Literature DB >> 9269047

Study of immunogenicity and virulence of bovine herpesvirus 1 mutants deficient in the UL49 homolog, UL49.5 homolog and dUTPase genes in cattle.

X Liang1, B Chow, L A Babiuk.   

Abstract

We previously reported that the bovine herpesvirus 1 (BHV 1) gene homologous to herpes simplex virus gene UL49 is dispensable; nevertheless, a mutant with the UL49 homolog (UL49 h) gene deletion exhibited significantly impaired growth in cell culture. To further evaluate the role of the UL49 h in virus infectivity in the natural host of BHV 1, the pathogenesis of the UL49 h negative mutant was studied in cattle. An additional mutant with a combined defect in UL49 h, UL49.5 h and dUTPase genes was also studied in parallel. We found that both mutants were avirulent in cattle inasmuch as intranasal (i.n.) administration of either mutants induced no apparent clinical disease, nor did animals receiving the mutants shed virus. Following i.n. inoculation with the mutants animals developed low levels of serum neutralizing (SN) antibodies, and were partially protected against wild-type BHV 1 challenge. Intramuscular immunizations with either mutant induced good SN titers, and moreover, they induced nearly complete protection against respiratory challenge with wild-type virus. The results from this study establish that BHV 1 UL49 h is an important virulence factor, and also suggest that deletion of the nonessential viral genes UL49 h, UL49.5 h and dUTPase may be useful in developing recombinant BHV 1 vaccines or BHV 1-based vaccine vectors.

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Year:  1997        PMID: 9269047     DOI: 10.1016/s0264-410x(97)00008-x

Source DB:  PubMed          Journal:  Vaccine        ISSN: 0264-410X            Impact factor:   3.641


  17 in total

1.  Herpes simplex virus glycoproteins gD and gE/gI serve essential but redundant functions during acquisition of the virion envelope in the cytoplasm.

Authors:  Aaron Farnsworth; Kimberly Goldsmith; David C Johnson
Journal:  J Virol       Date:  2003-08       Impact factor: 5.103

2.  Distinctions between bovine herpesvirus 1 and herpes simplex virus type 1 VP22 tegument protein subcellular associations.

Authors:  J S Harms; X Ren; S C Oliveira; G A Splitter
Journal:  J Virol       Date:  2000-04       Impact factor: 5.103

3.  Deletion of the herpes simplex virus VP22-encoding gene (UL49) alters the expression, localization, and virion incorporation of ICP0.

Authors:  Gillian Elliott; Wali Hafezi; Alison Whiteley; Emmanuelle Bernard
Journal:  J Virol       Date:  2005-08       Impact factor: 5.103

4.  The pseudorabies virus VP22 homologue (UL49) is dispensable for virus growth in vitro and has no effect on virulence and neuronal spread in rodents.

Authors:  T del Rio; H C Werner; L W Enquist
Journal:  J Virol       Date:  2002-01       Impact factor: 5.103

5.  Characterization of a UL49-null mutant: VP22 of herpes simplex virus type 1 facilitates viral spread in cultured cells and the mouse cornea.

Authors:  Carol Duffy; Jennifer H Lavail; Andrew N Tauscher; Elizabeth G Wills; John A Blaho; Joel D Baines
Journal:  J Virol       Date:  2006-09       Impact factor: 5.103

6.  Characterization of the nuclear localization and nuclear export signals of bovine herpesvirus 1 VP22.

Authors:  Chunfu Zheng; Robert Brownlie; Lorne A Babiuk; Sylvia van Drunen Littel-van den Hurk
Journal:  J Virol       Date:  2005-09       Impact factor: 5.103

7.  Bovine herpesvirus 1 tegument protein VP22 interacts with histones, and the carboxyl terminus of VP22 is required for nuclear localization.

Authors:  X Ren; J S Harms; G A Splitter
Journal:  J Virol       Date:  2001-09       Impact factor: 5.103

8.  Tyrosine phosphorylation of bovine herpesvirus 1 tegument protein VP22 correlates with the incorporation of VP22 into virions.

Authors:  X Ren; J S Harms; G A Splitter
Journal:  J Virol       Date:  2001-10       Impact factor: 5.103

9.  A UL47 gene deletion mutant of bovine herpesvirus type 1 exhibits impaired growth in cell culture and lack of virulence in cattle.

Authors:  Vladislav A Lobanov; Sheryl L Maher-Sturgess; Marlene G Snider; Zoe Lawman; Lorne A Babiuk; Sylvia van Drunen Littel-van den Hurk
Journal:  J Virol       Date:  2010-01       Impact factor: 5.103

10.  The simian varicella virus uracil DNA glycosylase and dUTPase genes are expressed in vivo, but are non-essential for replication in cell culture.

Authors:  Toby M Ward; Marshall V Williams; Vicki Traina-Dorge; Wayne L Gray
Journal:  Virus Res       Date:  2009-02-04       Impact factor: 3.303

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