The significant increase in demand for camel milk has led to a rapid increase in the number of Bactrian camels. However, the widespread occurrence of mastitis significantly impacts the development of the Bactrian camel milk industry and poses a public health risk. Despite this, there is a lack of research on the transcriptional response, immune response pathways, and changes in core genes of Bactrian camels with subclinical mastitis. This study aimed to reveal the changes in immune-related response pathways and gene transcription levels in Bactrian camels with subclinical mastitis by analyzing the blood transcriptional response after the occurrence of subclinical mastitis in natural conditions. This study focused on 7-year-old Bactrian camels and collected 2 mL of blood from the camels that tested positive with a 4-peak California Mastitis Test (CMT) and those that tested negative with a 3-peak CMT. RNA sequencing (RNA-Seq) technology was used to analyze gene expression in the blood samples. Gene expression was verified using quantitative reverse transcription polymerase chain reaction (RT-qPCR). Overall, 1722 differentially expressed genes were sequenced in the blood samples of CMT-positive and CMT-negative Bactrian camels, including 1061 upregulated and 661 downregulated genes. After conducting gene ontology functional enrichment, 453 differentially expressed genes were identified. We also discovered pathways such as immune response, the G-protein-coupled receptor signaling pathway, and internal signal transmission. Kyoto Encyclopedia of Genes and Genomes (KEGG) signaling pathway enrichment detected 668 differentially expressed genes annotated onto 309 metabolic pathways, with significantly enriched immune pathways including cytokine–cytokine receptor interaction, complex and coalescence cascades, natural killer cell-mediated cytotoxicity, and T helper type 17 cell differentiation, among others. Through a STRING protein interaction database and cytoscape analysis, it was found that core differentially expressed genes related to immunity included IL10, CCL5, IL1B, OSM, TNFRSF1B, IL7, and CCR3, among others. The RT-qPCR results for six randomly selected core differentially expressed genes showed that the RT-qPCR expression pattern was consistent with the RNA Seq results. The immune-related genes in Bactrian camels affected by subclinical mastitis are primarily concentrated in the immune response and the cytokine–cytokine receptor interaction pathway. Given the importance of these pathways and the connections among related genes, the immune genes within these pathways may play a crucial role in the pathogenesis of subclinical mastitis in Bactrian camels. This study provides a valuable reference for investigating the immune regulatory mechanisms of subclinical mastitis in Bactrian camels.

Subclinical mastitis is a critical disease affecting camel health and milk quality. However, research on shifts in milk bacterial communities following subclinical mastitis in camels is limited. We evaluated changes in bacterial communities following subclinical mastitis in Bactrian camels. Three portions of California Mastitis Test (CMT)-negative milk and five portions of CMT-positive milk were collected from each Jimunai County and Keping County using the CMT, and the bacterial community composition of the camel milk was analyzed using amplicon sequencing of the v34 region of the 16S rRNA gene. Subclinical mastitis induced genus-level differences in the core bacterial microbiota of Bactrian camel milk. To our knowledge, Delftia was identified in camel milk for the first time, predominantly in Jimunai County. Bacterial abundance in camel milk from Keping County was increased and altered. Alpha diversity analysis revealed that subclinical mastitis induced lower and higher bacterial abundance in milk from Jimunai County and Keping County, respectively, compared to that of healthy camels. Therefore, these findings provide direction for future research on pathogenic microorganisms for the prevention and control of subclinical mastitis in Bactrian camels.

Gastrointestinal parasitic diseases pose significant health risks to equine populations. This study investigated the epidemiological patterns of equine gastrointestinal parasites in Xinjiang by analyzing 83 fecal samples collected from Ili (n = 62) and Urumqi (n = 21) between August and November 2024. The modified McMaster technique was employed to quantify fecal egg counts (EPG) and was complemented by morphological identification to assess infection dynamics related to geography, breed specificity, and management practices. The results demonstrated an overall infection prevalence of 66.3% (55/83), with strongyles, Parascaris equorum, and Eimeria oocysts being present. Significant geographical variation was observed, with Ili exhibiting a higher prevalence (74.2%) compared to Urumqi (42.9%). Breed susceptibility analysis revealed that there was a 94.1% prevalence in Yili horses versus 42.9% in Kazakh horses. Pasture-managed herds showed markedly higher infection rates (94.1%) than stable-based systems (50.0%). Parasite community composition was dominated by strongyles (82.1%), followed by Triodontophorus spp. (27.7%) and P. equorum (2.4%). These findings highlight severe parasitic infection risks in Xinjiang’s grazing equids, underscoring the urgency of implementing targeted anthelmintic protocols to mitigate disease transmission.

Camels, vital to economies in Asia, Africa, and the Arabian Peninsula, have been domesticated for over 4000 years. They thrive in arid regions like Xinjiang, China, but face challenges from internal and external parasites, particularly gastrointestinal parasites, which impact health, meat and milk quality, and production efficiency. This study investigates the prevalence of gastrointestinal helminth infections in camels from five major regions in Xinjiang. We collected 435 fresh fecal samples and used the saturated saline flotation method and McMaster’s method for detection. Molecular examination followed. The overall prevalence was 18.2% (95% confidence interval [CI]: 14.7–22.2%), with Urumqi showing the highest prevalence (29%, 95% CI: 23.4–35.1%) compared to other regions (odds ratio [OR]: 4.62, 95% CI: 2.63–8.41%). Younger camels (≤3 years old) were more likely infected by the parasites after adjusting for the region differences (OR: 10.53, 5.12–24.65%). However, we found no evidence that the prevalence was different between male and female camels. PCR analysis identified Trichostrongylus spp., Chabertia ovina, and Haemonchus contortus as predominant parasites, with observed co-infections indicating a complex parasitic landscape. The findings provide essential epidemiological data for effective parasite control strategies.