ライフサイエンスコーパス: Canis

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

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

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

4 philum, Ehrlichia chaffeensis, and Ehrlichia canis.

5 f the larval stage of the roundworm Toxocara canis.

6 s, Epidermophyton floccosum, and Microsporum canis.

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

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

9 eeks in dogs experimentally infected with E. canis.

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

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

12 and the parasitic nematode of dogs, Toxocara canis.

13 16 with a Bartonella species, and 7 with B. canis.

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

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

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

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

18 22 persons), C. meleagridis (17 persons), C. canis (6 persons), C. felis (6 persons), and C. suis (1

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

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

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

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

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

24 Ehrlichia canis, an obligatory intracellular bacterium of monocyte

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

26 Both E. canis and an uncharacterized Rickettsia species appeared

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

51 philum antibodies but negative for Ehrlichia canis antibodies.

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

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

54 0 sera reacted with 44- to 110-kDa native E. canis antigens.

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

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

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

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

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

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

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

62 She was found to have Helicobacter canis bacteremia.

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

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

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

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

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

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

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

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

71 gs to engineer two variants of Streptococcus canis Cas9-Sc(++) and a higher-fidelity mutant HiFi-Sc(+

72 Ehrlichia canis causes a potentially fatal rickettsial disease of

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

95 The domestic canine (canis familiaris) is a growing novel model for human neu

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

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

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

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

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

101 s silvestris catus) outnumber domestic dogs (Canis familiaris).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

118 E. canis gp19 composition consists of five predominant amin

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

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

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

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

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

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

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

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

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

128 Ehrlichia canis has a small subset of major immunoreactive protein

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

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

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

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

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

134 V consisted of serum samples from 8 Brucella canis IFA-positive and 10 Rickettsia rickettsii IFA-posi

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

159 and reliable serodiagnostic antigens for E. canis infections.

160 Toxocara canis is a zoonotic parasite of major socioeconomic impo

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

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

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

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

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

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

167 28 genes from two geographically distinct E. canis isolates was completely conserved.

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

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

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

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

172 Coyotes (Canis latrans) are highly adaptable, medium-sized carniv

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

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

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

176 We used a population of captive coyotes (Canis latrans) to simulate urban human-coyote interactio

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

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

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

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

181 logical traits across populations of coyotes Canis latrans.

182 nteus], raccoon [Procyon lotor], and coyote [Canis latrans]).

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

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

185 In Alaska, gray wolves (Canis lupis), brown bears (Ursus arctos), and black bear

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

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

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

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

190 f (Canis lupus hudsonicus) and domestic dog (Canis lupus familiaris).

191 Extant Canis lupus genetic diversity can be grouped into three

192 ate the feasibility of this method for wolf (Canis lupus hudsonicus) and domestic dog (Canis lupus fa

193 iotelemetry and census data from grey wolves Canis lupus in the Upper Peninsula of Michigan, USA to r

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

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

196 bitat helps understand why some adult wolves Canis lupus may approach human settlements more than oth

197 ne elk (Cervus elaphus) responded to wolves (Canis lupus) and cougars (Puma concolor), and found that

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

199 establishment and kill rates of gray wolves (Canis lupus) are affected by the coexistence with brown

200 elaphus) to the risk of predation by wolves (Canis lupus) during winter in northern Yellowstone, USA.

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

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

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

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

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

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

207 016, a mummified carcass of an ancient wolf (Canis lupus) pup (specimen YG 648.1) was discovered in t

208 ults with field data for a system of wolves (Canis lupus) that prey on wild boar (Sus scrofa), a wild

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

210 Wolves (Canis lupus) would be expected to scavenge on subsidies

211 ual brown bears (Ursus arctos), gray wolves (Canis lupus), and wolverines (Gulo gulo).

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

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

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

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

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

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

218 % loss), snow leopard (P. uncia, 38%), wolf (Canis lupus, 77%) and dhole (Cuon alpinus, 95%) from pro

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

220 t where coyotes co-occurred with grey wolves Canis lupus.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

239 16 bp), the 14-repeat region (78%) of the E. canis P140 gene (1,620 bp), and a 2-repeat region from t

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

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

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

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

244 atient who developed CL following a Toxocara canis parasitism.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

284 Ehrlichia canis virB9 was cloned and expressed.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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