From the Department of Pathology & Laboratory Medicine (Castañeda-Mogollón, Doolan, Toppings, Amarasekara, Tran, Pillai), University of Calgary, Calgary, Alberta, Canada.
Department of Microbiology, Immunology, and Infectious Diseases (Castañeda-Mogollón, Doolan, Toppings, Pillai), University of Calgary, Calgary, Alberta, Canada.
Arch Pathol Lab Med. 2023 Jul 1;147(7):774-785. doi: 10.5858/arpa.2021-0636-OA.
CONTEXT.—: Clostridioides difficile infection (CDI) is the world-leading cause of infectious nosocomial diarrhea and pseudomembranous colitis. Antibiotics are the first line of treatment against CDI despite the high likelihood of antibiotic failure and/or recurrence. More data are needed to correlate clinical variables with 16S rRNA microbiome profiles in CDI-infected patients.
OBJECTIVE.—: To determine the relationship(s) between a patient's clinical factors and the stool bacteriome of CDI-positive patients and CDI-negative patients with diarrheal symptoms.
DESIGN.—: This study used stool samples and clinical data from 358 patients with nosocomial diarrhea, who were divided by their CDI diagnosis (CDI-negative: n = 180; CDI-positive; n = 178). The stool bacteriome was profiled by amplicon deep sequencing of the 16S rRNA gene, followed by correlating clinical data.
RESULTS.—: The stool bacteriome was significantly different by severity assessment regardless of CDI status. Phyla and species varied significantly by CDI diagnosis. Severity, defined as a serum white blood cell count greater than 15 cells/μL and/or a creatinine level greater than 1.5 mg/dL, correlated significantly with dysbiosis of the stool bacteriome profile of CDI-positive patients compared to CDI-negative patients. Serum white blood cell count was significantly higher in patients with bacterial dysbiosis, and high levels of creatinine were associated with low bacteriome diversity.
CONCLUSIONS.—: Clinical severity of CDI influences the stool microbiome of infected patients. To date, this study has the largest data set comparing 16S rRNA microbiome profiles and clinical variables between CDI-infected and noninfected individuals.
艰难梭菌感染(CDI)是全球导致医院获得性腹泻和伪膜性结肠炎的主要原因。尽管抗生素治疗失败和/或复发的可能性很高,但抗生素仍然是治疗 CDI 的一线药物。需要更多的数据来将临床变量与 CDI 感染患者的 16S rRNA 微生物组谱相关联。
确定患者的临床因素与 CDI 阳性患者和有腹泻症状的 CDI 阴性患者粪便细菌组之间的关系。
本研究使用了来自 358 名患有医院获得性腹泻的患者的粪便样本和临床数据,这些患者根据他们的 CDI 诊断(CDI 阴性:n = 180;CDI 阳性:n = 178)进行分组。通过扩增子深度测序 16S rRNA 基因对粪便细菌组进行了分析,并对临床数据进行了关联分析。
无论 CDI 状态如何,严重程度评估都显著改变了粪便细菌组。门和物种因 CDI 诊断而显著不同。严重程度,定义为血清白细胞计数大于 15 个细胞/μL 和/或肌酐水平大于 1.5 mg/dL,与 CDI 阳性患者的粪便细菌组谱的失调显著相关,与 CDI 阴性患者相比。细菌失调患者的血清白细胞计数明显升高,肌酐水平高与细菌组多样性低相关。
CDI 的临床严重程度影响感染患者的粪便微生物组。到目前为止,这项研究是比较 CDI 感染和非感染个体的 16S rRNA 微生物组谱和临床变量的最大数据集。