Preharvest sprouting (PHS) in wheat represents a major constraint to the production of high‐quality grain. Genetic variation for tolerance to PHS is associated with seed dormancy. The present study was initiated to detect homologous chromosome variation associated with seed dormancy genes in a PHS tolerant cultivar ‘Zenkojikomugi’ (Zen) and ‘Chinese Spring’ (CS) using the backcross reciprocal monosomic method. The most striking effect on variation in seed dormancy was associated with chromosome 3A, and followed by group 4 chromosomes. These chromosomes of Zen increased dormancy compared with the respective CS homologues. Chromosomes 2D and 7D of Zen, and 6A of CS seemed to contribute smaller positive effects on dormancy. Chromosomes 2A of CS and Zen, as well as 3B, were equally effective in enhancing dormancy. The chromosome 3 A factors were independent of the grain‐colour gene R‐A1 because Zen was found to carry the white‐grained R‐A1a allele, which was identical to that of CS, and there was no difference in dormancy between the reciprocal F1 seeds.

The protozoan parasite Babesia spp. invades into tick oocytes and remains in the offspring. The transovarial transmission phenomenon of Babesia in ticks has been demonstrated experimentally, but the molecular mechanisms remain unclear. Babesia invasion into oocytes occurs along with the progression of oogenesis. In the present study, 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. With a Haemaphysalis longicornis tick–Babesia ovata experimental model, the expression profiles of Akt, target of rapamycin, S6K, GATA, and Vg, Vg synthesis-related genes, and Vg receptor (VgR) and autophagy-related gene 6 (ATG6), Vg uptake-related genes, were analyzed using real-time PCR using tissues collected during the preovipositional period in Babesia-infected ticks. The expression levels of H. longicornis Vg-2 (HlVg-2) and HlVg-3 decreased in the fat body of Babesia-infected ticks 1 day after engorgement. In the ovary, HlVg-2 mRNA expression was significantly higher in Babesia-infected ticks than in uninfected ticks 1 and 2 days after engorgement and decreased 3 days after engorgement. HlVgR expression was significantly lower in Babesia-infected ticks than in uninfected ticks 2 and 4 days after engorgement. HlATG6 had a lower gene expression in Babesia-infected ticks compared to uninfected ticks 2 days after engorgement. Additionally, western blot analysis using protein extracts from each collected tissue revealed that H. longicornis Vg-2 (HlVg-2) accumulate in the fat body and hemolymph of Babesia-infected ticks. These results suggest that Vg uptake from the hemolymph to the ovary was suppressed in the presence of B. ovata. Moreover, HlVg-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. Taken together, our results suggest that accumulated HlVg-2 is associated with Babesia infection or transmission in the tick body. These findings, besides previous reports on VgR, provide important information to elucidate the transovarial transmission mechanisms of pathogens in tick vectors.

Although vaccines are one of the environmentally friendly means to prevent the spread of ticks, there is currently no commercial vaccine effective against Haemaphysalis longicornis ticks. In this study, we identified, characterized, localized, and evaluated the expression patterns, and tested the immunogenic potential of a homologue of Rhipicephalus microplus ATAQ in H. longicornis (HlATAQ). HlATAQ was identified as a 654 amino acid-long protein present throughout the midgut and in Malpighian tubule cells and containing six full and one partial EGF-like domains. HlATAQ was genetically distant (homology < 50%) from previously reported ATAQ proteins and was expressed throughout tick life stages. Its expression steadily increased (p < 0.001) during feeding, reached a peak, and then decreased slightly with engorgement. Silencing of HlATAQ did not result in a phenotype that was significantly different from the control ticks. However, H. longicornis female ticks fed on a rabbit immunized with recombinant HlATAQ showed significantly longer blood-feeding periods, higher body weight at engorgement, higher egg mass, and longer pre-oviposition and egg hatching periods than control ticks. These findings indicate that the ATAQ protein plays a role in the blood-feeding-related physiological processes in the midgut and Malpighian tubules and antibodies directed against it may affect these tissues and disrupt tick engorgement and oviposition.

Ticks are hematophagous arthropods and have a remarkable ability to transmit various parasites. Babesia ovata, a protozoan parasite that causes babesiosis in cattle, is transmitted from parent to offspring in Haemaphysalis longicornis. Although transovarial transmission is demonstrated experimentally, little is known about the molecular mechanisms of tick-Babesia in that phenomenon.

In the past decades, omics data including genomes, transcriptomes, and proteomes of ticks of medical and veterinary importance have become available worldwide as web-based resources. Additionally, laboratory colonies and cell lines of these ticks have been established and now become essential tools for the research advancement of ticks and tick-borne diseases.