Frontiers in cellular and infection microbiology · 2026
Genomic and transcriptomic analyses reveal a Gifsy-1 prophage-encoded virulence module associated with enhanced epithelial adhesion of Salmonella ST34 in Huzhou, China.
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Zhu Ling, Li Xiangchen, Zheng Lili, Zhou Lihua, Chen Zhenfa, Lin Yibin, Zhu Jianhua, Gao Junshun, Gao Junli, Cai Yunxiang, Qiang Xinhua
Аннотация
INTRODUCTION: Non-typhoidal Salmonella (NTS) is a leading cause of bacterial gastroenteritis worldwide, yet the pathogenic differences among co-circulating dominant clones remain poorly understood.
METHODS: A 7.5-year surveillance study (2017-2024) was conducted using NTS isolates from patients with acute diarrheal illness in Huzhou, China. Quantitative IEC-6 cell-based adhesion and invasion assays, comparative genomics, transcriptomic profiling, and protein-protein interaction network analysis were integrated to compare the dominant sequence types (STs).
RESULTS: Among 188 NTS isolates, 35 serotypes and 36 STs were identified. Three STs predominated: ST34 (26.1%, mainly monophasic S. Typhimurium), ST11 (15.4%, exclusively S. Enteritidis), and ST19 (13.3%, classical S. Typhimurium). ST34 showed significantly enhanced epithelial adhesion in IEC-6 cells, whereas increased invasion was observed only in comparison with ST11 and not with ST19. Comparative genomics and transcriptomics identified an intact Gifsy-1 prophage as an ST34-specific genetic element encoding the T3SS effectors GogB and SteE/SarA, with gogB and steE/sarA being the only virulence genes consistently upregulated in ST34 versus both ST11 and ST19. Protein-protein interaction network analysis positioned these effectors as peripheral components of a 14-member prophage-associated module. All 49 ST34 isolates carried the intact Gifsy-1 prophage, whereas ST19 isolates harbored only truncated versions and ST11 completely lacked this element. ST34 also carried a broad antimicrobial resistance gene repertoire, including frequent tetracycline and sulfonamide resistance determinants and sporadic detection of clinically important beta-lactamase genes.
DISCUSSION: These findings identify an intact Gifsy-1 prophage encoding GogB and SteE/SarA as a candidate module associated with enhanced epithelial adhesion in ST34, a dominant NTS lineage with an extensive antimicrobial resistance repertoire.
METHODS: A 7.5-year surveillance study (2017-2024) was conducted using NTS isolates from patients with acute diarrheal illness in Huzhou, China. Quantitative IEC-6 cell-based adhesion and invasion assays, comparative genomics, transcriptomic profiling, and protein-protein interaction network analysis were integrated to compare the dominant sequence types (STs).
RESULTS: Among 188 NTS isolates, 35 serotypes and 36 STs were identified. Three STs predominated: ST34 (26.1%, mainly monophasic S. Typhimurium), ST11 (15.4%, exclusively S. Enteritidis), and ST19 (13.3%, classical S. Typhimurium). ST34 showed significantly enhanced epithelial adhesion in IEC-6 cells, whereas increased invasion was observed only in comparison with ST11 and not with ST19. Comparative genomics and transcriptomics identified an intact Gifsy-1 prophage as an ST34-specific genetic element encoding the T3SS effectors GogB and SteE/SarA, with gogB and steE/sarA being the only virulence genes consistently upregulated in ST34 versus both ST11 and ST19. Protein-protein interaction network analysis positioned these effectors as peripheral components of a 14-member prophage-associated module. All 49 ST34 isolates carried the intact Gifsy-1 prophage, whereas ST19 isolates harbored only truncated versions and ST11 completely lacked this element. ST34 also carried a broad antimicrobial resistance gene repertoire, including frequent tetracycline and sulfonamide resistance determinants and sporadic detection of clinically important beta-lactamase genes.
DISCUSSION: These findings identify an intact Gifsy-1 prophage encoding GogB and SteE/SarA as a candidate module associated with enhanced epithelial adhesion in ST34, a dominant NTS lineage with an extensive antimicrobial resistance repertoire.