ライフサイエンスコーパス: Felis

1 ure (single monomer vs. tandemly repeated in Felis).

2 similar (97 to 99%) to "H. heilmannii" or H. felis.

3 eukin-10-deficient (IL-10(-/-)) mice with H. felis.

4 and the mice were orally inoculated with H. felis.

5 type (WT) C57BL/6 mice were infected with H. felis.

6 ion with Helicobacter pylori or Helicobacter felis.

7 nisms and evaluate the immune response to H. felis.

8 ainly CD4(+) for H. pylori and CD8(+) for H. felis.

9 cts mice against challenge with Helicobacter felis.

10 e to be designated a new species, Rickettsia felis.

11 nd congenic mice with a single isolate of H. felis.

12 h either Helicobacter pylori or Helicobacter felis.

13 a after infection of mice with H pylori or H felis.

14 n and IL-8Tg mice infected with Helicobacter felis.

15 urease B (ureB) gene of H. heilmannii and H. felis.

16 re positive for H. heilmannii and two for H. felis.

17 is of the sialome of cat flea Ctenocephaides felis.

18 og (2) genotypes, C. meleagridis (7), and C. felis (1).

19 re gavaged with H pylori SS1 or Helicobacter felis; 3 months later, stomachs, spleens, and sera were

20 s, 20 were qPCR positive for FHV-1, 7 for M. felis, 5 for FCV, 1 for C. felis, and 0 for B. bronchise

21 ridis (17 persons), C. canis (6 persons), C. felis (6 persons), and C. suis (1 person) infection.

22 than to that of the California strain of H. felis (84%).

23 ted to that of the Ohio-Florida strain of H. felis (89%) than to that of the California strain of H.

24 The relationship of Helicobacter felis, a bacterium observed in the stomachs of cats, to

25 ly described bacterium closely related to R. felis, a known human pathogen.

26 solates of A. fumigatus, A. viridinutans, A. felis, A. pseudoviridinutans, and A. wyomingensis but wa

27 vitro studies demonstrated that Helicobacter felis activates complement in normal mouse serum but not

28 erum from Rag2(-/-) mice, indicating that H. felis activates complement through the classical pathway

29 After treatment with Helicobacter felis Ag, DC were polarized to secrete interleukin-6 as

30 fection in a host infected with Helicobacter felis alters the natural outcome of T. gondii infection,

31 acteria were closely related to Helicobacter felis, although there was heterogeneity among the sequen

32 ri, Helicobacter heilmannii and Helicobacter felis among others.

33 Cytauxzoon felis, an emerging virulent protozoan parasite that infe

34 ar to those originating from C. psittaci, C. felis and C. caviae.

35 C57BL/6 (-/-)] were orally infected with H. felis and examined longitudinally using routine histolog

36 L/6-T-bet knockout (KO) litter mates with H. felis and examined the bacterial colonization, immune re

37 Chlamydophila felis and feline herpesvirus (FHV) are pathogens commonl

38 NS-GAS mice) were infected with Helicobacter felis and given the CCK2/gastrin receptor antagonist YF4

39 ori and non-Helicobacter pylori organisms H. felis and H. heilmannii and analyzed the association bet

40 and H. pylori and 1(20%) coinfected with H. felis and H. pylori (p = 0.15).

41 and H. pylori and 3(60%) coinfected with H. felis and H. pylori (p = 0.66).

42 that the major protein bands of Helicobacter felis and Helicobacter bizzozeronii, two Helicobacter sp

43 PRIL Tg mice were infected with Helicobacter felis and Helicobacter pylori and compared with noninfec

44 uce protective immunity against Helicobacter felis and Helicobacter pylori infection in mice.

45 C57BL/6 mice were infected with Helicobacter felis and received bacterial eradication therapy after 2

46 currence of high relative copy numbers of C. felis and severe clinical signs in all cats was seen.

47 complex prevents gastric colonization by H. felis and the inflammatory response.

48 ently (e.g., Bartonella henselae, Rickettsia felis), and their mechanisms of transmission and impact

49 r FHV-1, 7 for M. felis, 5 for FCV, 1 for C. felis, and 0 for B. bronchiseptica.

50 re positive for FHV, 97 were positive for C. felis, and 16 were positive for both pathogens.

51 e orally infected with a single strain of H. felis, and 2 and 11 weeks after infection, the mice were

52 argeted mice were infected with Helicobacter felis, and a series of adoptive transfer experiments was

53 virus (FCV), Mycoplasma felis, Chlamydophila felis, and Bordetella bronchiseptica.

54 diarrhea, only infections with C. canis, C. felis, and subtype family Id of C. hominis were associat

55 of the H. muris strains, four strains of H. felis, and two strains of Eperythrozoon suis were sequen

56 atusRickettsia amblyommii,"R. montanensis,R. felis, andR. belliiwere frequently identified species, a

57 ins of H. pylori, as well as in Helicobacter felis, another member of the same genus.

58 Sera were also evaluated for H. felis antibody by ELISA.

59 H. felis antral colonization remained stable over time amon

60 th C. hominis and C. parvum; C. canis and C. felis are responsible for only a small number of cases.

61 of recent reports have implicated Rickettsia felis as a human pathogen, paralleling the increasing de

62 d-type mice were colonized with Helicobacter felis, as a model of human H. pylori infection.

63 after challenge with either H. pylori or H. felis, as confirmed by the complete absence of any bacte

64 ygous mice were inoculated with Helicobacter felis at 6 weeks of age and compared at various time poi

65 e-linked immunosorbent assay (ELISA) with H. felis ATCC 49179 antigen were performed with 101 serum s

66 nd for 1 year after oral inoculation with H. felis (ATCC 49179).

67 C. felis became undetectable in some of the cats during or

68 etection of two genotypes of Ctenocephalides felis biting humans in New Jersey, USA.

69 le when paired with the MAT1-1 isolate of A. felis but not with any of the other species.

70 d IL-10(-/-) mice infected with Helicobacter felis by gastric lavage.

71 L/6 x 129SvEv)F1] mice were infected with H. felis by oral gavage and were assessed histologically an

72 A unique strain (S. felis C4) was isolated from feline skin that inhibited M

73 H. felis can induce a hypertrophic gastropathy in the C57BL

74 obacter pylori (H. pylori) in domestic cats (Felis cattus) less than 2 years of age has been well des

75 his method to the under-annotated genomes of Felis catus (domestic cat) and Bos taurus (cow).

76 mental and theoretical analysis reveals that Felis catus exploits fluid inertia to defeat gravity and

77 present predominantly in one felid species: Felis catus GHV 1 (FcaGHV1) in domestic cats, Lynx rufus

78 sent the earliest evidence for domestic cat (Felis catus L., 1758) from Kazakhstan, found as a well p

79 ary fibroblasts isolated from domestic cats (Felis catus) and pumas (Puma concolor) with FeLV and qua

80 e disease and mortality in the domestic cat (Felis catus) and serves as a natural model for HIV infec

81 It is known that domestic cat (Felis catus) APOBEC3Z3 (A3Z3), the ortholog of human APO

82 direction and retinal disparity in the cat (Felis catus) are all strongly related to the organizatio

83 Domestic cats (Felis catus) are known to develop cognitive impairment,

84 nce spanning 758,291 bp of the domestic cat (Felis catus) extended and classical class II region.

85 characterized the proteome of domestic cat (Felis catus) follicular fluid EVs (ffEV).

86 We show that the domestic cat (Felis catus) laps by a subtle mechanism based on water a

87 Urban domestic cat (Felis catus) populations can attain exceedingly high den

88 ated the susceptibility of the domestic cat (Felis catus) to CWD infection experimentally.

89 nal referentiality in a common domestic cat (Felis catus) vocalization, the authors conducted 2 exper

90 and DRB gene homologues of the domestic cat (Felis catus) were cloned and sequenced to compare the pa

91 stic felids, vocalizations by domestic cats (Felis catus) were compared with cries by their closest w

92 entify felid GHVs, we screened domestic cat (Felis catus), bobcat (Lynx rufus), and puma (Puma concol

93 GHVs present in the blood of domestic cats (Felis catus), bobcats (Lynx rufus), and pumas (Puma conc

94 uenced the red and green opsin cDNAs of cat (Felis catus), horse (Equus caballus), gray squirrel (Sci

95 of FIV have been described for domestic cat (Felis catus), puma (Puma concolor), lion (Panthera leo),

96 several closely related to the domestic cat (Felis catus).

97 auses an AIDS-like disease in domestic cats (Felis catus).

98 roduced species, particularly the feral cat, Felis catus, and European red fox, Vulpes vulpes, and ch

99 bp mitochondrial genome of the domestic cat, Felis catus, has been sequenced and conforms largely to

100 comparative gene maps, the feline gene map (Felis catus, Order Carnivora, 2N = 38) displays the high

101 Following H. felis challenge, addition of the adjuvant CpG ODN provid

102 FHV-1), feline calicivirus (FCV), Mycoplasma felis, Chlamydophila felis, and Bordetella bronchiseptic

103 H. felis colonization also was increased in Duoxa(+/-) mice

104 atment did not alter the overall level of H. felis colonization but did result in significant down-re

105 H. felis colonization was significantly greater in the iNOS

106 onounced gastric atrophy after short-term H. felis colonization with a similar extent of preneoplasia

107 H. felis colonized the mucus layer in the stomachs of Duoxa

108 A high percentage of free-ranging pumas (Felis concolor) are infected with feline lentiviruses (p

109 rresponding transmembrane segments of the H. felis CopA pump were identified by hydrophobicity analys

110 ch single-nucleotide polymorphisms in the C. felis cytb gene had been identified.

111 The C. felis cytb genotype cytb1 is associated with increased s

112 69 cats with cytauxzoonosis for which the C. felis cytb genotypes had been characterized previously.

113 design a PCR panel that could distinguish C. felis cytb1 from other cytochrome b genotypes.

114 The PCR panel identified C. felis cytb1 with 100% sensitivity and 98.2% specificity.

115 tovaquone, a ubiquinone analogue, targets C. felis cytochrome b (cytb), of which 30 unique genotypes

116 We characterized the C. felis cytochrome b gene (cytb) in cats with cytauxzoonos

117 C57BL/6 mice inoculated with Helicobacter felis develop gastritis by 4 weeks.

118 felis were monitored for the presence of C. felis DNA on ocular swabs by using real-time PCR and for

119 Since felids outside the genus Felis do not harbor enFeLV genomes, we hypothesized abse

120 otor task and sitting quietly in adult cats (Felis domestica).

121 um pratense 1 (Phl p 1) and the cat allergen Felis domesticus 1 (Fel d 1) greater than 3.5 Immuno Sol

122 st mite (Dermatophagoides farinae), and cat (Felis domesticus) allergens in home dust samples, and sp

123 The cat isocortex (Felis domesticus) shows a similar structure.

124 now we add the successful cloning of a cat (Felis domesticus) to this list.

125 Infection of IL-10(-/-) mice with H. felis elicited a severe chronic gastritis and a greatly

126 Infection of IL-10(-/-) mice with H. felis elicited severe gastritis.

127 The data suggest that H. pylori and H. felis employ conserved mechanisms of ATPase-dependent co

128 vitro, induction of oxidative defense by H. felis failed to prevent a direct bacteriostatic effect a

129 tion to its annoyance to pets and humans, C. felis felis is responsible for flea bite allergy dermati

130 The cat flea, Ctenocephalides felis felis, is the most important ectoparasite of domes

131 by experimental infection with Helicobacter felis, followed by antibiotic eradication therapy and su

132 mice chronically infected with Helicobacter felis for 2 mo with the SOM analogue octreotide resolved

133 eporter mice were infected with Helicobacter felis for 3 and 8 weeks.

134 ions from male C57BL/6 mice infected with H. felis for 6 months.

135 el(-/-) mice were infected with Helicobacter felis for 6 weeks or 12 months.

136 C57BL/6 wild-type mice were infected with H. felis for either 12 or 18 months.

137 The sequences of two strains of H. felis from cats in California were identical, as were th

138 enzymes DdeI and MnlI for distinguishing H. felis from closely related bacteria was examined.

139 6-bp DNA fragment of the 16S rRNA gene of H. felis from each of four experimentally infected cats at

140 rs from the numt previously described in the Felis genus in: (1) chromosomal location (F2-telomeric r

141 und in the genomes of related species of the Felis genus, previously shown to harbor enFeLVs.

142 elicobacter spp. revealed that all except H. felis grew in serum-free, unsupplemented F-12.

143 ld-type mice were infected with Helicobacter felis (H. felis) to induce gastritis.

144 ther helicobacters (H. canis, H. cineadi, H. felis, H. mustelae, H. nemestrinae, H. pullorum, H. pylo

145 te substantial antigenic homology between H. felis, H. pylori, and H. bizzozeronii.

146 the "H. heilmannii"-like organisms (HHLO) H. felis, H. salomonis, and H. bizzozeronii.

147 , or both, produced a specific fecal anti-H. felis IgA response, with the highest IgA levels occurrin

148 ection with T. gondii alters the specific H. felis immune response, converting a previously resistant

149 ombination developed increased serum anti-H. felis immunoglobulin G (IgG).

150 0 (57%), H. heilmannii in 17/250 (6%) and H. felis in 10/250 (4%), respectively.

151 , paralleling the increasing detection of R. felis in arthropod hosts across the globe, primarily in

152 whole-cell sonicate vaccine of Helicobacter felis in conjunction with cholera toxin as a mucosal adj

153 Cellular stress was induced with IR and H felis in Ikkbeta(Deltastom), Ikkbeta(F/F), and cis-NF-ka

154 The acquisition and persistence of R. felis in mosquitoes was demonstrated by quantitative PCR

155 ed with a Florida isolate of Haemobartonella felis in order to collect organisms and evaluate the imm

156 Challenge with H. felis increased the inflammatory response in the gastric

157 Infection with H. felis induced expression of Duox2 and Duoxa2 in the stom

158 The suppressed H. felis-induced gastric phenotype of Stat3(SA/SA) mice was

159 the role of CD73 in regulating Helicobacter felis-induced gastritis and colonization.

160 out mice have increased susceptibility to H. felis-induced gastritis, with enhanced gastric inflammat

161 d p53 hemizygous mouse model of Helicobacter felis-induced gastritis.

162 ced peritonitis, DSS-induced colitis, and H. felis-induced gastritis.

163 n of noggin in mice increased H pylori- or H felis-induced inflammation and epithelial cell prolifera

164 ative of an impaired Th1 component of the H. felis-induced inflammatory response when the influence o

165 of SPEM to the neoplastic process in the H. felis -infected C57BL/6 mouse, we have now studied the a

166 Natural bites from R. felis-infected An. gambiae were able to cause transient

167 lesterol levels were observed between the H. felis-infected and -uninfected iNOS-/- mice in this stud

168 ddition, a group of mosquitoes was fed on R. felis-infected BALB/c mice.

169 Gastritis in H. felis-infected CD73-/- mice was significantly worse than

170 In contrast, H. felis-infected IL-10(-/-) mice develop a severe hyperpla

171 In contrast to wild-type mice, H. felis-infected IL-10(-/-) mice had a marked increase in

172 H. felis-infected IL-10(-/-) mice may provide a model with

173 cter-associated gastric carcinogenesis in H. felis-infected mice on a uniform C57BL/6 background hous

174 ic Pdx1 expression was observed in either H. felis-infected or DMP777-treated mice.

175 nths of age, in comparison with Helicobacter felis-infected wild-type littermates.

176 us metaplasia in the fundic mucosa, while H. felis-infected wild-type mice had severe atrophic and me

177 cant reduction of gastric inflammation in H. felis-infected, as well as immunized/challenged, mice.

178 itude between 12 and 15 months of chronic H. felis infection (P = 0.167).

179 jective of this study was to determine if H. felis infection alters gastric histopathology, proinflam

180 Both H. felis infection and K-ras mutation induced upregulation

181 adjuvant and examined for the presence of H. felis infection and leukocyte infiltration into the gast

182 R is a sensitive technique for monitoring C. felis infection and the response to antibiotic treatment

183 Ure produces a long-lasting inhibition of H. felis infection but that residual bacteria may produce a

184 Chronic H. felis infection did not alter these proportions, but ora

185 infection, but in GECs by IR or long-term H felis infection during progression to dysplasia.

186 s indicate that, in the absence of MyD88, H. felis infection enhances the activation of non-canonical

187 Nlrc5(mo-KO) mice with chronic H felis infection had increased numbers of gastric B-cell

188 Persistent Helicobacter felis infection in (C57BL/6 x 129SvEv)F1 mice induces ch

189 These findings indicate that H. felis infection in cats induces lymphoid follicular hype

190 cilitated diagnosis and discrimination of H. felis infection in cats.

191 n the recent report of high prevalence of R. felis infection in patients with "fever of unknown origi

192 y regulate the epithelial consequences of H. felis infection in the stomach, while c-Rel-mediated sig

193 H. felis infection leads to increased apoptosis and altered

194 ogenesis, and novel experiments involving H. felis infection of bone marrow transplanted irradiated m

195 veloped to detect and quantify Chlamydophila felis infection of cats.

196 Helicobacter felis infection of INS-GAS mice led to accelerated (< or

197 s of the antrum and pyloric junction, but H. felis infection of the Apc mutant mouse does not lead to

198 on between hypergastrinemia and Helicobacter felis infection on gastric corpus carcinogenesis in FVB/

199 emia in mice can synergize with Helicobacter felis infection to induce gastric carcinoma.

200 A mouse model of Helicobacter felis infection was used to study possible genetic deter

201 T-bet KO mice respond to H. felis infection with a markedly blunted IL-1beta and TNF

202 as upregulated in myeloid cells with acute H felis infection, but in GECs by IR or long-term H felis

203 ted development of gastric pathology upon H. felis infection, but the mechanisms leading to this phen

204 Within 4 weeks of H. felis infection, there are striking alterations in the c

205 emia, and possible synergy with Helicobacter felis infection, were investigated in insulin-gastrin (I

206 was observed in BALB/c and C3H/HeJ after H. felis infection, whereas sPLA2 expression was absent in

207 -deficient Stat3(SA/SA) mice with chronic H. felis infection, which mimics human H. pylori infection

208 Within 4 weeks of H. felis infection, wild-type mice develop a mild, focal ch

209 by DMP-777 treatment, L-635 treatment, or H felis infection.

210 to ionizing radiation (IR) and Helicobacter felis infection.

211 the cytokine environment during Helicobacter felis infection.

212 with oral doxycycline will not eliminate C. felis infection.

213 a competent immune response to Helicobacter felis infection.

214 odel of Helicobacter pylori and Helicobacter felis infection.

215 protection of the gastric mucosa against H. felis infection.

216 ion-mediated protection against Helicobacter felis infection.

217 une-mediated gastric pathology seen after H. felis infection.

218 iency and STAT3 activation in response to H. felis infection.

219 evaluated histologically for magnitude of H. felis infection.

220 ecies has the potential to be a vector of R. felis infection.

221 epithelial pathology even 12 months after H. felis infection.

222 not increase the risk of H. heilmannii or H. felis infection.

223 be useful for the serologic diagnosis of H. felis infections in cats.

224 characterized the cat flea (Ctenocephalides felis) innate immune response to R. typhi Initially, we

225 The stomachs of all five H. felis-inoculated cats became colonized, as determined by

226 elopment of gastric atrophy and cancer in H. felis/INS-GAS mice, while the proton pump inhibitor show

227 Cytauxzoon felis is a virulent, tick-transmitted, protozoan parasit

228 t was concluded that gastritis induced by H. felis is associated with increased HbA(1c) levels in the

229 d Helicobacter that is closely related to H. felis, is associated with little or no gastritis, and sh

230 Using the Helicobacter felis mouse model or H. pylori mouse model, both prophyl

231 We have utilized the C57BL/6 Helicobacter felis mouse model to critically analyze the role of the

232 employed the well-characterized Helicobacter felis-mouse model.

233 African black-footed cats (Felis nigripes) are endangered wild felids.

234 After 3 months of infection with H felis, Nlrc5(mo-KO) mice developed gastric hyperplasia (

235 , and four gastric ulcer samples), 10 for H. felis (one gastritis, three duodenal ulcer, and six gast

236 Three were strains of H. felis, one was H. bilis, and one was a novel helicobacte

237 own that infection of mice with Helicobacter felis or induction of acute parietal cell loss with the

238 fed with either blood meal infected with R. felis or infected cellular media administered in membran

239 could be specifically attributed to FCV, M. felis, or C. felis were seen, although interpretation in

240 ples from 8 children with C. meleagridis, C. felis, or C. parvum dog genotype were tested for anti-hu

241 R assay, the minimum detectable number of H. felis organisms was determined to be between 50 and 704.

242 tly up-regulated in WT mice infected with H. felis (P < 0.05) but were slightly elevated or were at b

243 h1-associated IgG2c antibody responses to H. felis (P <0.0003); the Th2-associated IgG1 responses wer

244 All the H. heilmannii and H. felis PCR positive patients were also positive for H. py

245 l role throughout the evolution of the genus Felis, predating cat exposure to feline retroviruses.

246 Blood for H. felis purification was repeatedly collected from splenec

247 r to Gastrospirillum hominis or Helicobacter felis (referred to as gastrospirilla).

248 th 7 and 14 days of doxycycline decreased C. felis relative copy numbers and clinical signs rapidly.

249 are caused by host-specific C. canis and C. felis, respectively.

250 ed with Helicobacter pylori and Helicobacter felis, respectively.

251 cell-deficient TCRbetadelta-/- mice with H. felis resulted in high levels of colonization, but no de

252 on in the body of the stomach, lower anti-H. felis serum IgG antibody responses (although both the wi

253 nfected animalls developed sustained anti-H. felis serum immunoglobulin G antibody responses.

254 The co-occurrence of domestic cats (Felis silvestris catus) and wild felids in rural landsca

255 Worldwide, domestic cats (Felis silvestris catus) outnumber domestic dogs (Canis f

256 st-virus evolution.IMPORTANCE Domestic cats (Felis silvestris catus) were domesticated from wildcats

257 enetic linkage (GL) map of the domestic cat (Felis silvestris catus).

258 youngest feline ERV groups in domestic cats (Felis silvestris catus); some members are replication co

259 ment of paw preferences in the domestic cat, Felis silvestris catus, is explored.

260 closest wild relative, the African wild cat (Felis silvestris lybica).

261 979 domestic cats and their wild progenitors-Felis silvestris silvestris (European wildcat), F. s. ly

262 Here, we detected several ERV-DC loci in Felis silvestris silvestris Notably, a species-specific

263 we investigated ERV-DC in European wildcats (Felis silvestris silvestris) and detected four loci: ERV

264 The survival of indigenous European wildcat (Felis silvestris silvestris) populations can be locally

265 group represents a distinctive subspecies of Felis silvestris.

266 ed by 16S rRNA gene sequencing as Mycoplasma felis (six cases) and Mycoplasma gateae (one case).

267 ed controls (P = 0.0008 and P = 0.002 for H. felis sonicate and CT, respectively).

268 tection induced by oral immunization with H. felis sonicate and CT.

269 e proportions, but oral immunization with H. felis sonicate plus cholera toxin (CT) or with CT alone

270 this sequence data, we designed a set of H. felis-specific primers.

271 E. suis being most similar to that of the H. felis strain from California.

272 ession of the H2O2-inducible katA gene in H. felis that colonized Duoxa(-/-) mice, compared with that

273 One year after infection with H. felis, the wild-type and p53 hemizygous mice showed seve

274 critical regulator of R. typhi burden in C. felis These data suggest that targeting the IMD pathway

275 The untreated cats remained positive for C. felis throughout the trial; clinical signs were most sev

276 control mice were infected with Helicobacter felis to create a model of Helicobacter pylori infection

277 ce were infected with Helicobacter felis (H. felis) to induce gastritis.

278 While bioinformatics analysis of the C. felis transcriptome identified homologs to all of the Dr

279 Four SPF H. felis-uninfected cats served as controls.

280 ori and H. heilmannii was 17(6%) and with H. felis was 10(4%), respectively.

281 R. felis was also found in the cotton used for sucrose feed

282 The 16S rRNA gene of Haemobartonella felis was amplified by using universal eubacterial prime

283 R. felis was detected in mosquito feces up to day 14.

284 cing of PCR products of H. heilmannii and H. felis was done.

285 y cytokine expression, or colonization of H. felis was evaluated in CD73-deficient (CD73-/-) mice or

286 H. felis was inoculated by gastric intubation into SPF C57B

287 The prevalence of H. heilmannii and H. felis was low in our patients with dyspepsia.

288 Furthermore, R. felis was visualized by immunofluorescence in salivary g

289 er bacteria (H. pylori, H. hepaticus, and H. felis) was mediated not by TLR4 but rather by TLR2.

290 SvEv (B6129) mice infected with Helicobacter felis, we conducted a study to characterize H. pylori in

291 rons of Helicobacter pylori and Helicobacter felis were cloned by gene library screening.

292 ), IgG2a, and IgG2c antibody responses to H. felis were determined.

293 . pylori, an H. pylori cagE(-) mutant, or H. felis were killed 2-24 weeks postchallenge.

294 Fifteen cats infected with Chlamydophila felis were monitored for the presence of C. felis DNA on

295 cifically attributed to FCV, M. felis, or C. felis were seen, although interpretation in this cohort

296 rgastrinemic mice infected with Helicobacter felis were studied at multiple stages of gastric dysplas

297 l disease (colitis), and antibody levels (H. felis) were examined.

298 Helicobacter felis, which does not express CagA or VacA, causes chron

299 als immunized intranasally with sonicated H. felis with CT and CpG.

300 e were immunized with sonicated Helicobacter felis with CT and/or CpG ODN adjuvants.