A mixed population of Helicobacter pylori, Helicobacter bizzozeronii and “Helicobacter heilmannii” in the gastric mucosa of a domestic cat
Irish Veterinary Journal volume 67, Article number: 25 (2014)
The presence of Helicobacter within the gastric mucosa is responsible for producing pathology in many animal species, including man. Since humans have been shown to harbour many of the same bacterial species as domestic carnivores, concern over their zoonotic potential has been growing. Helicobacter pylori, a class 1 carcinogen responsible for cases of gastritis and gastric cancer in humans, produces similar pathology in pet carnivores and is considered an example of anthroponosis. The case here presented refers to a 13 year-old mixed breed spayed female cat seen at necropsy.
Stomach samples were analysed for the presence of Helicobacter spp. by cytology, histopathology and PCR. Mild mucosal atrophy was observed in the fundus and antrum, while lymphoplasmocytic infiltrates where noted in the lamina propria of the antrum. Helicobacter-like organisms were observed in the corpus and antrum, occupying gastric glands and surface mucosa. It was possible to detect Helicobacter spp., H. pylori, H. heilmannii and H. bizzozeronii in the fundus, corpus and antrum by PCR, while in the antrum PCR samples were positive for H. pylori.
The spayed female under study could represent either a yet un-described population of domestic cats infected with H. pylori or a case of anthroponosis.
Helicobacter pylori is a gram negative, urease positive, spiral bacteria classified by the World Health Organization as a class 1 carcinogen as its relationship to human gastritis and gastric cancer has been firmly established . The majority of the 32 species described to date are enteric microorganisms of mammals, while 12 species are gastric inhabitants. Four species are now considered to be common in the gastric mucosa of domestic carnivores, Helicobacter felis, Helicobacter bizzozeronii, Helicobacter salomonis, “Helicobacter heilmannii” types 1, 2 and 4 [2, 3], while the role of H. bilis’ as a primary gastric organism remains questionable. Although the pathogenic role of these species in gastritis and/or gastric cancer has yet to be firmly established in pets [4, 5], felines seem to be much more susceptible then canines . Gastric fibroses and atrophy have been linked to H. felis infection in cats  while the presence of lymphoid follicles and inflammation have been related to Helicobacter spp. and “H. heilmannii” senso lato colonization [8, 9].
It has been suggested that, similarly to H. pylori infected humans, the presence of H. heilmannii could play a role in feline alimentary lymphoma . There are several reasons for the growing concern regarding the zoonotic potential of these bacteria . Firstly, humans have been shown to harbour species other than H. pylori with pathological consequences; secondly, no environmental source for these bacteria has been found; and lastly, epidemiological studies have shown a link between animal contact and infection . Although H. pylori produces similar pathology in pet carnivores and in humans, this species has yet to be found in normal domestic carnivore populations [13, 14], making these cases good examples of anthroponosis [4, 6, 13]. However, Buczolits et al.  have identified two sequences from Helicobacter-like organisms 100% identical to H. pylori in the gastric mucosa of canines, re-kindling the debate on the role of pet carnivores in the transmission of this bacterium to humans. The present work describes the presence of H. pylori in a mixed population of Helicobacter species in the gastric mucosa of a domestic short-hair cat.
A 13 year-old mixed breed spayed female cat with a history of mammary tumors and pleural effusion, euthanized at the owners’ request, was presented for necropsy to the Pathology Department of the Faculty of Veterinary Medicine, University of Lisbon. The stomach was opened along the greater curvature, brush cytology was performed and four full thickness biopsies where obtained from the fundus, corpus and antrum for histopathology and PCR analyses. Brush cytologies where obtained using sterile, single use inoculation loops and stained with May-Grünwald-Giemsa. One biopsy from each gastric region was stored in 10% formalin for histology processing. A combined sample, comprising one sample from each region, and the remaining biopsies from the three regions were kept frozen at −80°C, until DNA extraction with Qiagen DNeasy® Blood & Tissue Kit, according to the manufacturer’s instructions. PCR reactions for Helicobacter spp., H. pylori, H. felis, H. heilmannii, H. bizzozeronii, H. salomonis and H. bilis were performed as previously described [3, 7, 16–19], using FidelTaq™ MasterMix (USB® Products – Affymetrix, Inc.). Reference strains H. pylori CCUG 17874 T, H. felis ATCC 49179, H. bizzozeronii CCUG 35045, H. salomonis CCUG 37845, H. bilis ATCC 51630 and H. heilmannii DNA (kindly provided by Professor K.W. Simpson) were used as positive controls. Biopsies for histopathology were imbedded in paraffin blocks, processed and stained with Hematoxylin and Eosin and with Giemsa.
Based on the World Small Animal Veterinary Association histopathological standards , mild mucosal atrophy was observed in the fundus and antrum, while moderate lymphoplasmocytic infiltrates were noted in the lamina propria of the antrum. Helicobacter-like organisms were observed in the corpus and antrum, occupying gastric glands and surface mucosa (Figure 1A), where colonization was classified as mild. Brush cytology was positive in the fundus and corpus (Figure 1B), but negative in the antrum. PCR performed using DNA extracted from the combined sample was positive for Helicobacter spp., H. pylori, H. heilmannii and H. bizzozeronii, originating 1200-bp, 298-bp, 580-bp and 420-bp amplicons, respectively (Figure 2). When tested individually, the three regions were positive for Helicobacter spp., H. heilmannii and H. bizzozeronii, while only the antrum was positive for H. pylori.
The presence of a Helicobacter mixed population has been previously described in feline gastric biopsies . Our finding of mild mucosal atrophy is consistent with other studies [6, 22]; however Simpson et al.  linked changes in the architecture of the gastric mucosa with the presence of H. felis, a species not found in this cat. H. heilmannii has been shown to alter gastric architecture but through epithelial proliferation and lymphoid follicular hyperplasia , not atrophy. It is possible however that the presence of H. pylori and H. bizzozeronii altered the pathogenic capacity of H. heilmannii as described for mixed infections of H. bizzozeroniiI/H. felis. The fact that the fundus and antrum were the most affected regions is consistent with others findings  and, although not characteristic, the presence of inflammation in the antrum is similar to that found in felines experimentally infected with H. pylori.
The occurrence of H. pylori in the gastric mucosa of felines has been only reported in a particular commercial breeder  but not in stray and domestic populations [13, 14, 24]. The spayed female under study could represent either a yet un-described population of domestic cats infected with H. pylori or a case of anthroponosis, as hypothesized by some authors [4, 5, 13]. Considering H. pylori’s ability to survive in water  and the tendency for keeping indoor/outdoor cats in Portugal, colonization of this animal through a contaminated water source must also be considered. It was not possible to determine whether human co-inhabitants were H. pylori positive or if the animal had outdoor access.
The presence of H. heilmannii in cats has been linked to various alterations in gastric mucosa  and alimentary lymphoma . Jergens et al.  have shown that treatment leads to the improvement of gastritis clinical signs and bacterial clearance, although histological signs of gastritis remain, suggesting a causal relationship similar to that seen in H. pylori infected humans . However, as other studies could not evidence such relationship, other factors such as the effect of mixed infections and the possibility of strain dependent virulence, should be considered. The presence of a mixed infection of H. heilmannii and H. pylori, as found in this cat, could explain the development of pathology in some animals and not in others infected only with H. heilmannii. Given H. pylori’s focal distribution pattern , the small sample size normally obtained through endoscopy and even biopsy  may explain the high rate of negative results for H. pylori.
The role played by Helicobacter in feline gastritis, associated or not with lymphoma, remains controversial. Several factors, such as the species of Helicobacter present, the virulence of the strain, and the genetic predisposition of the animal, should be further investigated in order to better understand their relation to clinical disease.
Polymerase chain reaction
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The authors would like to thank CIISA/FMV for their financial support (Project PEst-OE/AGR/U10276/2014, funded by FCT), Professor Kenneth W. Simpson for the kind donation of H. heilmannii DNA used as a positive control for PCR, Professor Maria Conceição Peleteiro for her expert advice, as well as and Tec. Sandra Carvalho for her assistance with histopathology and Tec. Carla Carneiro for her assistance in the bacteriology laboratory.
The authors declare that they have no competing interests.
RCT identified the patient, collected the gastric samples and performed brush cytology. RCT and MO carried out the laboratory processes that permitted the processing of samples for PCR analyses. HP performed the histopathology. RCT and CLV were involved in data acquisition, analysis and interpretation and the drafting of the manuscript. MMREN was involved in revising the manuscript, contributing to its intellectual content. All authors read and approved the final manuscript.
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Canejo-Teixeira, R., Oliveira, M., Pissarra, H. et al. A mixed population of Helicobacter pylori, Helicobacter bizzozeronii and “Helicobacter heilmannii” in the gastric mucosa of a domestic cat. Ir Vet J 67, 25 (2014). https://doi.org/10.1186/2046-0481-67-25