Biology subjects

Desnues, C.

Publications and source records attributed to Desnues, C..

5 recordsLinked to original sources

bioRxiv2022

"Quasigenus" among Phycodnaviridae: A diversity of chlorophyte-infecting viruses in response to a dense algal culture in a high-rate algal pond.

This study approaches a high rate algal pond (HRAP) culture by metagenomic sequencing of the viral DNA fraction, this includes the so-called giant virus fraction (phylum Nucleocytoviricota), with the goal of revealing viruses coexisting within an intensified algal culture. A wealth of interesting novel viruses is revealed, including members of Nucleocytoviricota, Lavidaviridae, and polinton-like viruses, which are taxa containing previously characterized algal viruses. Our sequencing results are coupled with a virus targeted qPCR study and 18S rDNA metabarcoding to elucidate potential virus-host interactions. Several species of green algae are identified (Chlorophyta), likely representing the alternating dominant populations during the year of study. Finally, we observe a bloom of viral diversity within the family Phycodnaviridae (Nucleocytoviricota), including highly related but non-identical genotypes, appearing in the HRAP in September and October 2018. This bloom is most likely the cause of a mass mortality event of the cultured algae that occurred during these same months. We hypothesize that these related Phycodnaviridae lineages selectively infect different strains of the same algal species of the Genus Picochlorum that have been identified in the HRAP by metabarcoding and coined this phenomenon a "quasigenus" by analogy to the RNA virus quasispecies concept.

evolutionary biology↗

bioRxiv2022

Integrated viral elements unveil the dual lifestyle of Tetraselmis spp. polinton-like viruses

In this study, we aimed at exploring horizontal gene transfer between viruses and Chlorodendraceae green algae (Chlorophyta) using available genomic and transcriptomic sequences for 20 algal strains. We identified a significant number of genes sharing a higher sequence similarity with viral homologues, thus signaling their possible involvement in HGTs with viruses. Further characterization showed that many of these genes were clustered in DNA regions of several tens to hundreds of kilobases in size, originally belonging to viruses related to known Tetraselmis spp. viruses (TetV and TsV). In contrast, the remaining candidate HGT genes were randomly dispersed in the algal genomes, more frequently transcribed and belonged to large multigene families. The presence of homologs in Viridiplantae suggested that these latter were more likely of algal rather than viral origin. We found a remarkable diversity Polinton- like virus (PLV) elements inserted in Tetraselmis genomes, all of which were most similar to the Tetrasemis striata virus TsV. The genes of PLV elements are transcriptionally inactive with the notable exception of the homologue of the TVSG_00024 gene of TsV whose function is unknown. We suggest that this gene may be involved in a sentinel process to trigger virus reactivation and excision in response to an environmental stimulus. Altogether, these results provide evidence that TsV- related viruses have a dual lifestyle, alternating between a free viral phase (i.e., virion) and a phase integrated into host genomes.

microbiology↗

bioRxiv2022

Identification of a new Inovirus in the absence of bacterial infection in the human virome

Viruses infecting bacteria, known as bacteriophages, represent the most abundant viral particles in the human body. They participate in the control of the human associated bacterial communities and play an important role in the dissemination of virulence genes. Here we present the identification of a new genetic element, named RIP1, in the human virome. RIP1 shares conserved structural genes with the single-stranded DNA viruses of the Inoviridae family. Furthermore structure-function studies identified nuclear subcellular localization of the RIP1 DNA replication/recombination machinery. Additional metagenomics analysis and polymerase chain reaction detected RIP1 in multiple body sites including blood, cerebrospinal pericardial and amniotic fluids, nasal swabs and feces in the absence of concomitant bacterial infection, uncovering inovirus phage persistence in the human virome.

microbiology↗

bioRxiv2019

Global Genetic Cartography of Urban Metagenomes andAnti-Microbial Resistance

We have created a global atlas of 4,728 metagenomic samples from mass-transit systems in 60 cities across 3 years. This is the first systematic, worldwide study cataloging the urban microbial ecosystem. We identify taxonomically-defined microorganisms collected across three years. This atlas provides an annotated, geospatial profile of microbial strains, functional characteristics AMR markers, and novel genetic elements, including 10,928 viral, 1302 bacteria, and 2 archaea novel species. We identify 4,424 species of urban microorganisms and a consistent "core" of 31 species found in nearly all samples that is largely distinct from any human commensal microbiome. Profiles of AMR genes show geographic variation in type and density. Together, these results constitute a high-resolution, global metagenomic atlas, which enables the discovery of new genetic components, highlights potential forensic applications, and provides an essential first draft of the global AMR burden of the worlds cities.

microbiology↗

bioRxiv2019

Global phylogeography and ancient evolution of the widespread human gut virus crAssphage

Microbiomes are vast communities of microbes and viruses that populate all natural ecosystems. Viruses have been considered the most variable component of microbiomes, as supported by virome surveys and examples of high genomic mosaicism. However, recent evidence suggests that the human gut virome is remarkably stable compared to other environments. Here we investigate the origin, evolution, and epidemiology of crAssphage, a widespread human gut virus. Through a global collaboratory, we obtained DNA sequences of crAssphage from over one-third of the worlds countries, and showed that its phylogeography is locally clustered within countries, cities, and individuals. We also found colinear crAssphage-like genomes in both Old-World and New-World primates, challenging genomic mosaicism and suggesting that the association of crAssphage with primates may be millions of years old. We conclude that crAssphage is a benign globetrotter virus that may have co-evolved with the human lineage and an integral part of the normal human gut virome.

microbiology↗