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Biology subjects

de Brito, A. F.

Publications and source records attributed to de Brito, A. F..

2 recordsLinked to original sources

Viral metagenomics of synanthropic urban bats: a surveillance strategy for uncovering potentially zoonotic viruses

Bats are natural reservoirs for diverse viruses, including coronaviruses, filoviruses, and paramyxoviruses, many leading to zoonotic spillover events and demanding an integrated surveillance. Here, we present a framework that leverages Brazils rabies passive surveillance program to detect bat-borne viruses. Using an algorithm to select representative specimens from 2,422 bats collected across Sao Paulo state, we submitted 150 paired lung and intestine samples to nanopore metagenomic sequencing. We detected 98 viral contigs from 12 families of public health relevance, including Arenaviridae, Coronaviridae, and Paramyxoviridae. Notably, the approach identified a previously unknown filovirus in bats in the Americas, validating the frameworks capacity for epidemic preparedness. These findings reveal an undetected viral diversity and demonstrate how existing animal surveillance can monitor pathogen threats. Crucially, in a workshop involving multisectoral One Health experts in Brazil, this framework was validated as a scalable model for national expansion, adapted for low- and middle-income countries (LMICs). One-sentence summary lineThe study introduces a viral surveillance method using metagenomics in bats, offering a scalable, cost-effective model for operationalizing One Health surveillance, especially relevant to low- and middle-income countries.

genomics↗

Sensing soluble uric acid by Naip1-Nlrp3 platform

The immune system can recognize microbes and sterile tissue damage. Among the damage-associated molecular patterns (DAMPs), uric acid is considered a major component which can trigger inflammation. It represents a breakpoint in the evolutionary history of humans as our ancestors lost the uricase gene, the enzyme responsible for its cleavage. High soluble uric acid (sUA) concentration is able to increase IL-1{beta} in murine, but not human macrophages. We observed that sUA increased the mRNA expression of Naip1 in murine macrophages, and, therefore, we hypothesized that the recognition of sUA can be made by a Naip1-Nlrp3 inflammasome platform. Additionally, we used genome-wide transcriptome analysis, functional analyses and structural modeling predictions and observed that virus-transduction of murine Naip1 into human macrophages induced IL-1{beta} after sUA stimulus, besides leading to fatty acid production and an inflammation-related response. Moreover, pharmacologic inhibition and genetic loss of Nlrp3 led to decreased IL-1{beta} production upon sUA stimulus. Surface plasmon resonance and quartz crystal microbalance showed that sUA is able to interact with Naip1. Naip could be a lost receptor for sUA in the evolutionary process and a better understanding of the immune modulatory function of sUA could lead to design rational novel anti-hyperuricemic therapies.

immunology↗