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. 2011 Aug;85(15):7594-602.
doi: 10.1128/JVI.00290-11. Epub 2011 Jun 1.

Genetic editing of herpes simplex virus 1 and Epstein-Barr herpesvirus genomes by human APOBEC3 cytidine deaminases in culture and in vivo

Rodolphe Suspène  1 , Marie-Ming Aynaud, Stefanie Koch, David Pasdeloup, Marc Labetoulle, Barbara Gaertner, Jean-Pierre Vartanian, Andreas Meyerhans, Simon Wain-Hobson
Affiliations

Genetic editing of herpes simplex virus 1 and Epstein-Barr herpesvirus genomes by human APOBEC3 cytidine deaminases in culture and in vivo

Rodolphe Suspène et al. J Virol. 2011 Aug.

Abstract

Human APOBEC3 cytidine deaminases target and edit single-stranded DNA, which can be of viral, mitochondrial, or nuclear origin. Retrovirus genomes, such as human immunodeficiency virus (HIV) genomes deficient in the vif gene and the hepatitis B virus genome, are particularly vulnerable. The genomes of some DNA viruses, such as human papillomaviruses, can be edited in vivo and in transfection experiments. Accordingly, herpesviruses should be no exception. This is indeed the case for herpes simplex virus 1 (HSV-1) in tissue culture, where APOBEC3C (A3C) overexpression can reduce virus titers and the particle/PFU ratio ∼10-fold. Nonetheless, A3A, A3G, and AICDA can edit what is presumably a small fraction of HSV genomes in an experimental setting without seriously impacting the viral titer. Hyperediting was found in HSV genomes recovered from 4/8 uncultured buccal lesions. The phenomenon is not restricted to HSV, since hyperedited Epstein-Barr virus (EBV) genomes were readily recovered from 4/5 established cell lines, indicating that episomes are vulnerable to editing. These findings suggest that the widely expressed A3C cytidine deaminase can function as a restriction factor for some human herpesviruses. That the A3C gene is not induced by type I interferons begs the question whether some herpesviruses encode A3C antagonists.

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Figures

Fig. 1.
Fig. 1.
Several human A3 enzymes may restrict HSV-1 replication and edit the genome. (A) Transfection of HeLa cells by 2.5 μg of plasmid DNA followed by HSV-1 infection. pv, empty vector. Titers are the means for triplicate experiments. (B) Dose-response relationship of supernatant titers as a function of A3C DNA concentration. The DNA concentration was maintained constant with the plasmid vector. (C) 3DPCR of HSV-1 DNA for all DNA transfections. The denaturation temperature (Td) is given across the top; M, molecular weight markers. The HSV-1 sequence between the primers is 410 bp in length. The white vertical bar indicates the minimal Td (93 to 93.8°C) for cloned wild-type HSV-1 DNA. Bands to lower temperature can be taken as prima facie evidence of cytidine deamination. (D) A selection of A3-edited HSV-1 genomes from the HeLa + pv transfection. For clarity, only 200 bp of the 410-bp ICP22 sequence are shown, while differences are scored with respect to the reference sequence (G → A, n = 25, 10,250 bp; C → T, n = 9, 3,690 bp). The positions in the HSV-1 strain 17 sequence are also given. To the right of each sequence is the total number of C → T transitions on the plus or minus (shown as G → A transitions) strand.
Fig. 2.
Fig. 2.
A3C levels can impact particle/PFU ratios for HSV-1. (A) Impact of active A3 constructs. (B) Impact of the A3C C957S inactive mutant. (C) Impact of A3C siRNA. (D) Western blot of V5-tagged A3C and β-actin loading control for uninfected HeLa cells at 48 h; lanes 1 and 2, 400 ng A3C-V5 tag plus 1 μg siRNA control; lanes 3 and 4, 400 ng A3C-V5 tag plus 1 μg siA3C RNA. Molecular mass markers (in kDa) are shown to the left.
Fig. 3.
Fig. 3.
Four human cytidine deaminases can hyperedit HSV-1 genomes. (A) Agarose gels of ICP22 3DPCR DNA products from HSV-1-infected quail QT6 cells expressing various A3 genes. The annotation is as for Fig. 1C. Stars indicate A3A, A3C, and A3G catalytic mutants. (B) 5′ dinucleotide context associated with editing on the plus and minus strands. Asterisks denote significant deviations from the expected values (χ2 test, P < 0.05) (QT6 + A3A, G → A, n = 24, 9,840 bp; C → T, n = 31, 12,710 bp; QT6 + A3C, G → A, n = 50, 20,500 bp; C → T, n = 78, 31,980 bp; QT6 + A3G, G → A, n = 32, 13,120 bp; C → T, n = 8, 3,280 bp; QT6 + AID, G → A, n = 9, 3,690 bp; C → T, n = 24, 9,840 bp). (C) TaqMan transcriptome analysis of the seven A3 genes from HeLa cells. The levels have been normalized to those of A3G (horizontal bar). nd, not detected.
Fig. 4.
Fig. 4.
HSV-1 genomes can be edited in vivo. (A) Agarose gels of ICP22 3DPCR DNA products from total DNA derived from pharyngeal washes or labial swabs. The annotation is as for Fig. 1C. (B) Frequency distribution of A3-edited HSV-1 sequences from patient P9. Since the cytidine composition of the two strands varies (32% plus strand; 35% minus strand), the % editing differs slightly (P9 G → A, n = 88, 36,080 bp; C → T, n = 21, 8,610 bp). (C) 5′ dinucleotide context associated with editing on the plus and minus strands for the collection of sequences from patient P9 (Td = 90.4 to 92.1°C). Asterisks denote significant deviations form the expected values (χ2 test, P < 0.05). Also shown are sequences derived at a higher Td (93.8 to 94.5°C) with 1 to 4 C → T transitions or 5 to 10 transitions pooled from all patients [Patients (1–4 mut.), n = 713, 292,330 bp; Patients (5–10 mut.), n = 10, 4,100 bp; P9, G → A, n = 94, 38,540 bp; C → T, n = 21, 8,610 bp]. (D) Frequency distribution of sequences derived at 93.8 to 94.5°C from all eight patients for both strands. The insets expand the region covering 4 to 55 bp.
Fig. 5.
Fig. 5.
Hyperediting of EBV genomes in EBV-immortalized human B cell lines. (A) Agarose gels of EBNA-1 3DPCR DNA products from total DNA derived from five EBV-immortalized human B cell lines. The annotation is as for Fig. 1C. The P1 to -3 lines are all ung−/−; Z is AICDA−/−, while T is an EBV-cell line from a normal patient without any known leukocyte defect. (B) A selection of hyperedited sequences from P1 to -3 and Z. To the right are the number and % of cytidine residues edited. Plus-strand hypermutants were not always recovered and hence were excluded from analyses. (C) Frequency distribution of A3-edited EBV sequences from four EBV-transformed cell lines. Only minus-strand editing was identified (P1, n = 32, 6,400 bp; P2, n = 21, 4,200 bp; P3, n = 19, 3,800 bp; Z, n = 72, 14,400 bp). (D) 5′ dinucleotide context associated with minus-strand editing. Asterisks denote significant deviations from the expected values (χ2 test, P < 0.05).
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