Molecular characterization of misidentified Plasmodium ovale imported cases in Singapore

被引:35
作者
Chavatte, Jean-Marc [1 ]
Tan, Sarah Bee Hui [1 ]
Snounou, Georges [2 ,3 ]
Lin, Raymond Tzer Pin Valentine [1 ,4 ,5 ]
机构
[1] Malaria Reference Ctr, Natl Publ Hlth Lab, Minist Hlth, Singapore 138623, Singapore
[2] Univ Paris 06, UPMC UMRS CR7, Univ Sorbonne, F-75005 Paris, France
[3] CNRS, INSERM, U1135, Ctr Immunol & Malad Infect CIMI Paris,ERL 8255, F-75013 Paris, France
[4] Natl Univ Singapore Hosp, Dept Lab Med, Singapore 119074, Singapore
[5] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Microbiol, Singapore 117545, Singapore
来源
MALARIA JOURNAL | 2015年 / 14卷
关键词
Plasmodium ovale curtisi; Plasmodium ovale wallikeri; Singapore; Imported cases; Misidentification; Morphology; Molecular characterization; HUMAN MALARIA PARASITE; RIBOSOMAL-RNA; INDUCED INFECTIONS; GENE; WALLIKERI; CURTISI; IDENTIFICATION; PHYLOGENY; SEQUENCES; TRAVELERS;
D O I
10.1186/s12936-015-0985-8
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: Plasmodium ovale, considered the rarest of the malaria parasites of humans, consists of two morphologically identical but genetically distinct sympatric species, Plasmodium ovale curtisi and Plasmodium ovale wallikeri. These parasites resemble morphologically to Plasmodium vivax with which they also share a tertian periodicity and the ability to cause relapses, making them easily misidentified as P. vivax. Plasmodium ovale infections are rarely reported, but given the likelihood of misidentification, their prevalence might be underestimated. Methods: Morphological and molecular analysis of confirmed malaria cases admitted in Singapore in 2012-2014 detected nine imported P. ovale cases that had been misidentified as P. vivax. Since P. ovale had not been previously officially reported in Singapore, a retrospective analysis of available, frozen, archival blood samples was performed and returned two additional misidentified P. ovale cases in 2003 and 2006. These eleven P. ovale samples were characterized with respect to seven molecular markers (ssrRNA, Potra, Porbp2, Pog3p, dhfr-ts, cytb, cox1) used in recent studies to distinguish between the two sympatric species, and to a further three genes (tufa, clpC and asl). Results: The morphological features of P. ovale and the differential diagnosis with P. vivax were reviewed and illustrated by microphotographs. The genetic dimorphism between P. ovale curtisi and P. ovale wallikeri was assessed by ten molecular markers distributed across the three genomes of the parasite (Genbank KP050361-KP050470). The data obtained for seven of these markers were compared with those published and confirmed that both P. ovale species were present. This dimorphism was also confirmed for the first time on: (1) two genes from the apicoplast genome (tufA and clpC genes); and, (2) the asl gene that was used for phylogenetic analyses of other Plasmodium species, and that was found to harbour the highest number of dimorphic loci between the two P. ovale species. Conclusion: Misidentified P. ovale infections are reported for the first time among imported malaria cases in Singapore. Genetic dimorphism between P. ovale curtisi and P. ovale wallikeri was confirmed using markers from the parasites' three genomes. The apparent increase of imported P. ovale since 2012 (with yearly detection of cases) is puzzling. Given decrease in the overall number of malaria cases recorded in Singapore since 2010 the 'resurgence' of this neglected species raises public health concerns.
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