Literature DB >> 18635142

The specific involvement of coat protein in tobacco mosaic virus cross protection.

J L Sherwood1, R W Fulton.   

Abstract

Nicotiana sylvestris infected by strains of tobacco mosaic virus (TMV) causing mosaic can be superinfected in the dark green leaf tissue, but not light green tissue, by necrotizing strains of TMV. The dark green tissue, however, is much less susceptible than healthy tissue, to some extent, even to unrelated viruses. The RNA of necrotizing strains of TMV was relatively more infectious than intact virus on mosaic than on healthy leaves and caused lesions in both light and dark green tissues. The same relationship was found in Nicotiana longiflora and, when the protecting strain in N. sylvestris could be used as a challenge, in Capsicum baccatum. The efficiency of superinfection by RNA was not found with viruses unrelated to TMV. When bentonite at 1 mg/ml, which is known to strip protein from TMV, was included in the inoculum of intact TMV it superinfected in the same manner as RNA. RNA of a necrotizing strain of TMV, encapsidated in brome mosaic virus protein and used as a challenge, superinfected in the same manner as RNA. When encapsidated in common TMV protein, however, it behaved as native virus. Cross protection apparently results from the prevention of uncoating of related challenge virus in light green tissue of N. sylvestris. Locally inoculated N. sylvestris leaves were insusceptible to challenge RNA or intact virus when the protecting virus was increasing. After increase ceased, RNA was more infectious than intact virus.

Entities:  

Year:  1982        PMID: 18635142     DOI: 10.1016/0042-6822(82)90072-1

Source DB:  PubMed          Journal:  Virology        ISSN: 0042-6822            Impact factor:   3.616


  13 in total

Review 1.  Genetic engineering of plants for virus resistance.

Authors:  F Gadani; L M Mansky; R Medici; W A Miller; J H Hill
Journal:  Arch Virol       Date:  1990       Impact factor: 2.574

2.  What history tells us XXIX. Transfers from plant biology: from cross protection to RNA interference and DNA vaccination.

Authors:  Michel Morange
Journal:  J Biosci       Date:  2012-12       Impact factor: 1.826

Review 3.  Engineering virus resistance in agricultural crops.

Authors:  P J van den Elzen; M J Huisman; D P Willink; E Jongedijk; A Hoekema; B J Cornelissen
Journal:  Plant Mol Biol       Date:  1989-09       Impact factor: 4.076

4.  Superinfection exclusion is an active virus-controlled function that requires a specific viral protein.

Authors:  Svetlana Y Folimonova
Journal:  J Virol       Date:  2012-03-07       Impact factor: 5.103

Review 5.  Coat protein-mediated resistance in transgenic plants.

Authors:  A F Hackland; E P Rybicki; J A Thomson
Journal:  Arch Virol       Date:  1994       Impact factor: 2.574

6.  The Matrix Protein of a Plant Rhabdovirus Mediates Superinfection Exclusion by Inhibiting Viral Transcription.

Authors:  Xin Zhou; Kai Sun; Xueping Zhou; Andrew O Jackson; Zhenghe Li
Journal:  J Virol       Date:  2019-09-30       Impact factor: 5.103

7.  Infection with strains of Citrus tristeza virus does not exclude superinfection by other strains of the virus.

Authors:  Svetlana Y Folimonova; Cecile J Robertson; Turksen Shilts; Alexey S Folimonov; Mark E Hilf; Stephen M Garnsey; William O Dawson
Journal:  J Virol       Date:  2009-11-18       Impact factor: 5.103

8.  The Coat Protein and NIa Protease of Two Potyviridae Family Members Independently Confer Superinfection Exclusion.

Authors:  Satyanarayana Tatineni; Roy French
Journal:  J Virol       Date:  2016-11-14       Impact factor: 5.103

9.  Improving the large scale purification of the HIV microbicide, griffithsin.

Authors:  Joshua L Fuqua; Valentine Wanga; Kenneth E Palmer
Journal:  BMC Biotechnol       Date:  2015-02-22       Impact factor: 2.563

10.  Developing an understanding of cross-protection by Citrus tristeza virus.

Authors:  Svetlana Y Folimonova
Journal:  Front Microbiol       Date:  2013-04-04       Impact factor: 5.640

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