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Patrick, B.

Publications and source records attributed to Patrick, B..

2 recordsLinked to original sources

Wild communities of Morpho butterflies reveal Spiroplasma endosymbiont with inflated genome size and peculiar evolution

AbstractThe evolution of endosymbiont genomes is likely influenced by the ecological interactions with their hosts. Here, we studied the evolution of Spiroplasma genomes, as well as their transmission patterns within and between Morpho butterflies sampled in the wild. Spiroplasma was detected in 4 out of 11 Morpho species studied and displayed a 3 times larger genome size as compared to Spiroplasma genomes documented in other hosts. This inflation in genome size is caused by massive and recent expansion of various mobile genetic elements and by the acquisition of new genes stemming from prophages. Interestingly, these new Spiroplasma genomes also revealed a peculiar evolution of toxin genes in plasmids that may enhance host resistance to parasites. Phylogenetic comparisons with Spiroplasma extracted from other plant and insect host suggest multiple independent colonization of Lepidoptera by Spiroplasma, and probable horizontal exchanges among distantly-related butterfly species occurring in South America. In contrast, resequencing data obtained for multiple populations of the two sister-species M. helenor and M. achilles living in sympatry over the majority of their distribution revealed an opposite prevalence (97% in M. achilles and 3% in M. helenor), suggesting low levels of transmission between these sympatric host- species. Reconciliation analysis of the phylogenetic relationships of mitochondrial genomes within M. achilles and Spiroplasma strains furthermore confirms predominant vertical transfers of the endosymbiont within species. Altogether, our results indicate persistent interactions between Spiroplasma symbiont and some Morpho species, as well as contrasted prevalence among sympatric host-species, consistent with an evolution of ecological interactions between the endosymbiont and its different hosts that may modify their genomic evolution.

evolutionary biology↗

Maternal diet disrupts the placenta-brain axis in a sex-specific manner

High maternal weight is associated with a number of detrimental outcomes in offspring, including increased susceptibility to neurological disorders such as anxiety, depression, and communicative disorders (e.g. autism spectrum disorders)1-8. Despite widespread acknowledgement of sex-biases in the prevalence, incidence, and age of onset of these disorders, few studies have investigated potential sex-biased mechanisms underlying disorder susceptibility. Here, we use a mouse model to demonstrate how maternal high-fat diet, one contributor to overweight, causes endotoxin accumulation in fetal tissue, and subsequent perinatal inflammation influences sex-specific behavioral outcomes in offspring. In male high-fat diet offspring, increased macrophage toll like receptor 4 signaling results in excess phagocytosis of serotonin neurons in the developing dorsal raphe nucleus, decreasing serotonin bioavailability in the fetal and adult brain. Bulk sequencing from a large cohort of matched first trimester human fetal brain, placenta, and maternal decidua samples reveals sex-specific transcriptome-wide changes in placenta and brain tissue in response to maternal triglyceride accumulation (a proxy for dietary fat content). Further, we find that fetal brain serotonin levels decrease as maternal dietary fat intake increases in males only. These findings uncover a microglia-dependent mechanism through which maternal diet may impact offspring susceptibility for neuropsychiatric disorder development in a sex-specific manner.

neuroscience↗