Volume 14, Number 11—November 2008
Use of Malaria Rapid Diagnostic Test to Identify Plasmodium knowlesi Infection
Reports of human infection with Plasmodium knowlesi, a monkey malaria, suggest that it and other nonhuman malaria species may be an emerging health problem. We report the use of a rapid test to supplement microscopic analysis in distinguishing the 5 malaria species that infect humans.
Recent reports of Plasmodium knowlesi infections in humans in Sarawak and Sabah in Borneo and in the Pahang Peninsula of Malaysia have focused attention on the potential of monkey malarias to be a human health issue (1,2). As much as 70% of malaria infections in regional hospitals in Borneo are the result of P. knowlesi infection; similar infections have been found in Thailand, the Philippines, and Singapore (3–5). To date, only patients in hospitals are being screened for the disease. To better understand the epidemiology of this apparent outbreak of P. knowlesi in humans, one needs a method to rapidly screen both monkeys and humans in areas of high disease prevalence, regardless of their present health status. Thus, a rapid test that could detect and distinguish among the primate malarias would not only benefit individual patients but would also provide an important epidemiologic tool to monitor the overall risk and prevalence of malaria.
We have known for nearly 8 decades that, under laboratory conditions, several monkey malarias are capable of infecting humans and that P. knowlesi can be transmitted to humans by mosquito bite (6,7). Work in Malaysia by a team from the National Institutes of Health nearly 50 years ago reported that transmission to humans was not occurring to any prevalent extent. Currently, we see major foci of the disease, which can be life-threatening. Although the current overall incidence of P. knowlesi infection in humans is low, an exacerbating problem is that it can be consistently misdiagnosed by microscopy as the more benign human malaria, P. malariae (1,2,8,9). The rapid replication rate of P. knowlesi and the resulting high level of parasitemia warrant immediate and aggressive treatment, whereas P. malariae does not. Although the use of PCR has been essential to defining the problem, a more rapid diagnosis would be an important tool for prompt medical treatment. Furthermore, incorporating the capability to detect P. knowlesi into existing rapid tests already capable of detecting the other 4 Plasmodium species that infect humans (P. falciparum, P. vivax, P. ovale, and P. malariae) would be beneficial.
P. knowlesi is transmitted by members of the Anopheles leucosphyrus group of mosquitoes that resides in the upper canopy of the forests in large areas of Southeast Asia; these Anopheles mosquitoes have infrequent contact with humans (10). With increasing encroachment into the forest areas to provide farmland, however, humans are likely to increase their exposure to this vector. The potential for P. knowlesi infection as well as other monkey malarias to expand into the human population is real. While the P. knowlesi parasite is carried by zoophilic mosquitoes, some monkey malarias such as P. cynomolgi and P. inui are transmitted by the same mosquito vectors that carry human malaria and therefore represent an even wider threat.
One important test developed for detecting human malarias is an antigen-capture test based on monoclonal antibodies (MAbs) to plasmodium lactate dehydrogenase (pLDH). The 4 human malarial LDH isoforms have been cloned, and >20 MAb have been raised that differentially recognize epitopes among the isoforms (11,12). The specificity of a subset of these antibodies is shown in Figure 1. Of the 4 human Plasmodium spp., antibodies such as 17E4 and 7G9 specifically bind only to P. falciparum LDH, whereas antibodies such as 11D9 and 13H11 bind only to P. vivax LDH.
Using this panel of antibodies, we show that we can distinguish P. knowlesi from P. malariae. P. knowlesi binds to both the “falciparum-specific” (17E4/7G9) and the “vivax-specific” (11D9/13H11) antibodies (Figure 1, panels A and B). Furthermore, P. knowlesi does not react with 10D12 (an antibody specific for P. ovale), 7E7 (an antibody that reacts strongly with P. malariae and weakly with P. falciparum), or 9C1 (an antibody that reacts exclusively with P. ovale and P. malariae). Detecting P. knowlesi in monkeys, which often are co-infected with several other malaria parasites, is also important and can be achieved with the same panel of antibodies. We have tested the reactivity of the P. falciparum–specific antibody (17E4/7G9) with the other monkey malarias known to be indigenous to Malaysia (P. cynomolgi, P. inui, and P. fieldi) and found that none react (Figure 1, panel C). This then serves as a basis for distinguishing P. knowlesi from the other prevalent forms of monkey malaria.
The unexpected pattern of antibody recognition on which we based our tests led us to examine the molecular basis of recognition (Figure 2). As expected, P. knowlesi LDH is highly similar to the known pLDH isoforms. We found that only a few residue differences could account for the epitope differences detected by the 17E4/7G9 and 11D9/13H11 antibodies. We first generated a 3-dimensional model of P. knowlesi LDH and then mapped surface-exposed residues that were uniquely shared by P. falciparum or P. vivax isoforms. The protein structure was calculated by using the structures of P. falciparum and P. vivax LDH (PDB: 2A94 and 2AA3) and the WURST threading server (13). Here, only a few patches of residues were found to describe the P. vivax–specific epitope, and only 1 residue (K115) was found to describe the P. falciparum–specific epitope (Figure 2, panel B). Thus, the existing MAbs perform well at distinguishing pLDH isoforms despite only a small number of different surface-exposed residues.
These data show that pLDH antibodies that detect P. falciparum and P. vivax can also be used to detect and distinguish P. knowlesi. The 1 major caveat is that a P. knowlesi infection cannot be distinguished from a mixed infection with both P. vivax and P. falciparum in the blood. Mixed infections of this description, however, are infrequent, as these species do not proliferate concurrently when both are present in the blood (14,15). Furthermore, any confusion would be resolved by microscopic examination of blood that, while inadequate to distinguish P. knowlesi and P. malariae, would serve to distinguish P. knowlesi from mixed infections.
Obviously, an antibody specific for P. knowlesi would be optimal if the threat of P. knowlesi increases. Although development of a specific antibody would be a considerable investment, our epitope analysis discussed here indicates that only small sequence differences in pLDH isoforms are required to generate antibody panels capable of uniquely distinguishing animal pLDH isoforms.
Dr McCutchan is head of the Regulation of Growth and Development Section of the Laboratory of Malaria and Vector Research at NIAID. His work on malaria, which spans over 25 years, has resulted in the publication of >100 manuscripts on such subjects as vaccine development, parasite diagnosis, and antimalaria drug development.
We thank Brenda Rae Marshall for editorial assistance.
This work was supported by the Intramural Research Program of the Division of Intramural Research, National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health.
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Suggested citation for this article: McCutchan TF, Piper RC, Makler MT. Use of malaria rapid diagnostic test to identify Plasmodium knowlesi infection. Emerg Infect Dis [serial on the Internet]. 2008 Nov [date cited]. Available from http://wwwnc.cdc.gov/eid/article/14/11/08-0840.htm
Comments to the Authors
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