Correction
28 May 2015: Camacho-Ortiz A, López-Barrera D, Hernández-García R, Galván-De los Santos AM, Flores-Treviño SM, et al. (2015) Correction: First Report of Clostridium difficile NAP1/027 in a Mexican Hospital. PLOS ONE 10(5): e0129079. https://doi.org/10.1371/journal.pone.0129079 View correction
Figures
Abstract
Background and Objective
Clostridium difficile NAP1/ribotype 027 is associated with severe disease and high mortality rates. Our aim was to determine the prevalence of NAP1/ribotype 027 among C. difficile isolates in a tertiary care hospital, and review the main clinical data.
Methods
We included 106 stool samples from 106 patients. Samples were tested for A&B toxins and were cultured on CCFA agar. The genes tcdA, tcdB, tcdC, cdtA, and cdtB were amplified using PCR in clinical isolates. The tcdA 3’-end deletion analysis, PCR-ribotyping, and pulsed-field gel electrophoresis (PFGE) were also performed. Stool samples that were positive for culture were tested by the GeneXpert C. difficile assay. Clinical data were collected.
Results
Thirty-six patients tested positive for A&B toxins; and 22 patients had positive culture for C. difficile, 14 of which tested positive for the A&B toxins and all 22 patients tested positive by the GeneXpert C. difficile assay. Risk factors included an average hospital stay of 16.1 days prior to toxin detection, average antibiotic use for 16.2 days, and a median of 3 antibiotics used. The 30-day crude mortality rate was 8.4%. Six of the 22 patients died, and 3 of those deaths were directly attributed to C. difficile infection. The majority of isolates, 90.9% (20/22), carried genes tcdB, tcdA, cdtA, and cdtB; and these strains carried the corresponding downregulator gene tcdC, with an 18-bp deletion. PFGE was performed on 17 isolates, and one main pattern was observed. Analysis of the ribotyping data showed similar results.
Citation: Camacho-Ortiz A, López-Barrera D, Hernández-García R, Galván-De los Santos AM, Flores-Treviño SM, Llaca-Díaz JM, et al. (2015) First Report of Clostridium difficile NAP1/027 in a Mexican Hospital. PLoS ONE 10(4): e0122627. https://doi.org/10.1371/journal.pone.0122627
Academic Editor: Markus M. Heimesaat, Charité, Campus Benjamin Franklin, GERMANY
Received: December 11, 2014; Accepted: February 23, 2015; Published: April 27, 2015
Copyright: © 2015 Camacho-Ortiz et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Data Availability: All relevant data are within the paper.
Funding: The authors have no support or funding to report.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Clostridium difficile is a Gram-positive anaerobic bacterium that is able to produce spores. This bacterial species causes a potentially fatal diarrheal disease due to the production of its principal virulence factors toxin A and toxin B, which are encoded by their genes tcdA and tcdB that are located on a 21-kilobase section of chromosomal DNA known as the pathogenicity locus (PaLoc). The tcdC gene is thought to encode a negative regulator of toxin production. Therefore, enhanced toxin production, and thus increased virulence, is often derived in strains with an aberrant tcdC genotype. In addition to toxins A and B, some strains also produce a third toxin known as binary toxin, encoded by ctdA and ctdB, located outside the PaLoc [1]. The spores of this anaerobic bacterium are widely distributed in hospital environments, and their ingestion by patients with an altered gut microflora contributes to colonization and disease [1,2].
The spectrum of C. difficile infection (CDI) is very wide, starting from asymptomatic carriage to severe diarrhea that may progress to pseudomembranous colitis and toxic megacolon. The epidemiology of C. difficile has changed in the past decade, and a new type has emerged: polymerase chain reaction (PCR) ribotype (RT) 027/North American Pulsed (NAP)-field type 01. Major outbreaks associated with this strain have been described since 2004, first in Canada followed by the USA and Europe [1,3–5]. C. difficile NAP1/027 is associated with a severe disease presentation and high morbidity and mortality rates; therefore, it presents a major clinical and financial burden [6]. In Latin America, this strain has been found in Costa Rica and more recently in Chile [7]. In Mexico, studies have shown the clinical characteristics of patients with CDI demonstrating a significant risks of developing CDI following the use of H2 blockers, if they had a prior hospitalization within 12 weeks of diagnosis, if they had been in the intensive care unit, prior use of cephalosporin’s, fluoroquinolones [7] and clindamycin [7] but genetic analysis of Mexican isolates have not been published. Thus, our aim was to determine the prevalence of NAP1/027 among C. difficile isolates in a tertiary care hospital, and review the main clinical data.
Material and Methods
Ethics Statement
This study was performed with the approval of the Local Ethics Committee of the School of Medicine of the Universidad Autónoma de Nuevo León (Approval MB11-007). Written informed consent approved by the Ethics Committee was obtained from all patients.
When applied, written informed consent was obtained from caretakers, or guardians on behalf of the minors enrolled in this study.
Study population and collection of data
From March 2011 through August 2012, 106 stool samples were analyzed from hospitalized patients aged 16 years or older. We enrolled patients with a hospital stay greater than 48 h or a recent hospitalization (in the previous 12 weeks) who developed diarrhea (3 or more depositions in the last 24h with a Bristol score of 6 or 7) and in whom there was no obvious explanation of the cause. All subjects agreed to participate in the study by signing an informed consent.
The demographic and clinical data collected in the study were age, gender, and length of hospital stay. In addition, the usage and dosage of antibiotics within the past 2 months were investigated as potential risk factors for CDI. Laboratory tests such as white blood cell (WBC) count, creatinine, and albumin were performed within 24 h of enrollment.
Detection of infection
The stool samples collected were tested for toxins using the ImmunoCard toxins A&B assay (Meridian Bioscience, Cincinnati, OH, USA). Furthermore, fecal samples were collected from patients and were treated with ethanol shock for 3 h prior to inoculation on cycloserine-cefoxitin fructose agar (CCFA). Incubation was achieved in an anaerobic atmosphere using a GasPak EZ anaerobe pouch system (Becton Dickinson, Sparks, MA, USA) at 37°C for 48 h; and anaerobic colonies were identified using catalase, Gram staining, and the Crystal Identification System (Becton Dickinson).
Analysis of clinical isolates
For all isolates, multiple PCR were performed to genotype tcdA, tcdB, cdtA, cdtB, tcdC. We also detected the deletion in the downregulator gene tcdC.
To obtain DNA form clinical isolates, five colonies were transferred into 200 μL of 100 mM Tris-HCl, 150 μg of lysozyme was added, and the mixture was incubated at 37°C overnight. Finally, genomic DNA was extracted with a standard phenol-chloroform-isoamyl alcohol protocol.
tcdA, tcdB, cdtA, and cdtB analysis
The genes tcdA, tcdB, cdtA, and cdtB were amplified using a multiplex PCR method [8]. The total volume was 25 μL, consisting of 2.5 μL of 10× PCR buffer, 100 ng of DNA, 3mM MgCl2, 200 μM of each dNTP, and 1 U of Taq polymerase (Bioline, London, UK), and the primers tcdA-F3345, tcdA-R3969, tcdB-F5670, tcdB-R6079A, tcdB-R6079B, cdtA-F739A, and cdtA-F739B were used (Table 1). Thermocycler conditions were as follows: 3 min at 94°C; then 35 cycles of 50 s at 94°C, 40 s at 56°C, and 50 s at 72°C; and a final extension of 3 min at 72°C.
tcdC analysis
PCR was performed to amplify the tcdC gene according to the method used by Spigaglia et al.(2002) [9]. The total volume was 25 μL, consisting of 2.5 μL of 10× PCR buffer, 100 ng of DNA, 3mM MgCl2, 200 μM of each dNTP, and 1 U of Taq polymerase. The primers used were C1 and C2 (Table 1). Thermocycler conditions were as follows: 5 min at 94°C; then 30 cycles of 1 min at 94°C, 1 min at 50°C, and 1 min at 72°C; and a final extension of 3 min at 72°C.
tcdC internal in-frame deletion analysis
For tcdC internal in-frame deletion analysis, PCR was performed as described by Persson et al.(2011) [8]. The total volume was 25 μL, consisting of 2.5 μL of 10× PCR buffer, 100 ng of DNA, 3mM MgCl2, 200 μM of each dNTP, and 1 U of Taq polymerase. The primers used were tcdC-F252 and tcdC-R415 (Table 1). Thermocycler conditions were as follows: 3 min at 94°C; then 35 cycles of 50 s at 94°C, 40 s at 56°C, and 50 s at 72°C; and a final extension of 3 min at 72°C.
tcdA 3’-end deletion analysis
For tcdA3’-end deletion analysis, the reaction mixture consisted of 25 μL, containing 2.5 μL of 10× PCR buffer, 100 ng of DNA, 3mM MgCl2, 200 μM of each dNTP, 1 U of Taq polymerase, and the primers NK9 and MNKV011 [10]. Thermocycler conditions were as follows: 6 min at 94°C; then 37 cycles of 20 s at 94°C, 30 s at 55°C, and 2 min at 60°C; and a final extension of 3 min at 60°C.
GeneXpert C. difficile
The Xpert C. difficile/Epi assay (Cepheid, CA) was performed as described by the manufacturer. Briefly, each stool sample positive for culture was transferred into a sample reagent vial. The vial was vortexed for 10 s, and the solution was pipetted into the cartridge by using a Pasteur pipette. The cartridge was placed on the Xpert instrument, and the assay was performed using the GeneXpert C. difficile assay program.
PCR-Ribotyping
Amplification reactions were performed according to the method described by Bidet et al.[11]. The reaction mixture consisted of 25 μL, containing of 2.5 μL of 10× PCR buffer, 100 ng of DNA, 3mM MgCl2, 200 μM of each dNTP, 1 U of Taq polymerase, and the primers 16S and 23S (Table 1). Thermocycler conditions were as follows: 6 min at 94°C; then 35 cycles of 1 min at 94°C, 1 min at 57°C, and 1 min at 72°C; and a final extension of 7 min at 72°C. Amplification products were subjected to electrophoresis through a 2.5% agarose gel stained with ethidium bromide for 6 h at 85 V and then analyzed on an ultraviolet table with the LabWorks Image Acquisition and Analysis Software Version 4.5.00.0 for Windows (UVP, Inc., Upland, CA, USA). C. difficile ATCC 9689 and ATCC 9689 were used as a control.
Pulsed-Field Gel Electrophoresis (PFGE)
PFGE was performed according to the method used by Alonso et al. (2002), with minor modifications [12]. A bacterial culture was grown in CCFA agar three times before starting, and then it was inoculated into fluid thioglycollate medium (FTM) and grown for 24 h at 37°C. Next, 2 mL of the FTM mixture was taken and centrifuged to obtain the bacterial pellet. The pellet was washed one time with 1 mL of cell suspension buffer and then resuspended in 410 μL of cell suspension buffer. Each bacterial suspension was mixed with 150 μL of 1.5% agarose and mixed thoroughly. The mixture was transferred to plug molds (35 μL for each plug) and allowed to solidify at 4°C for 10–15 min. The solidified plugs were incubated in 1 mg mL-1 lysozyme solution (100 μL of 25 mg mL-1 lysozyme stock plus 2.5 mL of lysozyme buffer) for 2 h at 37°C. The lysozyme was removed, and the plugs were rinsed with sterile water. The plugs were incubated with 20 U mL-1 proteinase K solution (100 μL of >600 U mL-1 proteinase K stock in 2.5 mL of proteinase K reaction buffer) at 50°C overnight (17 h). Then, the plugs were washed four times with 1× washing buffer for 30 min at room temperature with agitation. Next, the plugs were incubated for 1 h with 1 mL of 1× restriction enzyme buffer at room temperature and then overnight in 300 μL of 1× restriction enzyme buffer containing 30–50 U of the restriction enzyme SmaI at 30°C. After digestion, the buffer with the restriction enzyme was removed and the plugs were incubated for 30 min in 1× washing buffer. The plugs were loaded on a 1% agarose gel with 0.5× Tris-borate-EDTA buffer with thiourea (200 μM). Electrophoresis was run at 6 V for 22 h with pulse times starting at 1 s and ending at 35 s using the CHEF-DR III Pulsed-Field Electrophoresis System (Bio-Rad, Hercules, CA, USA).
Results
Clinical data of patients
During the 18-month surveillance period, we screened 106 patients with probable CDI, and 36 tested positive with the ImmunoCard assay. Furthermore, we found 22 patients with a positive culture for C. difficile, 14 of which tested positive with the Immuno Card assay and all 22 were positive by the GeneXpert assay. (Fig 1)
Of the 22 patients with a positive culture, 9 were women (40.9%) and the median age was 46.5 years old. Risk factors included an average hospital stay of 16.1 days prior to toxin detection, average antibiotic use for 13.5 days, and a median of 3 antibiotics used. The most common antibiotics used prior to toxin detection were third-generation cephalosporins (11/22), clindamycin (11/22), and flouroquinolones (7/22). Patients had a median of 9 stool movements per day. The average levels of peripheral leukocytes, albumin, and creatinine were 22,200 cells/mL, 2.0 g/dL, and 1.69 mg/dL, respectively. We observed differences in prior use of clindamycin and overall mortality between culture positive and culture negative patients (Table 2)
Treatment was combined (enteral vancomycin and IV metronidazole) in 9/22 (40.9%) patients, and 13/22 (59%) had monotherapy (10 metronidazole, 2 vancomycin, and 1 rifaximin). The overall 30-day crude mortality rate was 8.4% (9/106). Two patients required colectomies for treatment of CDI. Six of the 22 patients died, and 3 of those deaths were directly attributed to CDI.
Isolates
Twenty-two isolates were collected from 22 patients (mean age, 51.7 years old; range, 20–89 years old; 10 females, 12 males). Most of these isolates were collected from medical wards, but other wards such as trauma and intensive care units were also involved (Table 3). Toxin gene profiles were assessed based on PCR, and two profile types were noted. The majority of isolates, 90.9% (20/22), carried genes encoding enterotoxin, cytotoxin, and the binary toxins (tcdB, tcdA, cdtA, and cdtB); and these strains carried the corresponding downregulator gene tcdC, with an 18-bp deletion. The 20 stool samples from which these isolates were obtained tested positive for the toxigenic NAP1/027 strain: toxigenic C. difficile positive/presumptive NAP1/027 positive.
The remaining 9.1% (2/22) of the isolates were positive for tcdB, tcdA, and tcdC; had no deletion of the downregulator gene tcdC; and were negative for the binary toxin marker genes cdtB and cdtA (Table 3).
The 2 stool samples from which these isolates were obtained tested negative for the toxigenic NAP1/027 strain: toxigenic C. difficile positive/presumptive NAP1/027 negative.
PFGE was performed on 17 isolates, and one main pattern characteristic of NAP1 strain was observed. Only two isolates showed a different pattern (isolates 106 and 186).
Analysis of the ribotyping data showed similar results with a predominant ribotype characteristic of 027 strains and only two isolates showing a different pattern (isolates 106 and 186).
Discussion
C. difficile is an important nosocomial pathogen associated with diarrheal disease. In this paper, we present the first report of C. difficile ribotype NAP1/027 from Mexico.
One of the most used tests for the diagnosis of CDI is the ImmunoCard assay. In our study, we screened 106 patients with probable CDI, and 36 tested positive with the ImmunoCard assay. Interestingly, among the 22 patients with a positive culture for C. difficile, only 14 were positive by the ImmunoCard assay. According to the manufacturer, the ImmunoCard assay has a sensitivity of 95.2%, a specificity of 98.5%, and a negative predictive value of 99%. However, based on our results, the culture was not able to detect 12 infected patients and the ImmunoCard test missed 8 patients. Even though it was not our objective to evaluate the diagnostic tests, it seems that it is necessary to perform both for a more accurate diagnosis. Direct PCR from stool specimens is a widely used test for the diagnosis of CDI because it has high sensitivity, specificity, positive predictive value, and negative predictive value. In fact, PCR has been recommended as the preferred diagnostic test for CDI [13].
While no test is 100% sensitive and specific for the detection of C. difficile, cell cytotoxigenic and cytotoxin tests are the current gold standards. A bias of our study is that these tests are not still available in our laboratory for confirmation of the PCR results, we are already implementing this technique.
Previous work has determined that approximately one out of ten patients who acquire C. difficile will die [14] and that mortality associated with ribotype NAP1/027 infection increases with the patient’s age. A recent study has shown that 44.1% of infected patients were older than 65 years and that 8.1% of them died within 30 days after diagnosis [15]. In our study, 3 out of 22 patients (13.6%) died from CDI, with an average age of 67.6 years. If we consider all infected patients (n = 44) (36 toxin-positive patients plus 8 culture-positive, ImmunoCard-negative patients), we had a mortality rate directly attributed to CDI of 6.8% (3/44). In our study, we did not find a direct epidemiologic link between the CDI NAP1/027 cases.
C. difficile infection is also related with higher health care costs due to longer hospital stays [16]. It has been shown that hospital-acquired C. difficile infection significantly extends the duration of a patient’s stay in hospital [17]. Furthermore, C. difficile is most commonly a nosocomial infectious agent, with reservoirs being patients, healthcare workers, and the hospital environment; and the major risk for CDI is antibiotic exposure within the preceding 2–3 months [18]. The risk factors for our patients were a hospital stay of 16.1 days prior to toxin detection, average antibiotic use for 16.2 days, and a median of 3 antibiotics used.
Typing of C. difficile isolates is mostly based on one or more of three common typing schemes, including restriction enzyme analysis (the epidemic clone is type BI), PFGE (the epidemic clone is NAP1), and/or PCR ribotyping (the epidemic clone is ribotype 027). It has been described that PFGE exhibits better discriminatory power than PCR ribotyping, with D-values of 0.843 and 0.688, respectively [19]. In our study, we used both methodologies and both were able to show the clonal relationship of the isolates. However, PCR ribotyping is much easier to perform in the laboratory than PFGE analysis because it is less laborious.
A more severe disease presentation is more likely to be caused by ribotype NAP1/027 strains than by non-027 strains because ribotype NAP1/027 strains produce excessive amounts of toxins A and B as a result of tcdC deletion [4]. In our hospital, most of the isolates were ribotype NAP1/027 and were disseminated in several hospital wards; thus, special care should be taken to avoid the spread of this ribotype. In summary, the above findings represent the clonal spread of C. difficile in our institution, which mainly includes the ribotype NAP1/027 strain.
Clonal spread of C. difficile is a mayor concern in the healthcare environment and thus the isolation of C. difficile NAP1/027 requires an ongoing genetic surveillance for an early identification of new cases. Hospital policies regarding the use of clorine based disinfectants and earlier isolation precautions were reinforced after these findings.
These data confirm the emergence of C. Difficile in Mexico. Surveillance data are needed to assess the dissemination of this strain in the hospital and to establish risk factors related with the transmission of this bacterium in our healthcare facilities. This is the first report of C. difficile ribotype NAP1/027 in Mexico.
Author Contributions
Conceived and designed the experiments: ACO EGG. Performed the experiments: DLB SFT RHG AGS JLlD. Analyzed the data: EGG ACO FJBP HJMG JLlD. Contributed reagents/materials/analysis tools: ACO EGG. Wrote the paper: ACO EGG SFT DLB.
References
- 1. Elliott B, Chang BJ, Golledge CL, Riley TV (2007) Clostridium difficile-associated diarrhoea. Intern Med J 37: 561–568. pmid:17640189
- 2. Poutanen SM, Simor AE (2004) Clostridium difficile-associated diarrhea in adults. CMAJ 171: 51–58. pmid:15238498
- 3. Kuijper EJ, Coignard B, Tull P (2006) Emergence of Clostridium difficile-associated disease in North America and Europe. Clin Microbiol Infect 12 Suppl 6: 2–18. pmid:16965399
- 4. McDonald LC, Killgore GE, Thompson A, Owens RC Jr., Kazakova SV, Sambol SP et al. (2005) An epidemic, toxin gene-variant strain of Clostridium difficile. N Engl J Med 353: 2433–2441. pmid:16322603
- 5. Warny M, Pepin J, Fang A, Killgore G, Thompson A, Brazier J et al. (2005) Toxin production by an emerging strain of Clostridium difficile associated with outbreaks of severe disease in North America and Europe. Lancet 366: 1079–1084. pmid:16182895
- 6. Mylonakis E, Ryan ET, Calderwood SB (2001) Clostridium difficile—Associated diarrhea: A review. Arch Intern Med 161: 525–533. pmid:11252111
- 7. Hernandez-Rocha C, Barra-Carrasco J, Pizarro-Guajardo M, Ibanez P, Bueno SM, Sarker MR et al. (2012) Epidemic Clostridium difficile ribotype 027 in Chile. Emerg Infect Dis 18: 1370–1372. pmid:22840230
- 8. Persson S, Jensen JN, Olsen KE (2011) Multiplex PCR method for detection of Clostridium difficile tcdA, tcdB, cdtA, and cdtB and internal in-frame deletion of tcdC. J Clin Microbiol 49: 4299–4300. pmid:21976756
- 9. Spigaglia P, Mastrantonio P (2002) Molecular analysis of the pathogenicity locus and polymorphism in the putative negative regulator of toxin production (TcdC) among Clostridium difficile clinical isolates. J Clin Microbiol 40: 3470–3475. pmid:12202595
- 10. Kato H, Kato N, Katow S, Maegawa T, Nakamura S, Lyerly DM. (1999) Deletions in the repeating sequences of the toxin A gene of toxin A-negative, toxin B-positive Clostridium difficile strains. FEMS Microbiol Lett 175: 197–203. pmid:10386368
- 11. Bidet P, Barbut F, Lalande V, Burghoffer B, Petit JC (1999) Development of a new PCR-ribotyping method for Clostridium difficile based on ribosomal RNA gene sequencing. FEMS Microbiol Lett 175: 261–266. pmid:10386377
- 12. Alonso R, Martin A, Pelaez T, Marin M, Rodriguez-Creixems M, et al. Bouza E. (2005) An improved protocol for pulsed-field gel electrophoresis typing of Clostridium difficile. J Med Microbiol 54: 155–157. pmid:15673509
- 13. O'Horo JC, Jones A, Sternke M, Harper C, Safdar N (2012) Molecular techniques for diagnosis of Clostridium difficile infection: systematic review and meta-analysis. Mayo Clin Proc 87: 643–651. pmid:22766084
- 14. Oake N, Taljaard M, van Walraven C, Wilson K, Roth V, Forster AJ. (2010) The effect of hospital-acquired Clostridium difficile infection on in-hospital mortality. Arch Intern Med 170: 1804–1810. pmid:21059973
- 15. Pepin J, Valiquette L, Alary ME, Villemure P, Pelletier A, Forget K, et al. (2004) Clostridium difficile-associated diarrhea in a region of Quebec from 1991 to 2003: a changing pattern of disease severity. CMAJ 171: 466–472. pmid:15337727
- 16. Ghantoji SS, Sail K, Lairson DR, DuPont HL, Garey KW (2010) Economic healthcare costs of Clostridium difficile infection: a systematic review. J Hosp Infect 74: 309–318. pmid:20153547
- 17. Forster AJ, Taljaard M, Oake N, Wilson K, Roth V, van Walraven C. (2012) The effect of hospital-acquired infection with Clostridium difficile on length of stay in hospital. CMAJ 184: 37–42. pmid:22143235
- 18. Heinlen L, Ballard JD (2010) Clostridium difficile infection. Am J Med Sci 340: 247–252. pmid:20697257
- 19. Killgore G, Thompson A, Johnson S, Brazier J, Kuijper E, Pepin J et al. (2008) Comparison of seven techniques for typing international epidemic strains of Clostridium difficile: restriction endonuclease analysis, pulsed-field gel electrophoresis, PCR-ribotyping, multilocus sequence typing, multilocus variable-number tandem-repeat analysis, amplified fragment length polymorphism, and surface layer protein A gene sequence typing. J Clin Microbiol 46: 431–437. pmid:18039796