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Charrel, R. N.

Publications and source records attributed to Charrel, R. N..

3 recordsLinked to original sources

Newly identified genomic sequences establish benchmarks for proposed taxonomic classification of jingmenviruses

Jingmenviruses are a group of viruses related to orthoflaviviruses characterized by a segmented genome and multipartite organisation that have been detected worldwide in a wide range of hosts. As next-generation sequencing has become more affordable, increasing numbers of large-scale metagenomics studies have been published, alongside raw sequencing data. With the growing number of new jingmenvirus sequences identified in metagenomics data, it can be difficult to assess whether a new sequence is associated to a new virus species or to a strain of an existing species. In order to propose clear classification criteria for this group, we assembled a large jingmenvirus sequence database, from published and newly assembled sequences. Indeed, we screened data from studies that did not search for or report jingmenvirus sequences, looking for new strains of known jingmenvirus species. We then performed multiple sequence alignments and used the inferred percentage identity values to determine demarcation criteria based on the distribution of evolutionary distances upon pairwise comparisons. We report the identification of almost 60 libraries containing jingmenvirus sequences, in a wide range of sample types and geographical locations. Using these data and published jingmenvirus sequences, we have determined that to classify jingmenvirus sequences into virus species, at least four segments are required, on which eight cut-off values in percentage identity (nucleotide and amino acid) are used for demarcation. The ratification of this proposal would enhance consistency in virus taxonomy and provide a standardized framework for comparative genomics studies of jingmenviruses, a group that is yet under-characterised. ImportanceThere are currently no guidelines to classify jingmenvirus sequences which means sequences are associated to species with no ratified rationale, which can result in missed opportunities at better describing jingmenvirus genomics. In this study we propose criteria to provide a parsimonious framework for classifying jingmenvirus species based on current knowledge, and allow us to propose re-classification of some sequences and to identify outlier sequences which we recommend should be further characterised in vitro.

genomics↗

Detection of porcine enteric viruses (Kobuvirus, Mamastrovirus and Sapelovirus) in domestic pigs in Corsica, France

Many enteric viruses are found in pig farms around the world and can cause death of animals or important production losses for breeders. Among the wide spectrum of enteric viral species, porcine Sapelovirus (PSV), porcine Kobuvirus (PKoV) and porcine Astrovirus (PAstV) are frequently found in pig feces. In this study we investigated sixteen pig farms in Corsica, France, to evaluate the circulation of three enteric viruses (PKoV, PAstV-1 and PSV). In addition to the three viruses studied by RT-qPCR (908 pig feces samples), 26 stool samples were tested using the Next Generation Sequencing method (NGS). Our results showed viral RNA detection rates (i) of 62.0% [58.7-65.1] (n = 563/908) for PSV, (ii) of 44.8% [41.5-48.1] (n = 407/908) for PKoV and (iii) of 8.6% [6.8-10.6] (n = 78/908) for PAstV-1. Significant differences were observed for all three viruses according to age (P-value = 2.4e-13 for PAstV-1; 2.4e-12 for PKoV and 0.005 for PSV). The type of breeding was significantly associated with RNA detection only for PAstV-1 (P-value = 9.6e-6). Among the 26 samples tested with NGS method, consensus sequences corresponding to 10 different species of virus were obtained This study provides first insight on the presence of three common porcine enteric viruses in France. We also showed that they are frequently encountered in pigs born and bred in Corsica, which demonstrates endemic local circulation. ImportanceThis study provides important information in the comprehension of the epidemiology of different viruses circulating in swine farms. We have shown the great diversity of viruses that could be present in extensive farms. Moreover, to our knowledge, this is the first detection of these different viruses in France. So far, this study has to be considered as a first step in the study of enteric viruses in Corsican pig farms.

molecular biology↗

Evaluation of heating and chemical protocols for inactivating SARS-CoV-2

Clinical samples collected in COVID-19 patients are commonly manipulated in BSL-2 laboratories for diagnostic purpose. We used the French norm NF-EN-14476+A2 derived from the European standard EN-14885. To avoid the risk of exposure of laboratory workers, we showed that Triton-X100 must be added to guanidinium thiocyanate-lysis buffers to obtain a 6-log reduction of infectious virus. Although heating protocol consisting of 92{degrees}C-15min was more effective rather than 56{degrees}C-30min and 60{degrees}C-60min to achieve 6-log reduction, it is not amenable for molecular detection on respiratory specimens because of important decrease of detectable RNA copies in the treated sample vs untreated sample. The 56{degrees}C-30min and 60{degrees}C-60min should be used for inactivation of serum / plasma samples for serology because of the 5log10 reduction of infectivity and low viral loads in blood specimens.

microbiology↗