Establishment of an in vitro assay for assessing the effects of drugs on the liver stages of Plasmodium vivax malaria

• Published in: PloS one 2010-12, Vol.5 (12), p.e14275-e14275
• Main Authors: Chattopadhyay, Rana, Velmurugan, Soundarapandian, Chakiath, Chinnamma, Andrews Donkor, Lucy, Milhous, Wilbur, Barnwell, John W, Collins, William E, Hoffman, Stephen L
• Format: Article
• Language: English
• Subjects: Analysis; Animals; Anopheles - parasitology; Antimalarials - pharmacology; Armed forces; Assaying; Carcinoma, Hepatocellular - drug therapy; Carcinoma, Hepatocellular - parasitology; Cryopreservation; Culicidae; Developing countries; Developmental stages; Disease control; Disease Models, Animal; Disease prevention; Drug development; Drug screening; Drugs; Erythrocytes; Feasibility studies; Health aspects; Hepatocytes; Hepatocytes - drug effects; Hepatocytes - parasitology; Hepatoma; Humans; Immunoglobulins; Impact analysis; In Vitro Techniques; Infection; Infections; Infectious Diseases; Infectious Diseases/Neglected Tropical Diseases; Infectious Diseases/Tropical and Travel-Associated Diseases; Life cycle engineering; Life cycles; Liver; Liver - drug effects; Liver - metabolism; Liver cancer; Malaria; Malaria, Vivax - metabolism; Merozoites; Metabolites; Microscopy, Fluorescence - methods; Monkeys & apes; Mosquitoes; Pan troglodytes; Parasites; Photovoltaic cells; Plasmodium berghei; Plasmodium cynomolgi; Plasmodium falciparum; Plasmodium vivax; Plasmodium vivax - metabolism; Primaquine; Primaquine - pharmacology; Salivary Glands - metabolism; Solar cells; Sporozoites; Sporozoites - chemistry; Studies; Vector-borne diseases
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0014275

Plasmodium vivax (Pv) is the second most important human malaria parasite. Recent data indicate that the impact of Pv malaria on the health and economies of the developing world has been dramatically underestimated. Pv has a unique feature in its life cycle. Uninucleate sporozoites (spz), after invasion of human hepatocytes, either proceed to develop into tens of thousands of merozoites within the infected hepatocytes or remain as dormant forms called hypnozoites, which cause relapses of malaria months to several years after the primary infection. Elimination of malaria caused by Pv will be facilitated by developing a safe, highly effective drug that eliminates Pv liver stages, including hypnozoites. Identification and development of such a drug would be facilitated by the development of a medium to high throughput assay for screening drugs against Pv liver stages. We undertook the present pilot study to (1) assess the feasibility of producing large quantities of purified, vialed, cryopreserved Pv sporozoites and (2) establish a system for culturing the liver stages of Pv in order to assess the effects of drugs on the liver stages of Pv. We used primaquine (PQ) to establish this assay model, because PQ is the only licensed drug known to clear all Pv hepatocyte stages, including hypnozoites, and the effect of PQ on Pv hepatocyte stage development in vitro has not previously been reported. We report that we have established the capacity to reproducibly infect hepatoma cells with purified, cyropreserved Pv spz from the same lot, quantitate the primary outcome variable of infected hepatoma cells and demonstrate the inhibitory activity of primaquine on the infected hepatoma cells. We have also identified small parasite forms that may be hypnozoites. These data provide the foundation for finalizing a medium throughput, high content assay to identify new drugs for the elimination of all Pv liver stages.