Clostridioides difficile infection (CDI) is a frequent complication of cancer care. Patients with hematological malignancies and solid tumors, in addition to receiving their care in the outpatient oncology facilities, are frequently exposed to the inpatient hospital environment. As a result, they have increased risk of colonization with Clostridioides difficile spores, and under the selective antibiotic pressure on the intestinal microbiome, they can develop CDI. Reference Lee, Arguello and Jenq1 We aimed to characterize the molecular epidemiology of Clostridioides difficile strains causing colitis in order to better understand acquisition and transmission in a nonoutbreak setting in a cancer population.
Methods
We retrospectively studied cases of Clostridioides difficile colitis that occurred in patients with hematological malignancies or solid tumors at Roswell Park Comprehensive Cancer Center. Roswell Park is a 133-bed National Cancer Institute-designated Comprehensive Cancer Center in Buffalo, NY. The study was approved by Roswell Park’s Institutional Review Board. The study period extended from February to December 2016.
The patients’ charts were reviewed and data were collected on age, sex, underlying malignancy, and admission to intensive care unit. The presence of leukopenia (white blood cell count of ≤ 1.5 × 109/L), neutropenia (neutrophil count of ≤ 0.5 × 109/L), the level of creatinine and albumin, days of exposure to antibiotics, and proton pump inhibitors during the preceding 3 months were recorded. The incidence of CDI was estimated per 10,000 patient days of hospital admission.
Severe CDI was defined as disease associated with peripheral blood leukocytosis (white blood cell count of ≥15,000 cells/mL) and/or elevated serum creatinine (creatinine level >1.5 mg/dL). Reference McDonald, Gerding and Johnson2 Fulminant CDI was characterized by hypotension, ileus, or toxic megacolon. Reference McDonald, Gerding and Johnson2 Crude mortality was determined at 30 and 45 days after diagnosis of CDI.
Patients were tested for Clostridioides difficile when clinically indicated at the discretion of the treating physician. The diagnostic algorithm included initial detection of Clostridioides difficile Glutamate Dehydrogenase antigen and toxins A and B, using the C. Diff Quick Check Complete® immunoassay. If the Clostridioides difficile toxin was negative but the glutamate dehydrogenase antigen was positive, the sample was further tested by PCR using the BioFire® FilmArray® gastrointestinal panel. Reference McDonald, Gerding and Johnson2
All patients with positive results by either Clostridioides difficile toxin or PCR assays were placed on “contact plus” precautions that included strict contact isolation, handwashing with soap and water, and bleach terminal cleaning. Reference Muto, Jernigan and Ostrowsky3
Clostridioides difficile isolation and ribotyping were performed at the Department of Pathology at Washington University, St. Louis, MO. Clostridioides difficile was isolated from fecal samples with a previously described CCMB-TAL broth enrichment technique Reference Hink, Burnham and Dubberke4 and identified using VITEK MS MALDI-TOF MS. Ribotyping and identification of toxins A and B were performed as previously described. Reference Westblade, Chamberland and MacCannell5,Reference Antikainen, Pasanen and Mero6 The PCR-ribotyping was evaluated for genetic similarity using the DiversiLab Bacterial Barcodes software program (bioMérieux, Durham, NC) and compared to a reference library of ribotypes. Reference Westblade, Chamberland and MacCannell5 Three nontoxigenic Clostridioides difficile strains that were isolated from 3 patients with diarrhea but negative stool Clostridioides difficile toxin and PCR assays served as controls.
Results
The incidence of CDI was 0.29 cases per 10,000 inpatient days and remained stable throughout the study period. Of 111 episodes of CDI 66 stool samples were available and sent for isolation of Clostridioides difficile. Of 66 samples, 31 isolates were recovered in cultures and studied with molecular typing. The isolates corresponded to CDI in 30 patients with one patient having recurrent disease 2 weeks after completion of treatment. The demographics of 31 patients are provided in Table 1. Diagnosis was established by positive toxin and antigen assays in 19 (61.3%) cases and with PCR in 12 (38.7%) cases when toxin and antigen assays were discordant.
Demographics and Basic Characteristics of 31 Patients with Typable Clostridioides difficile Strains
Note. LEU, leukemia; LYM, lymphoma; TCT, transplantation and cellular therapy. ALL, acute lymphocytic leukemia; AML, acute myelocytic leukemia; MDS, myelodysplastic syndrome; HL, Hodgkin lymphoma; NHL, non-Hodgkin lymphoma; MM, multiple myeloma.
a Ovarian cancer, lung cancer, glioma.
The 31 isolates with available typing from patients with CDI represented 12 ribotypes. Twenty-five isolates (80.6%) belonged to 6 ribotypes, represented by 3–7 strains and the rest 6 (19.4%) were unique ribotypes. The most prevalent ribotype was 014/020 (n=7, 22.6%). Other ribotypes comprised 1/VPI/077/087 (n=5 in 4 patients, 12.9%), 05/015 and 015/046 (n=4 patients each, 12.9%), and 05/053 and 106/174 (n=3 patients each, 9.7%).
Three novel ribotypes were identified (designated as Novel A, B, and C). Novel ribotype A was a nontoxigenic strain and was identified in a control sample. Novel ribotype C possessed the cdtA and cdtB genes encoding for binary toxin. None of the 2 patients with toxigenic novel ribotypes presented with severe CDI and both responded to antibiotic therapy.
The hypervirulent ribotype 078 was detected in one patient while the cdtA and cdtB genes encoding for binary toxin were present in a total of 3 isolates (1 with novel ribotype C). None of these patients presented with severe disease, fulminant CDI, or associated mortality. The 027 ribotype was not detected in our cohort.
Evaluation of genetic similarity of ribotype band patterns showed 6 lineages of 2–5 isolates among 19 (63.3%) patients (Figure 1). These lineages corresponded to 5 out of 6 most common ribotypes. The exception was isolates of ribotype 106/174 of which SI was 90% to 94.9%. Epidemiological investigation showed occasional temporal and spatial overlap among several patients within the clusters.
Dendrogram illustrating the gel electrophoresis profiles of Clostridioides difficile isolates. Footnote of Figure 1: aIsolates R3, R50, and R52 are nontoxigenic control strains. bIsolates R32 and R40 originate from a patient with a recurrent episode of Clostridioides difficile colitis.
Discussion
The incidence of CDI among patients with malignancies is significantly higher than in the general population. Reference Lessa, Mu and Bamberg7,Reference Gorschluter, Glasmacher and Hahn8 In our cohort, CDI incidence was 0.29 cases per 10,000 inpatient days. During this period the incidence of Clostridioides difficile colitis remained steady, a pattern consistent with a nonoutbreak setting.
Molecular typing documented shared clones in the majority of patients (80.6%) in our cohort. The most common ribotypes were 014/020, followed by ribotypes 1/VPI/77/87, 05/015, and 015/046. Ribotype 014/020 is one of the most prevalent ribotypes with worldwide distribution Reference Collins, Sohn and Wu9 and an emerging ribotype in the United States. Reference Tickler, Goering and Whitmore10 Less is known about the 1/VPI/77/87 ribotype that in our cohort comprised a group of 5 isolates originating from 4 patients. No isolate carried the genes for the binary toxin. They all caused healthcare-associated CDI with 4 isolates falling under the same lineage, clustering over a period of 3 months. CDI associated with this ribotype was severe in 3 cases but responded to antibiotic therapy, except for one patient who was heavily treated with antibiotics and experienced a relapse.
The hypervirulent ribotype NAP1/027 was not detected in our cohort. Reference Lessa, Mu and Bamberg7 The hypervirulent ribotype 078 was detected in one patient and the cdtA and cdtB genes encoding for binary toxin were present in another 2 patients (1 with the novel ribotype C). None of these patients presented with severe or fulminant disease. Among the 3 novel ribotypes, novel ribotype A was a nontoxigenic strain identified in a control stool sample.
Limitations of our study include its retrospective nature, the single center data source, and failure to recover all isolates for ribotyping. The failure to recover many of the isolates for ribotyping was attributed to suboptimal processing of the specimens during interstate transfer to the reference laboratory for molecular typing, which led to overgrowth of competing commensal flora. It might also reflect the superior sensitivity of PCR leading to detection of nonclinically significant carriage of Clostridioides difficile or nonviable bacterial elements.
We demonstrated that in a nonoutbreak state when incidence rate of CDI remained stable CDI was caused by several Clostridioides difficile lineages. Lack of a predominant strain suggests community acquisition of C. difficile spores and demonstrates the value of molecular analysis rather than relying solely on days of hospitalization in defining hospital-acquired C. difficile infection.
Acknowledgments
Financial support
Funding for the isolation and ribotyping of Clostridioides difficile was provided to Washington University (WUSM), St. Louis, MO by Roswell Park Comprehensive Cancer Center, Buffalo, NY.
Competing interests
Research funding: C.-A.D. Burnham has received grants or contracts from Cepheid, bioMerieux, BioFire Diagnostics, Luminex, ThermoFisher, CDC, AHRQ, NIH, Selux, and Qiagen to Washington University School of Medicine (WUSM). B.H.S. has received research funding from Apellis and NextCure. Consultant or Advisory Role: C.-A.D. Burnham has received consulting fees from Cepheid, BioFire Diagnostics, Shionogi, and Pattern Bioscience paid to herself. Honoraria: C.-A.D. Burnham has received payment or honoraria for lectures, presentations, speakers, bureaus, manuscript writing, or educational events from Roche, Cepheid, BD, BioFire Diagnostics, Medavera, and Medscape paid to herself. B.H.S. is a member of Scientific Advisory Board for NextCure. Employment or Leadership: C.-A.D. Burnham has leadership or fiduciary role in the American Academy of Microbiology (ASM) and Clinical Laboratory Standards Institute (CLSI) for which she or her institution has not been compensated. Stock Ownership: None declared. Expert Testimony: None declared. Patents: None declared. Other Remuneration: None declared.
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