Clostridium difficile in faeces from healthy dogs and dogs with diarrhea
© Wetterwik et al.; licensee BioMed Central Ltd. 2013
Received: 22 November 2012
Accepted: 28 February 2013
Published: 12 March 2013
This study was conducted to evaluate the faecal occurrence and characterization of Clostridium difficile in clinically healthy dogs (N = 50) and in dogs with diarrhea (N = 20) in the Stockholm-Uppsala region of Sweden.
Clostridium difficile was isolated from 2/50 healthy dogs and from 2/20 diarrheic dogs. Isolates from healthy dogs were negative for toxin A and B and for the tcdA and tcdB genes. Both isolates from diarrheic dogs were positive for toxin B and for the tcdA and tcdB genes. The C. difficile isolates from healthy dogs had PCR ribotype 009 (SE-type 6) and 010 (SE-type 3) whereas both isolates from dogs with diarrhoea had the toxigenic ribotype 014 (SE-type 21). One of the isolates from healthy dogs was initially resistant to metronidazole.
This study revealed presence of toxigenic C. difficile in faecal samples of diarrheic dogs and low number of non- toxigenic isolates in healthy dogs from Uppsala-Stockholm region in Sweden. However, more comprehensive studies are warranted to investigate the role of C. difficile in gastrointestinal disease in dogs.
KeywordsClostridium difficile Dog Faeces Toxins Ribotyping Antibiotic resistance pattern
The role of C.difficile in gastrointestinal disease in dogs is not yet defined. Moreover, interspecies transmission of C. difficile has also been suggested. The virulence of C. difficile is mainly related to the presence of two exotoxins, A and B that are encoded by tcd A and tcd B genes, respectively. In addition, some strains express a binary toxin (CDT).
The aim of the present study was to evaluate the presence of C. difficile in faeces from healthy and diarrheic dogs in the Stockholm-Uppsala region, Sweden. Toxin production, ribotyping and antibiotic resistance pattern of the isolates was also revealed.
Material and methods
Animals and sampling
Faecal samples from 50 healthy, randomly selected, and 20 diarrheic dogs (8 months-12 years old, median age 5 years) of varying breeds and from different households were investigated. Eighteen of the diarrheic dogs were hospitalized due to acute gastrointestinal disease involving diarrhea, whereas the remaining two dogs were outpatients and sampled at veterinary clinics. Use of systemic antibiotics within the last three months was recorded in a questionnaire for the healthy dogs. Samples were collected directly upon defecation. To prevent contamination, 10–20 g of faeces was collected with a spoon and stored in a sterile plastic sampling tube. The samples were kept refrigerated, and processed in the laboratory within 12 h after collection.
Culture conditions and bacteriological analysis
Faecal samples were plated onto C. difficile agar (CM0601 Oxoid, Basingstoke, UK) and used to inoculate C. difficile enrichment broth. Clostridium difficile agar was supplemented with moxalactam and norfloxacin (SR0173E Oxoid) and 5% horse blood (National Veterinary Institute, SVA, Uppsala, Sweden), and incubated anaerobically for 48 h at 37°C. Clostridium difficile broth was prepared with the ingredients for CM0601 (agar excluded), supplemented with moxalactam and norfloxacin. Briefly, 5 g of each faecal sample was added to 10 mL broth and mixed by vortex and incubated anaerobically at 37°C for 10 days. After incubation, the suspension was streaked onto C. difficile agar and Fastidious Anaerob Agar (FAA agar, SVA, Uppsala, Sweden) containing 5% horse blood and incubated for 48 h.
Identification of the isolates
Clostridium difficile was tentatively identified on the basis of Gram stain and morphology, characteristic horse manure odour, L-proline aminopeptidase activity (Oxoid), and then confirmed by the latex agglutination test (C. difficile test kit DR1107A, Oxoid).
Toxin detection of C. difficile
Toxin A detection was performed on fresh faeces, within 12 h after sampling, using the C. difficile toxin A test (TD 0970A, Oxoid Ltd). Positive control (C. difficile strain ATCC 43255) and negative control were included in each experiment, according to the instructions of the manufacturer. Detection of toxin B was performed by inoculation of isolates into C. difficile broth. The sterile culture filtrates (48 h incubation at 37°C under anaerobic condition) were used in the Vero cell assay as previously described.
Detection of C. difficile toxin A and toxin B genes
Presence or absence of toxin A and toxin B genes were evaluated by using PCR amplification of the A3 and B1 fragments using primer pairs and PCR protocol described by Rupnik. The analysis was performed on C. difficile isolates.
PCR ribotyping of C. difficile
PCR ribotyping was performed according to Stubbs et al. with modifications described by Svenungsson et al.. The type was given according to the international nomenclature by using the ribotype nomenclature of the Cardiff Anaerobe Reference Laboratory (Cardiff, Wales, UK), or when reference isolates were missing, as SE-type (Swedish type).
Antibiotic resistance pattern of the isolates
Ribotypes, tcdA/tcdB and antibiotic susceptibility patterns with MIC values (mg/L) of C. difficile isolated from dogs in Sweden
tcd A & tcd B
Clostridium difficile was isolated from 2 of the 50 healthy dogs and from 2 of the 20 diarrheic dogs investigated. Clostridium difficile was isolated both from primary culture and from the enrichment broth after 10 days of incubation, except the isolate no. 56 that was recovered only after enrichment.
Toxin production of C. difficile
Both C. difficile isolates (no. 56 and 61) from diarrheic dogs were toxin B producers, and were positive for the tcd A and tcd B genes (Table 1). However, samples from both dogs were negative on the initial C. difficile toxin A test performed on fresh faeces. Faeces from 4 additional diarrheic dogs tested positive for toxin A test but bacteria were not isolated from these samples. The C. difficile isolates (no. 35 and 38) from healthy dogs were negative for the tcd A and tcd B genes (Table 1). Culture filtrates from these samples were negative for toxin B, and all faeces from the animals from which the isolates were obtained were negative for toxin A.
The isolates from healthy dogs were classified as PCR ribotype 009/SE-type 6 (isolate no. 35) and 010/SE-type 3 (isolate no. 38), whereas both isolates from diarrheic dogs had PCR ribotype 014/ SE-type 21 (Table 1).
Antibiotic treatment of the dogs and resistance pattern of the isolates
Two of the healthy dogs investigated were treated with metronidazole and amoxicillin with clavulanic acid respectively, within three months before sampling. The isolate no. 35 was isolated from the dog that was treated with metronidazole, and this isolate was initially resistant to high levels of metronidazole: 64 mg/L (Table 1). However, high level metronidazole resistance was not maintained; subsequent subcultures following recovery from frozen storage were resistant to between 2 and 8 mg/L of antibiotic. Isolate no. 38 was isolated from a dog without history of antibiotic treatment, and this strain did not show elevated resistance to the antibiotics tested. Seven of the 20 diarrheic dogs were treated with antibiotics at the animal hospital or within 3 months before sampling. Antibiotic treatments in these dogs included amoxicillin (N = 1), ampicillin (N = 2) and metronidazole (N = 2), metronidazole and amoxillin with clavulanic acid (N = 1), amoxicillin, ampicillin and metronidazole (N = 1). Isolate no. 56 was from a dog treated with metronidazole during hospital stay. Isolate no. 61 was isolated from a dog treated (at the hospital), during recurrent diarrheic episodes, with ampicillin, metronidazole and amoxicillin respectively. One of the dogs that tested positive for the presence of toxin A, but was culture negative, had been treated with metronidazole and amoxicillin with clavulanic acid. Resistance patterns of the isolates are shown in Table 1.
Clostridium difficile was isolated in 2/50 of the healthy dogs and in 2/20 of the diarrheic dogs. Additionally, toxin A was detected in the faeces of diarrheic dogs and toxigenic bacteria were only isolated from diarrheic dogs, whereas toxin A was not detected in the faeces of any healthy dogs. Both isolates from healthy dogs were PCR negative for the tcd A and tcd B toxin genes. In four diarrheic dogs toxin A was detected in faeces samples but C. difficile was not isolated. On the other hand the C. difficile isolated from faeces of two diarrheic dogs were cdtA/cdtB positive but negative in the initial toxin A test performed on fresh faeces. Possible explanations for this phenomenon could be that C. difficile is a strict anaerobe bacterium and the recovery and cultivation of the microorganism can be difficult. Also, the bacteria can be present in the faeces although in very small number and therefore, in some cases, undetectable. Furthermore, very little is known about the actual excretion of toxins in the different phases of C. difficile colonisation/infection. This factor could also explain the negative results in the initial toxin A test.
There is wide variation in the reported C. difficile carriage rate among household pets. Different studies describes occurrence of C. difficile in faecal samples of dogs ranging from 0% to 21%[9–12]. Both toxigenic and non-toxigenic isolates are reported. Several factors may contribute to these discrepancies, including different methods of isolation and detection, prior use of antibiotics, geographical location, age or breed of animals.
Both isolates from diarrheic dogs had the toxigenic ribotype 014 associated with clinical disease in humans, while isolates from healthy dogs revealed nontoxigenic PCR ribotypes 009 and 010. Ribotype 010 is occasionally isolated from human faeces in Sweden while type 009 is uncommon, whereas ribotype 014 is commonly detected in clinical specimens from human patients in Sweden.
Evidence of antibiotic resistance in C. difficile isolates from humans is growing, but reports of antibiotic resistant strains from dogs are rare[13, 16]. Marks and Kather reported that all C. difficile isolated from diarrheic and nondiarrheic dogs were susceptible to metronidazole and vancomycin, leading to the recommendation that these drugs are appropriate for use in treating infection. However, in our study, one of the C. difficile isolates from a healthy dog (no. 35), treated with metronidazole, was initially resistant to metronidazole (MIC = 64 mg/L). The dog from which this isolate originated was treated for gingivitis with metronidazole one month before sampling. The high level of metronidazole resistance in this purified strain was unstable and decreased to 2 mg/L, which may be due to the absence of continual antibiotic selection. This phenomenon has been reported by Pelaez et al. and Huang et al. on human isolates and is not fully understood. The lack of continuous selection in vitro might lead to loss of resistance. Genetic determinants of resistance in C. difficile are not known but may be on an unstable plasmid that is lost without continuous selection. Metronidazole unresponsive C. difficile infection has been discussed as an emerging problem in humans but resistance against metronidazole has not to our knowledge previously been reported in C. difficile isolates from dogs.
In conclusion, our work contributes to the growing evidence on the occurrence of toxigenic and nontoxigenic C. difficile in dogs. This study revealed presence of toxigenic C. difficile in faecal samples of diarrheic dogs and low number of non- toxigenic isolates in healthy dogs. However, more comprehensive studies are warranted to investigate the role of C. difficile in gastrointestinal disease in dogs. Also, the finding of toxigenic ribotype 014 in diarrheic dogs might imply a potential zoonotic risk. In addition, one C. difficile isolate was initially resistant to metronidazole, and acquisition of resistance to this common drug of choice in dogs should be considered in veterinary clinical practice.
The authors wish to thank Dr. Thomas Åkerlund for scientific comments and suggestions on the manuscript, and Ingela Alefjord for excellent technical assistance and Prof. Richard Zuerner for his critical comments and suggestions during the final part of preparation of the manuscript.
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