Susceptibility of Panamanian Aotus lemurinus lemurinus to sporozoite-induced Plasmodium falciparum (Santa Lucia) infection

Citation
Ra. Gramzinski et al., Susceptibility of Panamanian Aotus lemurinus lemurinus to sporozoite-induced Plasmodium falciparum (Santa Lucia) infection, AM J TROP M, 61(1), 1999, pp. 19-25
Citations number
23
Categorie Soggetti
Envirnomentale Medicine & Public Health","Medical Research General Topics
Journal title
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE
ISSN journal
00029637 → ACNP
Volume
61
Issue
1
Year of publication
1999
Pages
19 - 25
Database
ISI
SICI code
0002-9637(199907)61:1<19:SOPALL>2.0.ZU;2-P
Abstract
Aotus monkeys are good models for erythrocyte-induced Plasmodium falciparum and P. vivax infections and have been extensively used in malarial drug an d vaccine development. Recently, it has been shown that certain species of Aotus can be infected with sporozoites, and that the degree of susceptibili ty varies among species. We demonstrate here that Panamanian Aotus lemurinu s lemurinus are susceptible to a sporozoite-induced infection, opening the possibility that this species of Aotus could be used as models for testing the efficacy of pre-erythrocytic P. falciparum vaccines and drug candidates directed at the pre-erythrocytic stages of P. falciparum and P. vivax mala ria. In this species, we compared sporozoite infection rates. Two of four a nimals splenectomized prior to infection with sporozoites developed patent parasitemias. Seven of eight animals splenectomized either 7 or 35 days aft er infection became parasitemic. Additionally, we used a P. falciparum-spec ific polymerase chain reaction (PCR) method to detect the early appearance of parasitized erythrocytes in the blood prior to detection by conventional microscopy, and found that the parasitemia was detected first in five anim als by the PCR method, first in three animals by blood film, with one paras itemia detected simultaneously. We also demonstrated the feasibility of inf ecting monkeys located in Panama with sporozoites isolated at an insectary in Atlanta, thus documenting the feasibility of similar studies where the i nsectary and monkey colony are not in the same location. A subsequent attem pt to infect these monkeys using sporozoites was not successful, suggesting that this model of human malaria is not yet ready for routine use in vacci ne or drug efficacy screening. This model merits further study because of t he importance of testing pre-erythrocytic P. falciparum malaria vaccines an d drugs in animals.