Genomic representation predicts an asymptotic host adaptation of bat coronaviruses using deep learning

Coronaviruses (CoVs) are naturally found in bats and can occasionally cause infection and transmission in humans and other mammals. Our study aimed to build a deep learning (DL) method to predict the adaptation of bat CoVs to other mammals. The CoV genome was represented with a method of dinucleotid...

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Veröffentlicht in:Frontiers in microbiology 2023-05, Vol.14, p.1157608-1157608
Hauptverfasser: Li, Jing, Tian, Fengjuan, Zhang, Sen, Liu, Shun-Shuai, Kang, Xiao-Ping, Li, Ya-Dan, Wei, Jun-Qing, Lin, Wei, Lei, Zhongyi, Feng, Ye, Jiang, Jia-Fu, Jiang, Tao, Tong, Yigang
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Sprache:eng
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Zusammenfassung:Coronaviruses (CoVs) are naturally found in bats and can occasionally cause infection and transmission in humans and other mammals. Our study aimed to build a deep learning (DL) method to predict the adaptation of bat CoVs to other mammals. The CoV genome was represented with a method of dinucleotide composition representation (DCR) for the two main viral genes, and . DCR features were first analyzed for their distribution among adaptive hosts and then trained with a DL classifier of convolutional neural networks (CNN) to predict the adaptation of bat CoVs. The results demonstrated inter-host separation and intra-host clustering of DCR-represented CoVs for six host types: Artiodactyla, Carnivora, Chiroptera, Primates, Rodentia/Lagomorpha, and Suiformes. The DCR-based CNN with five host labels (without Chiroptera) predicted a dominant adaptation of bat CoVs to Artiodactyla hosts, then to Carnivora and Rodentia/Lagomorpha mammals, and later to primates. Moreover, a linear asymptotic adaptation of all CoVs (except Suiformes) from Artiodactyla to Carnivora and Rodentia/Lagomorpha and then to Primates indicates an asymptotic bats-other mammals-human adaptation. Genomic dinucleotides represented as DCR indicate a host-specific separation, and clustering predicts a linear asymptotic adaptation shift of bat CoVs from other mammals to humans via deep learning.
ISSN:1664-302X
1664-302X
DOI:10.3389/fmicb.2023.1157608