The alveolin IMC1h is required for normal ookinete and sporozoite motility behaviour and host colonisation in Plasmodium berghei

• Published in: PloS one 2012-07, Vol.7 (7), p.e41409-e41409
• Main Authors: Volkmann, Katrin, Pfander, Claudia, Burstroem, Charlotte, Ahras, Malika, Goulding, David, Rayner, Julian C, Frischknecht, Friedrich, Billker, Oliver, Brochet, Mathieu
• Format: Article
• Language: English
• Subjects: Animals; Antigens; Aquatic insects; Biology; Blood; Cell division; Cell Line, Tumor; Cell migration; Clonal deletion; Colonization; Defects; Dermis; Gene Knockout Techniques; Glands; Gliding; Heat shock proteins; Hepatocytes - parasitology; Hepatoma; Host-Parasite Interactions; Infections; Kinases; Life Cycle Stages; Liver; Liver - parasitology; Malaria; Mammals; Mechanical properties; Medicine; Mice; Mosquitoes; Motility; Movement; Parasites; Pellicle; Plasmodium; Plasmodium berghei; Plasmodium berghei - cytology; Plasmodium berghei - growth & development; Plasmodium berghei - metabolism; Plasmodium berghei - physiology; Plasmodium falciparum; Proteins; Protozoan Proteins - genetics; Protozoan Proteins - metabolism; Rodents; Salivary glands; Salivary Glands - parasitology; Sporozoites; Sporozoites - cytology; Sporozoites - metabolism; Studies; Time Factors; Trypanosoma brucei; Vector-borne diseases; Zygote - cytology; Zygote - metabolism; Zygotes
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0041409

Alveolins, or inner membrane complex (IMC) proteins, are components of the subpellicular network that forms a structural part of the pellicle of malaria parasites. In Plasmodium berghei, deletions of three alveolins, IMC1a, b, and h, each resulted in reduced mechanical strength and gliding velocity of ookinetes or sporozoites. Using time lapse imaging, we show here that deletion of IMC1h (PBANKA_143660) also has an impact on the directionality and motility behaviour of both ookinetes and sporozoites. Despite their marked motility defects, sporozoites lacking IMC1h were able to invade mosquito salivary glands, allowing us to investigate the role of IMC1h in colonisation of the mammalian host. We show that IMC1h is essential for sporozoites to progress through the dermis in vivo but does not play a significant role in hepatoma cell transmigration and invasion in vitro. Colocalisation of IMC1h with the residual IMC in liver stages was detected up to 30 hours after infection and parasites lacking IMC1h showed developmental defects in vitro and a delayed onset of blood stage infection in vivo. Together, these results suggest that IMC1h is involved in maintaining the cellular architecture which supports normal motility behaviour, access of the sporozoites to the blood stream, and further colonisation of the mammalian host.