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Poon, L. L.

Publications and source records attributed to Poon, L. L..

2 recordsLinked to original sources

The impact of clade B lineage 5 MERS coronaviruses spike mutations from 2015 to 2023 on virus entry and replication competence

Middle East respiratory syndrome coronavirus (MERS-CoV) is an emerging coronavirus that can cause zoonotic disease in humans with lethal severe viral pneumonia. Dromedary camels are the source of zoonotic infection. As of June 2025, MERS-CoV has resulted in a total of 2626 reported cases, 36% of these being fatal. The number of reported human cases has been on a decreasing trend since 2016 and reached a minimum level during the COVID-19 pandemic. The reason for the reduction of cases is unclear and may be multifactorial. We hypothesized that mutations accumulating in the virus spike protein may have reduced zoonotic potential. Here, we investigate the impact of recently emerged virus spike-protein mutations on virus replication competence using pseudoviruses and replication-competent recombinant viruses. We found that two spike variants detected in 2019 show a reduced cell entry and lower viral replication in human cells. However, spike variants detected in 2023 sequences, did not show significant changes in cell entry and viral replication. All the MERS-CoV spikes tested showed a cell-entry pathway preference via the cell-surface TMPRSS2 route. Our data suggests that spike protein mutations are not a major determinant of the fewer MERS-CoV human cases observed. Author SummaryMERS-CoV is identified by the World Health Organization (WHO) as a potential pandemic candidate. The ability of coronaviruses to mutate and adapt in new hosts raises concerns about the impact of virus genetic changes on human zoonotic potential. There has been a notable decline in human MERS cases reported to the WHO since 2018, but the underlying reasons remain unclear. Here, we focus on investigating whether the recently emerged virus spike mutations may contribute to this observation. We found that while some spike mutations detected in 2019 reduce cell entry and viral replication, more recent viruses do not share this phenotype. This study highlighted a need for comprehensive genomic surveillance and phenotyping of recent MERS-CoV isolates to understand the potential role, if any, of other non-spike virus mutations on viral zoonotic competence and to explore alternate hypothesis, such as cross-reactive immunity from COVID-19 contributing to reduced human MERS-CoV disease.

microbiology↗

Long non-coding RNA BCAR4 is required for efficient influenza A virus replication

Long non-coding RNAs (lncRNAs) regulate diverse biological processes, including influenza A virus (IAV) infection. However, the understanding of lncRNAs in IAV infection is limited. By using both bioinformatic analyses and virological assays, we showed that lncRNA BCAR4 expression can be highly induced by infection of multiple different IAV subtypes. BCAR4 was required for the propagation of IAV infection. Genetic inactivation of BCAR4 inhibited IAV growth. Investigation of the IAV infection cycle revealed a suppressed IAV viral RNA transcription and replication, and attenuated viral protein synthesis in the BCAR4-deficient cells. BCAR4 potentially interacted with cellular splicing-associated proteins and the activation of BCAR4 was associated with influenza viral NS segment. These findings suggest the important role of lncRNA BCAR4 in regulation of IAV infection. ImportanceLong non-coding RNAs (lncRNAs) serve as critical regulators in the biological processes of influenza A virus (IAV) infection. However, how lncRNAs engage IAV infection remains unclear. Here we show BCAR4 as highly universally induced lncRNA in infection of multiple different IAV subtypes. Deletion of BCAR4 reduced IAV multiplication. In the IAV infection cycle, BCAR4 deficiency decreased IAV viral RNA transcription, replication and viral protein biosynthesis. BCAR4 was potentially binding to the host RNA splicing associated protein, and the IAV viral NS segment is required for the activation of BCAR4. Our results highlight important regulation of BCAR4 in IAV infection.

microbiology↗