Differential expression of TLR and CXCR genes in mammary HC11 cells challenged with Bacillus cereus and Bacillus subtilis: Implications for mastitis resistance.

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Title: Differential expression of TLR and CXCR genes in mammary HC11 cells challenged with Bacillus cereus and Bacillus subtilis: Implications for mastitis resistance.
Authors: Dilla Yanthi, Nova1 nova.dy@gmail.com, Anggraeni, Anneke2 ria.anneke@yahoo.co.id, Said, Syahruddin3 syahruddinsaid01@gmail.com, Sugiyono Saputra2 sugiyonosaputra@gmail.com, Soejoedono, Retno Damayanti4 retnodmail@yahoo.com, Muladno, Muladno5 muladno@gmail.com, Herlina, Nina3 nina.herlina.0212@gmail.com, Fauziah, Ima6 imafauziah37@gmail.com, Nugroho, Herjuno Ari1 herjunoari@gmail.com, Nasrulloh, Mukh Fajar1 fajarnashrulloh@gmail.com, Tiffarent, Rida1 ridatiffarent@gmail.com
Source: Veterinary World. Apr2025, Vol. 18 Issue 4, p1014-1024. 11p.
Document Type: Article
Subjects: Gram-positive bacterial infections, Interleukin-1, Gene expression, Bacillus cereus, Cell receptors, Mastitis, Chemokine receptors, Bovine mastitis
Author-Supplied Keywords: Bacillus subtilis
chemokine receptors
gene expression
HC11 cells
innate immunity
mastitis
toll-like receptors
Abstract: Background and Aim: Mastitis remains a major health challenge in dairy cattle, often caused by Gram-positive pathogens. Toll-like receptors (TLRs) and chemokine receptors (CXCRs) play essential roles in the innate immune response of mammary epithelial cells (MECs). However, the differential expression of these genes in response to specific mastitis-causing Bacillus spp. has not been comprehensively evaluated. This study aimed to characterize the temporal gene expression patterns of TLR and CXCR family members in murine mammary epithelial HC11 cells exposed to Bacillus cereus and Bacillus subtilis, thereby providing insights into their immunological roles in mastitis pathogenesis. Materials and Methods: HC11 cells were cultured and infected with B. cereus and B. subtilis (5 × 10⁷ colony-forming units/mL) and incubated at 37°C with 95% O2 and 5% CO2 for 48 h in RPMI 1640 medium supplemented with serum and antibiotics. Gene expression of interleukin (IL)-6, IL-8, TLR2, TLR4, IL-1 alpha (IL-1α), and CXCR1 was evaluated by quantitative real-time polymerase chain reaction at 0, 6, 12, 24, 48, and 72 h post-infection. Expression levels were normalized to glyceraldehyde-3-phosphate dehydrogenase and analyzed using ΔCt methods and Spearman correlation. Results: TLR2 exhibited a biphasic expression pattern, with early upregulation followed by suppression, while TLR4 showed higher expression in response to B. subtilis than B. cereus. IL-6 displayed prolonged expression under B. subtilis challenge but was transient under B. cereus exposure. IL-1α showed consistent expression across both bacterial challenges, suggesting its potential as a stable biomarker for mastitis susceptibility. CXCR1 exhibited delayed but sustained expression, indicative of its role in secondary neutrophil recruitment. IL-8 expression correlated with early immune activation and chemotactic signaling. Conclusion: The immune response of HC11 MECs to Gram-positive bacterial infection is gene-and pathogen-specific. TLR and CXCR genes show distinct temporal profiles, underscoring their utility in understanding epithelial-driven immune defense. These findings provide molecular insights into mastitis pathogenesis and identify IL-1α, IL-6, and CXCR1 as promising targets for genetic selection and therapeutic intervention. [ABSTRACT FROM AUTHOR]
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Author Affiliations: 1Research Center for Applied Microbiology, Research Organization for Life Sciences and Environment, National Research and Innovation Agency, Cibinong Science Center, Jl. Raya Jakarta - Bogor KM. 46, Cibinong, Bogor 16911, West Java, Indonesia
2Research Center for Animal Husbandry, Research Organization for Agriculture and Food, National Research and Innovation Agency, Cibinong Science Center, Jl. Raya Jakarta - Bogor KM. 46, Cibinong, Bogor 16911, West Java, Indonesia
3Research Center for Applied Zoology, Research Organization for Life Sciences and Environment, National Research and Innovation Agency, Cibinong Science Center, Jl. Raya Jakarta - Bogor KM. 46, Cibinong, Bogor 16911, West Java, Indonesia
4Division of Medical Microbiology, School of Veterinary Medicine and Biomedical Sciences, Bogor Agricultural University (IPB University), Jl. Agatis, Kampus IPB Dramaga, Bogor 16680, West Java, Indonesia
5Department of Animal Production and Technology, Faculty of Animal Science, Bogor Agricultural University (IPB University), Jl. Agatis, Kampus IPB Dramaga, Bogor 16680, West Java, Indonesia
6Research Centre for Veterinary Science, Research Organization for Health, National Research and Innovation Agency, Cibinong Science Center, Jl. Raya Jakarta - Bogor KM. 46, Cibinong, Bogor 16911, West Java, Indonesia
ISSN: 0972-8988
DOI: 10.14202/vetworld.2025.1014-1024
Accession Number: 185024075
Database: Veterinary Source
Description
Abstract:Background and Aim: Mastitis remains a major health challenge in dairy cattle, often caused by Gram-positive pathogens. Toll-like receptors (TLRs) and chemokine receptors (CXCRs) play essential roles in the innate immune response of mammary epithelial cells (MECs). However, the differential expression of these genes in response to specific mastitis-causing Bacillus spp. has not been comprehensively evaluated. This study aimed to characterize the temporal gene expression patterns of TLR and CXCR family members in murine mammary epithelial HC11 cells exposed to Bacillus cereus and Bacillus subtilis, thereby providing insights into their immunological roles in mastitis pathogenesis. Materials and Methods: HC11 cells were cultured and infected with B. cereus and B. subtilis (5 × 10⁷ colony-forming units/mL) and incubated at 37°C with 95% O2 and 5% CO2 for 48 h in RPMI 1640 medium supplemented with serum and antibiotics. Gene expression of interleukin (IL)-6, IL-8, TLR2, TLR4, IL-1 alpha (IL-1α), and CXCR1 was evaluated by quantitative real-time polymerase chain reaction at 0, 6, 12, 24, 48, and 72 h post-infection. Expression levels were normalized to glyceraldehyde-3-phosphate dehydrogenase and analyzed using ΔCt methods and Spearman correlation. Results: TLR2 exhibited a biphasic expression pattern, with early upregulation followed by suppression, while TLR4 showed higher expression in response to B. subtilis than B. cereus. IL-6 displayed prolonged expression under B. subtilis challenge but was transient under B. cereus exposure. IL-1α showed consistent expression across both bacterial challenges, suggesting its potential as a stable biomarker for mastitis susceptibility. CXCR1 exhibited delayed but sustained expression, indicative of its role in secondary neutrophil recruitment. IL-8 expression correlated with early immune activation and chemotactic signaling. Conclusion: The immune response of HC11 MECs to Gram-positive bacterial infection is gene-and pathogen-specific. TLR and CXCR genes show distinct temporal profiles, underscoring their utility in understanding epithelial-driven immune defense. These findings provide molecular insights into mastitis pathogenesis and identify IL-1α, IL-6, and CXCR1 as promising targets for genetic selection and therapeutic intervention. [ABSTRACT FROM AUTHOR]
ISSN:09728988
DOI:10.14202/vetworld.2025.1014-1024