# Preliminary Transcriptomic Insights into the Combined Pathogenesis of Avian Leukosis Virus and Salmonella pullorum Co-Infection

**Authors:** Min Tan, Rong Ran, Cheng Liu, Tao Xie, Keshan Zhang, Qigui Wang, Xi Lan, Haiwei Wang

PMC · DOI: 10.3390/vetsci13030283 · Veterinary Sciences · 2026-03-18

## TL;DR

This study explores how two poultry diseases interact at the genetic level, revealing key genes and pathways involved in their combined effects.

## Contribution

The study identifies novel differentially expressed genes and pathways in co-infected chickens, offering new molecular insights into poultry disease interactions.

## Key findings

- Co-infected chickens showed significant differences in gene expression compared to single-infected groups.
- Genes related to extracellular matrix–receptor interactions, PPAR signaling, and calcium ion signaling were enriched.
- RT-qPCR confirmed the upregulation of MAPK10 and SQLE and downregulation of FOXG1 in co-infected chickens.

## Abstract

Co-infection with avian leukemia and Pullorum Disease poses a serious threat to poultry health. However, the combined pathogenic mechanism remains unclear, and no commercial vaccines or effective drugs are available. This study used transcriptome sequencing to identify differentially expressed genes and pathways related to immunity and tumorigenesis. The findings provide new insights into the co-infection mechanism and offer a theoretical basis for developing integrated control strategies in the poultry industry.

Co-infection with avian leukemia and Pullorum Disease severely compromises poultry health, yet its pathogenic mechanisms remain unclear. We employed transcriptome sequencing to analyze gene expression changes and enriched pathways in kidney, spleen, and liver tissues of Chongqing Chengkou mountain chickens under single-infection (avian leukemia virus or Pullorum Disease) and co-infection conditions. Significant differences were observed in the number and pathways of differentially expressed genes between co-infected and single-infected groups. These genes were predominantly enriched in pathways involving extracellular matrix–receptor interactions, PPAR signaling, and calcium ion signaling. RT-qPCR validation confirmed significant upregulation of MAPK10 and SQLE, alongside downregulation of genes such as FOXG1. This study identifies multiple differentially expressed genes and pathways associated with immunity and tumorigenesis, providing crucial molecular insights into the regulatory mechanisms underlying avian leukemia and Pullorum Disease co-infection.

## Full-text entities

- **Genes:** HRH1 (histamine receptor H1) [NCBI Gene 100858928], LOC101747704 (uncharacterized LOC101747704) [NCBI Gene 101747704], LOC107049046 (60S ribosomal protein L17) [NCBI Gene 107049046], RPS3A (ribosomal protein S3A) [NCBI Gene 422477] {aka RPS3AE}, JAG1 (jagged canonical Notch ligand 1) [NCBI Gene 396043], ACOX1 (acyl-CoA oxidase 1) [NCBI Gene 417366], IL4 (interleukin 4) [NCBI Gene 416330] {aka IL-4, Interleukin-4}, NGFR (nerve growth factor receptor) [NCBI Gene 425805] {aka TNFRSF16}, FOXG1 (forkhead box G1) [NCBI Gene 2290] {aka BF1, BF2, FHKL3, FKH2, FKHL1, FKHL2}, INFG (interferon gamma) [NCBI Gene 396054] {aka IFNG}, DHCR24 (24-dehydrocholesterol reductase) [NCBI Gene 424661], MSMO1 (methylsterol monooxygenase 1) [NCBI Gene 422423] {aka SC4MOL}, PPARA (peroxisome proliferator activated receptor alpha) [NCBI Gene 374120] {aka PPAR}, PPARA (peroxisome proliferator activated receptor alpha) [NCBI Gene 5465] {aka NR1C1, PPAR, PPAR-alpha, PPARalpha, hPPAR}, SQLE (squalene epoxidase) [NCBI Gene 420335], PCSK1 (proprotein convertase subtilisin/kexin type 1) [NCBI Gene 769230] {aka PC1}, CYP51A1 (cytochrome P450 family 51 subfamily A member 1) [NCBI Gene 420548] {aka CYP51}, CPT1A (carnitine palmitoyltransferase 1A) [NCBI Gene 423118] {aka CPT1, L-CPT1}, IGF2 (insulin like growth factor 2) [NCBI Gene 395097] {aka IGF-II}, CYSLTR2 (cysteinyl leukotriene receptor 2) [NCBI Gene 428071], RPS3 (ribosomal protein S3) [NCBI Gene 419069], MAPK10 (mitogen-activated protein kinase 10) [NCBI Gene 5602] {aka JNK3, JNK3A, PRKM10, SAPK1b, p493F12, p54bSAPK}, RPL18A (ribosomal protein L18a) [NCBI Gene 417823] {aka chRPL18}, FDFT1 (farnesyl-diphosphate farnesyltransferase 1) [NCBI Gene 422038], EDNRA (endothelin receptor type A) [NCBI Gene 373908], COL1A1 (collagen type I alpha 1 chain) [NCBI Gene 395532], FDPS (farnesyl diphosphate synthase) [NCBI Gene 425061] {aka FPS}, FN1 (fibronectin 1) [NCBI Gene 396133] {aka FN}, MYL6 (myosin, light chain 6, alkali, smooth muscle and non-muscle) [NCBI Gene 100996929], SQLE (squalene epoxidase) [NCBI Gene 6713]
- **Diseases:** cancer (MESH:D009369), Avian Leukosis Virus Infection (MESH:D001353), reproductive disorders (MESH:D060737), viral (MESH:D014777), inflammation (MESH:D007249), S. pullorum infection (MESH:D012480), avian typhoid infection (MESH:D014435), Co (MESH:D060085), white diarrhea infection (MESH:D003967), infectious diseases (MESH:D003141), AL (MESH:D007938), bacterial infections (MESH:D001424), tumorigenesis (MESH:D063646), death (MESH:D003643), PD (MESH:D004194), -infection (MESH:D007239), bleeding (MESH:D006470), injury to (MESH:D014947)
- **Chemicals:** PBS (MESH:D007854), amino acid (MESH:D000596), steroid (MESH:D013256), acylamide (MESH:D020106), terpenoid (MESH:D013729), sodium pentobarbital (MESH:D010424), fatty acid (MESH:D005227), cholesterol (MESH:D002784), calcium (MESH:D002118), lipid (MESH:D008055)
- **Species:** Salmonella enterica subsp. enterica serovar Pullorum (no rank) [taxon 605], Arthrospira sp. LV (species) [taxon 2231211], Avian leukemia virus (no rank) [taxon 11946], Avian leukosis virus (no rank) [taxon 11864], Gallus gallus (bantam, species) [taxon 9031], Avian leukosis virus ev/J (no rank) [taxon 1401444], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

15 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13030694/full.md

## References

36 references — full list in the complete paper: https://tomesphere.com/paper/PMC13030694/full.md

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Source: https://tomesphere.com/paper/PMC13030694