1. 1.

    This article systematically reviews research on m6A and COVID-2019 infection;

  2. 2.

    This article proposes potential future research directions on the relationship between m6A and COVID-2019 infection in the context of existing research.

Open Questions

  1. 1.

    This article suggests a mathematical model based on m6A-related genes for the prediction of COVID-2019 infection;

  2. 2.

    This article proposes a treatment strategy for COVID-2019 infection based on m6A-related pathways.


The novel coronavirus is an RNA virus that belongs to the family Coronaviridae and is a close relative of the severe acute respiratory syndrome (SARS) and the Middle East respiratory syndrome (MERS), whose full name is Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) [1]. This virus is the pathogen causing coronavirus disease 2019 (COVID-19) [2]. COVID-19 is a highly infectious and lethal disease that is majorly transmitted between individuals through respiratory droplets and contact routes and has caused hundreds of millions of infections and millions of deaths worldwide, for which there is no specific treatment [3,4,5,6,7].Some drugs, such as remdesivir, chloroquine, and hydroxychloroquine, have been used in the treatment of COVID-19 [8], but their efficacy and safety still require further research. Currently, COVID-19 patients are mainly treated with supportive care, including oxygen therapy, fluid infusion, and organ support, which aims to enable patients to recover as well as possible [9]. It has become a hot research topic to investigate the pathogenesis of COVID-19 at the molecular level and identify reliable therapeutic targets.

N6-methyladenosine (m6A) is a common RNA modification and widely exists in cells [10]. m6A involves the addition of methyl groups to RNA molecules and plays an important role in biological processes such as transcription, translation, and splicing of RNA [11,12,13] . Recently, mounting evidence has revealed that m6A methylation modifications are closely related to virus infection [14,15,16,17,18,19]. As many studies demonstrated, m6A methylation can affect cellular function through various mechanisms during the occurrence of hepatitis virus, human immunodeficiency virus type 1, and SARS-CoV-2 infection to adapt to the life cycle demands of the virus [15, 16, 18, 20,21,22,23]. In turn, m6A methylation can also have an impact on viral infection, affecting the life cycle and pathogenicity of the virus [20, 24, 25] Therefore, elucidating the specific mechanism of m6A methylation in COVID-19 virus infection is important for the prevention and treatment of COVID-19.

RNA m6A methylation

Overview of m6A

RNA m6A methylation refers to a methylation modification that occurs at the nitrogen-6 position of the adenine (A) base on RNA molecules, which is widely found in eukaryotic ribosomal messenger RNA (mRNA), transfer RNA (tRNA), RNA (rRNA), and noncoding RNA (ncRNA) and has been shown to be important in regulating various biological processes of RNA [10, 26, 27]. As one of the most common RNA modifications, m6A methylation occurs mainly in the shared sequence RRACH (R = G or A; H = A, C, or U) and is mostly enriched in the stop codon, 3' untranslated region, and long internal exons, which is dynamically reversible under the regulation of various modifying enzymes, such as methyltransferases (writers), demethylases (erasers), and methylated readers (readers) [28]. m6A methylation is catalyzed by methyltransferases. Furthermore, two methyltransferases have been identified to be involved in m6A methylation, including methyltransferase-like 3 (METTL3) and METTL14 [29]. In addition, other proteins, such as WTAP, KIAA1429, and RBM15, are also implicated in the mediation of m6A methylation [30]. m6A readers are a class of proteins that recognize and bind to m6A-modified RNAs, which include many proteins, such as YTHDC1, YTHDC2, YTHDF1, YTHDF2, YTHDF3, HNRNPC, and IGF2BP1 [31]. These proteins can regulate biological processes of RNA, including transcription, splicing, translation, and degradation [31,32,33]. Demethylases can reverse the m6A methylation of RNA by reducing the m6A modification to A. A variety of demethylases have been identified, including FTO and ALKBH5, which are involved in RNA metabolism and regulation and are essential for maintaining RNA stability and function [33]. m6A recognition factors are a class of RNA structural domains capable of recognizing and binding to m6A modifications, which consist of YTHDC1, YTHDC2, YTHDF1, YTHDF2, and YTHDF3. Moreover, m6A recognition factors participate in the recognition and interaction to RNA and modulate the local structure and interaction of RNA [34].

m6A and COVID-2019 infection

Effects of m6A methylation on COVID-2019 infection

Accumulating evidence has unraveled that m6A modification is crucial for the transmission and pathogenicity of COVID-2019. For instance, Liu et al. found that m6A modification was deregulated in host cells infected with SARS-CoV-2 and re-localized by viral infection, thereby increasing the abundance of m6A in cells [17]. Campos et al. identified the methylation of m6A transcripts in African green monkey Vero cells and human Calu-6 cells infected with SARS-CoV-2 with RNA sequencing and analyzed the results with nonparametric statistics and two computational methods (m6anet and EpiNano), which showed higher levels of m6A methylation in the RNA of infected cells [35]. This study verifies that the effect of SARS-CoV-2 virus infection on cell function is associated with m6A methylation. Qiu et al. observed downregulation of m6A-related genes in blood leukocytes from COVID-2019 patients [36]. In addition, a study by Li et al. showed that the m6A methylation gene METTL3 was significantly downregulated and inflammatory genes were upregulated in lung tissues of patients with severe COVID-2019 than in those of healthy individuals [16]. Additionally, Lu et al. analyzed the expression of 9 writers, 15 readers, and 2 erasers for m6A modification in healthy individuals and COVID-2019 patients and observed that the expression of WTAP, RBM15, HNRNPC, YTHDC1, FMR1, HNRNPA2B1, ELAVL1, and YTHDF3 was markedly higher but the expression of RBM15B, IGFBP2, and IGF2BP1 was substantially poorer in COVID-2019 patients than in healthy individuals, illustrating that the above targets may be associated with the regulation of m6A on COVID-2019 infection [37] (Fig. 1). Subsequent research further validated that SARS-CoV-2 infection altered the epigenetic transcriptome of m6A in lymphocytes, especially in those from patients with severe disease, and that it could enhance RBM15 m6A modification to regulate host immune responses [38].

Fig. 1
figure 1

The overview of m6A RNA methylation modification in blood lymphocytes of patients infected with SARSCoV-2, including writers, readers, and erasers.

The pathogenesis of severe respiratory infections caused by novel coronaviruses is associated with a disorder of the pro-inflammatory/anti-inflammatory response and immune imbalance, with immune system overreaction, excessive apoptosis and depletion of immune cells, immunosuppression, and immunoparalysis as the main immunopathological manifestations. For instance, prior research revealed that patients with severe COVID-2019 had high levels of pro-inflammatory cytokines than patients with moderate COVID-2019, indicating that high levels of pro-inflammatory cytokines are associated with the poor prognosis of COVID-2019 patients [39, 40]. Braun et al. found peak reactivity of CD35 T cells in 4% of COVID-2019 patients and 19% of healthy controls, illustrating the existence of T cell cross-reactivity which may prevent SARS-CoV-2 infection to some extent [41]. Because persistent inflammatory factor storms serve as one of the most dangerous factors in the COVID-19 pandemic, pro-inflammatory cytokines such as IL-1α, IL-1β, IL-6, and TNF-α play a key role in COVID-19 development. Recent studies have indicated that m6A modification can affect SARS-CoV-2 infection by regulating the antiviral response of immune cells. A previous study exhibited that METTL3 was downregulated in host cells after SARS-CoV-2 infection to decrease m6A levels in viral and host genes, thus enhancing retinoic acid-inducible gene-I binding and the expression of downstream innate immune pathways and inflammatory genes, suggesting that human immune responses play an important role in COVID-2019 infection [42]. A study by Du et al. unraveled that deletion of the m6A-related target METTL14 or YTHDF1 in macrophages predisposed infected mice to inflammatory factor storms, resulting in higher mortality from infection, which illustrated m6A as a pivotal mechanism regulating inflammatory factor storms [43]. In summary, the immune response participates in the development and progression of COVID-2019. As an important biomolecule, m6A not only is essential for gene expression, translation, and regulation but also exerts important physiological functions in various aspects of immune responses in the body. The role of m6A in the immune system has been investigated, which provides not only a novel perspective for the in-depth understanding of the biological function of m6A but also a critical reference for exploring the occurrence, transmission, prevention, and control of COVID-2019 [44,45,46]. However, there is a lack of research on the association of m6A with immune responses in COVID-2019 infections. In this context, further research is warranted to characterize the regulatory mechanism of m6A in immune cells and the potential molecular mechanism of interactions between m6A and COVID-2019 infection-related immune responses, thus providing new ideas and approaches for the treatment and prevention of COVID-2019.

Effect of m6A methylation modification on the evolution of SARS-CoV-2

It has been demonstrated that m6A methylation modifications also play a crucial role in the transmission and evolution of SARS-CoV-2. Liu et al. used RNA immunoprecipitation sequencing for sequencing of the m6A methylation profiles in SARS-CoV-2-infected human and monkey cells and systematic bioinformatics analysis and found the dynamic distribution pattern of m6A modifications in the SARS-CoV-2 genome and that m6A modifications were also widely present on the negative-strand RNAs as replication intermediates. Further, the researchers used the more precise m6A individual-nucleotide-resolution cross-linking and immunoprecipitation technique to identify m6A sites at single-base resolution on SARS-CoV-2 genomic RNA and identified eight m6A sites at single-base resolution, and more importantly, phylogenetic analysis unveiled that a series of mutant strains carrying specific m6A modification site emerged in different regions of the world. Functional experiments confirmed that the m6A methyltransferase METTL3/14 and the demethylase ALKBH5 negatively/positively regulated the replication of the SARS-CoV-2 genome, respectively, and that a decrease in the m6A reading protein YTHDF2 also promoted viral replication and infectivity. As this result indicated, SARS-CoV-2 infection not only elevates m6A contents in the host genome and changes the overall methylation profile. Meanwhile, SARS-CoV-2 can also use cellular enzymes for its own methylation to generate an evolutionary pressure to adapt the viral DRACH sequence, thus becoming more similar to the cellular sequence to successfully evade the killing effect of interferon. In conclusion, m6A modifications affect the interaction between the host and SARS-CoV-2 [17]. The research by Wyler et al. also revealed that m6A methylation is vital for virus-host interactions [47]. It was found in the research by Zhang et al. that METTL3A expression was increased and its distribution in cells was changed after SARS-CoV-2 infection. This research also confirmed the effect of METTL3 on viral replication by knocking down or overexpressing METTL3 through transfection with short hairpin RNA or plasmids [25].

m6A methylation modifications and diagnosis of SARS-CoV-2 infection

The importance of m6A in COVID-2019 infection was previously confirmed. Accordingly, molecular mechanisms underlying m6A can be used for the development of new preventive and therapeutic options for COVID-2019. In the study by Lu et al., a model to predict the risk of COVID-2019 was constructed by screening m6A-related genes, which successfully predicted the degree of risk of COVID-2019 infection and had a high validity [48]. In the study by Qing et al., 18 basic m6A methylation enzymes were identified, among which the eight optimal m6A methylation enzymes were selected to predict the occurrence of COVID-2019 with a random forest model which had high-accuracy prediction capability [41]. As a result, the risk of COVID-2019 infection can be assessed by constructing a linear model of m6A-related genes. In addition, Dong et al. used LASSO and multivariate Cox regression analyses to determine prognostic factors for patients with COVID-2019 and found that hypertension, increased neutrophil-to-lymphocyte ratio, and elevated NT-proBNP were significantly associated with the poor in-hospital prognosis of COVID-2019 patients. The model involving these three factors effectively predicted the in-hospital survival of COVID-2019 patients, which, therefore, is expected to be applied to the clinical management of COVID-2019 [49]. Therefore, the prediction models of m6A-related genes constructed based on clinical symptoms would be expected to more accurately predict disease onset and progression in the early stages of COVID-2019 infection.

m6A methylation modification and treatment of SARS-CoV-2 infection

As reported, m6A-related regulators in SARS-CoV-2 infection provide new strategies for the development of vaccines and antiviral drugs. Specifically, m6A modification-related genes are knocked down or overexpressed to reduce viral virulence, thus designing attenuated vaccine viruses. Additionally, the mechanisms of m6A modification can be utilized as a new target for antiviral therapy, such as the method investigated by Aik et al. [50]. Malacrida et al. [51] reported a variety of m6A demethylation-related small molecules, such as N-oxalylglycine (NOG), 2,4-Pyridinedicarboxylic acid (2,4-PDCA), IOX3, and MV1035, providing ideas for the development of drugs involving m6A-related targets. Liu et al. found that knockdown of METTL3, METTL14, and YTHDF2 increased viral replication, whereas knockdown of ALKBH5 repressed SARS-CoV-2 infection [17]. Therefore, drugs targeting these relevant targets can be more effective in treating COVID-2019 infection. A study by Zannella et al. exhibited that emodin enhanced interference with the replication of β-coronavirus replication, particularly SARS-CoV-2, and that its strong activity of anti-SARS-CoV-2 was associated with m6A pathways [52]. There are some reports on the antiviral effects of m6A-related small molecule drugs (such as NOG, 2,4-PDCA, IOX3, and imidazobenzoxazin-5-thione MV1035) against other viruses. Nevertheless, the development of m6A-related small molecule drugs against SARS-CoV-2 requires more in-depth research, which helps to increase the efficacy of treatment of COVID-2019 infection and provides novel ideas and methods to prevent similar outbreaks.

Conclusion and outlook

With the global outbreak of the COVID-2019 epidemic, tremendous attention has been paid to the association between m6A methylation and COVID-2019 infection, and the involved mechanisms are being intensively explored. Although m6A methylation has been revealed to play a critical role in COVID-2019 infection, the detailed regulatory mechanisms still need in-depth studies. In addition, the development of m6A-related small molecule drugs against SARS-CoV-2 is also an important field, which needs to be intensively researched for more rapid and effective treatment of COVID-2019 infection to make a greater contribution to global human health security. In addition to the development of drugs targeting m6A methylation, research on other m6A-related molecular targets, such as reader proteins and demethylases, are also promising targets for vaccines and therapies against COVID-2019. In addition, as the understanding of m6A methylation gradually deepens, new therapeutic strategies may emerge, such as modulation of the immune response or suppression of inflammation by regulating m6A methylation modifications. Therefore, more vaccines and treatments targeting m6A methylation against COVID-2019 are expected to be developed in the future, providing new strategies and methods to control COVID-2019 outbreaks.