Articles

Analysis of enzymatic digestion pattern of two open reading frames of Varciella-Zoster genome from Kuwaiti patients using the RFLP technique

Abstract

Background and Objectives: Varicella–Zoster virus (VZV) is a human herpes virus that usually attacks young children and commonly causes chicken pox (Varicella). Following primary infection, a lifelong latent infection is established. The virus often reactivates during adulthood or senesces to cause shingles (Zoster). Little is known regarding the genotypes of Varicella in Kuwait. The aim of this study was to genotype Varicella samples collected from patients in Kuwait.
Materials and Methods: Samples from 60 cases of chicken pox were typed. The DNA extraction was performed using the commercially available DNA extraction kit. Two sets of oligonucleotide primers were used to amplify the intervening sequences with polymerase chain reaction to identify VZV DNA in clinical samples. The BglI and PstI endonucleases were used to digest. The PCR amplicons for PCR-RFLP typing.
Results: Relatively consistent restriction enzyme digestion profiles for different VZV strains were observed. Limited genetic differences between VZV samples were found. Three VZV strains were identified (A, B and C) with type B representing 86.6%, type A 11.7% and type C being 1.7%. We found that distinct restriction fragment length polymorphism isolates from the same origin or nationality were very similar.
Conclusion: Varicella strains with cutting sites for both enzyme PstI and BglI (typeB) were more prevalent. Molecular amplification of viral DNA by PCR and restriction digestion could be used for VZV typing as an alternative method to serological assays.

Davison AJ, Scott JE. The complete DNA sequence of varicella-zoster virus. J Gen Virol 1986; 67: 1759-1816.

Dumas AM, Geelen JL, Weststrate MW, Wertheim P, van der Noordaa J. XbaI, PstI, and BglI restriction enzyme maps of the two orientations of the varicella- zoster virus genome. J Virol 1981; 39: 390-400.

HayakawaY, Yamamoto T, Yamanishi K, Takahashi M. Analysis of varicella-zoster virus DNAs of clinical isolates by endonuclease HpaI. J Gen Virol 1986; 67:1817-1829.

Hondo R, Yogo Y. Strain variation of R5 direct repeats in the right-hand portion of the long unique segment of varicella-zoster virus DNA. J Virol 1988; 62: 2916-2921.

Straus SE, Hay J, Smith H, Owens J. Genome differences among varicella-zoster virus isolates. J Genl Virol 1983;64: 1031-1041.

Takada M, Suzutani T, Yoshida I, Matoba M, Azuma M. Identification of varicella-zoster virus strains by PCR analysis of three repeat elements and a PstI-site- less region. J Clin Microbiol 1995; 33: 658-660.

-Takayama M, Takayama N,. Inoue N, Kameoka Y.Application of long PCR method of identification of variations in nucleotide sequences among varicella- zoster virus isolates.-J Clin Microbiol 1996; 34: 2869-74.

Fairley CF, Miller E. Varicella epidemiology: a changing scene? J Infect Dis 1966; 174 (Suppl. 3): S314-S319.

Adams SG, Dohner DE, Gelb LD. Restriction fragment differences between the genomes of the Oka varicella vaccine virus and American wild-type varicella-zoster virus. J Med Virol 1989; 29: 38-45.

Gelb LD, Dohner DE, Gershon AA, Steinberg SP, Waner JL, Takahashi M, et al. Molecular epidemiology of live, attenuated varicella virus vaccine in children with leukemia and normal adults. J Infect Dis 1987;155: 633-640.

Straus SE, Reinhold W, Smith HA, Ruyechan WT, Henderson DK, Blaese RM, et al. Endonuclease analysis of viral DNA from varicella and subsequent zoster infections in the same patient. N Engl J Med 1984; 311:1362-1364.

Gray GC, Palinkas LA, Kelley PW. Increasing evidence of varicella hospitalizations in United States Army and Navy personnel: are today’s teenagers more susceptible? Should recruits be vaccinated? Pediatrics 1990; 86:867-873.

Ragozzino MW, Melton LJ 3rd, Kurland LT, Chu CP, Perry HO. Population-based study of herpes zoster and its sequelae. Medicine (Baltimore) 1982; 61: 310-316.

Lee BW. Review of varicella zoster seroepidemiology in India and Southeast Asia. Trop Med and Int Health 1998; 3: 886-890.

Lolekha S, Tanthiphabha W, Sornchai P, Kosuwan P, Sutra S, Warachit B, et al. Effect of climatic factors and population density on varicella zoster virus epidemiology within a tropical country. A J of Trop Med and Hyg 2001; 64: 131-136.

Carr MJ, McCormack GP, Crowley B. Genetic variation in clinical varicella-zoster virus isolates collected in Ireland between 2002 and 2003. J Med Virol 2004; 73:131-136.

Loparev VN, Gonzalez A, Deleon-Carnes M, Tipples G, Fickenscher H, Torfason EG, et al. Global identification of three major genotypes of varicella-zoster virus: longitudinal clustering and strategies for genotyping. J Virol 2004; 78: 8349-8358.

Muir WB, Nichols R, Breuer J. Phylogenetic analysis of varicella-zoster virus: evidence of intercontinental spread of genotypes and recombination. J Virol 2002;76: 1971-1979.

ChowVT, Wan SS, Doraisingham S, Ling AE.Comparative analysis of the restriction endonuclease profiles of the Dumas and Singapore strains of varicella- zoster virus. J Med Virol 1993; 40: 339-342.

Takayama M, Takayama N. Long PCR amplification of varicella-zoster virus DNA in clinical specimens from the patients with varicella and herpes zoster. Kansenshogaku Zasshi 2002; 76: 347-354.

LaRussa P, Lungu O, Hardy I, Gershon A, Steinberg SP, Silverstein S. Restriction fragment length polymorphism of polymerase chain reaction products from vaccine and wild-type varicella-zoster virus isolates. J Virol 1992;66: 1016-1020.

Loparev V, Argaw T, Krause P, Takayama M, Schmid Ds. Improved identification and differentiation of varicella-zoster virus (VZV) wild-type strains and an attenuated varicella vaccine strain using a VZV open reading frame 62- based PCR. J Clin Microbiol 2000;38: 3156-60.

Norberg P, Liljeqvist JA, Bergstrom T, Sammons S, Schmid DS, Loparev VN. Complete-genome phylogenetic approach to varicella-zoster virus evolution: genetic divergence and evidence for recombination. J Virol 2006; 80: 9569-9576.

Peters GA,. Tyler SD, Grose C, Severini A, Gray MJ, Upton C, et al. A full-genome phylogenetic analysis of varicella-zoster virus reveals a novel origin of replication-based genotyping scheme and evidence of recombination between major circulating clades. J Virol 2006; 80: 9850-9860.

Beards G, Graham C, Pillay D. Investigation of vesicular rashes for HSV and VZV by PCR. J Med Virol 1998;54: 155-157.

Dahl H, Marcoccia J, Linde A. Antigen detection: the method of choice in comparison with virus isolation and serology for laboratory diagnosis of herpes zoster in human immunodeficiency virus-infected patients. J Clin Microbiol 1997; 35: 347-349.

Perez JL, Garcia A, Niubo J, Salva J, Podzamczer D, Martin R. Comparison of techniques and evaluation of three commercial monoclonal antibodies for laboratory diagnosis of varicella-zoster virus in mucocutaneous specimens. J Clin Microbiol 1994; 32: 1610-1613.

Soushi S, Ozawa H, Matsuhashi M, Shimazaki J, Saga U, Kurata T. Demonstration of varicella-zoster virus antigens in the vitreous aspirates of patients with acute retinal necrosis syndrome. Ophthalmology 1988; 95:1394-1398.

Quinlivan M, Hawrami K, Barrett-Muir W, Aaby P, Arvin A, Chow VT, et al. The molecular epidemiology of varicella-zoster virus: evidence for geographic segregation. J Infect Dis 2002; 186: 888-894.

LaRussa P, Steinberg S, Arvin A, Dwyer D, Menegus M, Rekrut K, et al. Polymerase chain reaction and restriction fragment length polymorphism analysis of varicella-zoster virus isolates from the United States and other parts of the world. J Infect Dis 1998; 178: S64-S6.

Davis CL, Field D, Metzgar D, Saiz R, Morin PA,.Smith IL, Spector SA, Wills C. Numerous length polymorphisms at short tandem repeats in human cytomegalovirus. J Virol 1999; 73: 6265-6270.

Umene K, Yoshida M. Genomic characterization of two predominant genotypes of herpes simplex virus type 1. Arch Virol 1993; 131: 29-46.

Faga B, Maury W, Bruckner DA, Grose C. Identification and mapping of single nucleotide polymorphisms in the varicella-zoster virus genome. Virology 2001; 280: 1-6.

Sauerbrei A, Eichhorn U, Gawellek S, Egerer R,Schacke M, Wutzler P, et al. Molecular characterization of Varicella-Zoster Virus trains in Germany and Differentiation from the Oka Vaccine Strain. J Med Virol 2003; 71: 313-319.

Mori C, Takahara R, Toriyama T, Nagai T, Takahashi M, Yamanishi K. Identification of the Oka strain of the live attenuated varicella vaccine from other clinical isolates by molecular epidemiologic analysis. J Infect Dis 1998; 178: 35-38.

Hawrami K, Breuer J. Analysis of United Kingdom wild- type strains of varicella-zoster virus: differentiation from the Oka vaccine strain. J Medl Virol 1997; 53: 60-2.

Loparev V, Martro E, Rubtcova E, Rodrigo C, Piette JC, Caumes E, et al. Towards universal varicella-zoster virus genotyping: diversity of VZV strains from France and Spain. J Clin Microbiol 2007; 45: 559-563.

Sergeev N, Rubtcova E, Chizikov V, Schmid DS, Loparev VN. New mosaic subgenotype of varicella- zoster virus in the USA: VZV detection and genotyping by oligonucleotide-microarray. J Virol Methods 2006; 136: 8-16.

LoparevVN, Argaw T, Krause PR, Takayama M, Schmid DS. Improved identification and differentiation of varicella-zoster virus (VZV) wild-type strains and an attenuated varicella vaccine strain using a VZV open reading frame 62-based PCR. J Clin Microbiol 2000;38: 3156-3160.

Gershon AA, Forghani B (1995). Varicella-zoster virus.In: Lennette EH, Lennette DA, Lennette ET. Diagnostic procedures for viral, rickettsial, and chlamydial infections. 7th ed. New York, NY, Marcel Dekker, pp.601-613.

Files
IssueVol 4 No 4 (2012) QRcode
SectionArticles
Keywords
Genotyping Kuwait RFLP Restriction enzymes Varicella

Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
How to Cite
1.
Qasem JA, Al-Fadhli MA, Saraya MA, Thomas J. Analysis of enzymatic digestion pattern of two open reading frames of Varciella-Zoster genome from Kuwaiti patients using the RFLP technique. Iran J Microbiol. 1;4(4):191-197.