Plasmodium knowlesi Reinfection in Human

To the Editor: In 2004, a large number of patients infected with Plasmodium knowlesi (simian malarial species) were reported in Sarawak, Malaysia (1). P. knowlesi infection was also reported in Peninsular Malaysia (2). Here we report a case of human P. knowlesi reinfection. Phylogenetic sequence analysis shows that the first and second infections were caused by different strains of P. knowlesi.

To the Editor: In 2004, a large number of patients infected with Plasmodium knowlesi (simian malarial species) were reported in Sarawak, Malaysia (1). P. knowlesi infection was also reported in Peninsular Malaysia (2).
Here we report a case of human P. knowlesi reinfection. Phylogenetic sequence analysis shows that the fi rst and second infections were caused by different strains of P. knowlesi.
The patient was a 41-yearold businessman from Peninsular Malaysia. He was fi rst admitted to the hospital in October 2009 with a 4-day history of fever, chills, and headache. His symptoms started ≈2 weeks after a 4-wheel-drive expedition with overnight camping in a jungle in Raub in the state of Pahang. Initial examination showed thrombocytopenia and hepatitis, and P. knowlesi malaria was subsequently confi rmed with nested PCR by using diagnostic primers for Plasmodium small subunit (SSU) rRNA as described (3). He recovered fully after a treatment course of oral quinine plus doxycycline.
The patient was readmitted to the hospital on June 11, 2010, with a 5-day history of fever and chills and rigors, followed by epigastric pain, nausea, and vomiting. His symptoms began 15 days after another 4-wheel-drive expedition with overnight camping in a jungle in Tanjung Malim in the state of Perak. Laboratory investigations showed severe thrombocytopenia. Falciparum malaria was diagnosed initially on the basis of blood fi lm examination with 1% parasitemia. The patient was administered oral mefl oquine (750 mg) followed by 500 mg and 250 mg at 6 hours and 12 hours, respectively. His parasitemia level increased from 1.0% to 2.5% despite treatment with mefl oquine. Oral quinine and doxycycline were initiated. However, renal function deteriorated further, and acute hemolysis was evident. Oral quinine was changed to intravenous quinine infusion, and oral combination of artemether and lumefantrine was added. Intermittent hemodialysis was initiated, and 1 unit each of packed erythrocyte cells and whole blood were transfused. Parasitemia eventually cleared on June 16, 2010. PCR confi rmed P. knowlesi in the patient's blood sample.
P. knowlesi has a 24-hour asexual life cycle, resulting in daily schizont rupture, which leads to high parasitemia levels. Delay in appropriate treatment, as seen in the second infection of the patient in our study, can cause severe conditions, such as thrombocytopenia, acute renal failure, and hemolysis (4).
To confi rm the reinfection, blood samples collected from the patient at the fi rst and second infections were reexamined. Giemsa-stained thin and thick blood fi lms showed 2.0% and 2.5% parasitemia for the fi rst and second infections, respectively. Some parasites showed morphologic features resembling those of P. falciparum ring forms and P. malariae trophozoite band forms.
We confi rmed the P. knowlesi in the fi rst and second infections by PCR, sequencing and analysis of the highly variable csp gene (5), and SSU rRNA. The nucleotide sequences of the gene were aligned by using ClustalW and analyzed by using MEGA4 software (6). The csp gene of the isolate from the fi rst infection (denoted as Pkpah-1) was 1,217 nt, whereas the gene of the isolate from the second infection (denoted as Pkprk-1) contained 1,277 nt. This difference was due to the absence of 2 repetitive sequences 1314 Emerging Infectious Diseases • www.cdc.gov/eid • Vol. 17, No. 7, July 2011 Figure. Phylogenetic tree based on nucleotide sequences of small subunit rRNA of Plasmodium knowlesi isolates from Peninsular Malaysia (Pkpah-1, Pkprk-1, KAL-1) and surrounding regions (denoted by GenBank accession nos.). The tree was constructed by using the maximum-parsimony method. The percentage of replicate trees in which the associated isolates cluster together in the bootstrap test (10,000 and 1,000 replicates, no differences were observed) is shown next to the branches. Phylogenetic analysis was conducted by using MEGA4 (6). Scale bar indicates nucleotide substitutions per site.
(5′-GTGGAGCAAATGCAGGACA ACCGAATGCAG-3′;5′-AGCAA AT G C A G G A C A A C C G A AT GCAGAAGG-3′) in the csp gene of Pkpah-1. Furthermore, the alignment showed 21 variable sites between the genes. Phylogenetic analysis based on SSU rRNA sequences indicated that Pkpah-1 and Pkprk-1 formed a cluster, which was more related to P. knowlesi isolates from Thailand than to isolates from Sarawak, a Malaysian state in Borneo Island (Figure). Another isolate from Peninsular Malaysia, KAL-1, was also grouped with Pkpah-1 and Pkprk-1. The KAL-1 isolate was detected in a traveler from Finland returning from Peninsular Malaysia in 2007 (7). P. knowlesi infection does not relapse because the parasite has no liver hypnozoite stage (8). Reinfection and recrudescence are not uncommon in malaria. The fi nding in the patient reported here indicates reinfection rather than recrudescence as confi rmed by PCR genotyping. He acquired his infection while jungle trekking in Raub in October 2009 and was reinfected in Tanjung Malim in June 2010 (the great-circle distance between the 2 locations is 38.61 km). This case shows that immunity toward P. knowlesi infection is strain specifi c as has been observed in other malaria species (9). P. knowlesi is a nonhuman primate malaria species, and humans are accidental hosts when they go into areas where macaques dwell. P. knowlesi can cause reinfection and can potentially be severe in areas where it is endemic. Travelers to forested areas of endemicity should be advised to take strict antimosquito measures and prophylaxis. Physicians should be aware that P. knowlesi infection is a vital differential diagnosis in febrile travelers with a recent travel history to forested areas in Southeast Asia.

Antibody to Arenaviruses in Rodents, Caribbean Colombia
To the Editor: The ≈20 recognized arenaviruses in the Americas are hosted by rodents of the family Cricetidae; 1 exception may be hosted by a bat (genus Artibeus, family Phyllostomidae) (1). Pichindé virus, hosted by Oryzomys albigularis, was described from animals in the Pichindé Valley near Cali, Colombia (2), and antibody reactive to Pichindé virus was found in 2 of 82 serum samples from humans in the same area. No studies of arenavirus infection in rodents or humans have been conducted in Colombia since 1971. Although Pichindé virus is not associated with human disease, Guanarito virus, which is hosted by Zygodontomys brevicauda, the short-tailed cane mouse (3,4), causes Venezuelan hemorrhagic fever in the Venezuelan state of Portuguesa (5). This state borders on Colombia, and Z. brevicauda is a common species in Caribbean Colombia. Our aim was to determine the prevalence of antibody to arenaviruses among wild rodents in this region.