Chiggers (chigger mites) and gamasid mites are two groups of ectoparasites on rodents, and they can be the vectors or potential vectors of scrub typhus and hemorrhagic fever with renal syndrome (HFRS), while Bower’s white-toothed rat (Berylmys bowersi) can serve as the reservoir host of the diseases. Based on field investigations at 117 survey sites of southwest China, a total of 2512 mites were collected from 55 B. bowersi rats. Under a microscope, these mites were taxonomically identified as 56 distinct species, comprising 37 chigger mite species and 19 gamasid mite species. The mite infestation burdens on B. bowersi were heavy, with a high prevalence (P_M = 85.45%), mean abundance (MA = 45.67), and intensity (MI = 53.45). Of 56 mite species identified, 7 are vectors of scrub typhus and HFRS. Of the seven vector mite species, Leptotrombidium scutellare was one of dominant chigger species, with a higher infestation index on rats (P_M = 21.82%, MA = 7.76) than the other six vector mite species. The sex ratio of female gamasid mites was higher than that of males. The number and infestation of adult gamasid mites were higher than those of immature mites. The infestation indexes of mites on B. bowersi hosts varied with the host’s sex and age and fluctuated along different environmental gradients. The association coefficient (V) showed a slight positive association between chiggers and gamasid mites, suggesting that these two groups of mites may coexist on B. bowersi rats. Spearman correlation coefficients showed positive correlations among some dominant and vector mite species, indicating that some mite species tend to select the same hosts. A total of 69 mite species (47 chigger mite species and 22 gamasid mite species) on B. bowersi were estimated by species rarefaction and extrapolation curves. In conclusion, Berylmys bowersi has a high susceptibility to mite infestation, and it has the potential to harbor abundant mites, with heavy mite burdens. The occurrence of vector mite species, especially L. scutellare (the dominant species), increases the potential risk of transmission and the focus persistence of scrub typhus and HFRS in southwest China.

Ascodipteron bat flies are specialized parasites of bats, but their diversity and parasite ecology in China remain poorly understood. We surveyed hipposiderid bats at ten localities in Yunnan Province, China, combining morphological identification, mitochondrial cytochrome c oxidase subunit I (COI) barcoding, and ecological analyses. Among 226 bats, 58 were infested; 72 neosomic females were collected, and 14 representative specimens were sequenced. Morphology, COI genetic distances, Assemble Species by Automatic Partitioning (ASAP), and maximum-likelihood phylogenetic analysis supported three taxa: A. phyllorhinae, A. sanmingense, and an undescribed Ascodipteron sp. Within-taxon COI distances were 0.199–0.512%, whereas between-taxon distances were 6.303–12.118%. Overall prevalence was 25.66%, and prevalence and mean parasite abundance varied among host species. Evidence for host-species differences in parasitism depended strongly on the absence of infestation in Hipposideros gentilis. Estimated associations of body condition with infestation occurrence and parasite abundance were positive but uncertain, and no clear associations were detected for the site-level environmental variables examined. These findings expand current knowledge of Ascodipteron diversity and host-associated parasitism in Yunnan and provide an integrative basis for further studies of species identification, host use, and parasite ecology in this genus.

Malaria pathogenesis involves complex immunopathological mechanisms that hinder early diagnosis and effective treatment. This study integrates multi-omics data and experimental models to identify host-derived biomarkers and elucidate their functional roles. By combining human transcriptomic datasets, weighted gene co-expression network analysis (WGCNA), and machine learning (LASSO, SVM, RF), we identified C1QB as a key hub gene. In human data, C1QB was significantly upregulated in both training and validation cohorts (AUC 0.983 and 0.970). Single-gene GSEA and immune infiltration analyses linked C1QB to apoptosis, inflammation, and altered immune cell composition, including increased activated dendritic cells and neutrophils, and decreased naïve B cells and CD8⁺ T cells. In a murine malaria model (Plasmodium berghei ANKA), C1QB expression rose as early as day one post-infection, preceding detectable parasitemia. Immunohistochemistry revealed C1QB accumulation in the liver and spleen. Single-cell RNA sequencing in the murine model confirmed monocyte-predominant expression, and scTenifoldKnk analysis suggested its role in immune regulation. Crucially, inhibiting C1q in mice via antibody intervention alleviated malaria-induced inflammation, tissue damage, and apoptosis, indicating that C1QB/C1q actively contributes to immunopathology. AI-based drug prediction and molecular docking further supported its therapeutic potential. Collectively, our findings establish C1QB as a dual biomarker and pathogenic driver in malaria, with diagnostic and therapeutic implications. Further studies are required to validate direct target engagement and clarify upstream regulatory mechanisms.