Abstract
ABSTRACTThe impact ofClostridioides difficilestrain diversity on the severity of intestinal infection and diarrhea remains unclear. The RT027/ST1 strain is highly prevalent and has been associated with more severe disease and increased toxin production. Previous studies using antibiotic-treated mice, however, have demonstrated that the severity of diarrhea and colonic inflammation caused by clinical RT027/ST1C. difficileisolates cultured from different patients is isolate-specific and varies from avirulent to lethal. Herein we demonstrate that increased flagellar expression is associated with increased in vivo virulence. While sequencing the flagellar operon did not identify differences between high and low virulence isolates, high virulence was associated with strains encoding higher proportions of the phase variable flagellar switch in the ON mode. We found that the proportion of bacteria with the switch in the ON mode correlates with maximum weight loss, a readout for virulence in mice. Further analysis of flagellar switch sequences identified variant inverted repeat (IR) sequences, with 40% of isolates having lost one A or T in the IR compared to the genome ofC. difficileR20291. The isolates with the R20291 IR sequence have increased virulence compared to those with variant IR (p = 3.2e-05) and these isolates have markedly reduced ability to invert the flagellar switch. Our results suggest that a restricted capacity to invert the flagellar switch during infection is associated with reduced virulence ofC. difficileRT027/ST1 strains and may account for some of the inconsistent associations betweenC. difficileinfection and disease severity in patients.IMPORTANCEC. difficileRT027/ST1 has been associated with high virulence. However, variable virulence among ST1 isolates has also been observed. Recent studies have shed light on the impacts of the gut microbiota and host immunity duringClostridioides difficileinfection (CDI). Beyond that, determining the genetic factors ofC. difficileregulating virulence is essential for a successful CDI diagnosis and treatment. Here, we report a strong association between the flexibility of the flagellar switch and the virulence ofC. difficile. Specifically, the inverted repeats of the flagellar switch correlate with switch flexibility. Overall, our study explores variations inC. difficilevirulence and highlights the potential of using flagellar switch inverted repeats as an easily accessible genetic trait to predict pathogen virulence.
Publisher
Cold Spring Harbor Laboratory
Reference63 articles.
1. CDC. 2019. Antibiotic Resistance Threats in the United States Atlanta GUSDoHaHS, CDC; 2019.,
2. CDC. 2020. 2020 Annual Report.
3. Clostridium difficile: its disease and toxins
4. Mechanism of action of Clostridium difficile toxin B: role of external medium and cytoskeletal organization in intoxicated cells;Eur J Cell Biol,1989
5. Internalization of Clostridium difficile cytotoxin into cultured human lung fibroblasts;Biochim Biophys Acta,1983