Obihiro University of Agriculture and Veterinary Medicine
National Research Center for Protozoan Diseases
Ticks are obligatory hematophagous arthropods and are known to be important vectors of Babesia and Theileria parasites to vertebrates. I am interested in the molecular mechanisms underlying nutrient metabolism in unfed or fed ticks and oogenesis in female ticks. Moreover, using ticks infected with parasites, we are studying the relationship between the transmission of parasites and the nutrient metabolism of ticks. I aim to contribute to the development of new methods for controlling ticks and tick-borne pathogens through tick biology and physiology research.

Presenter of 2 Presentations

Video On-Demand

ESTABLISHMENT OF THE TICK BIOBANK FOR THE APPLICATION TO VECTOR BIOLOGY RESEARCH AND THE DEVELOPMENT OF TICK CONTROL METHODS (ID 1499)

Session Type
Video On-Demand
Date
08/21/2022
Session Time
18:00 - 21:00
Room
Video On-Demand
Lecture Time
19:30 - 19:50
Onsite or Pre-Recorded
Pre-Recorded
03. Parasites of domestic and wild animals

PRE-RECORDED: THE ROLES OF OOGENESIS-RELATED MOLECULES IN BABESIA-INFECTED HAEMAPHYSALIS LONGICORNIS (ID 753)

Session Type
03. Parasites of domestic and wild animals
Date
08/26/2022
Session Time
09:00 - 10:30
Room
Hall B4.M5+6
Lecture Time
09:50 - 09:55
Presentation Icon
Pre-Recorded Presentation
Onsite or Pre-Recorded
Pre-Recorded

Abstract

Introduction

The phenomenon of the transovarial transmission of Babesia parasites in ticks has been demonstrated experimentally, however, the molecular mechanisms are still unclear. To find the key tick factor(s) for Babesia transmission, we focused on molecules involved in yolk protein precursor (vitellogenin; Vg) synthesis and Vg uptake, which are crucial events in tick oogenesis.

Methods

With a tick–Babesia experimental model, the expression profiles of Haemaphysalis longicornis Vg synthesis-related genes and Vg uptake-related genes were examined after the semiartificial mouse skin membrane feeding of Babesia-infected bovine red blood cells. Based on the expression profiles, Vg gene silencing was conducted and the existence of Babesia DNA in the ovary and hemolymph was assessed.

Results

The expression levels of Vg-2 and Vg-3 decreased in the fat body of Babesia-infected ticks at 1 day after engorgement (DAE). In the ovary, Vg-2 mRNA expression was significantly higher in Babesia-infected ticks than in uninfected ticks at 1 and 2 DAE and decreased at 3 DAE. VgR expression was significantly lower in Babesia-infected ticks than in uninfected ticks at 2 and 4 DAE. ATG6 had a lower gene expression in Babesia-infected ticks compared to uninfected ticks at 2 DAE. Western blot analysis revealed that H. longicornis Vg-2 accumulates in the fat body and hemolymph of Babesia-infected ticks. Moreover, Vg-2 knockdown ticks had a lower detection rate of B. ovata DNA in the ovary and a significant reduction of B. ovata DNA in the hemolymph compared with control ticks.

Conclusions

Vg uptake from the hemolymph to the ovary was suppressed in the presence of B. ovata and that accumulated Vg-2 is associated with Babesia infection or transmission in the tick body.

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