Co-infection of phylogenetically distinct nucleocytoviruses in Acanthamoeba castellanii cells.

IF 2.2 4区 生物学 Q3 MICROBIOLOGY
Daichi Morimoto, Ryoma Usutani, Naohisa Tateishi, Yusaku Funaoka, Michiko Takahashi, Keizo Nagasaki
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引用次数: 0

Abstract

Nucleocytoviruses have extraordinarily large double-stranded DNA genome, including a set of highly conserved genes for viral reproduction. Meanwhile, nucleocytoviruses supposedly acquire new genes from cellular organisms and different lineages of nucleocytovirus, leading to their evolution. Although horizontal gene transfer among nucleocytoviruses is thought to occur in cells simultaneously infected by distinct nucleocytoviruses, it remains unknown which combination of lineages can co-infect a host cell. Here, we performed co-infection experiments using cedratvirus, megavirus, mollivirus, and pandoravirus. By transmission electron microscopy, we observed Acanthamoeba castellanii cells incorporating two distinct viral species in all six combinations. Furthermore, A. castellanii cell incorporating all four viral species was observed. In these experiments, a simultaneous increase in viral particles was observed for the combination of mollivirus and pandoravirus, pandoravirus and cedratvirus, mollivirus and cedratvirus, and megavirus and cedratvirus. Furthermore, transcription levels of cedratvirus and megavirus genes in the co-infected culture were significantly lower than those in the mono-infected culture based on time-course experiments, suggesting that distinct nucleocytoviruses may compete for viral reproduction. This is the first report experimentally demonstrating that co-infection of distinct nucleocytoviruses occurs in a A. castellanii cell.

系统发育上不同的核细胞病毒在棘阿米巴细胞中的共感染。
核细胞病毒具有非常大的双链DNA基因组,包括一组用于病毒繁殖的高度保守的基因。同时,核细胞病毒可能从细胞生物和不同的核细胞病毒谱系中获得新的基因,从而导致它们的进化。虽然核细胞病毒之间的水平基因转移被认为发生在同时被不同核细胞病毒感染的细胞中,但仍不清楚哪些谱系组合可以共同感染宿主细胞。在这里,我们使用巨病毒、鼹鼠病毒和潘多拉病毒进行了联合感染实验。通过透射电镜,我们观察到棘阿米巴castellanii细胞在所有六种组合中含有两种不同的病毒。此外,还观察到A. castellanii细胞含有所有四种病毒。在这些实验中,观察到mollivirus和pandoravirus、pandoravirus和cedratvirus、mollivirus和cedratvirus、megavirus和cedratvirus结合时,病毒颗粒数量同时增加。此外,根据时间过程实验,在共同感染的培养物中,巨病毒和巨病毒基因的转录水平明显低于单独感染的培养物,这表明不同的核细胞病毒可能会竞争病毒的繁殖。这是首次用实验证明不同核细胞病毒在黄颡鱼细胞中同时感染的报道。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Fems Microbiology Letters
Fems Microbiology Letters 生物-微生物学
CiteScore
4.30
自引率
0.00%
发文量
112
审稿时长
1.9 months
期刊介绍: FEMS Microbiology Letters gives priority to concise papers that merit rapid publication by virtue of their originality, general interest and contribution to new developments in microbiology. All aspects of microbiology, including virology, are covered. 2019 Impact Factor: 1.987, Journal Citation Reports (Source Clarivate, 2020) Ranking: 98/135 (Microbiology) The journal is divided into eight Sections: Physiology and Biochemistry (including genetics, molecular biology and ‘omic’ studies) Food Microbiology (from food production and biotechnology to spoilage and food borne pathogens) Biotechnology and Synthetic Biology Pathogens and Pathogenicity (including medical, veterinary, plant and insect pathogens – particularly those relating to food security – with the exception of viruses) Environmental Microbiology (including ecophysiology, ecogenomics and meta-omic studies) Virology (viruses infecting any organism, including Bacteria and Archaea) Taxonomy and Systematics (for publication of novel taxa, taxonomic reclassifications and reviews of a taxonomic nature) Professional Development (including education, training, CPD, research assessment frameworks, research and publication metrics, best-practice, careers and history of microbiology) If you are unsure which Section is most appropriate for your manuscript, for example in the case of transdisciplinary studies, we recommend that you contact the Editor-In-Chief by email prior to submission. Our scope includes any type of microorganism - all members of the Bacteria and the Archaea and microbial members of the Eukarya (yeasts, filamentous fungi, microbial algae, protozoa, oomycetes, myxomycetes, etc.) as well as all viruses.
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