Miller C S, Jacob R J, Hiser D G
Department of Oral Health Science, L. P. Markey Cancer Center, University of Kentucky College of Dentistry, Lexington.
Oral Surg Oral Med Oral Pathol. 1993 May;75(5):602-9. doi: 10.1016/0030-4220(93)90234-u.
Replication of herpes simplex virus type 1 was enhanced in fibroblast cultures when cells were ultraviolet irradiated 12 to 48 hours before infection. Maximum enhancement (340% increase) occurred at exposures of 9.6 J/m2 in DNA-repair competent fibroblasts. Repair deficient xeroderma pigmentosum cells responded to lower ultraviolet exposures (1.6 to 5.6 J/m2) with lower levels of enhancement (37% to 140%). Ultraviolet irradiation of host cells before infection increased viral DNA synthesis, but did not alter the ability of the cell to adsorb virus. Prostaglandins were not shown to contribute to the process. These results suggest that ultraviolet-enhanced replication of herpes simplex virus may be associated with DNA-repair activities, and that ultraviolet-enhanced herpes simplex virus replication should be further examined for its contribution to herpes simplex virus recurrence in vivo.
当在感染前12至48小时对细胞进行紫外线照射时,单纯疱疹病毒1型在成纤维细胞培养物中的复制增强。在具有DNA修复能力的成纤维细胞中,当暴露剂量为9.6 J/m2时出现最大增强(增加340%)。DNA修复缺陷的着色性干皮病细胞对较低的紫外线照射剂量(1.6至5.6 J/m2)有反应,增强水平较低(37%至140%)。感染前对宿主细胞进行紫外线照射会增加病毒DNA合成,但不会改变细胞吸附病毒的能力。未显示前列腺素参与该过程。这些结果表明,紫外线增强的单纯疱疹病毒复制可能与DNA修复活性有关,并且应进一步研究紫外线增强的单纯疱疹病毒复制对体内单纯疱疹病毒复发的作用。