Department of Biology, New Mexico State University, Las Cruces, New Mexico; Laboratory of Infectious Diseases, National Institutes of Allergy and Infectious Diseases, Bethesda, Maryland; Center for Tropical Diseases, Department of Pathology and Center for Biodefense and Emerging Infectious Diseases, University of Texas Medical Branch, Galveston, Texas; Institute for Human Infections and Immunity and Center for Tropical Diseases, University of Texas Medical Branch, Galveston, Texas; Tulane National Primate Research Center, Tulane University, Covington, Louisiana
Department of Biology, New Mexico State University, Las Cruces, New Mexico; Laboratory of Infectious Diseases, National Institutes of Allergy and Infectious Diseases, Bethesda, Maryland; Center for Tropical Diseases, Department of Pathology and Center for Biodefense and Emerging Infectious Diseases, University of Texas Medical Branch, Galveston, Texas; Institute for Human Infections and Immunity and Center for Tropical Diseases, University of Texas Medical Branch, Galveston, Texas; Tulane National Primate Research Center, Tulane University, Covington, Louisiana.
Am J Trop Med Hyg. 2014 Oct;91(4):672-6. doi: 10.4269/ajtmh.13-0492. Epub 2014 Aug 4.
The four serotypes of mosquito-borne dengue virus (DENV-1, -2, -3, and -4) that circulate in humans each emerged from an enzootic, sylvatic cycle in non-human primates. Herein, we present the first study of sylvatic DENV infection dynamics in a primate. Three African green monkeys were inoculated with 10(5) plaque-forming units (pfu) DENV-2 strain PM33974 from the sylvatic cycle, and one African green monkey was inoculated with 10(5) pfu DENV-2 strain New Guinea C from the human cycle. All four monkeys seroconverted (more than fourfold rise in 80% plaque reduction neutralization titer [PRNT80]) against the strain of DENV with which they were inoculated; only one (33%) of three monkeys infected with sylvatic DENV showed a neutralizing antibody response against human-endemic DENV. Virus was detected in two of three monkeys inoculated with sylvatic DENV at low titer (≤ 1.3 log10pfu/mL) and brief duration (≤ 2 days). Clinical signs included rash and elevated aspartate aminotransferase (AST) and alanine aminotransferase (ALT) levels.
在人类中传播的四种虫媒登革热病毒(DENV-1、-2、-3 和 -4)均起源于非人类灵长类动物的地方性、森林性循环。在此,我们首次研究了灵长类动物中的森林性 DENV 感染动态。三只非洲绿猴接种了来自森林性循环的 10(5)噬菌斑形成单位(pfu)DENV-2 株 PM33974,一只非洲绿猴接种了 10(5)pfu 来自人类循环的 DENV-2 株新几内亚 C。四只猴子均针对接种的 DENV 株发生血清转化(80%蚀斑减少中和试验滴度[PRNT80]升高四倍以上);仅三名感染森林性 DENV 的猴子中的一名(33%)对人源性流行的 DENV 产生了中和抗体反应。在接种森林性 DENV 的三只猴子中的两只猴子中,病毒以低滴度(≤1.3log10pfu/mL)和短暂时间(≤2 天)检测到。临床症状包括皮疹和天门冬氨酸转氨酶(AST)和丙氨酸转氨酶(ALT)水平升高。