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Wenz, C.

Publications and source records attributed to Wenz, C..

2 recordsLinked to original sources

Exposure to pyrethroid insecticides modulates immunity of Anopheles against Plasmodium falciparum

Transmission of malaria parasites relies on the blood-feeding behaviour of female Anopheles mosquitoes and can be prevented by vector control methods. Particularly, the usage of pyrethroid-containing insecticide-treated nets (ITNs) remains a cornerstone of malaria prevention. Whilst ITNs are primarily designed to induce mosquito mortality, their impact on parasite development, particularly in the context of pyrethroid resistance, is poorly understood. Our study reveals that sub-lethal pyrethroid exposure triggers systemic increases in reactive oxygen and nitrogen species reducing transmission efficacy of Plasmodium falciparum. Production of reactive nitrogen species in granulocytes induces their proliferation and primes mosquito immunity through activation of a non-canonical immune deficiency (IMD) pathway, leading to increased nitration around the midgut epithelium and subsequent ookinete destruction. These findings highlight an overlooked secondary mode of action for pyrethroids and reinforces the importance of sustained pyrethroid usage in ITNs, even in the face of high-levels of pyrethroid resistance in mosquitoes.

molecular biology↗

An Sfi1-like centrin-interacting centriolar plaque protein affects nuclear microtubule homeostasis.

Malaria-causing parasites achieve rapid proliferation in human blood through multiple rounds of asynchronous nuclear division followed by daughter cell formation. Nuclear divisions critically depend on the centriolar plaque, which organizes intranuclear spindle microtubules. The centriolar plaque consists of an extranuclear compartment, which is connected via a nuclear pore-like structure to a chromatin-free intranuclear compartment. Composition and function of this non-canonical centrosome remain largely elusive. Centrins, which reside in the extranuclear part, are among the very few centrosomal proteins conserved in Plasmodium falciparum. Here we identify a novel centrin-interacting centriolar plaque protein. Conditional knock down of this Sfi1-like protein (PfSlp) caused a growth delay in blood stages, which correlated with a reduced number of daughter cells. Surprisingly, intranuclear tubulin abundance was significantly increased, which raises the hypothesis that the centriolar plaque might be implicated in regulating tubulin levels. Disruption of microtubule homeostasis caused polymerization of excess microtubules and aberrant mitotic spindles. Time-lapse microscopy revealed that this prevented or delayed spindle extension. Our study thereby identifies a novel extranuclear centriolar plaque factor and establishes a functional link to the intranuclear compartment of this divergent eukaryotic centrosome.

cell biology↗