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Rapid and precise identification and discrimination of causative pathogens are required in the treatment of infectious diseases. Quantitative real-time PCR is used to detect and identify infectious viruses before treatment. Although it is an established modality, results take several hours, even in well-equipped hospitals. It is difficult to simultaneously detect many pathogen types because only a single-virus genome can be amplified per PCR. Recently, an AI-based nanopore machine has been used to identify individual viruses based on electrical conductivity. Here, we recognized a single virus using an AI-based detection system and successfully identified viral particles in clinical samples without the need for any prior treatment. We used a nanopore detector and discriminated among viruses using an AI-based waveform analysis. The efficacy of the AI nanopore detector as an on-site clinical analysis device was validated in cultured herpesvirus samples, and its discrimination capability was verified with clinical samples. The AI nanopore analysis of cultured viruses revealed that and within the same family can be distinguished with a relatively high accuracy. The AI nanopore rapidly detected viral particles and can be useful as an on-site clinical diagnosis tool. We demonstrated the multiplex discrimination of herpetic viruses in clinical ocular samples, proving that the AI nanopore is an ultra-high-speed and highly sensitive detection tool that can be used in various medical fields.
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http://dx.doi.org/10.1093/pnasnexus/pgaf161 | DOI Listing |
Microbiol Spectr
September 2025
Department of Cell Biology, Kyoto Pharmaceutical University, Kyoto, Japan.
Kaposi's sarcoma-associated herpesvirus (KSHV) belongs to the Gammaherpesvirinae subfamily. During the lytic phase of herpesviruses, viral capsids form in the host cell nucleus, and the replicated viral genome is packaged into these capsids. The herpesviral genome is replicated as a precursor head-to-tail concatemer consisting of tandemly repeated genomic units, each flanked by terminal repeats (TRs).
View Article and Find Full Text PDFJ Biomed Sci
September 2025
Virology and Vaccine Immunology, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.
Background: Enteroviruses, including Coxsackie B (CVB) viruses, can cause severe diseases such as myocarditis, pancreatitis, and meningitis. Vaccines can prevent these complications, but conserved non-neutralizing epitopes in the viral capsid may limit their effectiveness. The immunodominant PALXAXETG motif, located in the VP1 N-terminus, is a highly conserved region in enteroviruses that elicits non-neutralizing antibody responses.
View Article and Find Full Text PDFDev Comp Immunol
September 2025
Guangdong Key Laboratory of Animal Conservation and Resource Utilization, Institute of Zoology, Guangdong Academy of Sciences, Guangzhou, Guangdong, China.
Sorting nexin 27 (Snx27), a member of the sorting nexin (SNX) family, plays crucial roles in cell signaling, organelle motility, protein sorting and membrane remodeling/trafficking. While existing studies have focused on the functions of SNXs in mammalian viral diseases and immune regulation, little is known about fish-encoded SNXs, particularly their regulatory roles in aquatic virus infection. In this study, we characterized the Snx27 from the orange-spotted grouper (Epinephelus coioides) and found that it facilitates the in vitro release of Singapore grouper iridovirus (SGIV), as evidenced by the detection of viable virions in the culture supernatants of SGIV-infected grouper spleen (GS) cells.
View Article and Find Full Text PDFPLoS Pathog
September 2025
Department of Molecular Biology, Princeton University, Princeton, New Jersey, United States of America.
Hepatitis C virus (HCV) exhibits a narrow species tropism, causing robust infections only in humans and experimentally inoculated chimpanzees. While many host factors and restriction factors are known, many more likely remain unknown, which has limited the development of mouse or other small animal models for HCV. One putative restriction factor, the black flying fox orthologue of receptor transporter protein 4 (RTP4), was previously shown to potently inhibit viral genome replication of several ER-replicating RNA viruses.
View Article and Find Full Text PDFMicrobiol Spectr
September 2025
Institute of Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing, China.
Modulating cell endocytosis activity to reduce host susceptibility to virus represents a promising strategy for antiviral drug development. In this study, we reveal that lactate transporter SLC16A3 is a critical host factor for reducing diverse virus invasion. By performing metabolomics, proteomics, and thermal proteome profiling experiments, AP1G1, a pivotal protein involved in cellular endocytosis, was indiscriminately screened as a chaperone of SLC16A3.
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