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Ito, J.

Publications and source records attributed to Ito, J..

At least 19 recordsLinked to original sources

Quantitative host-response mapping enables phenotypic profiling of viruses detected by virome sequencing

Animal-derived viruses have repeatedly caused human outbreaks, motivating efforts to identify and characterize viruses circulating in animals. Virome sequencing has accelerated animal virus discovery, but phenotypic characterization remains difficult to scale. Although generated for viral detection, virome RNA-seq data also capture host transcriptional responses to infection. Here, we developed ViroChart, a comparative transcriptomic framework that quantifies activities across biological pathways and maps diverse mammalian host responses into a common, interpretable low-dimensional space. ViroChart enables clustering of infected samples by host response pattern and quantitative assessment of host response similarity between samples. In virome data sets from wild and farmed animals, some lung samples infected with poorly characterized betacoronaviruses showed host responses resembling those induced by viruses capable of causing fatal disease. ViroChart also revealed host-response heterogeneity in natural infections: among rats with zoonotic rodent-borne viruses, most showed weak responses, consistent with asymptomatic infection, but some showed pronounced inflammation characteristic of acute infection. ViroChart thus enables phenotypic characterization and prioritization of newly detected viruses by leveraging the same RNA-seq data from which their genomes were detected.

microbiology↗

Poxvirus gene repertoires are shaped by expansion-biased birth-and-death dynamics and genome architectural constraints

Poxviruses (family Poxviridae) are DNA viruses with exceptionally large genomes containing hundreds of genes. Yet the evolutionary processes contributing to their numerous gene repertoires remain insufficiently understood. Here, we inferred ortholog groups of genes across 58 poxvirus genomes and comprehensively analyzed gene gain, gene duplication, gene loss, horizontal gene transfer, and synteny conservation. Across poxviruses, coding capacity scaled linearly with genome length. Gene repertoires evolved through birth-and-death dynamics but generally expanded because gene gain cumulatively exceeded gene loss and gained genes subsequently underwent further duplication. Gene gain and duplication were concentrated in the terminal regions of most poxvirus genomes. In viral lineages whose gene repertoires expanded extensively, terminal-region expansion was accompanied by further accumulation of duplicated genes within the otherwise conserved central genomic regions. The phylogenetic placement of the bird-infecting genus Avipoxvirus, together with evidence that several horizontally acquired genes originated from mammals, raises the possibility of a mammalian origin for Avipoxvirus. Altogether, our findings reveal that poxvirus gene repertoire evolution is shaped by expansion-biased birth-and-death dynamics and genome architectural constraints.

evolutionary biology↗

A rapidly deployable CRISPR-Cas3 diagnostic platform for emerging RNA viruses

Rapidly converting viral genome information into deployable molecular tests remains a major challenge in outbreak preparedness. We developed CONAN-SWIFT (Simple Workflow for Isothermal Field Testing), a sequence-to-test platform that integrates computational assay design, reverse-transcription loop-mediated isothermal amplification, CRISPR-Cas3 detection, reagent lyophilization and lateral-flow readout. Sequence-guided assays for Andes virus and Bundibugyo virus were established within approximately three weeks and extended to four additional filoviruses. A web-based designer supported crRNA selection, and systematic RT-LAMP primer optimization improved amplification performance. Recombinant Escherichia coli-expressed Cascade enabled standardized preparation of lyophilized Cas3-detection reagents, which were combined with a battery-operated isothermal device. The portable system detected as few as 10 input RNA copies per reaction within approximately 40 min. It also detected viral RNA and biologically contained, replication-incompetent Ebola virus in spiked human blood and concentrated wastewater. These findings establish the analytical feasibility of a rapidly adaptable CRISPR-Cas3 engineering framework for decentralized detection of emerging RNA viruses.

bioengineering↗

Genetic interaction between Adgrg6 and Sox9 reveals a feedforward mechanism for postnatal spinal stability

Adolescent idiopathic scoliosis (AIS) is the most common spinal disorder in children and is best understood as a complex polygenic condition. Genome-wide association studies (GWAS) have identified several AIS risk loci, including regions near ADGRG6 and SOX9, yet the functional mechanisms underlying AIS heritability remain poorly defined. Here, we use spatial transcriptomics to characterize altered gene expression in the spine of a conditional Adgrg6 mutant mouse model of AIS (Adgrg6-cKO), revealing reduced expression of Sox9 and several components of extracellular matrix organization in the intervertebral disc. We further show that SOX9 occupies regions of open chromatin within the Adgrg6 locus in cells isolated from the mouse intervertebral disc. Finally, we demonstrate a strong genetic interaction between Adgrg6-cKO and a hypomorphic Sox9 allele that increases both the penetrance and severity of AIS-like pathology in mice. Collectively, these findings support a self-reinforcing feedforward regulatory circuit, where Adgrg6 and Sox9 are co-regulated to maintain extracellular matrix gene expression in the annulus fibrosus and paraspinal tissues. These findings provide mechanistic insight into the functional significance of AIS-associated GWAS loci near ADGRG6 and SOX9 and establish combined Adgrg6-Sox9 insufficiency as a tractable model of polygenic scoliosis susceptibility. O_LIAdgrg6 maintains Sox9 and extracellular matrix gene expression in the intervertebral disc C_LIO_LISOX9 directly occupies open chromatin at the Adgrg6 locus in SOX9 skeletal cells C_LIO_LIAdgrg6 and Sox9 genetically interact to increase scoliosis incidence and severity C_LIO_LICombined loss of Adgrg6 and Sox9 drives ectopic cartilage formation and reduced vertebral bone mineral density in the thoracic spine C_LI

developmental biology↗

Novel African Rhinolophus bat ACE2 sequences reveal the determinants of Afro-Eurasian sarbecovirus entry

Sarbecoviruses, including SARS-CoV and SARS-CoV-2, are frequently linked to Rhinolophus bats as their putative natural reservoirs. Angiotensin-converting enzyme 2 (ACE2), a host carboxypeptidase widely expressed in mammalian tissues, plays a critical role in sarbecovirus infection by serving as the cellular receptor for the viral spike (S) protein. Given recent human outbreaks and pandemics caused by members of sarbecoviruses, and the wide distribution of Rhinolophus bats, it is essential to maintain surveillance of these viruses while improving our understanding of their interactions with bat hosts, particularly the ACE2 receptor. However, while Rhinolophus bats from Asia have been relatively well studied, African Rhinolophus bats remain underrepresented and require further investigation. In this study, five Rhinolophus bat lung samples were obtained from Zambia, and ACE2 genes from these individuals were cloned and sequenced. We further evaluated the susceptibility of ACE2 variants to a panel of sarbecoviruses, revealing key residues that influence viral infectivity. ACE2 polymorphism was observed among Rhinolophus simulator individuals, revealing multiple ACE2 genotypes within the sampled population. However, R. simulator ACE2s did not permit infection by the clade 3 Afro-Eurasian sarbecoviruses tested in this study. Notably, RhGB01 and BM48-31 virus utilized only Rhinolophus blasii ACE2. Mutational analyses further suggested that ACE2 residues 31 and 41 play important roles in modulating spike-ACE2 interactions. This study reports 4 unique ACE2 sequences of R. simulator and R. blasii, and provides new insights into the molecular interactions between African Rhinolophus species ACE2s and the S protein of sarbecoviruses circulating in Africa and Europe. ImportanceAs putative natural reservoirs of sarbecoviruses, including SARS-CoV and SARS-CoV-2, Rhinolophus bats play a critical role in the emergence of zoonotic coronaviruses, making it essential to understand their interactions with these viruses for future pandemic preparedness. While Asian Rhinolophus bats have been relatively well studied, African species remain underrepresented, highlighting the need for further investigation. In this study, we cloned and sequenced ACE2 genes of five Rhinolophus bats collected in Zambia, Africa. We identified ACE2 polymorphism among Rhinolophus simulator individuals, although this variation was not associated with susceptibility to the clade 3 Afro-Eurasian sarbecoviruses examined. In addition, we identified key ACE2 residues that govern SARS-CoV-2 spike-ACE2 interactions and contribute to distinct infectivity patterns across species. These findings expand our understanding of the molecular determinants of sarbecovirus host range and support improved surveillance and risk assessment of emerging coronaviruses.

microbiology↗

Experimental SARS-CoV-2 infection using horseshoe bats

Horseshoe bats are known as the natural reservoir of sarbecoviruses. To understand how horseshoe bats coexist with sarbecoviruses in nature, experimental infection can provide direct evidence. However, in vivo infection studies using horseshoe bats have been lacking because of the difficulty of maintaining insectivorous bats in a laboratory setting. Here, we established a stable husbandry system for greater horseshoe bats (Rhinolophus ferrumequinum) and performed experimental infection with SARS-CoV-2. In contrast to Syrian hamsters which showed substantial viral replication, infected horseshoe bats exhibited low-level but persistent viral replication in the lung without overt disease. Histological analyses revealed that inflammatory lesions in the bat lungs were spatially restricted and temporally delayed compared with those in hamsters. Transcriptomic analyses further showed preferential activation of tissue repair pathways but limited inflammatory responses following infection. Notably, bats expressed several interferon-stimulated genes prior to infection. Our results suggest that a host strategy combining constitutive antiviral state, limited inflammation and enhanced tissue repair may result in controlled viral replication without overt disease, likely enabling horseshoe bats to coexist with sarbecoviruses.

microbiology↗

Host innate immune response profiling reveals hidden viral infections across diverse animal species

Virus discovery using RNA-seq data from wildlife and livestock offers a powerful strategy for identifying unknown pathogens with pandemic potential. However, conventional approaches rely on homology-based searches that have limited sensitivity for highly divergent viruses, are computationally intensive at scale, and cannot distinguish true infections from contamination. Viral infection induces interferon-stimulated genes (ISGs), key components of the frontline antiviral defense, and their expression serves as a robust indicator of viral infection. Here, we developed a host-response-based virus discovery framework that rapidly quantifies ISG expression and predicts viral infection status. Applying this framework to [~]210,000 RNA-seq data sets from diverse mammalian and avian species, we identified hidden viral infections across diverse hosts, including those caused by highly divergent viruses missed by a conventional approach. Our framework complements existing virus discovery strategies by adding host innate immune response context and enabling computationally efficient prescreening for scalable viral surveillance. HighlightsO_LIHost response-based virus discovery in wildlife and livestock RNA-seq data C_LIO_LIQuantify interferon-stimulated gene (ISG) expression and predict viral infection C_LIO_LIAnalysis of [~]210,000 RNA-seq data sets reveals hidden viral infections C_LIO_LIDetects highly divergent viruses and scalable viral surveillance through rapid prescreening C_LI

microbiology↗

A Quality Measure for Repeating Multiple-Unit Spike Patterns

We propose a quality measure for spatio-temporal spike patterns (STPs) in multiple-neuron recordings. In such recordings, repeating STPs or pattern repetitions (PRs) are often found, with many of these generated by chance. To rule those out, statistical tests have been developed to discriminate the unlikely from the more likely PRs. This statistical problem is complicated by the fact that there are several obvious quality criteria for a PR, such as the size (the number of spikes) of the pattern and the number of its occurrences. Here, we propose a canonical way of combining several criteria (which we collect in the so-called signature of the pattern) into a single quality measure, based on the unlikeliness of the pattern. This measure is defined mathematically, and a formula for its computation is derived for stationary spike trains. It can be used to compare PRs. Since spike trains are not stationary in practice, we discuss, for two experimental data sets, how well the stationary formula correlates with the defined quality measure as determined from simulations. The results encourage the use of the stationary formula or also some simpler, related formulas as proxies for the quality, for the comparison of PRs and also for statistical tests that avoid the multiple testing problem incurred by using several quality criteria. Based on our results, we propose a few test statistics, i.e., random variables on the space of multi-unit spike trains with an appropriate null-hypothesis distribution, to evaluate STPs with less computational and sampling efforts.

neuroscience↗

The effect of data preprocessing on spike correlation analysis results

In recent years, an increasing number of large electrophysiological data sets have become publicly available, thereby providing researchers with the opportunity to analyze spike train data without conducting their own experiments. While this is undoubtedly a positive development, it increases the need for proper documentation on how the data were collected and what preprocessing was performed on the data, since interpreting analysis results in ignorance of these pieces of information can lead to wrong conclusions. An important preprocessing step is the removal of artifacts from the recordings. Electrophysiological recordings are particularly susceptible to electrical cross-talks between recording channels, resulting in artifact spikes that are coincident in multiple channels on the time scale of the data sampling rate, i.e., 1/30 ms in popular setups. The removal by signal whitening is only possible if also the raw sampled data are available, thus to eliminate this type of artifact is to remove all coincident spikes on the recording time scale to definitely avoid artifact spikes. However, given the lack of the "ground truth", this step has the potential to eliminate, in conjunction with the artifacts, components of the data that are pertinent to the research objective. In this study, we use a modified version of the Unitary Event Analysis and demonstrate that such preprocessing results in significantly lower correlations than expected by chance even on longer time scales. We also propose a method to correct for the bias introduced by this preprocessing. Thus, slight changes in the preprocessing have potentially strong impact on analysis results and methods need to consider these effects.

neuroscience↗

Plant-specific tau class glutathione transferases safeguard against lipid oxidation stress through dual detoxification of lipid peroxides and reactive carbonyl species

O_LIOxidation of membrane lipids results in the formation of lipid peroxides (LOOHs) and reactive carbonyl species (RCS), that induce lipid oxidation stress in plants. The plant-specific tau class of glutathione transferases (GSTUs) possess both LOOH peroxidase and RCS-conjugating activities, but their overall contribution to stress tolerance remains unclear. C_LIO_LIWe systematically examined 16 GSTU isozymes of Arabidopsis thaliana and found that all catalysed glutathione-dependent reduction of LOOHs. GSTU17, showing the highest activity, recognized five different isomers of linoleic acid-derived hydroperoxides within comparable catalytic efficiencies. C_LIO_LIT-DNA mutants lacking GSTU3, GSTU17, GSTU18, GSTU19 or GSTU25--isoforms with strong conjugation activities toward acrolein, 4-hydroxynonenal or crotonal--displayed enhanced sensitivity to photooxidative stress, indicating that detoxification of RCS is crucial for oxidative protection. C_LIO_LITranscriptome analyses revealed that exposure to RCS (crotonal, 2-pentenal or 2-hexenal) strongly induced 12 GSTU genes, while other GST classes showed little response. Collectively, these results demonstrate that GSTUs function as a major enzymatic system mitigating lipid oxidation stress in A. thaliana through the combined detoxification of lipid peroxides and their reactive carbonyl products. C_LI

plant biology↗

Humoral immunity induced by LP.8.1 monovalent vaccines against a broad range of SARS-CoV-2 variants including XEC, NB.1.8.1, XFG, and BA.3.2

In the spring of 2025, multiple SARS-CoV-2 Omicron JN.1 subvariants were circulating, with LP.8.1 among the major variants. Pharmaceutical companies such as Pfizer/BioNTech, Moderna, and Novavax/Takeda adopted monovalent LP.8.1 for their 2025-2026 season vaccines, following recommendations issued by the WHO in May 2025. As of November 2025, SARS-CoV-2 variants including LP.8.1, XEC, NB.1.8.1, and XFG--all designated as variants under monitoring--were circulating. In terms of the spike gene, these recent variants as well as LP.8.1 are derived from JN.1. Moreover, BA.3.2, a BA.3 descendant with multiple mutations in the spike gene, has recently emerged and exhibits robust immune evasion. In Japan, the rollout of the LP.8.1-based vaccination has progressed since the end of September 2025. We previously reported the humoral immunity induced by the XBB.1.5-based monovalent vaccine in 2023 and the JN.1-based monovalent vaccine in 2024 in the Japanese population. Here, we investigated the efficiency of humoral immunity induced by two LP.8.1-based vaccines, the mRNA vaccine from Pfizer/BioNTech and the recombinant protein-based vaccine from Novavax/Takeda, in Japan. We performed neutralization assays using sera obtained from individuals who received the LP.8.1 mRNA vaccine from Pfizer/BioNTech (N=29) or the LP.8.1 recombinant protein vaccine from Novavax/Takeda (N=20) with pseudoviruses harboring spike proteins of B.1.1, BA.5, XBB.1.5, JN.1, LP.8.1, XEC, NB.1.8.1, XFG and BA.3.2. In both mRNA and protein-based vaccinee groups, the change in 50% neutralizing titer (NT50) against variants that were predominant before JN.1 (i.e., B.1.1, BA.5 and XBB.1.5) were smaller than those against JN.1 and its subvariants, including LP.8.1, XEC, NB.1.8.1 and XFG. Consistent with recent studies, neutralizing antibodies against BA.3.2 were induced by both vaccines. However, the induction fold change of BA.3.2 was smaller than those of JN.1 and its subvariants. Next, we tested humoral immune response of participants who received both JN.1-based vaccine in 2024 and LP.8.1-based vaccine in 2025 (N=15). Approximately a year after the JN.1-based vaccination, neutralization titer has waned against all variants tested. However, when we compare the NT50s of pre-vaccination sera between 2025 and 2024, those in 2025 against all variants except for B.1.1 were significantly higher than those last year. This suggests that the cross-neutralizing antibodies induced by JN.1-based vaccination were still maintained for a year. Furthermore, the neutralization abilities against the JN.1 sublineages tested and BA.3.2 were significantly reboosted after the LP.8.1-based vaccination. Our study shows immune boosting by the LP.8.1-based vaccine is effective in achieving cross-neutralization against a broad range of JN.1 sublineages in a JN.1-naive population and in recalling waning humoral immunity against these subvariants.

microbiology↗

Osteochondrogenic Transdifferentiation of Vascular Smooth Muscle Cells and Microenvironmental Dynamics in Medial Arterial Calcification

BackgroundVascular calcification, particularly medial arterial calcification (MAC), considerably affects cardiovascular mortality. Current treatments are limited because of the unclear molecular mechanisms of MAC. This study aimed to establish an MAC mouse model using O-ring-induced transverse aortic constriction (OTAC) and to identify critical genes, pathways, and cellular interactions involved in MAC formation by combining lineage tracing technology and single-cell RNsA sequencing (scRNA-seq). MethodsWe developed an OTAC mouse model to mimic MAC. Adult C57BL/6J male mice underwent OTAC, and subsequent analyses were performed at various intervals. Histological and immunohistochemical evaluations were conducted to observe changes in vascular smooth muscle cells (VSMCs). Lineage tracing was used to confirm the origin of osteochondrogenic cells in the tunica media. Additionally, scRNA-seq was performed to capture the dynamic changes in VSMCs and other cell types involved in MAC development. ResultsOsteochondrogenic cells and the subsequent MAC in OTAC mice were observed using histological evaluations. Immunohistochemistry showed time-dependent decreases in -SMA expression and increases in SOX9 and RUNX2 expression in VSMCs. Lineage tracing using Myh11CreERT2;ROSA26-EGFP mice confirmed that osteochondrogenic cells originated from contractile VSMCs. scRNA-seq confirmed osteochondrogenic transdifferentiation of VSMCs and highlighted dynamic changes in surrounding cells involved in calcification-related and inflammatory processes. ConclusionThe OTAC method enabled a comprehensive understanding of the microenvironmental dynamics during MAC progression at the single-cell level. This powerful model provides a robust platform for future therapeutic intervention research. Graphic Abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=140 SRC="FIGDIR/small/684711v1_ufig1.gif" ALT="Figure 1"> View larger version (58K): org.highwire.dtl.DTLVardef@c64634org.highwire.dtl.DTLVardef@12b0b9aorg.highwire.dtl.DTLVardef@106c5b4org.highwire.dtl.DTLVardef@19dd4f4_HPS_FORMAT_FIGEXP M_FIG C_FIG

cell biology↗

Genetic diversity in horseshoe bat ACE2 and sarbecovirus spike proteins mutually shape one another

Angiotensin-converting enzyme 2 (ACE2) serves as the entry receptor for a wide diversity of sarbecoviruses naturally harboured by horseshoe bats (genus Rhinolophus). Despite the extensive circulation of these viruses in many horseshoe bat species, the potential interactions between virus and receptor evolution remain poorly understood. We sampled individuals of the intermediate horseshoe bat (Rhinolophus affinis) across Vietnam and identified 15 genotypes of ACE2 proteins, 10 of which are previously unreported. Phylogenetic analysis and infectivity assays with a panel of 36 sarbecovirus spike proteins indicated that the R. affinis ACE2 phylogeny has geographic structuring and genotypes originating from different geographic regions exhibit distinct infectivity phenotypes. We detected site-specific positive selection on ACE2 site 24 with the associated substitutions largely affecting the receptors sarbecovirus infectivity profile. Together, our findings suggest that the R. affinis within-species ACE2 diversity has likely been shaped through selection by past sarbecovirus infection. Similarly on the virus end, we use mutagenesis assays and structural analysis through cryo-EM, to delineate the proximal evolution of the Ra22QT77 spike defined by specialization to the ACE2 genotypes of horseshoe bats found in and near southern Vietnam, where the virus was sampled. Our findings contribute to a better understanding of host-sarbecovirus co-evolution dynamics and provide valuable insights into the receptor usage determinants of these viruses. HighlightsO_LIWe identify a total of 15 ACE2 genotypes in R. affinis bats from Vietnam. C_LIO_LIACE2 intraspecific polymorphism is geographically separated and associated with distinct sarbecovirus infectivity. C_LIO_LISite 24 of R. affinis ACE2 experiences positive selection and controls susceptibility to sarbecoviruses. C_LIO_LIBat ACE2s and sarbecovirus spikes are bidirectionally shaped by each others evolution. C_LI

microbiology↗

Camsap3-Mediated Microtubules Maintain Transzonal Projections Essential for Germline-Soma Communication during Ovarian Follicle Maturation in Mice

Oocytes are surrounded and nursed by layers of maternal somatic granulosa cells (GCs) in ovarian follicles. Within a follicle, GCs extend actin-containing transzonal projections (TZPs) to an oocyte across the zona pellucida to establish communication. In contrast, microtubules have rarely been observed in some TZPs, and their significance in TZP organisation and functions for follicular maturation remain largely unknown. Here, using super-resolution microscopy, we visualised the presence of microtubules alongside F-actin in most TZPs. Knockout (KO) mice of the microtubule minus-end binding protein Camsap3 (calmodulin-regulated spectrin-associated protein 3) exhibited infertility with fewer developing late-stage follicles. In earlier stages of Camsap3-KO follicles, the number of TZPs was reduced compared to that in wild-type follicles, and microtubules in TZPs were disorganised, which led to a decrease in physical contact between GCs and oocytes. We also found that TZP morphology in wild-type follicles transforms over time during follicle development, and Camsap3 modulates TZP morphology by assisting the organisation of microtubules as well as F-actin. Our findings thus suggest that Camsap3-mediated microtubules play a crucial role in governing the number and morphology of TZPs to ensure successful follicle development for the production of fertile oocytes.

cell biology↗

Integrative modeling of seasonal influenza evolution via AI-powered antigenic cartography

Seasonal influenza viruses evade host immunity through rapid antigenic evolution. Antigenicity is assessed by serological assays and typically visualized as antigenic maps, which represent antigenic differences among virus strains. However, conventional maps cannot directly infer the antigenicity of unexamined variants from their genotypes. Here, we present PLANT, a protein language model that projects influenza A/H3N2 viruses onto an antigenic map using HA protein sequences. Using PLANT-based cartography, we show that (i) H3N2 antigenic evolution accelerates during periods of disrupted global circulation, (ii) antigenic novelty accounts for a substantial portion of viral fitness advantage, and (iii) vaccine strains are often antigenically distant from circulating viruses. We further propose a PLANT-based framework for selecting vaccine strains with improved antigenic match than the WHO-recommended strains. This study provides a statistical foundation for integrated modeling of viral genotype, antigenicity, and fitness, offering quantitative insights into seasonal influenza virus evolution and supporting rational vaccine design.

microbiology↗

A non-spike nucleocapsid R204P mutation in SARS-CoV-2 Omicron XEC enhances inflammation and pathogenicity

The global circulation of SARS-CoV-2 in human populations has driven the emergence of Omicron subvariants, which have become highly diversified through recombination. In late 2024, SARS-CoV-2 Omicron XEC variant emerged from the recombination of two JN.1 progeny, KS.1.1 and KP.3.3, and became predominant worldwide. Here, we investigated virological features of the XEC variant. Epidemic dynamics modeling suggested that spike substitutions in XEC mainly contribute to its increased viral fitness. Additionally, four licensed antivirals were effective against XEC. Although the fusogenicity of XEC spike is comparable to that of the JN.1 spike, the intrinsic pathogenicity of XEC in hamsters was significantly higher than that of JN.1. Notably, we found that the nucleocapsid R204P mutation of XEC enhanced inflammation through NF-{kappa}B activation. Recent studies suggest that the evolutionary potential of spike protein is reaching its limit. Indeed, our findings highlight the critical role of non-spike mutations in the future evolution of SARS-CoV-2.

microbiology↗

Molecular basis of sarbecovirus evolution and receptor tropism in natural hosts, potential intermediate hosts, and humans

The spike protein of many sarbecoviruses binds to the angiotensin-converting enzyme 2 (ACE2) receptor and facilitates viral entry. The diversification of the sarbecovirus spike gene and the mammalian ACE2 gene suggests that sarbecoviruses and their hosts have co-evolved, and the genetic diversity in these genes affects the host tropism of sarbecoviruses. Better comprehending the evolutionary potential of sarbecoviruses can lead to preparedness for the next pandemic. However, the host tropism of sarbecoviruses is not fully understood. Here, we performed round-robin pseudovirus infection assays using 53 sarbecoviruses and ACE2s from 17 mammals to elucidate the ACE2 tropism of sarbecoviruses in natural hosts, potential intermediate hosts and humans. We determined the factors responsible for the ACE2 tropism of sarbecoviruses through structural, phylogenetic analyses, and infection experiments, revealing which substitutions can expand the host range of sarbecoviruses. These results highlight the mechanisms modulating host tropism throughout sarbecovirus evolution.

microbiology↗

Inferring context-specific site variation with evotuned protein language models

Multiple sequence alignments (MSAs) have been traditionally used for making inferences about site-specific diversity in proteins. Recent advancements in the field of artificial intelligence have highlighted the potential of protein language models (pLMs) to capture similar protein properties. Unlike MSAs, pLMs can make inferences from single sequences, without the need for a set of aligned sequences. In this study, we introduce a novel, pLM-based metric, termed pLM entropy, to assess protein site conservation and variability. We test this metric using versions of two popular pLMs (ESM-2 and protT5) fine-tuned on the diversity of different Influenza A virus serotype hemagglutinin proteins. Our study demonstrates how our pLM entropy metric can capture which sites are more likely to change in a specific sequence context and how fine-tuning pLMs on a set of evolutionarily related proteins (evotuning) can improve the models understanding of the groups diversity.

evolutionary biology↗