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Memórias do Instituto Oswaldo Cruz

Print version ISSN 0074-0276On-line version ISSN 1678-8060

Mem. Inst. Oswaldo Cruz vol.95 n.3 Rio de Janeiro May/Jun. 2000

http://dx.doi.org/10.1590/S0074-02762000000300011 

SHORT COMMUNICATION

Aotus infulatus Monkey is Susceptible to Plasmodium falciparum Infection and May Constitute an Alternative Experimental Model for Malaria

Vol. 95(3): 363-365, May/Jun. 2000

Leonardo JM Carvalho, Salma G Oliveira*, Francisco A Alves**,
Maria CO Brígido**, José APC Muniz**, Claudio T Daniel-Ribeiro/+

Laboratório de Pesquisas em Malária, Departamento de Imunologia, Instituto Oswaldo Cruz, Av. Brasil 4365, 21045-900 Rio de Janeiro, RJ, Brasil *Serviço de Parasitologia, Instituto Evandro Chagas, Fundação Nacional de Saúde, Av. Almirante Barroso 492, Belém, PA, Brasil **Centro Nacional de Primatas, FNS, BR316 km 7 s/no, Ananindeua, PA, Brasil

Aotus is one of the WHO-recommended primate models for studies in malaria, and several species can be infected with Plasmodium falciparum or P. vivax. Here we describe the successful infection of the species A. infulatus from eastern Amazon with blood stages of P. falciparum. Both intact and splenectomized animals were susceptible to infection; the intact ones were able to keep parasitemias at lower levels for several days, but developed complications such as severe anemia; splenectomized monkeys developed higher parasitemias but no major complications. We conclude that A. infulatus is susceptible to P. falciparum infection and may represent an alternative model for studies in malaria.

Key words: Aotus infulatus - Plasmodium falciparum - malaria - primate model

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The neotropical non-human primate Aotus has long been known as a model for human malaria because it can support infection by human malaria parasites, including Plasmodium falciparum and P. vivax (Collins 1994). A. lemurinus griseimembra from northern Colombia is reported to be highly susceptible to both sporozoite and erythrocytic stage infection (Hershkovitz 1983, Collins et al. 1996), but the difficulties in obtaining this species (export has been prohibited) have led to the search, in countries other than Colombia, for other species within the genus Aotus as alternative models for malaria. Species belonging to both the Gray Neck (e.g. A. lemurinus lemurinus and A. vociferans) and the Red Neck (e.g. A. nancymai and A. azarae boliviensis) groups have been used, especially for vaccine and drug studies. A. lemurinus lemurinus from Panama has been recently reported as supporting sporozoite infection with the Santa Lucia strain of P. falciparum (Gramzinski et al. 1999). The Red Neck species A. infulatus is endemic in eastern Amazon (Pieczarka & Nagamachi 1988) and exclusive of the Brazilian territory; this species presents a karyotype and fur pattern similar to A. azarae boliviensis, but despite Pieczarka and coworkers have been proposing that both may form a single species (Pieczarka et al. 1993), the original classification by Hershkovitz (1983), based on differences in karyotype, fur pattern and geographical distribution, has been maintained to date. The susceptibility to plasmodial infection varies among species bearing different karyotypes. Splenectomized A. azarae boliviensis has been reported to be highly susceptible to different strains of P. falciparum (Collins et al. 1986) but, to our knowledge, A. infulatus from eastern Amazon has not been approached as a potential model for malaria. Here, we describe the successful infection of A. infulatus by assexual erythrocytic stages of P. falciparum, thus indicating that this species may be an alternative to others within the genus Aotus for research in malaria.

A. infulatus monkeys used in the present study were all bred in captivity and maintained in the Brazilian National Primate Center (Cenp). The colony was originally formed in 1984 with Aotus monkeys captured in both sides of Tocantins river, eastern Amazon, during flooding of Tucuruí dam's lake. They were classified as A. infulatus, and a number of them were karyotyped; they were shown to be homogeneous, presenting 2n chromosome numbers of 49 for males and 50 for females (Pieczarka & Nagamachi 1988). Most of the rescued animals were released in safe places and a number of them were taken to Cenp and gave origin to the present colony. Five monkeys (three males and two females), two of them splenectomized (one male and one female), were inoculated intravenously with 1x106 P. falciparum-parasitized red blood cells (pRBC), having a clear predominance of ring forms and young trophozoites (FVO strain, a kind gift of Dr Socrates Herrera, Univalle, Cali, Colombia). Parasitized RBC were obtained from a donor A. infulatus previously inoculated with a thawed cryostabilate. Parasitemia was daily followed up by the examination of Giemsa-stained thick and thin blood films and expressed in terms of percentage of pRBC in relation to the total number of RBC. Hematocrit was evaluated each 3-4 days (pre-infection values ranged from 44% to 62%; median: 48%). Whenever necessary, monkeys were treated with a single dose of mefloquine (15 mg/kg), which, in all cases, caused immediate drop in parasitemia and a clearance of parasites within 1-4 days.

First parasites were detected in thick smears on day 4 of infection, both in the splenectomized and in the intact monkeys. Parasitemia grew then exponentially in the following days, until reaching values near 1% (around day 7 for most monkeys _ Fig. 1a). From then, parasitemia kept growing although in a non-geometrical basis and was apparently assynchronous. Mature forms were commonly observed; in some cases the percentage of schizonts reached 15% of all forms in peripheral blood, and that of mature trophozoites up to 20%, though the rule was the clear predominance of ring and young trophozoites. Common features of young trophozoites were double chromatin and peripheric localization in the RBC.

Body (rectal) temperature was followed from day 2 to 10 (Fig. 1b). Pre-infection temperatures ranged from 38.5°C to 40°C; in the first days, there was considerable variation in individual temperatures but, from day 7 on, all monkeys (both splenectomized and intact) showed a synchronous variation in rectal temperature: at each two days, temperatures peaked at 41-41.5°C, decreasing to nearly 40°C on the day after. This observation suggests that P. falciparum in this model probably keeps a periodicity similar to that observed in humans.

In the absence of previous data of infection with malaria parasites in this particular species of Aotus, we evaluated both intact and splenectomized monkeys. In the two splenectomized ones, parasitemia reached more than 5% on day 10; one monkey was treated on this day and the other, left untreated for longer, supported well high parasite load (parasitemia of 26% on the day of treatment _ day 16) without developing signs of clinical disease or of severe anemia (hematocrit of 35% on day 18).

One of the three intact monkeys also reached a 5% parasitemia on day 10 and was treated. The second one showed an apparent control of parasite growth, with a 2% parasitemia on day 10, but presented clinical signs of disease (prostration) on this day and was treated as well. The third one showed no clinical disease and controlled well the parasitemia, which was relatively stable around 2% up to day 17; on day 18, parasitemia rose to 5.5%, and the monkey was treated. This intact animal showed signs of weakness and, despite keeping low parasitemia, developed severe anemia by day 18 (13% hematocrit). After having cleared the parasitemia, this animal received a blood transfusion but died a few days later. The three monkeys treated on day 10 showed, at that moment, the following hematocrits: 37% (splenectomized), 38% and 46% (intact).

The fact that the intact monkey (in contrast to the splenectomized one) left untreated developed severe anemia in spite of having low parasitemia may represent an additional evidence that spleen controls parasite growth probably by destroying large numbers of RBC, and that other mechanisms such as bone marrow depression, which may depend on the presence of the spleen, might also take place (Ferreira-da-Cruz & Daniel-Ribeiro 1996). Despite this possible deleterious effect, the spleen plays a crucial role in immunity against malaria and a decision for working with splenectomized animals should be carefully considered in any experimental procedure, since the use of intact animals may provide more reliable data in models that are, by definition, artificial. In any case, each infected individual must be closely followed up hematologically and treated before developing life-threatening severe anemia.

In the present work, both intact and splenectomized A. infulatus were shown to be susceptible to P. falciparum infection, though at different degrees (splenectomized animals had higher susceptibility, as expected). Accordingly, splenectomized A. azarae boliviensis, which presents a karyotype similar to A. infulatus, is also highly susceptible to P. falciparum infection (Collins et al. 1986). Taken together, these data indicate that A. infulatus can be a suitable model for P. falciparum malaria, at least for erythrocytic stages. However, testing a larger number of animals with different inocula is necessary to determine more precisely several parameters, such as: pre-patent periods, course of infection and its pathological consequences. Other approaches should include: definition of the susceptibility of this species to other P. falciparum isolates as well as to P. vivax, and attempts to infect A. infulatus with sporozoites. The establishment of A. infulatus as a reliable model for studies in malaria would be welcome in view of the numerous restrictions imposed for malaria vaccine and drug development and testing worldwide.

 

bul1.gif (879 bytes)  REFERENCES

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Fig. 1

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The authors dedicate this paper in honor of the Instituto Oswaldo Cruz, on the occasion of the centenary of its foundation, 25 May 1900.

Financial support: Instituto Oswaldo Cruz, Fiocruz; Centro Nacional de Primatas; European Commission _ Primate Vaccine Evaluation Network.

+Corresponding author. Fax: +55-21-280.1589. E-mail: ribeiro@ioc.fiocruz.br and recipient of a fellowship from the Conselho de Desenvolvimento Científico e Tecnológico, CNPq.

Received 5 October 1999

Accepted 28 December 1999

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