Plasmodium vivax Seroprevalence in Bred Cynomolgus Monkeys, China

To the Editor: Malaria caused by Plasmodium spp. is one of the most prevalent parasitic diseases in the world, especially in tropical countries. P. vivax represents the second most prevalent of malaria species. Therefore, as measures to control the high death rates in humans caused by P. falciparum become more effective, P. vivax is likely to become the primary malaria threat (1). In P. vivax infection, the main clinical signs and symptoms are fever, chills, nausea and vomiting, generalized body pain and fatigue, toxic shock and pulmonary edema, retinal hemorrhage, renal failure, uremic encephalopathy, and thrombocytopenia (2–6). Because of their phylogenetic proximity to humans, nonhuman primates have been used extensively as animal models of human diseases (7). Thousands of workers come in contact with monkeys, but little information about the prevalence of P. vivax in bred cynomolgus monkeys (Macaca fascicularis) is available worldwide. The objective of our investigation was to examine whether P. vivax seroprevalence is present in bred cynomolgus monkeys in the People’s Republic of China. A total of 328 blood samples were collected by venous puncture during June 2008–September 2009. Of these, 224 blood samples were from 4 nonhuman primate centers in Guangxi Zhuang Nationality Autonomous Region and 108 blood samples were from 2 nonhuman primate centers in Guangdong Province. All of the cynomolgus monkeys were caged. Each cage has 2 rooms, 1 indoors and 1 outdoors. The monkeys spend ≈10 hours in the outdoor room each day during the daytime. The age and sex of monkeys are listed in the Table. Serum samples were separated and stored at –20°C before testing. Serum samples were tested for P. vivax antibodies by using a commercially available ELISA kit (Tiancheng Yiliu Co., Ltd, Shanghai, China), according to the manufacturer’s instructions. This kit uses biotinylated anti–P. vivax as a coating antigen and is specifi cally for monkeys. Positive and negative control serum samples were provided in the kit and included in each test. Those samples with doubtful results were retested. Differences in the seroprevalence of P. vivax in bred cynomolgus monkeys according to sex and area were analyzed by using the χ2 test in SPSS 13.0 standard version for Windows (SPSS Inc., Chicago, IL, USA). The differences were considered to be statistically signifi cant when the p value obtained was <0.05. The total prevalence of anti–P. vivax antibodies in bred cynomolgus monkeys in southern China was 3.4% (11/328), which was lower than the prevalence of anti–P. vivax antibodies in captured monkeys (Alouatta seniculus, Saguinus midas, and Pithecia pithecia) in French Guiana (8). The prevalence in female monkeys (3.1%, 5/161) was slightly lower than that in male monkeys (3.6%, 6/167); the seroprevalence of 3.6% (8/224) in Guangxi Zhuang Nationality Autonomous Region was slightly higher than that in Guangdong Province (2.9%, 3/104) (Table), but these differences were not signifi cant (p>0.05). A total of 52 monkey serum samples from nonhuman primate center E in Guangdong Province were found seronegative for P. vivax antibodies (Table). The difference in prevalence of P. vivax antibodies in different nonhuman primate centers may be related to differences in ecologic and geographic conditions, climate conditions, as well as in the management practices. All of the nonhuman primate centers are surrounded by hills or paddy fi elds, and the environment is favorable for Anopheles mosquitoes. The mosquito control measures, including the use of antimosquito insecticides and good drainage facilities for preventing water collection on the ground, were better executed at nonhuman primate center E than at the other nonhuman primate centers.