ヒト細胞に侵入可能なコウモリ由来コロナウイルスを特定(UK scientists identify bat coronavirus that can enter human cells)

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2026-04-22 英国研究イノベーション機構(UKRI)

UK Research and Innovationの支援による研究で、ヒト細胞に侵入可能なコウモリ由来コロナウイルスが特定された。研究チームはウイルスのスパイクタンパク質を解析し、ヒト細胞受容体と結合できる能力を確認。現時点でヒトへの感染や流行が確認されたわけではないが、種間感染(スピルオーバー)の潜在的リスクを示す重要な知見とされる。この成果は、新興感染症の監視やパンデミック予防に向けたリスク評価の高度化に貢献する。今後は感染性や伝播能力の詳細な検証が必要とされる。

<関連情報>

コウモリのアルファコロナウイルスはヒトのCEACAM6を利用して細胞に侵入する Heart-nosed bat alphacoronaviruses use human CEACAM6 to enter cells

Giulia Gallo,Antonello Di Nardo,Doreen Lugano,Adam J. Roberts,Bernadette Ataku Kutima,Moses Okombo,Aghnianditya Kresno Dewantari,Florence M. M. Buckley,Gavin J. Wright,James Nyagwange,Bernard Agwanda,Stephen C. Graham & Dalan Bailey
Nature  Published:22 April 2026
DOI:https://doi.org/10.1038/s41586-026-10394-x

ヒト細胞に侵入可能なコウモリ由来コロナウイルスを特定(UK scientists identify bat coronavirus that can enter human cells)

Abstract

Identifying viruses with zoonotic potential on the basis of their ability to enter human cells is a critical component of pandemic prediction, prevention and preparedness. Here using a computational approach that retains maximum phylogenetic diversity, we selected an optimal subset of alphacoronavirus spike proteins to screen against broad coronavirus receptor libraries. Most of the selected spike proteins did not use any of the established coronavirus receptors. However, the pseudotyped spike protein of Cardioderma cor (heart-nosed bat) coronavirus KY43 (CcCoV-KY43) could enter human cells. Using a recombinant CcCoV receptor-binding domain (RBD) and a human receptor screening platform, we identified direct interactions with the human CEACAM proteins CEACAM3, CEACAM5 and CEACAM6. Overexpression of human CEACAM6—a protein widely expressed in the human lung—conferred permissivity to otherwise refractory human cells. A crystal structure showed that the RBD binds the amino-terminal IgV-like domain of human CEACAM6. Immune surveillance studies using sera of individuals from the Taveta region of Kenya, where CcCoV-KY43 was identified, did not show significant evidence of recent spillover. Wider characterization of alphacoronaviruses related to CcCoV-KY43 showed that human CEACAM6 is used by two other CcCoVs collected in Kenya. Moreover, there was more restricted nonhuman CEACAM6 tropism for viruses isolated from Rhinolophus bats from Russia and China. Thus, alphacoronaviruses that use CEACAM6 are probably geographically widespread, and viruses from East Africa show potential for transmission to humans.

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