A conserved trypanosomatid differentiation regulator controls substrate attachment and morphological development inTrypanosoma congolense

Abstract

AbstractTrypanosomatid parasites undergo developmental regulation to adapt to the different environments encountered during their life cycle. InTrypanosoma brucei, a genome wide selectional screen previously identified a regulator of the protein family ESAG9, which is highly expressed in stumpy forms, a morphologically distinct bloodstream stage adapted for tsetse transmission. This regulator, TbREG9.1, has an orthologue inTrypanosoma congolense, despite the absence of a stumpy morphotype in that parasite species, which is an important cause of livestock trypanosomosis. RNAi mediated gene silencing of TcREG9.1 inTrypanosoma congolensecaused a loss of attachment of the parasites to a surface substrate in vitro, a key feature of the biology of these parasites that is distinct fromT. brucei. This detachment was phenocopied by treatment of the parasites with a phosphodiesterase inhibitor, which also promotes detachment in the insect trypanosomatidCrithidia fasciculata. RNAseq analysis revealed that TcREG9.1 silencing caused the upregulation of mRNAs for several classes of surface molecules, including transferrin receptor-like molecules, immunodominant proteins, and molecules related to those associated with stumpy development inT. brucei. Depletion of TcREG9.1 in vivo also generated an enhanced level of parasites in the blood circulation consistent with reduced parasite attachment to the microvasculature. The morphological progression to insect forms of the parasite was also perturbed. We propose a model whereby TcREG9.1 acts as a regulator of attachment and development, with detached parasites being adapted for transmission.Author summaryTrypanosoma congolenseis a major cause of livestock trypanosomosis in sub-Saharan Africa where it contributes to lost economic productivity and poverty. These parasites differ in two key respects from the better-studied African trypanosomes,Trypanosoma brucei. Firstly,T. congolenseadheres to surfaces in vitro and in the vaculature in vivo. Secondly, they lack a morphologically distinct transmission stage equivalent to the stumpy form ofT. brucei. In the current work we identify aT congolenseorthologue of a key developmental regulator inT. brucei, REG9.1, previously identified by a genome-wide RNAi screen. By RNA interference in transgenicT. congolensewe demonstrate that TcREG9.1 functions both in parasite adherence in vitro and in vivo, and also in parasite development. The work provides a first insight into the unusual adherence and developmental biology ofT. congolenseand also suggests a possible model for how these characteristics interact to promote disease spread.