Literature DB >> 2876051

Comparison of restriction site polymorphisms among clinical isolates and laboratory strains of human cytomegalovirus.

S H Chandler, J K McDougall.   

Abstract

We have compared HindIII and EcoRI restriction sites in the long and short unique regions of the human cytomegalovirus (HCMV) genome among 20 low passage clinical isolates and four high passage laboratory strains (AD169, Davis, Towne, UW-1). This was done by hybridizing digested DNA on Southern blots with a series of subgenomic cloned fragments of AD169. Fourteen HindIII sites were conserved and three fragments (O, V, W) co-migrated among all strains. Nine HindIII sites found in AD169 were absent in one or more other strains. Eight additional HindIII sites were identified and three more hypothesized by the appearance of slightly smaller fragments. Sixteen EcoRI sites were conserved and six fragments (c, Y, S, W, B, R) co-migrated among all strains. Twelve EcoRI sites were absent or in altered locations and at least seven additional sites were identified in one or more strains. Although no two of these strains were identical throughout the genome, identical patterns of variation in a given region frequently occurred in multiple strains. Polymorphisms occurred throughout the entire genome, including the region specifying immediate early functions. All strains studied showed an identical fragment which hybridized to the transforming fragment of AD169. These restriction site polymorphisms may in the future serve as convenient markers for identification of functional variation among HCMV strains.

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Year:  1986        PMID: 2876051     DOI: 10.1099/0022-1317-67-10-2179

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


  15 in total

1.  Modification of specific regions of the human cytomegalovirus genome during in vitro passage.

Authors:  C Hamelin; M Dion
Journal:  Can J Infect Dis       Date:  1990

Review 2.  Molecular biology of cytomegalovirus.

Authors:  V C Emery; P D Griffiths
Journal:  Int J Exp Pathol       Date:  1990-12       Impact factor: 1.925

3.  A cytomegalovirus protein with properties of herpes simplex virus ICP8: partial purification of the polypeptide and map position of the gene.

Authors:  G W Kemble; A L McCormick; L Pereira; E S Mocarski
Journal:  J Virol       Date:  1987-10       Impact factor: 5.103

4.  Comparative sequence analysis of human cytomegalovirus strains.

Authors:  R Lehner; T Stamminger; M Mach
Journal:  J Clin Microbiol       Date:  1991-11       Impact factor: 5.948

5.  A polymorphic region of the human cytomegalovirus genome encoding putative glycoproteins.

Authors:  S Watanabe; M Shinkai; S Hitomi; H Kozuka; S Kimura; K Shimada; R Hondo; N Yamaguchi
Journal:  Arch Virol       Date:  1994       Impact factor: 2.574

6.  Molecular and biological characterization of new strains of murine cytomegalovirus isolated from wild mice.

Authors:  T W Booth; A A Scalzo; C Carrello; P A Lyons; H E Farrell; G R Singleton; G R Shellam
Journal:  Arch Virol       Date:  1993       Impact factor: 2.574

7.  Localization of the human cytomegalovirus 2.7-kb major early beta-gene transcripts by RNA in situ hybridization in permissive and nonpermissive infections.

Authors:  T C Wu; W A Lee; M C Pizzorno; W C Au; Y J Chan; R H Hruban; G M Hutchins; G S Hayward
Journal:  Am J Pathol       Date:  1992-11       Impact factor: 4.307

8.  Strain-specific neutralization of human cytomegalovirus isolates by human sera.

Authors:  M Klein; K Schoppel; N Amvrossiadis; M Mach
Journal:  J Virol       Date:  1999-02       Impact factor: 5.103

9.  Human cytomegalovirus clinical isolates carry at least 19 genes not found in laboratory strains.

Authors:  T A Cha; E Tom; G W Kemble; G M Duke; E S Mocarski; R R Spaete
Journal:  J Virol       Date:  1996-01       Impact factor: 5.103

10.  Comparative analysis of human cytomegalovirus a-sequence in multiple clinical isolates by using polymerase chain reaction and restriction fragment length polymorphism assays.

Authors:  J A Zaia; G Gallez-Hawkins; M A Churchill; A Morton-Blackshere; H Pande; S P Adler; G M Schmidt; S J Forman
Journal:  J Clin Microbiol       Date:  1990-12       Impact factor: 5.948

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