ライフサイエンスコーパス: Canis

1 ing behavior of the smooth dogfish (Mustelus canis).

2 s, Epidermophyton floccosum, and Microsporum canis.

3 y 10% are conserved in the more divergent T. canis.

4 nant major outer membrane P30 proteins of E. canis.

5 ocalized mainly on the morula membrane of E. canis.

6 eeks in dogs experimentally infected with E. canis.

7 ly in the periplasm of E. chaffeensis and E. canis.

8 the isolates are most closely related to S. canis.

9 16 with a Bartonella species, and 7 with B. canis.

10 ntracellular bacterium closely related to E. canis.

11 specimens strongly recognized the rP30 of E. canis.

12 ontained a partial 30-kDa protein gene of E. canis.

13 tions of Ehrlichia chaffeensis and Ehrlichia canis.

14 f E. chaffeensis, and a 30-kDa protein of E. canis.

15 and the parasitic nematode of dogs, Toxocara canis.

16 s and the complete TR (24 amino acids) in E. canis.

17 m types were observed, including one from S. canis.

18 samples were positive for a new strain of E. canis.

19 philum, Ehrlichia chaffeensis, and Ehrlichia canis.

20 the 22 samples that were IFA positive for E. canis, 100% reacted with rP43, 96% reacted with rP28, an

21 rlichia chaffeensis (1,644 bp) and Ehrlichia canis (2,064 bp) encode proteins of 548 to 688 amino aci

22 Phylogenetic analysis among the three E. canis 30-kDa proteins and the major surface proteins of

23 re divided into four clusters and the two E. canis 30-kDa proteins are closely related but that the t

24 22 persons), C. meleagridis (17 persons), C. canis (6 persons), C. felis (6 persons), and C. suis (1

25 esults, 15 dogs were infected with Ehrlichia canis, 9 with Ehrlichia chaffeensis, 8 with Ehrlichia ew

26 e proteins in E. chaffeensis (75-kDa) and E. canis (95-kD) whole-cell lysates and supernatants were i

27 Ehrlichia canis, a small obligately intracellular, tick-transmitte

28 E. canis, a widely recognized agent of canine ehrlichiosis,

29 Inoculation with M. canis also decreased major histocompatibility complex cl

30 Ehrlichia canis, an obligatory intracellular bacterium of monocyte

31 ion identified the isolates as Streptococcus canis, an organism normally associated with animal hosts

32 Both E. canis and an uncharacterized Rickettsia species appeared

33 associated with C. hominis and C. parvum; C. canis and C. felis are responsible for only a small numb

34 these animals are caused by host-specific C. canis and C. felis, respectively.

35 Ehrlichia canis and E. chaffeensis are tick-borne obligatory intra

36 tations in a 28- and a 27-kb locus in the E. canis and E. chaffeensis genomes, respectively.

37 Western blot analysis of E. canis and E. chaffeensis lysates with the anti-rMmpA ser

38 a major outer membrane proteins (OMPs) of E. canis and E. chaffeensis.

39 ence of a single copy of the mmpA gene in E. canis and Ehrlichia chaffeensis but not in the human gra

40 the cytoplasm of the reticulate forms of E. canis and Ehrlichia chaffeensis but was notably found on

41 Immunoreactive proteins of Ehrlichia canis and Ehrlichia chaffeensis that have been character

42 Da major immunoreactive protein (gp19) of E. canis and identified the corresponding TR-containing ort

43 he major immunoreactive 36-kDa protein of E. canis and the corresponding ortholog of E. chaffeensis (

44 experimentally or naturally infected with E. canis and were previously demonstrated to contain antibo

45 skate Raja erinacea and the dogfish Mustelus canis), and a jawless fish (the lamprey Petromyzon marin

46 affeensis, < or =67.3% identity to P30 of E. canis, and < or =63.1% identity to MAP1 of C. ruminantiu

47 oreactive to an Ehrlichia sp., 16 to Babesia canis, and 25 to Bartonella vinsonii, and 22 seroconvert

48 pe), B. canis subsp. vogeli, B. canis subsp. canis, and B. canis subsp. rossi DNA in blood samples fr

49 pe), B. canis subsp. vogeli, B. canis subsp. canis, and B. canis subsp. rossi DNA in canine blood sam

50 Brucella abortus, B. melitensis, B. suis, B. canis, and B. ovis-using whole-genome comparisons.

51 marine mammal isolates (no species name), B. canis, and B. suis, confirmed that all but the latter tw

52 ences of Brucella abortus, B. melitensis, B. canis, and B. suis.

53 pathogens, Ehrlichia chaffeensis, Ehrlichia canis, and Cowdria ruminantium, that have multiple hyper

54 tested (Anaplasma phagocytophilum, Ehrlichia canis, and Rickettsia rickettsii), but the sample was hi

55 mans: Ehrlichia chaffeensis, E. sennetsu, E. canis, and the agent of human granulocytic ehrlichiosis.

56 acter bilis, one clustered with Helicobacter canis, and the remaining pattern was closely related to

57 genes from Neosartorya fischeri, Microsporum canis, and Trichophyton tonsurans were shown to be able

58 philum antibodies but negative for Ehrlichia canis antibodies.

59 tions between rP30 and the whole purified E. canis antigen were compared in the dot immunoblot assay.

60 festations in dogs seroreactive to Ehrlichia canis antigens by indirect immunofluorescent antibody te

61 T-helper 1-type response was elicited to E. canis antigens consisting of immunoglobulin G2 antibodie

62 dies that reacted with E. chaffeensis and E. canis antigens in a pattern different from that of human

63 quantity identified major immunoreactive E. canis antigens recognized early in the infection as the

64 ecific primers, sick dogs seroreactive to E. canis antigens were determined to be infected with four

65 0 sera reacted with 44- to 110-kDa native E. canis antigens.

66 ion process, the structure of Bc28.1 from B. canis appears unrelated to the previously published stru

67 are needed to determine the importance of H. canis as a primary enteric pathogen in cats and the role

68 g and 16S rRNA gene sequencing identified S. canis associated with ulcer infections in dog owners.

69 choeri CCUG 48324(T), 97.9% similarity to S. canis ATCC 43496(T), and 97.8% similarity to S. ictaluri

70 The golden jackal of Africa (Canis aureus) has long been considered a conspecific of

71 k-transmitted pathogens, including Ehrlichia canis, Babesia canis, Babesia gibsonii, or spotted fever

72 athogens, including Ehrlichia canis, Babesia canis, Babesia gibsonii, or spotted fever group ricketts

73 She was found to have Helicobacter canis bacteremia.

74 eared to be a new species, with Helicobacter canis being the most genetically similar species.

75 -Brucella melitensis, Brucella suis-Brucella canis, Brucella ovis, and Brucella ceti.

76 , B. canis subsp. rossi, and B. canis subsp. canis but not mammalian DNA.

77 and nymphs) were separately infected with E. canis by feeding on the infected dogs.

78 ehrlichiosis cases that were positive for E. canis by immunofluorescent antibody test and in various

79 rated to contain antibodies reactive with E. canis by indirect immunofluorescence assays.

80 iated with diarrhea, only infections with C. canis, C. felis, and subtype family Id of C. hominis wer

81 Mycoplasma canis can infect many mammalian hosts but is best known

82 Streptococcus dysgalactiae and Streptococcus canis cannot be distinguished when only Lancefield typin

83 Ehrlichia canis causes a potentially fatal rickettsial disease of

84 These data suggest that rMAP2 of E. canis could be used as a recombinant test antigen for th

85 te cell line DH82 at 25 degrees C than in E. canis cultivated at 37 degrees C.

86 on of the remaining paralogs was lower in E. canis cultivated in dog monocyte cell line DH82 at 25 de

87 lts were correct, except for one Microsporum canis culture containing two colony variants, which coul

88 rlichia chaffeensis and p30 gene locus of E. canis despite marked divergence between genera in the st

89 a's largest terrestrial predator, the dingo (Canis dingo), could be a driver of shrub encroachment in

90 s the first molecular characterization of E. canis directly from naturally infected ticks.

91 of Smilodon fatalis (saber-toothed cats) and Canis dirus (dire wolves).

92 be infected with four Ehrlichia species: E. canis, E. chaffeensis, E. equi, and E. ewingii.

93 cluding Anaplasma phagocytophilum, Ehrlichia canis, E. chaffeensis, E. ewingii, Rickettsia rickettsii

94 Coinfection with three Ehrlichia species (E. canis, E. ewingii, and E. equi) was documented for one d

95 hat both dogs were coinfected with Ehrlichia canis, E. platys, and E. equi.

96 hia phagocytophila but not against Ehrlichia canis, Ehrlichia ewingii, B. burgdorferi, or Coxiella bu

97 iptional activity of a five gene locus in E. canis encoding homologous, but non-identical, p28 genes.

98 ed MmpA was cloned by screening an Ehrlichia canis expression library with convalescent dog sera, whi

99 ion of the telomerase catalytic subunit from Canis familiaris (dog), dogTERT.

100 CNTFRalpha was RH mapped to CFA 11 (Canis familiaris autosome 11) in the dog, a region showi

101 Now, advances in genomics have made Canis familiaris genetically tractable and poised to off

102 The recently discovered Canis familiaris papillomavirus (PV) type 2 (CfPV2) prov

103 ously neglected species - domesticated dogs (Canis familiaris) - may allow researchers to do just tha

104 Allergy to the domestic dog (Canis familiaris) affects 5-10% of the population in aff

105 in bark frequency and context between dogs (Canis familiaris) and wolves (Canis lupus) has led some

106 in behavioural tendency in the domestic dog (Canis familiaris) are well established, the phenomenon w

107 functions are specific for the domestic dog (Canis familiaris) data.

108 Allergy to dog (Canis familiaris) is a worldwide common cause of asthma

109 traits and the skeleton of the domestic dog (Canis familiaris) is arguably the best system in which t

110 Detection dogs (Canis familiaris) located owl pellets accumulated under

111 y draft genome sequence of the domestic dog (Canis familiaris), together with a dense map of single n

112 h is familiar and relevant to domestic dogs (Canis familiaris), who are known to perceive both segmen

113 The domestic dog, Canis familiaris, is an excellent model species in which

114 acterized in recently available genomes from Canis familiaris, Macaca mulatta, P. troglodytes and Rat

115 iants (CNVs) in the modern domesticated dog, Canis familiaris, which exhibits considerable morphologi

116 , a disjunctive syllogism), task-naive dogs (Canis familiaris; n=19) and 4- to 6-year-old children (H

117 nvestigated by comparing Can f 1 (major dog [Canis familiaris] allergen) levels in hair and coat samp

118 predicted three-dimensional structure of E. canis Fbp demonstrated conservation of important Fbp fam

119 E. canis Fbp had a molecular mass (38 kDa) consistent with

120 E. canis Fbp was homologous to a family of periplasmic Fbp'

121 The identification of two isolates of S. canis from a relatively small sample set suggests that t

122 sequence conservation of p30-10 genes for E. canis from diverse geographic regions.

123 Differentiation of Brucella canis from other Brucella species are mainly performed t

124 Carbohydrate profiles differentiated B. canis from the other three Brucella species due to the a

125 cleotide sequences from the unique Ehrlichia canis gene, p30, to facilitate studies that require moni

126 plete genome sequencing revealed that the E. canis genome consists of a single circular chromosome of

127 nly forming a monophyletic clade when the B. canis genome was included.

128 of multiple copies of these genes in the E. canis genome.

129 A new MLVA-13Bc method for B. canis genotyping was established by combining eight newl

130 ssay is a highly discriminatory assay for B. canis genotyping, and can serve as a useful molecular ep

131 E. canis gp19 composition consists of five predominant amin

132 andem repeats that are not present in the E. canis gp19 gene (414 bp).

133 E. canis gp19 has substantial carboxyl-terminal amino acid

134 The E. canis gp200 gene (4,263 bp; 1,421 amino acids) was clone

135 E. canis gp36 and E. chaffeensis gp47 were differentially e

136 lated synthetic peptide repeat units from E. canis gp36 and E. chaffeensis gp47 were substantially le

137 E. canis gp36 was recognized by early acute-phase antibodie

138 t signals from eight other helicobacters (H. canis, H. cineadi, H. felis, H. mustelae, H. nemestrinae

139 humans, the other five being H. pullorum, H. canis, "H. rappini," H. fennelliae, and H. cinaedi.

140 at units, and the 140-kDa protein gene of E. canis has 14 nearly identical, tandemly arranged 108-bp

141 Ehrlichia canis has a small subset of major immunoreactive protein

142 it is not likely a primary neuropathogen, M. canis has the capacity to influence meningoencephalitis

143 ng rough species, Brucella ovis and Brucella canis, has confused interpretation.

144 Ehrlichia chaffeensis and E. canis have a small subset of tandem repeat (TR)-containi

145 major merozoite surface antigens of Babesia canis have been described as a 28-kDa membrane protein f

146 pp. were identified from three (Helicobacter canis, Helicobacter winghamensis, and MIT 99-5504).

147 neotomae are nonpathogenic to humans and B. canis human infections are rare.

148 E. canis immunodominant 30-kDa major outer membrane protein

149 ELISA format using 141 serum samples from E. canis immunofluorescent antibody (IFA)-positive and IFA-

150 ogical culture were positive for Microsporum canis in all cases.

151 The unexpected presence of M. canis in brains of dogs with idiopathic meningoencephali

152 The assay was used to detect E. canis in canine carrier blood and in experimentally infe

153 This is the first observation of H. canis in cats and raises the possibility that H. canis,

154 B9, indicating that VirB9 was produced by E. canis in dogs and was antigenic.

155 virB9 was transcribed by E. canis in dogs, ticks, and cell culture.

156 mpared with the prominence given to Toxocara canis in dogs.

157 study revealed transcription of p30-10 by E. canis in naturally infected ticks and sequence conservat

158 rom nondiarrheic cats, the causal role of H. canis in producing the diarrhea could not be proven.

159 nd to contain antibodies against rMAP2 of E. canis in the ELISA.

160 ult in underestimation of the presence of S. canis in the human population.

161 whether dogs and ticks are infected with E. canis in Venezuela and, if so, whether this is the same

162 E. canis, in addition, had a 6.9-kb locus which contained a

163 ified in Ehrlichia chaffeensis and Ehrlichia canis, including three molecularly and immunologically c

164 iptionally active in in-vitro cultures of E. canis incubated at the vertebrate host (37 degrees C) an

165 s were detected by Northern blotting from E. canis infected DH82 cells, indicating that the genes are

166 tope strongly recognized by serum from an E. canis-infected dog.

167 sb) proteins were recognized by sera from E. canis-infected dogs but not from E. chaffeensis-infected

168 with clinical illness and with concurrent B. canis infection (by PCR).

169 t that dogs serve as a reservoir of human E. canis infection and that R. sanguineus, which occasional

170 is the first molecular identification of E. canis infection in dogs from Peru.

171 and dog were diagnosed with Cryptosporidium canis infections during the same period.

172 and reliable serodiagnostic antigens for E. canis infections.

173 Toxocara canis is a zoonotic parasite of major socioeconomic impo

174 Toxocara canis is better recognized as a cause of human toxocaria

175 Babesia canis is the agent of the canine babesiosis in Europe.

176 rucella abortus, Brucella suis, and Brucella canis) is problematic for many clinical laboratories tha

177 uantitatively (P < 0.01) among strains of M. canis isolated from canine brain tissue or mucosal surfa

178 Only B. suis and B. canis isolates clustered together and could not be disti

179 and attempted emm typing of 5 Streptococcus canis isolates from a recent population-based surveillan

180 The four S. canis isolates shared highly homologous alleles but were

181 28 genes from two geographically distinct E. canis isolates was completely conserved.

182 sgalactiae subsp. equisimilis isolates, 4 S. canis isolates) to represent each emm type identified, i

183 les from 22 U.S. states, resulting in 229 B. canis isolates.

184 s derived from a sequence conserved among E. canis isolates.

185 otype groups were identified from the 229 B. canis isolates.

186 The recent revelations that coyotes (Canis latrans) can excrete N. caninum oocysts in their f

187 Among 109 coyotes (Canis latrans) from central coastal California, 31 anima

188 Over the past century, coyotes (Canis latrans) have undergone a pervasive range expansio

189 black bears (Ursus americanus) and coyotes (Canis latrans).

190 ed deer (Odocoileus virginianus) and coyote (Canis latrans).

191 wolves Canis lupus are known to kill coyotes Canis latrans, and coyotes, in turn, may kill foxes Vulp

192 mutation also causes melanism in the coyote, Canis latrans, and in Italian gray wolves, and hence our

193 s in cats and raises the possibility that H. canis, like H. hepaticus and H. bilis in mice, can cause

194 Ehrlichia and Cowdria spp.: p30 of Ehrlichia canis (< or =71.3%), p28 of E. chaffeensis (< or =68.3%)

195 me from regions outside the natural range of Canis lupus (the dog's wild ancestor) and where dogs wer

196 For example, in North America, grey wolves Canis lupus are known to kill coyotes Canis latrans, and

197 o primary species studied, the domestic dog (Canis lupus familiaris) and the Tasmanian devil (Sarcoph

198 The domestic dog (Canis lupus familiaris) has been used in biomedical rese

199 nover in cooperatively breeding grey wolves (Canis lupus Linnaeus 1758).

200 in prey composition and kill rate for wolves Canis lupus living on the Northern Range (NR) of Yellows

201 postcranial skeletal morphologies of wolves (Canis lupus) and coyotes (C. latrans) from Pleistocene-a

202 between dogs (Canis familiaris) and wolves (Canis lupus) has led some researchers to conclude that b

203 itment and population growth of grey wolves (Canis lupus) in Denali National Park and Preserve, Alask

204 rs of data from a long-term study of wolves (Canis lupus) in Yellowstone National Park, USA, to evalu

205 The gray wolf (Canis lupus) is a widely distributed top predator and an

206 The gray wolf (Canis lupus) is one of the few large predators to surviv

207 or 732 moose (Alces alces) killed by wolves (Canis lupus) over a 50-year period in Isle Royale Nation

208 omyzon marinus) tracked for 12 h and a wolf (Canis lupus) tracked for 1 year.

209 (NCEs) of an active predator, the grey wolf (Canis lupus), by simultaneously tracking wolves and the

210 xplored multiple linkages among grey wolves (Canis lupus), elk (Cervus elaphus), berry-producing shru

211 In wolves (Canis lupus), empirical evidence for density-dependent s

212 jackals aligned more closely to gray wolves (Canis lupus), which is surprising given the absence of g

213 nce, and foraging in the presence of wolves (Canis lupus).

214 mange (Sarcoptes scabiei) among grey wolves (Canis lupus).

215 However, melanism in the gray wolf, Canis lupus, is caused by a different melanocortin pathw

216 se serum antibody responses to whole-cell E. canis lysates and recombinant p28, gp140, and gp200 were

217 Ehrlichia canis major immunoreactive proteins of 36 and 19 kDa eli

218 gen-rich shell of the red supergiant star VY Canis Majoris (VY CMa).

219 well explored, although recent studies of VY Canis Majoris have resulted in the identification of HCO

220 Because S. canis may be incorrectly identified (published biochemic

221 rsity of Ehrlichia chaffeensis and Ehrlichia canis may involve independent or differential expression

222 s [n = 2], Pasteurella canis [n = 2], and N. canis [n = 1]) are discussed.

223 d isolates (P. dagmatis [n = 2], Pasteurella canis [n = 2], and N. canis [n = 1]) are discussed.

224 The 28-kDa E. chaffeensis and 30-kDa E. canis native proteins were recognized by 25 IFA-positive

225 ith exposure to canine parvovirus, Ehrlichia canis, Neospora caninum and perhaps rabies virus, but no

226 d in the presence of an MmpA band only in E. canis, not in E. chaffeenesis.

227 nd was closely related (99.9%) to that of E. canis Oklahoma.

228 DE was similar to the profiles of VHE and E. canis Oklahoma.

229 been attributed to infection with either E. canis or Ehrlichia ewingii.

230 a chaffeensis, Ehrlichia sennetsu, Ehrlichia canis, or their host cells.

231 with DNA extracted from E. chaffeensis-, E. canis-, or E. phagocytophila-infected samples, confirmin

232 source of contamination in an event of a B. canis outbreak.

233 Like the E. chaffeensis p120, the E. canis p120 contains tandem repeat units.

234 The overall amino acid sequence of the E. canis p120 is 30% homologous to that of E. chaffeensis p

235 lotting demonstrated that the recombinant E. canis p120 reacted with convalescent sera from dogs with

236 16 bp), the 14-repeat region (78%) of the E. canis P140 gene (1,620 bp), and a 2-repeat region from t

237 eins reacted with E. chaffeensis P120 and E. canis P140, respectively.

238 previously demonstrated that recombinant E. canis p28 and the 140- and 200-kDa glycoproteins gp140 a

239 The amino acid homology of the E. canis P28 proteins ranged from 51 to 74%.

240 4), Ehrlichia chaffeensis p28-OMP, Ehrlichia canis p30, and Ehrlichia ruminantium MAP1, and has been

241 atient who developed CL following a Toxocara canis parasitism.

242 During 2010 and 2016, 377 B. canis PCR-positives were identified from 6,844 canine bl

243 eous cell line, or consistent patterns of M. canis polyvalent antigen distribution in canine meningoe

244 of the 16S rRNA genes from six additional E. canis-positive dog blood specimens and from three pooled

245 h 26.3% identity to a hypothetical Ehrlichia canis protein with no known function.

246 nfection, additional major immunoreactive E. canis proteins were identified, including the 28-, 47-,

247 eported the cloning of two immunoreactive E. canis proteins, P28 and P140, that were applicable for s

248 naturally or experimentally infected with E. canis recognized the recombinant protein.

249 te was detected on the E. chaffeensis and E. canis recombinant proteins, including the two-repeat pol

250 brane protein genes of E. chaffeensis and E. canis, respectively.

251 The draft genome of T. canis should provide a useful resource for future molecu

252 d group size/composition in Ethiopian wolves Canis simensis in the Bale Mountains, Ethiopia, using fi

253 to be a novel species; the name Penicillium canis sp. nov. is proposed.

254 provision themselves and their hunting dogs (Canis sp.) throughout the year.

255 ses, in addition to hybridization with other Canis species.

256 PCR analysis using E. canis-specific primers revealed that 17 of the 55 dog bl

257 e invasive disease, the genome of Mycoplasma canis strain PG14(T) from a dog's throat was compared to

258 LVA methods are limited in discriminating B. canis strains.

259 subsp. vogeli, B. canis subsp. rossi, and B. canis subsp. canis but not mammalian DNA.

260 (Asian genotype), B. canis subsp. vogeli, B. canis subsp. canis, and B. canis subsp. rossi DNA in blo

261 (Asian genotype), B. canis subsp. vogeli, B. canis subsp. canis, and B. canis subsp. rossi DNA in can

262 subsp. vogeli, B. canis subsp. canis, and B. canis subsp. rossi DNA in blood samples from infected do

263 subsp. vogeli, B. canis subsp. canis, and B. canis subsp. rossi DNA in canine blood samples.

264 (Asian genotype), B. canis subsp. vogeli, B. canis subsp. rossi, and B. canis subsp. canis but not ma

265 entiate Babesia gibsoni (Asian genotype), B. canis subsp. vogeli, B. canis subsp. canis, and B. canis

266 discriminate B. gibsoni (Asian genotype), B. canis subsp. vogeli, B. canis subsp. canis, and B. canis

267 A genes from B. gibsoni (Asian genotype), B. canis subsp. vogeli, B. canis subsp. rossi, and B. canis

268 sent study we cloned a new immunoreactive E. canis surface protein gene of 1,170 bp, which encodes a

269 The nematode Toxocara canis survives for years in mammalian tissues, and when

270 Human toxocariasis, caused by Toxocara canis, T. cati, and T. vitulorum of dogs, cats and rumin

271 Da major outer membrane protein of Ehrlichia canis, the agent of canine ehrlichiosis, is the major an

272 ously culture isolated a strain of Ehrlichia canis, the causative agent of canine ehrlichiosis, from

273 cephalus sanguineus ticks transmit Ehrlichia canis, the etiologic agent of canine ehrlichiosis.

274 f cats in the possible zoonotic spread of H. canis to humans.

275 oduce a draft genome and transcriptome of T. canis to support future biological and biotechnological

276 f these gene products in pathogenesis and E. canis transmission as well as in designing a rational va

277 -rich regions in the acidic C terminus of E. canis TRP95 but not in E. chaffeensis TRP75.

278 E. chaffeensis TRP75 and E. canis TRP95 were immunoprecipitated with anti-pTyr antib

279 ates and comparison with sequences of the S. canis type strain and other related streptococci of anim

280 e S. halichoeri type strain, 84.6% to the S. canis type strain, and 83.8% to the S. ictaluri type str

281 sis were examined for infection of Ehrlichia canis using PCR, multiplex real-time PCR, and DNA sequen

282 Ehrlichia canis virB9 was cloned and expressed.

283 ajor antigenic protein 2 (MAP2) of Ehrlichia canis was cloned and expressed.

284 The analogous gene of p120 in Ehrlichia canis was cloned, sequenced, and expressed.

285 erric ion-binding protein (Fbp) of Ehrlichia canis was identified and its iron-binding capability was

286 notypic, and 16S rRNA analyses, Helicobacter canis was isolated from Bengal cats with and without chr

287 ing Campylobacter helveticus, and because H. canis was isolated from nondiarrheic cats, the causal ro

288 Pasteurella canis was the most common isolate of dog bites, and Past

289 hyton rubrum, Trichophyton tonsurans, and M. canis-was excellent.

290 Two DNA fragments of E. canis were amplified by PCR with two primer pairs based

291 immunoreactive protein (gp200) of Ehrlichia canis were defined.

292 rucella abortus, Brucella suis, and Brucella canis were extracted and distributed to participating la

293 Adult M. canis were held for 5 days in a current-day control (405

294 teins of Ehrlichia chaffeensis and Ehrlichia canis were identified which restored DsbA activity in co

295 Pasteurella dagmatis and Neisseria canis were repeatedly isolated from the sputum of a pood

296 Eleven out of 14 paralogs in E. canis were transcribed in increasing numbers and transcr

297 own genes, and secA in the omp cluster in E. canis were transcriptionally active in the monocyte cult

298 s infected with microorganisms other than E. canis, were seronegative.

299 e 30-kDa major outer membrane proteins of E. canis will greatly facilitate understanding pathogenesis

300 We presented a small shark species, Mustelus canis, with carefully timed and measured odor pulses dir