • Cytology • Developmental biology • Evolutionary biology • Genetics • Molecular biology • Phylogeny • Physiology.
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