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New deadly virus may be 'bat bug'

New deadly virus may be 'bat bug' | Virology News | Scoop.it

"Bats may be the source of a new Sars-like virus which killed a man in Saudi Arabia, according to an analysis of the coronavirus' genome.

Two other people have been infected and one, who was flown to the UK for treatment in September, is still in intensive care.

Experts, writing in the journal mBio, said the virus was closely related to other viruses in bats.

It is thought the virus does not pass readily from one person to another.

Coronaviruses are a family of viruses ranging from the common cold to the Sars (severe acute respiratory syndrome) virus. They infect a wide range of animals."

 

I repeat: fear the bat...there are lots of them, and they have a LOT of viruses that can infect people.

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The subgenomic promoter of brome mosaic virus folds into a stem–loop structure capped by a pseudo-triloop that is structurally similar to the triloop of the genomic promoter

The subgenomic promoter of brome mosaic virus folds into a stem–loop structure capped by a pseudo-triloop that is structurally similar to the triloop of the genomic promoter | Virology News | Scoop.it

In brome mosaic virus, both the replication of the genomic (+)-RNA strands and the transcription of the subgenomic RNA are carried out by the viral replicase. The production of (−)-RNA strands is dependent on the formation of an AUA triloop in the stem–loop C (SLC) hairpin in the 3′-untranslated region of the (+)-RNA strands. Two alternate hypotheses have been put forward for the mechanism of subgenomic RNA transcription. One posits that transcription commences by recognition of at least four key nucleotides in the subgenomic promoter by the replicase. The other posits that subgenomic transcription starts by binding of the replicase to a hairpin formed by the subgenomic promoter that resembles the minus strand promoter hairpin SLC. In this study, we have determined the three-dimensional structure of the subgenomic promoter hairpin using NMR spectroscopy. The data show that the hairpin is stable at 30°C and that it forms a pseudo-triloop structure with a transloop base pair and a nucleotide completely excluded from the helix. The transloop base pair is capped by an AUA triloop that possesses an extremely well packed structure very similar to that of the AUA triloop of SLC, including the formation of a so-called clamped-adenine motif. The similarities of the NMR structures of the hairpins required for genomic RNA and subgenomic RNA synthesis show that the replicase recognizes structure rather than sequence-specific motifs in both promoters.

 

BMV!! I worked on bromoviruses in general and BMV in particular from 1977 to around 1985, and collected every paper on them - and especially the mol biol. It was always obvious, once the sequences were known, that origins of replication and the subgenomic promoter were not sequence-delimited - and now we see that it's a structure. Cool stuff!!


Via Hiroyuki Mizumoto, Jeanmarie Verchot Virologist
Ed Rybicki's comment, June 23, 2012 4:21 AM
BMV!! I worked on bromoviruses in general and BMV in particular from 1977 to around 1985, and collected every paper on them - and especially the mol biol. It was always obvious, once the sequences were known, that origins of replication and the subgenomic promoter were not sequence-delimited - and now we see that it's a structure. Cool stuff!!