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Barros, G.

Publications and source records attributed to Barros, G..

2 recordsLinked to original sources

Incorporation of ChiA into AcMNPV occlusion bodies and its implications for oral infectivity

Baculoviruses are insect-specific viruses primarily employed in biological pest control and recombinant protein expression. As biopesticides, they offer numerous advantages over chemical pesticides and hold significant potential for application in integrated pest management (IPM). However, their slower action compared to conventional synthetic strategies has limited their widespread adoption. This study aimed to investigate the impact of incorporating a viral protein, AcChiA chitinase, which disrupts the gut peritrophic membrane of susceptible insects, into AcMNPV occlusion bodies in trans. This was achieved through the development of an insect cell line that facilitates the passive incorporation of this protein. The presence of ChiA was detected in dissolved occlusion bodies (OBs) preparations from infected transgenic lines, in a method-dependent manner, with the stronger signals observed in chimeric polyhedra. It is hypothesized that ChiA in OBs will increase peritrophic membrane permeability and facilitate primary infection. In bioassays, OBs produced in ChiA-expressing lines were associated with higher larval mortality than OBs produced in Sf9, consistent with a ChiA-mediated effect. Notably, the addition of ChiA proteins from stably transformed insect cell lines improved infection rates, particularly in recombinant baculoviruses, which exhibited a significant reduction in occlusion-derived virion (ODV) occlusion. This underscores the critical role of these proteins in the oral infection process. Consequently, it was possible to incorporate the ChiA protein from stably transformed insect cell lines into wild-type and recombinant baculovirus occlusion bodies, paving the way for potential applications in IPM with AcMNPV.

bioengineering↗

The ubiquitin conjugase Rad6 mediates ribosome pausing during oxidative stress

Oxidative stress causes K63-linked ubiquitination of ribosomes by the E2 ubiquitin conjugase, Rad6. How Rad6-mediated ubiquitination of ribosomes affects global translation, however, is unclear. We therefore performed Ribo-seq and Disome-seq in Saccharomyces cerevisiae, and found that oxidative stress caused ribosome pausing at specific amino acid motifs, and this also led to ribosome collisions. However, these redox pausing signatures were lost in the absence of Rad6 but did not depend on the ribosome-associated quality control (RQC) pathway. We also found that Rad6 is needed to inhibit overall translation in response to oxidative stress and its deletion leads to increased expression of antioxidant genes. Finally, we observed that the lack of Rad6 leads to changes during translation initiation that affect activation of the integrated stress response (ISR) pathway. Our results provide a high-resolution picture of the gene expression changes during oxidative stress and unravel an additional stress response pathway affecting translation elongation. HIGHLIGHTSO_LIRad6 is required for sequence-specific ribosome pausing under oxidative stress. C_LIO_LIRad6 affects translation independently of the RQC pathway. C_LIO_LICells lacking Rad6 show dysregulated translational repression upon oxidative stress. C_LIO_LILoss of Rad6 leads to altered activation of the ISR pathway. C_LI

molecular biology↗