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maaroufi, H.

Publications and source records attributed to maaroufi, H..

4 recordsLinked to original sources

Certain Aquatic Eukaryotes Harbor an OLD-Like Immune Defense System

Key elements of eukaryotic antiviral immunity are evolutionarily conserved with prokaryotic anti-phage defense systems. The Overcoming Lysogenization Defect (OLD) anti-phage defense system is well characterized in prokaryotes but has remained unknown in eukaryotes. Here, the old-like genes are identified in certain aquatic eukaryotes, including the SAR supergroup, Filasterea, Chytridiomycota, and some metazoan lineages (Placozoa, Cnidaria, Spiralia, Hemichordata, and Cephalochordata). Within molluscs, old-like genes are present in bivalves but absent in gastropods and cephalopods. Interestingly, the filasterean Capsaspora owczarzaki, an endosymbiont of the gastropod Biomphalaria glabrata, encodes putative secreted OLD-like proteins, suggesting it may provide its host with symbiont-mediated antiviral protection. Genomic and transcriptomic analyses revealed that old-like genes vary in copy and intron number and are expressed in some eukaryotic lineages. OLD-like proteins retain key structural features but exhibit a different topology from that of prokaryotes. Structural predictions reveal homodimeric dsDNA-bound architectures analogous to that of the Bacillus cereus VD045 GajA OLD homodimer. Furthermore, phylogenetic analysis divided OLD-like proteins into three distinct clusters, one of which likely represents an ancient inheritance from the ancestral Promethearchaeota (formerly Asgard archaea) host. Together, these findings highlight an unexpected presence of old-like genes in certain aquatic eukaryotes, offering new insights into their evolutionary history and potential role in antiviral defense.

bioinformatics↗

The N764K and N856K mutations in SARS-CoV-2 Omicron S protein generate potential cleavage sites for SKI-1/S1P protease

Spike (S) protein is a key protein in coronaviruses life cycle. SARS-CoV-2 Omicron BA.1 variant of concern (VoC) presents an exceptionally high number of 30 substitutions, 6 deletions and 3 insertions in the S protein. Recent works revealed major changes in the SARS-CoV-2 Omicron biological properties compared to earlier variants of concern (VoCs). Here, these major changes could be explained, at least in part, by the mutations N764K and/or N856K in S2 subunit. These mutations were not previously detected in other VoCs. N764K and N856K generate two potential cleavage sites for SKI-1/S1P serine protease, known to cleave viral envelope glycoproteins. The new sites where SKI-1/S1P could cleave S protein might impede the exposition of the internal fusion peptide for membrane fusion and syncytia formation. Based on the human protein atlas, SKI-1/S1P protease is not found in lung tissues (alveolar cells type I/II and endothelial cells), but present in bronchus and nasopharynx. This may explain why Omicron has change of tissue tropism. Viruses have evolved to use several host proteases for cleavage/activation of envelope glycoproteins. Mutations that allow viruses to change of protease may have a strong impact in host range, cell and tissue tropism, and pathogenesis.

bioinformatics↗

SARS-CoV-2 Encodes a PPxY Late Domain Motif that is Known to Enhance 1 Budding and Spread in Enveloped RNA Viruses

The current COVID-19 (Coronavirus Disease-2019) pandemic is affecting the health and/or socioeconomic welfare of almost everyone in the world. Finding vaccines and therapeutics is therefore urgent, but elucidation of the molecular mechanisms that allow some viruses to cross host species boundaries, becoming a threat to human health, must also be given close attention. Here, analysis of all proteins of SARS-CoV-2 revealed a unique PPxY Late (L) domain motif, 25PPAY28, in a spike (S) protein inside a predicted hot disordered loop subject to phosphorylation and binding. PPxY motifs in enveloped RNA viruses are known to recruit Nedd4 E3 ubiquitin ligases and ultimately the ESCRT complex to enhance virus budding and release, resulting in higher viral loads, hence facilitating new infections. Interestingly, proteins of SARS-CoV-1 do not feature PPxY motifs, which could explain why SARS-CoV-2 is more contagious than SARS-CoV-1. Should an experimental assessment of this hypothesis show that the PPxY motif plays the same role in SARS-CoV-2 as it does in other enveloped RNA viruses, this motif will become a promising target for the development of novel host-oriented antiviral therapeutics for preventing S proteins from recruiting Nedd4 E3 ubiquitin ligase partners.

bioinformatics↗

Novel anionic cecropins from the spruce budworm feature a poly-L-aspartic acid C-terminus

Cecropins form a family of amphipathic -helical cationic peptides with broad-spectrum antibacterial properties and potent anticancer activity. The emergence of bacteria and cancer cells showing resistance to cationic antimicrobial peptides (CAMPs) has fostered a search for new, more selective and more effective alternatives to CAMPs. With this goal in mind, we looked for cecropin homologs in the genome and transcriptome of the spruce budworm, Choristoneura fumiferana. Not only did we find paralogs of the conventional cationic cecropins (Cfcec+), our screening also led to the identification of previously uncharacterized anionic cecropins (Cfcec-), featuring a poly-L-aspartic acid C-terminus. Comparative peptide analysis indicated that the C-terminal helix of Cfcec- is amphipathic, unlike that of Cfcec+, which is hydrophobic. Interestingly, molecular dynamics simulations pointed to the lower conformational flexibility of Cfcec- peptides, relative to that of Cfcec+. Phylogenetic analysis suggests that the evolution of distinct Cfcec+ and Cfcec- peptides may have resulted from an ancient duplication event within the Lepidoptera. Our analyses also indicated that Cfcec- shares characteristics with entericidins, which are involved in bacterial programmed cell death, lunasin, a peptide of plant origins with antimitotic effects, and APC15, a subunit of the anaphase-promoting complex. Finally, we found that both anionic and cationic cecropins contain a BH3-like motif (G-[KQR]-[HKQNR]-[IV]-[KQR]) that could interact with Bcl-2, a protein involved in apoptosis; this observation is congruent with previous reports indicating that cecropins induce apoptosis. Altogether, our observations suggest that cecropins may provide templates for the development of new anticancer drugs. Graphical abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=70 SRC="FIGDIR/small/307702v2_ufig1.gif" ALT="Figure 1"> View larger version (23K): org.highwire.dtl.DTLVardef@ba988dorg.highwire.dtl.DTLVardef@757d76org.highwire.dtl.DTLVardef@18009b5org.highwire.dtl.DTLVardef@fd71d3_HPS_FORMAT_FIGEXP M_FIG C_FIG HighlightsO_LIGenes encoding novel anionic cecropins (Cfcec-), featuring a C-terminal poly-L-aspartic acid, were found in the genome of the spruce budworm, Choristoneura fumiferana. C_LIO_LIDivergence between Cfcec+ and Cfcec- could be the result of an ancient duplication event within the Lepidoptera. C_LIO_LIThere is an apparent relationship between motifs observed in cecropin peptides and apoptosis. C_LIO_LIAnionic cecropins from the spruce budworm display characteristics suggesting they could have anticancer activity C_LI

bioinformatics↗