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Barrero, R. A.

Publications and source records attributed to Barrero, R. A..

2 recordsLinked to original sources

VIPER-seq: Protein-mediated small RNA enrichment enhances plant virus detection at low viral abundance

Early and accurate detection of viral infections is critical for effective disease management and biosecurity programs. High-throughput sequencing technologies have emerged as powerful tools for plant disease diagnostics. In particular, sequencing of virus-derived small RNAs (vsiRNAs) enables the simultaneous detection of both known and novel viral agents. Compared with other approaches, small RNA sequencing (sRNA-seq) can offer superior sensitivity because it is less affected by the abundance of host messenger and ribosomal RNAs (mRNA and rRNA, respectively), and because sRNAs are generally more stable than longer RNA molecules. However, the sensitivity of sRNA-seq can be compromised by the presence of abundant endogenous small RNAs, which dilute the viral signal and hinder pathogen detection, particularly in low-titre infections. Here, we present VIPER-seq (Viral small RNA Isolation by Protein-mediated Enrichment and Recovery sequencing), a method that exploits sRNA-binding proteins to enrich vsiRNAs prior to high-throughput sequencing. Using cucumber seeds infected with cucumber green mottle mosaic virus (CGMMV), we demonstrate that VIPER-seq substantially enhances the detection of infected plant material compared with conventional sRNA-seq. The increased sensitivity is particularly evident under low-titre infection conditions, demonstrating the utility of VIPER-seq for the early detection of viral infections and its potential to strengthen plant disease diagnostics, seed health testing, and biosecurity surveillance programs.

molecular biology↗

Temperature alters gene expression in mosquitoes during arbovirus infection

Arthropod-borne viruses (arboviruses) such as dengue, Zika and chikungunya constitute a significant proportion of the global disease burden. The principal vector of these pathogens is the mosquito Aedes (Ae.) aegypti, and its ability to transmit virus to a human host is influenced by environmental factors such as temperature. However, exactly how ambient temperature influences virus replication within mosquitoes remains poorly elucidated, particularly at the molecular level. Here, we use chikungunya virus (CHIKV) as a model to understand how the host mosquito transcriptome responds to arbovirus infection under different ambient temperatures. We exposed CHIKV-infected mosquitoes to 18 {degrees}C, 28 {degrees}C and 32 {degrees}C, and found higher temperature correlated with higher virus replication levels, particularly at early time points post-infection. Lower ambient temperatures resulted in reduced virus replication levels. Using RNAseq, we found that temperature significantly altered gene expression levels in mosquitoes, particularly components of the immune response. The highest number of significantly differentially expressed genes in response to CHIKV was observed at 28 {degrees}C, with a markedly more muted effect observed at either lower (18 {degrees}C) or higher (32 {degrees}C) temperatures. At the higher temperature, the expression of many classical immune genes, including Dicer-2 in the RNAi pathway, was not substantially altered in response to CHIKV. Upregulation of Toll, IMD and JAK-STAT pathways was only observed at 28 {degrees}C. Time post infection also led to substantially different gene expression profiles, and this effect varied depending upon the which temperature mosquitoes were exposed to. Taken together, our data indicate temperature significantly modulates mosquito gene expression in response to infection, potentially leading to impairment of immune defences at higher ambient temperatures.

microbiology↗