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Salmonella enterica serovar Enteritidis (S. Enteritidis) is a common zoonotic pathogen that not only causes gastroenteritis or death of livestock and poultry but also poses a serious threat to human health, causing severe economic losses to the poultry industry and society. Herein, RNA-sequencing (RNA-seq) was used to analyze the transcriptome variation of chicken cecum at four different time points (1, 3, 7, and 14 days) following S. Enteritidis infection. There were 529, 1477, 476, and 432 differentially expressed genes (DEGs) in the cecum at four different days post-infection (dpi), respectively. The DEGs were significantly enriched in various immune-related pathways on 3 dpi and 7 dpi, such as cytokine-cytokine-receptor interaction and Toll-like receptor signaling pathway. DEGs were significantly enriched in several metabolic pathways on 14 dpi. Gene ontology (GO) enrichment of DEGs showed that up-regulated genes were significantly enriched in immune-related terms on 3 and 7 dpi. On 14 dpi, up-regulated genes were mainly enriched in the signaling-related terms, while the down-regulated genes were primarily enriched in the metabolic-related terms. Based on weighted gene co-expression network analysis (WGCNA), the key modules related to energy, non-coding processes, immunity, and development-related functions were identified at 1, 3, 7, and 14 dpi, respectively, and 5, 8, 6, and 5 hub genes were screened out, respectively. This study demonstrated that the chicken cecal transcriptome regulation responding to S. Enteritidis infection is time-dependent. The regulation of S. Enteritidis infection in chickens is coordinated by multiple systems, mainly involving immunity, metabolism, and signal transduction. Both 3 and 7 dpi are key time points for immune response. As the infection progresses, metabolism-related pathways were increasingly identified. This change reflects the dynamic adjustment between immune response and metabolism in Jining Bairi chickens following S. Enteritidis infection. These results suggested that starting from 3 dpi, the chickens gradually transition from an immune response triggered by S. Enteritidis infection to a state where they adapt to the infection by modulating their metabolism.
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http://dx.doi.org/10.1016/j.psj.2025.104773 | DOI Listing |
Front Microbiol
August 2025
Hebei Key Laboratory of Preventive Veterinary Medicine, Hebei Normal University of Science & Technology, Qinhuangdao, China.
Background: has the ability to adapt to variable environments by modulating metabolism. The Tricarboxylic Acid Cycle (TCA), as a core metabolic process, is critical for the environmental adaptation and infection process of . Fumarate reductase FrdA is an important enzyme in the TCA cycle, mainly catalyzing the conversion of fumarate to succinate.
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September 2025
Research Unit in Microbial Food Safety and Antimicrobial Resistance, Department of Veterinary Public Health, Faculty of Veterinary Science, Chulalongkorn University, Bangkok, Thailand.
In Southeast Asia, most antimicrobial resistance (AMR) data on have been generated at the phenotypic level, while insights into the genetic characteristics of AMR and virulence genes remain limited. This study aimed to further characterize AMR isolates carrying plasmid-associated virulence genes in Thailand and neighboring countries. A total of 366 isolates were collected from pigs ( = 265), pork ( = 69), and humans ( = 32) across Thailand, Lao People's Democratic Republic, Cambodia, and Myanmar.
View Article and Find Full Text PDFFood Microbiol
January 2026
Laboratory of Agrifood Research and Innovation (LAPIAgro), Graduate Program in Animal Science, Pontifical Catholic University of Paraná, Curitiba, Paraná, Brazil. Electronic address:
The wide diversity of Salmonella serotypes poses challenges for traditional serotyping methods, which are labor-intensive and unsuitable for high-throughput testing, particularly in food safety contexts. Hence, this study aimed to develop and validate a real-time PCR method for detecting Salmonella spp., identifying the major public health serotypes (S.
View Article and Find Full Text PDFPoult Sci
August 2025
Food and Feed Safety Research Unit, Southern Plains Agricultural Research Center, Department of Agriculture - Agricultural Research Service, College Station, TX 77845, United States; Department of Animal and Food Sciences, University of Delaware, Newark, DE 19716, United States. Electronic address:
Inducing inflammation in response to pathogen infection is known to be an energy-intensive process. An extended state of inflammation in production animals can be detrimental to performance parameters. Here, we compare two doses of a microencapsulated thymol-based feed additive blend and two different antibiotics in the context of a Salmonella Enterica subsp.
View Article and Find Full Text PDFMolecules
August 2025
Department of Animal Science, University of Wyoming, Wyoming, WY 82071, USA.
The growing demand for natural preservatives has driven interest in essential oils (EOs) from medicinal and aromatic plants. This study examines the potential of EOs from six wild populations of Albanian , specifically subsp. , , and species, to be utilized for food conservation, among other possible uses.
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