@article{mbs:/content/journal/jgv/10.1099/0022-1317-81-3-639, author = "Andrei, Graciela and Snoeck, Robert and De Clercq, Erik and Esnouf, Robert and Fiten, Pierre and Opdenakker, Ghislain", title = "Resistance of herpes simplex virus type 1 against different phosphonylmethoxyalkyl derivatives of purines and pyrimidines due to specific mutations in the viral DNA polymerase gene", journal= "Journal of General Virology", year = "2000", volume = "81", number = "3", pages = "639-648", doi = "https://doi.org/10.1099/0022-1317-81-3-639", url = "https://www.microbiologyresearch.org/content/journal/jgv/10.1099/0022-1317-81-3-639", publisher = "Microbiology Society", issn = "1465-2099", type = "Journal Article", abstract = "Drug-resistant strains of herpes simplex virus type 1 (HSV-1) were selected under the pressure of (S)-3-hydroxy-2-phosphonylmethoxypropyl (HPMP) derivatives of cytosine (HPMPC, cidofovir) and adenine (HPMPA) and 2-phosphonylmethoxyethyl (PME) derivatives of adenine (PMEA, adefovir) and 2,6-diaminopurine (PMEDAP). HPMPC-resistant (HPMPCr) and HPMPAr strains were cross-resistant to one another, but they remained sensitive to foscarnet (PFA), acyclovir (ACV) and the PME derivatives, while the PMEAr and PMEDAPr strains showed cross-resistance to PFA and ACV. The PMEAr, PMEDAPr and PFAr mutants all revealed a single nucleotide change resulting in a Ser-724 to Asn mutation within the conserved region II of the DNA polymerase. Two HPMPAr clones and one HPMPCr clone possessed single amino acid changes in the DNA polymerase (HPMPAr clone D1, Leu-1007 to Met; HPMPAr clone B5, Ile-1028 to Thr; HPMPCr clone C3, Val-573 to Met). The HPMPCr clone A4 contained two mutations, Ala-136 to Thr and Arg-700 to Met. The mutation at position 136, located outside the catalytic domain of the enzyme, was not detected in other HPMPCr clones, suggesting that this mutation may not be responsible for the resistant phenotype. Residue 573 is located within the 3′→5′ exonuclease editing domain close to the catalytically important residues Tyr-577 and Asp-581. Similarly, residue 700 is located in the palm subdomain of the catalytic domain, adjacent to the Asp residues 717, 886 and 888 that are vital for polymerase activity. The HPMPAr mutations at residues 1007 and 1028, beyond the last conserved region, still fall within the thumb subdomain of the catalytic domain. The different drug-resistant mutants varied in neurovirulent behaviour, the HPMPCr strains showing reduced neurovirulence compared with the wild-type.", }