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High frequency of toxigenic Clostridium difficile and Clostridium perfringens coinfection among diarrheic patients at health care facility-onset (HCFO) and community-onset (CO) centers in Bogotá, Colombia
- Alex J. Forero†1, 2,
- Marina Muñoz†1, 3,
- Milena Camargo4,
- Sara C. Soto-De León5,
- Dora I. Ríos-Chaparro1,
- Claudia Birchenall6,
- Darío Pinilla6,
- Juan M. Pardo6,
- Diego F. Josa7,
- Manuel A. Patarroyo4, 8 and
- Juan D. Ramírez1Email authorView ORCID ID profile
© The Author(s) 2019
- Received: 11 April 2019
- Accepted: 29 May 2019
- Published: 3 June 2019
The aim of this study was to evaluate the frequency of toxigenic C. difficile and C. perfringens infections at health care facility-onset (HCFO) and community-onset (CO), in two health care centers (HCC) in Bogotá, Colombia. A total of 220 stool samples from patients presenting diarrhea acquired at HCFO or CO were analyzed by several PCR tests.
We found that 65.5% (n = 144) of the population had C. difficile infection, followed by toxigenic C. difficile with 57.3% (n = 126), and finally toxigenic C. perfringens with a frequency of 32.7% (n = 72).
This study is the first molecular detection and characterization of C. difficile and C. perfringens in HCFO and CO in Latin America and demonstrates a relevant frequency of these two species, including coinfection and strikingly diverse toxigenic profiles, especially in the CO.
- Clostridium perfringens
- Clostridium difficile
- Health care facility onset
Clostridium difficile is one of the most studied clostridial species, as it leads to developing diarrhea associated with the use of antibiotics at the hospital level . The main virulence factors of C. difficile are Toxin A (TcdA) and Toxin B (TcdB), belonging to the large family of Clostridial toxins with glucosyltransferase activity . These toxins are encoded by genes located in a region of the chromosome of approximately 20 Kb, which constitutes the pathogenicity locus (PaLoc). Some strains of C. difficile can produce a third toxin called binary, which is encoded by a chromosomal region called CdtLoc, located downstream of PaLoc, which contains the cdtA and cdtB genes, coding for its two components, in addition to a regulator for these genes (cdtR) .
On the other hand, diarrhea can also be caused by C. perfringens, a species that is widely distributed in various hosts and environments, and that has been related to histotoxic and intestinal infections in animals and humans. C. perfringens has been identified in humans as the main etiologic agent of gas gangrene, also being able to cause other complications such as diarrheal disease associated with food poisoning, necrotizing enteritis, and other nonspecific gastrointestinal manifestations . Historically, it has been considered that C. perfringens produces the following four main toxins: alpha (CPA), beta (CPB), epsilon (ETX), and iota (ITX). However, recently some authors have added two more toxins to its toxin repertoire: enterotoxin (CPE), and necrotic enteritis B-like (NetB) toxin; all these toxins can be differentially produced  and determine the clinical spectrum of infection by this species . CPA is recognized as the main virulence factor in humans, causing hemolytic and dermonecrotic effects, characteristic of clostridial myonecrosis, which can be lethal . Different gene regions coding for the above toxins have been previously implemented for C. perfringens molecular detection. The cpa gene encoding for CPA, has been described as the best molecular target, which is located in a stable region of the genome present in the seven identified toxinotypes (A–G), according to the most recent reclassification of the species .
The importance of these two pathogens in terms of public health mediated by the broad toxigenic arsenal, leads to the need to evaluate the coinfection frequency (defined as a positive result simultaneously for the two species). In this context, this study aimed at determining the frequency of C. perfringens and C. difficile (any type or toxigenic specifically) present in health care facility-onset (HCFO) or community-onset (CO) diarrhea, at two health care centers in Bogotá, Colombia.
A total of 220 stool samples from patients with diarrhea , were collected during the period from September 2015 to April 2017 at two health care centers (HCC), located in the city of Bogotá, Colombia [the Hospital Universitario Mayor—Méderi (HCC-1) and the Fundación Clínica Shaio (HCC-2)]. Participant selection (HCFO and CO groups) was carried out following the guidelines of the Society for Healthcare Epidemiology of America and the Infectious Diseases Society of America .
Molecular detection and toxinotyping of C. difficile and C. perfringens
The clostridial species were identified using several conventional polymerase chain reaction (PCR) tests. Two sets of consensus primers targeting constitutive genes coding for the 16S ribosomal subunit (rRNA-16S) and for the glutamate dehydrogenase enzyme (GDH) as reported elsewhere [8, 9] were initially used for C. difficile detection (toxigenic or non-toxigenic). Subsequently, the toxigenic profiles of the C. difficile positive samples were determined using six independent amplification tests, four of them directed to the PaLoc regions that code for the main toxins of C. difficile [10, 11], and the other two to the CdtLoc, where the coding regions for the binary toxin are located . A positive result for any of these genes led to the assignment in the ‘tox_C. difficile’ category. In the case of C. perfringens, the detection was carried out by conventional PCR directed to the cpa gene, as reported elsewhere , considered as an indicator of the presence of ‘tox_C. perfringens’.
Descriptive analyses were carried out to determine the frequencies in terms of percentages with respect to the total population, for each event of interest. χ2 tests were performed to identify potential associations between the variables analyzed. A binomial logistic regression analysis was used to estimate the association between infection by C. perfringens, C. difficile or tox_C. difficile (taken as dependent variables) and the different factors evaluated (hospital center and hospital stay) taken as independent variables within the analysis. Additionally, the strength of association between the existing coinfections (C. perfringens and C. difficile, C. perfringens and tox_C. difficile) was calculated using odds ratios (ORs) with their corresponding 95% confidence intervals (CIs). The adjustment of the ORs (AdOR) was carried out from hospital (HCC-1 and HCC-2) and place of stay (HCFO and CO), as confounding variables. All analyses were performed using STATA14® (StataCorp LLC, College Station, TX, USA). The level of significance was established at p < 0.05.
Frequency of C. difficile/C. perfringens infection and/or coinfection
In addition, the distribution of infections according to the stay (HCFO and CO) and the hospital of origin of the patients (HCC-1 and HCC-2) was determined. At the HCFO level, infections were higher for the three species in the patients from the HCC-1 healthcare center compared to HCC-2, the distribution observed for C. difficile being statistically significant (p = 0.0250) (Fig. 1b). For CO patients, C. difficile infections were higher in HCC-2 compared to HCC-1 (p = 0.2285), in contrast to C. perfringens whose infections were higher than those observed in HFCO. In community patients from HCC-1, the frequency of occurrence was higher than that observed for HCC-2 (p = 0.2810). A similar pattern was found for the distribution of tox_C. difficile between hospital centers which was statistically significant (p = 0.0001) (Fig. 1c).
Logistic regression modeling showing the relationship between a positive result for infection and the hospital and acquisition of infection
C. perfringens infection
C. difficile infection
Toxigenic C. difficile infection
Health care center
The present study identified the frequency of C. difficile (general and tox_ C. difficile), but also tox_C. perfringens in two HCCs of Bogotá, Colombia through molecular detection . It is important to note that previous reports indicate frequent development of diarrhea in individuals in whom the microbiota has been altered by the effect of antimicrobial agents, favoring the proliferation of pathogens such as those belonging to the genus Clostridium . This could explain the presence of tox_C. perfringens in HCFO diarrhea. However, the results reported in this study indicate greater frequency of infection in patients with CO diarrhea (Fig. 1), which could be related either to the established association of infection by this species with diarrheal disease caused by food poisoning , or with the presence of some other factor that could be involved with the development of dysbiosis and acquiring the role of a pathogen . Although, due to the lack of clinical and sociodemographic information of the individuals included in this study, it is not possible to establish an association of causality between the presence of C. perfringens or C. difficile in patients with diarrhea in Colombia. We found interesting associations between C. perfringens and C. difficile (AdOR: 2.05 CI 95% 1.07–3.93) (Fig. 3). This suggests that coinfection plays a relevant role in the population. Future studies should consider both species in terms of clinical and sociodemographic data which might provide novel insights regarding the impact of both species in a particular population.
One limitation of our study was the inability to recover the isolates and conduct molecular characterization using genome sequencing or Multilocus Sequence Typing. Therefore, we encourage the scientific community to develop novel studies in the region aimed at unraveling the molecular features of these two species. The findings herein identified represent a baseline about the high coexistence of these two Clostridial species towards depicting the epidemiological panorama in the country and Latin-America.
We thank Clara Lina Salazar from Universidad de Antioquia for providing the reference strain of C. perfringens. We also thank Analisa Avila, ELS, of Edanz Group (http://www.edanzediting.com/ac) for editing a draft of this manuscript.
The Departamento Administrativo de Ciencia, Tecnología e Innovación (Colciencias) financed the PhD program to MM within the framework of the National Program for Promoting Research Training (sponsorship call 617). This work was funded By DIRECCIÓN DE INVESTIGACIÓN E INNOVACIÓN from Universidad del Rosario.
AJF, MM, DIRC and JDR: led the project and contributed to definition of experimental approach. MC, SCS, MM and JDR: analyzed the results and conducted the statistical analyzes. CB, DP, JMP, DFJ and MAP: led the clinical component, from the inclusion of samples to analysis of the results at the epidemiological level. MAP and JDR: revised the final version. All authors read and approved the final manuscript.
Ethics approval and consent to participate
An initial study aimed to detect C. difficile infections in fecal samples from patients with diarrhea was approved by the Universidad del Rosario’s Research Ethics Committee (Approval Act No. 290, July 27, 2015). In addition, an addendum was approved, which authorized the additional use of samples for research purposes aimed at the description and characterization of any microorganisms present in the human gastrointestinal tract (Approval Act No. 312 April 28, 2016). All patients (adult) signed the written informed consent.
Consent for publication
The authors declare that they have no competing interests.
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