Increased frequency of specific locus mutation following human cytomegalovirus infection

Thomas Albrecht, Michael P. Fons, Cheng Z. Deng, Istvan Boldogh

Research output: Contribution to journalArticle

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Abstract

The effect of human cytomegalovirus (HCMV) infection on the frequency of mutations at the hypoxanthine-guanine phosphoribosyl transferase (hprt) locus was studied in Chinese hamster lung V79 cells. When V79 cells were infected with HCMV (strain AD169) at multiplicities of 0.1 to 50 plaque forming units (PFU) per cell the presumptive mutation frequency, as determined by the number of 6-thioguanine-resistant (TG(r)) colonies, was increased up to 16.8-fold (P < 0.005), depending on the multiplicity of infection. Increases in the mutation frequency at the hprt locus were also observed for other laboratory adapted HCMV strains (C-87, Davis) and for low passage clinical isolates (82-1, 84-2). The expression time required for the maximum increase in TG' colonies was 3 days and was consistent among the HCMV strains evaluated in this study. UV-irradiation of HCMV stock up to a dose of 9.6 x 104 ergs/mm2 increased the mutation frequency, but further exposure to UV light or to heat (56(r) for 30 min) significantly decreased the frequency of TG(r)-resistant colonies, suggesting that expression of HCMV genes was involved in the mutation process. HCMV-induced TG(r) cells demonstrated substantially reduced (> 96%) incorporation of [3H]hypoxanthine. PCR analysis of the hprt locus demonstrated deletions in 9 of 19 HCMV-induced TG(r) colonies randomly selected for further study, while 2 of 17 spontaneously developed TG(r) colonies demonstrated deletions. Although insertions were not detected in spontaneously developed clones, 3 of 19 HCMV-induced TG(r) clones had insertions in the hprt gene. Neither HCMV-specific DNA sequences nor HCMV-specific proteins were detected in the TG(r) clones obtained after HCMV infection. Infection of V79 cells with HCMV also increased their sensitivity to mutation with N-methyl-N'-nitro-N-nitrosoguanidine, giving a synergistic enhancement of the mutation frequency. These results indicate that HCMV infection has the capacity to induce mutations in the cellular genome and increase the sensitivity of infected cells to mutation by genotoxic chemicals. Although inactivated HCMV particles are responsible for a modest increase in the mutation frequency, expression of HCMV genes is associated with a substantial enhancement of the mutation frequency.

Original languageEnglish (US)
Pages (from-to)48-61
Number of pages14
JournalVirology
Volume230
Issue number1
DOIs
StatePublished - Mar 31 1997

Fingerprint

Cytomegalovirus Infections
Cytomegalovirus
Mutation
Thioguanine
Mutation Rate
Hypoxanthine
Guanine
Transferases
Clone Cells
Methylnitronitrosoguanidine
Cricetulus
Genes
Genome
Polymerase Chain Reaction
Lung

ASJC Scopus subject areas

  • Virology
  • Infectious Diseases

Cite this

Increased frequency of specific locus mutation following human cytomegalovirus infection. / Albrecht, Thomas; Fons, Michael P.; Deng, Cheng Z.; Boldogh, Istvan.

In: Virology, Vol. 230, No. 1, 31.03.1997, p. 48-61.

Research output: Contribution to journalArticle

Albrecht, Thomas ; Fons, Michael P. ; Deng, Cheng Z. ; Boldogh, Istvan. / Increased frequency of specific locus mutation following human cytomegalovirus infection. In: Virology. 1997 ; Vol. 230, No. 1. pp. 48-61.
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abstract = "The effect of human cytomegalovirus (HCMV) infection on the frequency of mutations at the hypoxanthine-guanine phosphoribosyl transferase (hprt) locus was studied in Chinese hamster lung V79 cells. When V79 cells were infected with HCMV (strain AD169) at multiplicities of 0.1 to 50 plaque forming units (PFU) per cell the presumptive mutation frequency, as determined by the number of 6-thioguanine-resistant (TG(r)) colonies, was increased up to 16.8-fold (P < 0.005), depending on the multiplicity of infection. Increases in the mutation frequency at the hprt locus were also observed for other laboratory adapted HCMV strains (C-87, Davis) and for low passage clinical isolates (82-1, 84-2). The expression time required for the maximum increase in TG' colonies was 3 days and was consistent among the HCMV strains evaluated in this study. UV-irradiation of HCMV stock up to a dose of 9.6 x 104 ergs/mm2 increased the mutation frequency, but further exposure to UV light or to heat (56(r) for 30 min) significantly decreased the frequency of TG(r)-resistant colonies, suggesting that expression of HCMV genes was involved in the mutation process. HCMV-induced TG(r) cells demonstrated substantially reduced (> 96{\%}) incorporation of [3H]hypoxanthine. PCR analysis of the hprt locus demonstrated deletions in 9 of 19 HCMV-induced TG(r) colonies randomly selected for further study, while 2 of 17 spontaneously developed TG(r) colonies demonstrated deletions. Although insertions were not detected in spontaneously developed clones, 3 of 19 HCMV-induced TG(r) clones had insertions in the hprt gene. Neither HCMV-specific DNA sequences nor HCMV-specific proteins were detected in the TG(r) clones obtained after HCMV infection. Infection of V79 cells with HCMV also increased their sensitivity to mutation with N-methyl-N'-nitro-N-nitrosoguanidine, giving a synergistic enhancement of the mutation frequency. These results indicate that HCMV infection has the capacity to induce mutations in the cellular genome and increase the sensitivity of infected cells to mutation by genotoxic chemicals. Although inactivated HCMV particles are responsible for a modest increase in the mutation frequency, expression of HCMV genes is associated with a substantial enhancement of the mutation frequency.",
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