| Literature DB >> 34140500 |
Masateru Taniguchi1, Shohei Minami2, Chikako Ono2,3, Rina Hamajima2, Ayumi Morimura4, Shigeto Hamaguchi4,5, Yukihiro Akeda2,4,5, Yuta Kanai2, Takeshi Kobayashi2, Wataru Kamitani6, Yutaka Terada7, Koichiro Suzuki8, Nobuaki Hatori8, Yoshiaki Yamagishi4,5,9, Nobuei Washizu10, Hiroyasu Takei11, Osamu Sakamoto11, Norihiko Naono11, Kenji Tatematsu12, Takashi Washio12, Yoshiharu Matsuura13,14, Kazunori Tomono15,16.
Abstract
High-throughput, high-accuracy detection of emerging viruses allows for the control of disease outbreaks. Currently, reverse transcription-polymerase chain reaction (RT-PCR) is currently the most-widely used technology to diagnose the presence of SARS-CoV-2. However, RT-PCR requires the extraction of viral RNA from clinical specimens to obtain high sensitivity. Here, we report a method for detecting novel coronaviruses with high sensitivity by using nanopores together with artificial intelligence, a relatively simple procedure that does not require RNA extraction. Our final platform, which we call the artificially intelligent nanopore, consists of machine learning software on a server, a portable high-speed and high-precision current measuring instrument, and scalable, cost-effective semiconducting nanopore modules. We show that artificially intelligent nanopores are successful in accurately identifying four types of coronaviruses similar in size, HCoV-229E, SARS-CoV, MERS-CoV, and SARS-CoV-2. Detection of SARS-CoV-2 in saliva specimen is achieved with a sensitivity of 90% and specificity of 96% with a 5-minute measurement.Entities:
Mesh:
Year: 2021 PMID: 34140500 DOI: 10.1038/s41467-021-24001-2
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919