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Ferraz, T.

Publications and source records attributed to Ferraz, T..

4 recordsLinked to original sources

Exploring the Evolution of the Cariogenic Oral Pathobiont Streptococcus mutans Using Ancient DNA

The oral pathobiont Streptococcus mutans can contribute to dental caries development through metabolism of dietary carbohydrates. Adoption of carbohydrate-rich agricultural diets is associated with increased prevalence of dental caries in archaeological populations; however, the evolutionary impact of changing subsistence strategies on cariogenic microbes like S. mutans remains to be explored. Here, we use a novel hybridization capture reagent to generate genome-wide ancient DNA data from a global set of 75 S. mutans strains spanning the last 8,000 years. Most virulence-associated genes predate the origins of agriculture; however, we highlight loci regulating genetic competence, bacteriocin production, and biofilm formation which are absent in 5 strains from pre-agricultural ancient hunter-gatherers, suggesting that their acquisition may have been associated with adaptation to carbohydrate-rich agricultural diets. Together, our study highlights ancient DNA as a promising tool for exploring the dynamic interplay between subsistence strategy, microbes, and dental pathology in human populations through time.

evolutionary biology↗

Combined Metabolic and Viral Insults in Pregnancy Disrupt Specific Placental Nutrient Transporter Systems in Mice

The placenta adapts to support nutrient transport to meet the demands of the growing fetus. Maternal obesity and viral infection are associated with adverse fetoplacental development. How co-exposure affects placental morphology and nutrient transport across gestation remains unclear. We hypothesise that co-exposure would have a greater impact on placental morphology and nutrient transporter expression than either of the exposures alone. C57BL/6J mice were fed a control (CON) or high-fat (HF) diet before and throughout pregnancy and exposed to poly(I:C) or vehicle at gestational days (GD) 12.5, 15.5, or 18.5. Placental morphology, folate and fatty acid transporter mRNA expression and localisation were evaluated by haematoxylin and eosin staining, immunohistochemistry (reported as % immunoreactivity (ir)-area stained), and qPCR, respectively. At GD12.5, HF diet associated with reduced junctional zone (JZ) and labyrinth zone (LZ) area and increased maternal blood space, followed by reduced fetal blood space at GD15.5 and increased JZ and LZ area size by GD18.5. HF diet and viral infection independently associated with increased placental Fat/Cd36 mRNA expression at GD12.5. However, HF diet and infection associated with increased ir-FR- while HF diet alone decreased ir-PCFT at GD12.5. By GD15.5, HF diet associated with reduced placental ir-FR- but increased ir-PCFT. At GD18.5, infection associated with reduced Rfc1 mRNA expression. HF diet and infection associated with greater prevalence of SGA and LGA fetuses, particularly at GD18.5. Obesity and infection independently and synergistically disrupted placental morphology and nutrient transporter expression in a zone- and gestational age-specific manner, with consequences for fetal growth across gestation.

developmental biology↗

Maternal High Fat Diet and Acute Viral Mimic Exposure Impact Placental Inflammation, Lipid Peroxidation, and Cellular Dynamics Across Mouse Pregnancy

Maternal obesity and viral infection induce placental inflammation, but how their co-exposure influence fetoplacental development remains unclear. We hypothesized that maternal high fat (HF) diet and viral infection would independently induce placental inflammation and lipid peroxidation, reduce antioxidant defence, and cellular turnover. Further, HF diet would compromise placental capacity to adapt to infection. Female C57BL/6J mice were fed a control (CON) or 62% HF diet six weeks before and throughout pregnancy and injected with poly(I:C) (viral mimic) or vehicle (VEH) 24h before sacrifice at gestational days (GD) 12.5, 15.5, and 18.5 (n=5-8/group/GD). Placental inflammasome (NLRP3), oxidative stress (4-HNE), antioxidant defence (GPx-4), and cellular proliferation-to-death ratio (Ki-67, Caspase-3) were assessed by immunohistochemistry, and mRNA expression of Tlr3, Irf3, Tlr4, Tirap, and Il-1{beta} were measured by qPCR. Data were analysed by linear mixed models (p[≤]0.05). At GD12.5, infection was associated with increased Tlr3 mRNA and immunoreactive (ir)-4-HNE, and reduced ir-GPx-4 expression in the placental labyrinth zone (LZ). By GD15.5, HF diet was associated with increased ir-NLRP3 in both LZ and junctional zones (JZ). Exposure to infection alone and co-exposure to HF diet and infection further increased LZ ir-NLRP3. At GD18.5, HF diet was associated with increased Tirap and Il-1{beta} mRNA expression, ir-4-HNE in the JZ and ir-Caspase-3 in the LZ. Maternal HF diet and infection exert distinct effects on the placenta across gestation, suggesting that maternal overnutrition might reduce the placentas capacity to handle adverse exposures, which may increase susceptibility to poor fetal outcomes.

developmental biology↗

Rapid expansion of synaptic complexity as a key contributor to cognitive growth in early humans

Primates have been evolving for over 50 million years. At some point, humans made an unusually large evolutionary leap, giving rise to abilities like the creation of tools, intricate art and complex language. The neuronal synapse, a key player in information processing and brain plasticity, has largely been ignored as a potential factor in this process. Here we used the genomic databases of ancestral hominins to compare the expression levels of 995 genes expressed in the human nervous system among archaic (6 Neanderthal, 2 Denisovan) and modern humans (62 African Modern Human). We searched in the 95th top p-value for variants whose derived alleles had a frequency [&ge;]90% in modern and <10% in archaic humans. We then used the STRING database to perform protein-protein interaction networks on the 95th top p-value for the variants. We identified genetic variants in 15 genes, and in two (STX16 and UBASH3B), the allele frequency was significantly higher in modern versus archaic humans. These genes have previously been associated with critical cellular (proliferation, differentiation, migration, survival) and synaptic (exocytosis, synaptic vesicle fusion) processes, supporting the idea that changes in synaptic structure and function may have played a key role in the development of human cognition.

evolutionary biology↗