Literature DB >> 1919522

Non-replicating deletion mutants of brome mosaic virus RNA-2 interfere with viral replication.

L E Marsh1, G P Pogue, U Szybiak, J P Connell, T C Hall.   

Abstract

Naturally occurring defective interfering RNAs (DI-RNAs) and satellite RNAs greatly reduce the accumulation of their helper virus in vivo, but often modulate symptom expression in an unpredictable manner. Deletion mutants Nc/S, Na/M and Sa/Nc + M/S, derived from brome mosaic virus (BMV) RNA-2, failed to replicate when co-inoculated with BMV RNAs-1 and -2 to barley protoplasts. However, the inoculum RNA corresponding to these deletion mutants was extremely stable and could have been mistaken for plus-strand progeny had minus-strand progeny analysis been omitted. These results accentuate the need for such tests in evaluating the ability of mutant viral sequences to replicate. One of the mutants, Nc/S, effectively interfered with the accumulation of BMV RNAs-1 and -2 in barley protoplasts. This non-replicating interfering RNA was termed NRI RNA-2 Nc/S. When present with RNAs-1 and -2 at low inoculum amounts (1 microgram), NRI RNA-2 Nc/S reduced replication of RNA-2, the parental RNA, by 63% and preferentially interfered with minus-strand RNA accumulation. At higher levels (4 micrograms), it completely displaced replication of both RNAs-1 and -2. Mutations eliminating translation of a truncated p2a protein from NRI RNA-2 Nc/S did not alleviate the interference effect, demonstrating that a defective replicase protein was not responsible for the decreased accumulation of genomic RNA. At an NRI RNA: genomic RNA inoculum molar ratio of 1:1, NRI RNA-2 Nc/S reduced the accumulation of all helper virus RNAs by 55%. Since this reduction was seen for both wild-type RNA-3 and delta SGP RNA-3, a deletion mutant of RNA-3 that lacks the subgenomic promoter necessary for coat protein expression, it was evident that the effective interference mediated by NRI RNA-2 Nc/S was not mitigated by encapsidation. The ability of the NRI RNAs to mimic satellite DI RNAs in depressing helper virus replication suggests that their expression in transgenic plants may provide a new and widely applicable approach for inducing resistance to viral infection.

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Year:  1991        PMID: 1919522     DOI: 10.1099/0022-1317-72-10-2367

Source DB:  PubMed          Journal:  J Gen Virol        ISSN: 0022-1317            Impact factor:   3.891


  7 in total

Review 1.  Strategies to protect crop plants against viruses: pathogen-derived resistance blossoms.

Authors:  T M Wilson
Journal:  Proc Natl Acad Sci U S A       Date:  1993-04-15       Impact factor: 11.205

2.  Artificial defective interfering RNAs derived from RNA 2 of beet necrotic yellow vein virus.

Authors:  A Hehn; S Bouzoubaa; G Jonard; H Guilley; K E Richards
Journal:  Arch Virol       Date:  1994       Impact factor: 2.574

3.  Broad-spectrum protection against tombusviruses elicited by defective interfering RNAs in transgenic plants.

Authors:  T Rubio; M Borja; H B Scholthof; P A Feldstein; T J Morris; A O Jackson
Journal:  J Virol       Date:  1999-06       Impact factor: 5.103

4.  The requirement for a 5' stem-loop structure in brome mosaic virus replication supports a new model for viral positive-strand RNA initiation.

Authors:  G P Pogue; T C Hall
Journal:  J Virol       Date:  1992-02       Impact factor: 5.103

5.  Identification of domains in brome mosaic virus RNA-1 and coat protein necessary for specific interaction and encapsidation.

Authors:  R Duggal; T C Hall
Journal:  J Virol       Date:  1993-11       Impact factor: 5.103

Review 6.  Comparison of the replication of positive-stranded RNA viruses of plants and animals.

Authors:  K W Buck
Journal:  Adv Virus Res       Date:  1996       Impact factor: 9.937

Review 7.  Molecular studies of genetic RNA-RNA recombination in brome mosaic virus.

Authors:  J J Bujarski; P D Nagy; S Flasinski
Journal:  Adv Virus Res       Date:  1994       Impact factor: 9.937

  7 in total

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