Helicobacter pullorum in Chickens, Belgium

Helicobacter pullorum is present in approximately one third of the chickens in Belgium.

Almost no data are available on the prevalence of this species in poultry. Research that could generate these data is hampered by the fastidious growth requirements of H. pullorum and the phenotypic similarity between member species of the genera Helicobacter and Campylobacter (3,4,12). H. pullorum in chickens has been studied on only 2 occasions when the organism was detected by using isolation (4,7). Furthermore, no valid epidemiologic research methods have been recommended.
This study's objective was to determine the occurrence of H. pullorum in broilers by using both polymerase chain reaction (PCR) and isolation. In addition, amplified fragment length polymorphism profiling (AFLP) was conducted to investigate the genetic relatedness between H. pullorum isolates.

Sample Origin
Samples from the gastrointestinal tracts and livers of 110 broiler chickens, 10 per flock (flock number 1-11), collected at a poultry abattoir, were studied. Each gastrointestinal tract and liver sample was deposited in a separate waterproof plastic bag. Samples were taken from the liver, cecum, jejunum, and colon for PCR and isolation within 3 hours after collection. All samples were stored at -20°C and -70°C for PCR and isolation, respectively, until further analysis, as described below.

PCR and Gel Electrophoresis
DNA was extracted from ≈25 mg cecum, colon, jejunum, and liver tissue with a commercial tissue kit (DNeasy Tissue Kit, Qiagen, Venlo, the Netherlands). A PCR assay amplifying a 447-bp fragment of the 16S rRNA gene of H. pullorum was then used for detection purposes (1). From each sample, 2 µL template was added to 8 µL

Helicobacter pullorum in Chickens, Belgium
Technologies), a final primer concentration of 0.5 µmol/L, and sterile distilled water. The conditions used for the amplifications were the following: an initial denaturation at 94°C for 5 min, followed by 35 cycles of denaturation at 94°C for 1 min, annealing at 60°C for 90 s, elongation at 72°C for 90 s, and a final elongation at 72°C for 5 min. Five microliters of the PCR products of each sample were mixed with 3 µL of sample buffer 5× (50% glycerol, 1 mmol cresol red) and were subjected to electrophoresis through an agarose gel containing 1.5% Multi Purpose agarose (Boehringer, Mannheim, Germany) and 50 ng ethidium bromide in per milliliter 1× Tris-acetate ethylenediaminetetraacetic acid buffer (Amresco, Solon, OH, USA), pH 8. As molecular size marker, the Gene Ruler 100-bp DNA ladder plus (MBI Fermentas, St. Leon-Rot, Germany) was used. Electrophoresis was implemented at a constant voltage of 170 V in 0.5× Tris-acetate ethylenediaminetetraacetic buffer for 75 min. The gels were visualized by using the Image Master VDS (Pharmacia Biotech, Puurs, Belgium).

Isolation of H. pullorum
Recovery of H. pullorum isolates was attempted on all positive samples in the PCR analysis described above. The samples (200 mg) for isolation of H. pullorum were placed in a 1.5-mL tube with 400 µL of a mixture of 7.5 g glucose, 25 mL brain heart infusion broth (Oxoid, Basingstoke, England), and 75 mL sterile inactivated horse serum, and then homogenized. The various isolates were inoculated on brain heart infusion agar that was supplemented with 10% horse blood, amphotericin B 20 µg/mL (Fungizone, Bristol-Myers Squibb, Epernon, France), and Vitox (Oxoid) (blood agar). A modified filter technique of Steele and McDermott (13) was then used. Briefly, a sterile cellulose acetate membrane filter (0.45 µm) was applied with a sterile pair of tweezers directly onto the surface of the agar. When the filter was totally absorbed on the agar, ≈300 µL of the mixture was placed in the middle of the filter. After at least 1 hour of incubation at 37°C and 5% CO 2 , the filter was removed with a sterile pair of tweezers and the filtrate was streaked on the agar with a loop. Incubation was conducted in microaerobic conditions (5% H 2 , 5% CO 2 , 5% O 2, and 85% N 2 ) at 37°C for a minimum of 3 days. Very small, gray-white, hemolytic colonies were selected and purified on a blood agar plate. The colonial form and phenotypic characteristics (gram-negative, slightly curved rod, catalase and oxidase positive, and indoxyl acetate negative) of the isolates were used for presumptive identification. Confirmation was based on PCR and sequencing of a 447-bp fragment of the 16S ribosomal RNA gene, as described below.

Analysis of Nucleotide Sequences
The PCR product of the retrieved H. pullorum isolates was purified with the Qiaquick purification kit (Qiagen) and sequenced by using the same primers applied in the assay with the BigDye Terminator cycle sequencing kit (Applied Biosystems, Lennik, Belgium). Sequencing products were run on the ABI prism 3100 Genetic Analyzer (Applied Biosystems) by using 50-cm capillaries filled with Performance-Optimized-Polymer 6. The electrophoregrams were exported and converted to the Kodon software package (Applied Maths, Sint-Martems-Latem, Belgium). Sequences were compared to published H. pullorum 16S rRNA sequences obtained from GenBank (accession nos. AY631956, L36143, and L36144) by using BLAST software (available from http://www.ncbi.nlm.nih. gov/blast/).

AFLP
Twenty-two poultry and 3 human isolates were fingerprinted by using AFLP (Table 1). These included 16 isolates from flock numbers 5 and 9 screened in this study. In addition, 4 samples previously isolated from broilers' cecal droppings and the boots from another flock's farmer, 4 reference strains (2 of chicken and 2 of human), and 1 human strain isolated from diarrheic stool in our laboratory were included for comparison.

Direct Selective PCR Amplification of Diluted Ligation
Five microliters of the diluted ligation reaction were applied in the PCR assay. The primers used in this assay were BGL2F-0, 5′-GAG TAC ACT GTC GAT CT-3′ (FAM labeled, 5′-end) and CSP6I-A, 5′-GAG CTC TCC AGT ACT ACA-3′ (15). The PCR conditions were as follows: an initial denaturation at 94°C for 3 min; 35 cycles of denaturation at 94°C for 1 min, annealing at 54°C for 1 min, and elongation at 72°C for 90 s; and a final elongation at 72°C for 10 min.

Capillary Electrophoresis
PCR products were run on the ABI prism 3100 Genetic Analyzer (Applied Biosystems) by using the Fragile X Rox-1000 size standard and 50-cm capillaries filled with Performance-Optimized-Polymer 6. Electropherograms were analyzed with Genemapper U 3.5 Software (Applied Biosystems).

Numerical Analyses of AFLP Profiles
The program BioNumerics version 2.5 (Applied Maths) was used to perform numerical analyses of AFLP profiles. Strain relationships were inferred by use of the Pearson product-moment correlation coefficient and unweighted pair-group with mathematical average (UPGMA) clustering and depicted in a dendrogram (16).

PCR
In Table 2, the number of H. pullorum DNA-positive samples originating from the intestinal tract and liver is shown. In 4 flocks, all samples were negative for H. pullorum. In the other 7 flocks, positive samples were found. In the cecum and colon, a PCR reaction for H. pullorum was positive in 33.6% and 31.8% of the samples, respectively. In total, 10.9% of jejunum and 4.6% of liver samples were positive for H. pullorum.

Isolation of H. pullorum
Eight H. pullorum cecum isolates from flock number 5 and 8 H. pullorum cecum isolates from flock number 9 were obtained. The sequences of the amplified 447-bp fragment of the H. pullorum 16S ribosomal RNA gene isolates showed a similarity of 98%-100% to those from GenBank (accession nos. AY631956, L36142, and L36143).

AFLP
AFLP analysis showed that isolates from each of the individual flocks examined clustered according to their flock of origin. The remaining chicken isolates and human strains each displayed a unique profile (Figure).

Conclusion
This study shows that H. pullorum is present in 33.6% of the cecal samples of broiler chickens collected at a poultry slaughterhouse during evisceration by using PCR. This microorganism was found in 7 of 11 flocks; 4 flocks were negative. Burnens et al. found a prevalence rate of 4% upon sampling cecal contents of broilers (7). The organism was detected by isolation. Considering the fastidious nature of this organism, this finding could explain this markedly lower percentage of positive birds. Additionally, in our study, cecal tissue, rather than cecal contents, was examined for the organism. Microorganisms related to H. pullorum adhere closely to the mucosa of the gastrointestinal tract. The phylogenetically related microorganism, C. jejuni, may tightly adhere to the brush borders of the intestine in chickens (17,18). The same phenomenon has also been documented for H. pylori in the stomach (19).
Comparing our study results to those obtained by Atabay et al. (4), the latter group found a higher occurrence of H. pullorum (60%) on poultry carcasses. This apparent discrepancy could be due to cross-contamination with cecal contents on the surface of broiler carcasses during poultry processing (4,8). Furthermore, contamination of the chicken body surface may occur during transportation to the abattoir. Fecal excretion of Campylobacter spp. may be increased because of stress during transportation and consequently may contaminate carcasses (20).
H. pullorum DNA was detected in only 5 (4.6%) liver and 11 (10.9%) jejunal samples, as opposed to 35 (31.8%) colonic and 37 (33.6%) cecal samples. Hence, one may assume that the lower segments of the intestinal tract are the predominant colonization sites for H. pullorum in broiler chickens. H. pullorum may gain access to the liver by retrograde transfer from the duodenum. Alternatively, it may translocate from the gut lumen to the portal circulation.
H. pullorum has been associated with vibrionic hepatitis in laying hens, both macroscopically and microscopically (7). In our study, no gross pathologic lesions were seen in the livers during sampling (data not shown).
Our modest isolation rate of H. pullorum from cecal samples may have been the result of examining frozen, as opposed to fresh, samples. However, we successfully recovered 16 isolates from 2 flocks, allowing (for the first time, to our knowledge) some analysis of the etiology of H. pullorum in broiler flocks to be undertaken. We used AFLP profiling for this purpose, a highly discriminatory method that has been successfully applied to molecular epidemiologic studies of several related species, including H. pylori (21,22), Arcobacter spp. (15), and Campylobacter spp. (23,24). Isolates from each of the individual flocks clustered according to their flock of origin, indicating a clonal relationship. In contrast, field and reference strains isolated from different hosts or geographic sources displayed a distinctive pattern. These data suggest that AFLP profiling has considerable potential for molecular epidemiologic studies of H. pullorum for the noted related species.
Several authors have suggested that H. pullorum has zoonotic potential and is involved in the pathogenesis of diarrhea and chronic liver diseases in humans (2,8,10,11). Retail raw poultry meats and other poultry products may constitute vehicles for human H. pullorum infections through carcass contamination, as previously reported for Arcobacter and Campylobacter species (8,(25)(26)(27). Concerning health monitoring, PCR may be helpful in detecting this pathogen not only in intestinal tissue but also in broiler chicken cecal droppings.
In conclusion, this study shows that H. pullorum is a frequent intestinal colonizer of broiler chickens. PCR and isolation are useful tools to detect the species in intestinal tissue and in cecal droppings. AFLP profiling appears to be useful for molecular epidemiologic studies of this species.