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Is zoonotic Plasmodium vivax malaria an obstacle for disease elimination?



The groundwork for malaria elimination does not currently consider the potential of Plasmodium zoonotic cycles that involve non-human primates (NHPs) in sylvatic environments. Since vivax malaria is less responsive to control measures, finding Plasmodium vivax infected NHPs adds even more concern.


Both Free-living monkeys in forest fragments inside the urban area and captive monkeys from a local zoo had blood samples tested for Plasmodium species.


In this study, among the Neotropical monkeys tested, three (4.4%), one captive and two free-living, were found to be naturally infected by P. vivax.


This important finding indicates that it is necessary to estimate the extent to which P. vivax NHP infection contributes to the maintenance of malaria transmission to humans. Therefore, the discussion on wildlife conservation and management must be incorporated into the malaria elimination agenda.


The world is joining forces, though not just to control malaria cases, but also to try to eliminate this disease, which is an important cause of death in economically disadvantaged countries. The World Malaria Report 2020 [1] and the Global Technical Strategy for Malaria 2016–2030 [2] both list some biological challenges and have identified the threats involved in eliminating malaria, such as parasite resistance to anti-malarials, vector control and asymptomatic or undiagnosed people, and these are the focus of discussions. However, these discussions may be missing one important target, i.e., that of the wild animal reservoir.

Plasmodium falciparum, Plasmodium malariae, Plasmodium ovale, and Plasmodium vivax are the main parasites transmitted by mosquito vectors of the genus Anopheles and cause malaria in humans. This transmission cycle of malaria theoretically makes it easier to fight this disease since it does not involve a wild animal reservoir, compared to other pathogens that have a complex cycle because they can infect more than one vertebrate host. The evolution of malaria parasites highlights their propensity to switch hosts; both P. vivax and P. falciparum first arose as human pathogens after a host switch from great apes in Africa [3, 4]. It is common knowledge that the transmission of P. vivax and P. falciparum occurs between infected mosquitoes and humans; however, some research groups have identified the possibility of a malaria reservoir in non-human primates [5, 6]. Zoonotic malaria transmission occurs in forests environments, during the close contact between humans and the mosquitoes that feed on Plasmodium-infected non-human primates (NHPs), and this is increasing due to habitat destruction and human encroachment into NHP habitats [7].

Plasmodium cynomolgi, and mainly Plasmodium knowlesi, are parasites that typically infect forest monkeys in Asia, but they can also cause zoonotic malaria when humans enter this parasite cycle. Another two Plasmodium species that can cause zoonotic malaria in Latin America are Plasmodium brasilianum and Plasmodium simium [8,9,10]. These zoonotic infections can be misdiagnosed during microscopy because the morphology of these parasites is similar to that of P. malariae and P. vivax, respectively [3, 11]. These pairs of parasites, P. brasilianum/P. malariae and P. simium/P.vivax, also have a very close genetic relationship. Plasmodium vivax came from Africa and, based on genomic data, there is a hypothesis that P. simium originated from humans infected with P. vivax that was transferred to New World monkeys [8, 12]. There is also an unresolved question of the host transfer and whether P. brasilianum in platyrrhines is a result of the cross-species transfer of P. malariae that was brought to the New World [3, 13] or whether they are in fact one species [14].

In 2019, Brazil was responsible for 19% of all reported malaria cases in the Americas, and 99.9% of all reported Brazilian malaria cases are from the endemic Amazon region. Furthermore, more than 80% of the cases in Brazil were caused by P. vivax [1]. Despite this, there is a substantial number of autochthonous cases reported in the extra-Amazonian region; 1,047 cases were reported in this area between 2006 and 2016 [15]. It is important to highlight that P. simium has only been reported in NHPs of the Atlantic Forest on the southern and southeastern states of the Brazilian coast [6, 16], though it can also infect humans, which evidences the exchange of parasitic species between NHPs and humans [9, 11]. Thus, the aim of this study is to screen NHPs in Manaus, in the Brazilian Amazon, for identification of Plasmodium infection, including the differential diagnosis of P. simium.


In a study in Manaus, Amazonas state, Brazil, free-living monkeys were captured in forest fragments inside the urban area using Tomahawk Live (Tomahawk, Wisconsin, USA) traps baited with fruit. Blood samples were collected via femoral vein puncture (1–1.5 mL), and samples were then transported to the laboratory. The animals were maintained in cages and were held overnight and then released in the early morning of the next day at the site of capture. It is important highlight that all animals seemed healthy and none appeared to be in need of veterinary medical assistance. Captive monkeys from a local zoo also had blood samples taken.

It was possible to carry out blood smears for 40% of the samples, but all samples had DNA extraction from blood using the QIAamp DNA Blood Mini Kit (Qiagen, Hilden, Germany), according to the manufacturer’s instructions. The molecular diagnosis was performed using nested PCR targeting the 18 S small subunit (SSU) rRNA and the mitochondrial coxI gene [15, 17]. The nested PCR reactions targeting the 18 S SSU used the protocol and primers described by Snounou et al. for diagnosis of Plasmodium species infecting humans [17]. The primers described for P. malariae were employed to identify P. brasilianum infections in NHPs and the primers for P. vivax were used to identify P. simium infections in NHPs, since these primers do not discriminate among these two pairs of Plasmodium species. The differential diagnosis of P. simium in relation to P. vivax was based on the nested PCR of the coxI gene fragment and subsequent enzymatic digestion, using primers and the protocol described by Alvarenga et al. [15].

In the PCR assays, the following were used as positive controls: (i) P. falciparum DNA from 3D7 strain in vitro culture (IRR-FIOCRUZ MINAS) [15]; (ii) P. vivax DNA, from a patient previously diagnosed by microscopy and nested PCR [15]; (iii) P. simium DNA from an acute infection in an NHP with parasitaemia confirmed by optical microscopy (BL10) [18]; (iv) P. brasilianum DNA from the Malaria Research and Reference Reagent Resource Center (MR4–ATCC, USA). The negative control was from non-human primates from areas without malaria transmission.

DNA sequencing was performed as described by Alvarenga et al. [15], using mitochondrial coxI gene PCR products, which resulted in sequences that covered both single nucleotide polymorphisms (SNPs) that are considered specific to P. simium [15]. Plasmodium simium differs from the closely related P. vivax in two unique single nucleotide polymorphisms (SNPs) in the mitochondrial genome, at positions 3535 (T > C) and 3869 (A > G) [18]. The differential diagnosis of P. simium in relation to P. vivax was based on the nested PCR of a coxI gene fragment and subsequent enzymatic digestion, using the primers and the protocol described by Alvarenga et al. [15].

The polymorphism at position 3535 generated a new restriction enzyme site for HpyCH4III, and the digestion of the amplified fragment resulted in two fragments of similar lengths (118 and 126 bp), where “T” in P. vivax, as well in all other Plasmodium species tested, is substituted by a “C” in P. simium [15].

The fragments were electrophoretically separated in an automatic DNA sequencer (ABI 3730, ThermoFisher). Sequences were aligned using the ClustalW software in the Bioedit package [19] and Chromas software [20].

Evolutionary history was inferred by using the maximum-likelihood method and the Tamura-Nei model [21]. The proportion of sites in which at least 1 unambiguous base is present in at least 1 sequence for each descendent clade is shown next to each internal node in the tree. Evolutionary analyses were conducted in MEGA X [22].


None of the blood smears were positive in the microscopy examination. DNA from 88 samples obtained from 68 NHPs (20 samples were from recapture) (Table 1) was screened for Plasmodium spp. using two nested PCR methods. There was no amplification for the 18 S gene; however, three samples (4.4%) were positive in the nested PCR for the coxI mitochondrial gene of Plasmodium spp, of them only one had blood smears carry out and analysed but was negative. After restriction enzyme digestion, the profile of the fragments suggested non-P. simium samples (Fig. 1). The P. vivax infection was confirmed using nested PCR/RFLP and sequencing, alignment of partial mitochondrial cytochrome c oxidase subunit I (coxI) gene sequences of P. vivax isolated from one captive (H47) and two free-living NHPs had 100% identification with GeneBank sequences from P. vivax (MG571499.1; MG571498.1) (Fig. 2). Three out of the 68 NHPs, which were two free living Saguinus bicolor from the forest fragment of the Federal University of Amazonas (UFAM)—one male (H52) and one female (H73), and one captive Saimiri sciureus female (H47) from the army zoo—Centro de Instrução de Guerra na Selva (CIGS) (Fig. 2). The first two had two samples collected at different points in time, but just one sample of each was positive. (H52) was captured for the first time in October 2018 and recaptured in July 2019, and only the first sample was positive. (H73) was captured for the first time in June 2019 and the second sample, which was collected 46 days later, was positive.

Table 1  Non-human primates included in the study


Three samples amplified from Neotropical NHPs using nested PCR of coxI gene fragments were sequenced in both strands, and the consensus sequences were compatible with P. vivax species. This is an important finding when trying to evaluate zoonotic vivax infection, and may help us to begin to understand the real role of NHPs in malaria transmission in the Americas. In 2019, in the western Brazilian Amazon, Silva et al. detected P. vivax and P. falciparum DNA in 2.04% (2/98) and 4.08% (4/98), respectively, of Neotropical primates in captivity, using another protocol [23]. These authors described two individual Saguinus bicolor were tested, and one of them was positive for P. falciparum, however 12 Saimiri sciureus were screened for Plasmodium, but none were positive [23]. In a study carried out in 1966, using intracardiac or subcutaneous inoculation, three Saimiri sciureus were experimentally infected with the pooled sporozoites from three specimens of Anopheles cruzi, though all of them were negative on daily examination of thick blood smears [11].

In Colombia, molecular analysis found Neotropical NHPs that were positive for Plasmodium spp.; P. falciparum was detected in two fecal samples of Alouatta seniculus, while Cebus versicolor, Ateles hybridus and Alouatta seniculus were infected with P. vivax/simium, and these last two species and Aotus griseimembra had fecal samples that were positive for P. malariae/brasilianum. Blood samples were also tested in this study, and one Ateles hybridus and one Alouatta seniculus were positive for P. vivax/simium, while these same two species plus Aotus griseimembra and Cebus versicolor were positive for P. malariae/brasilianum [24]. The present paper shows novel results in regards to the species Saguinus bicolor. These are important since, in the majority of previous studies, positive results for P. vivax in NHPs were only serological finds and indistinguishable positive PCR results for P. vivax/P. simium [25, 26].

Plasmodium vivax and P. simium can be misdiagnosed due to their morphological and molecular similarity. Malaria caused by P. simium is apparently restricted to regions of the Atlantic Forest on the coast of southeastern and southern Brazil [6]; despite this, it was possible to identify three NHPs with P. vivax using differential diagnosis. Identification of human malaria parasites in NHPs in the north of this country gets deserves attention since a zoonotic cycle for P. vivax in the Americas has not yet been considered due to a lack of scientific evidence. Sampling was performed in Manaus, capital of the Amazonas state and located in the middle of the tropical rainforest (− 3.044653 S, − 60.1071907 W), where more than 2 million people coexist with malaria. Besides socioeconomic difficulties, there are nuances in vivax malaria that complicate all efforts towards malaria elimination in this region, such as its hypnozoite form that causes late relapses, the existence of drug resistant parasites [27] and the loss of social importance since people have become used to living with the disease [28]. It may be that the animal reservoir could be one more obstacle for malaria elimination.

The richness of Neotropical primate species (Platyrrhini) is evidenced by the 171 species in 20 genera and five families [29]; however, there is a big knowledge gap in relation to which species can be infected with Plasmodium species, for how long and their importance in the parasite cycle. In addition, the presence of parasites in the blood of NHPs demands attention and discussion, since NHPs represent an animal reservoir in the vivax malaria cycle and, as such, the risk this presents should return to the discussion agenda.

Three primates (two free living and one captive) that were captured in small forest fragments in the urban area were P. vivax positive. In another study, the presence of two Anopheles species was identified at the CIGS zoo, namely Anopheles matogrossensis and Anopheles nimbus, although they are not species associated with human malaria transmission, which reinforces the results present here and strengthens the hypothesis of a zoonotic cycle. In addition, An. nimbus and Anopheles triannulatus were identified at UFAM [30]. The latter, An. (Nysorhynchus) triannulatus, is considered to be a secondary human malaria vector in some areas in Brazil [31, 32] and a dominant vector in the east of Loreto, Peru [33]. These areas in which vectors and potential vectors were collected (CIGS and UFAM) are the same areas that the primates were found to be positive for P. vivax between 2018 and 2019.

Since Saguinus bicolor is a critically endangered species [34], it is necessary to carry out studies aimed at the impacts that Plasmodium infection can cause on animal health and the conservation of this primate species, which is endemic to Manaus [35].


The data shown here reinforce and bring into question again the possibility of a non-human reservoir of P. vivax in the Amazon, which is worrisome since P. vivax is the agent of the greatest number of cases of malaria in the Americas. Knowledge regarding the disease cycle is essential in order to plan measures for mitigation, as well as for defining targets that help us to achieve the ultimate goal, which is, of course, malaria elimination. The assessment of the frequency of P. vivax infection in NHPs and the evaluation of the ecological importance of these primates as the parasite’s reservoir are urgent measures, and the questions presented herein need to be included in the agenda of further studies. As such, it remains to be determined whether wildlife management as a component of malaria elimination programmes is necessary.

Fig. 1
figure 1

Differential diagnosis of Plasmodium simium infection using nested PCR followed by a digestion with HpyCH4III restriction enzyme. H47 captive Saimiri sciureus, H52 and H73 free-living Saguinus bicolor. 3% agarose gel stained with ethidium bromide. MM:1 kb Plus Ladder (ThermoFischer). D: Digested PCR Product; ND: Undigested PCR product; PCPs: Plasmodium simium; PCPv: Plasmodium vivax; NC: Negative Control

Fig. 2
figure 2

Phylogenetic tree constructed using the maximum-likelihood method with partial mitochondrial sequences of Plasmodium isolates. Plasmodium vivax isolated from NHPs from Brazilian Amazonia: two of them Saguinus bicolor (H52 and H73) and one Saimiri sciureus (H47); P. vivax isolated from human from Amazon region: PvPV/RO1 and PvPV/RO2 (Porto Velho, Rondonia), PvGuy (Guyana), PvAri/RO (Ariquimedes, Rondônia), PvVen (Venezuela), PvFrGui (French Guiana); P. simium isolated from captive (2098, 2302, 3636) and free living NHPs (J9, J11, MB) from Atlantic forest. All P. simium and P. vivax sequences used here were sequenced by Alvarenga et al. 2018. Accession number at Genbank sequences from P. simium, P. vivax, P. brasilianum, P. malariae, P. falciparum, Plasmodium berghei and Plasmodium yoelii are included in the name of each sequence. The three new sequences obtained here are marked by an asterisk. Figures represent whether the host of each isolate is a human or a non-human primate

Data availability

Data analysed during this study is included in this published article and dataset used and/or analysed during current study are available from corresponding author on demand.


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The authors would like to thank Centro de Instrução de Guerra na Selva (CIGs) for their support in NHP collections.


This research was funded by an International Collaborations in Infectious Disease Research (ICIDR) grant, U01 AI115577, which was awarded to NV by the National Institutes of Health and by Fundação de Amparo à Pesquisa do Estado do Amazonas—via Call No. 006/2019 - UNIVERSAL AMAZONAS.

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BAC wrote the initial draft of the manuscript. MG, ERC, ASMM and IJMP captured the NHPs. DB, MO, DAMA and ELS tested the samples. GCM, CFAB, DAMA, MTL and BAC analyzed the test results. MVGL, NV, GCM, DAMA, CFAB and WM reviewed and edited the manuscript. All the authors read and approved the final version of manuscript.

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Correspondence to Bárbara Aparecida Chaves.

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This study was certified by the System of Authorization and Information on Biodiversity (SISBIO), protocol number: 57003-4, issued on 27th July, 2017. The protocol was submitted to and approved by the Research Ethics Committee on Animal Use (CEUA) of the Fundação de Medicina Tropical Doutor Heitor Vieira Dourado (FMT-HVD) (protocol number: 003188, issued 30th October, 2017), as well as by the Institutional Animal Care and Use Committee of the University of Texas Medical Branch (UTMB) (protocol no. 1706039, issued: 1st June, 2017).

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Chaves, B.A., de Alvarenga, D.A.M., Pereira, M.d.C. et al. Is zoonotic Plasmodium vivax malaria an obstacle for disease elimination?. Malar J 21, 343 (2022).

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  • Plasmodium vivax
  • Malaria
  • Zoonotic cycle
  • Malaria elimination
  • Non-human primates