ライフサイエンスコーパス: subsp

1 sus and five clonal groups for M. abscesssus subsp. bolletii, with just one clone detected in two pat

2 essus subsp. bolletii (n = 24), M. abscessus subsp. abscessus (n = 6), Mycobacterium fortuitum (n = 3

3 MIC90 values for 81 isolates of M. abscessus subsp. abscessus and 12 isolates of M. abscessus subsp.

4 esence of two clonal groups for M. abscessus subsp. abscessus and five clonal groups for M. abscesssu

5 susceptibility breakpoints for M. abscessus subsp. abscessus be changed from </=2 to </=4 mug/ml and

6 ness of macrolides for treating M. abscessus subsp. abscessus infections.

7 . massiliense and 15% to 20% of M. abscessus subsp. abscessus isolates renders these species intrinsi

8 lated U.S. and Western European M. abscessus subsp. abscessus isolates that are genetically distinct

9 Sequencing of the erm gene of M. abscessus subsp. abscessus will predict inducible macrolide suscep

10 imately 20% of U.S. isolates of M. abscessus subsp. abscessus.

11 and a nonfunctional erm gene in M. abscessus subsp. massiliense and 15% to 20% of M. abscessus subsp.

12 scessus subsp. abscessus and 13 M. abscessus subsp. massiliense isolates identified by whole-genome s

13 p. abscessus and 12 isolates of M. abscessus subsp. massiliense were 8 mug/ml and 4 mug/ml, respectiv

14 rately identified 41 Mycobacterium abscessus subsp. abscessus and 13 M. abscessus subsp. massiliense

15 rolide resistance in Mycobacterium abscessus subsp. abscessus, calling into question the usefulness o

16 cies identified were Mycobacterium abscessus subsp. bolletii (n = 24), M. abscessus subsp. abscessus

17 We found that F. x ananassa subsp. cuneifolia populations consisted of both parental

18 died the natural hybrid (Fragaria x ananassa subsp. cuneifolia) between two sexually dimorphic octopl

19 um longum: subsp. infantis (B. infantis) and subsp. longum (B. longum).

20 Mycoplasma mycoides subsp. capri (Mmc) and subsp. mycoides (Mmm) are important ruminant pathogens w

21 acebo, the single-species product B animalis subsp lactis or L reuteri significantly reduced duration

22 cebo (placebo group, n = 365) or B. animalis subsp. lactis at a dose of 10(9) colony-forming units/d

23 oides ovatus was out-competed by B. animalis subsp. lactis Bl-04 in mixed cultures growing on raffino

24 this study show that the use of B. animalis subsp. lactis failed to prevent nosocomial infections in

25 y improve H(2)O(2) resistance in B. animalis subsp. lactis strains.

26 iet), and probiotic, Bfidobacterium animalis subsp. lactis (Bb12) (final dose verified at 10(5) colon

27 us rhamnosus GG and Bifidobacterium animalis subsp lactis BB-12 (total cell count per capsule, 1.3 x

28 us rhamnosus GG and Bifidobacterium animalis subsp lactis BB-12 did not significantly reduce antibiot

29 cillus acidophilus, Bifidobacterium animalis subsp lactis, Faecalibacterium prausnitzii, Bacteroides

30 The FMPP contained Bifidobacterium animalis subsp Lactis, Streptococcus thermophiles, Lactobacillus

31 pensions containing Bifidobacterium animalis subsp. lactis (B. lactis) HN019 was topically administer

32 asei 01); QB - with Bifidobacterium animalis subsp. lactis (BB 12); and QC, co-culture with the three

33 s acidophilus LA-5, Bifidobacterium animalis subsp. lactis BB-12 and Propionibacterium jensenii 702.

34 from the probiotic Bifidobacterium animalis subsp. lactis Bl-04 binds alpha-(1,6)-linked glucosides

35 -galactosidase from Bifidobacterium animalis subsp. lactis Bl-04.

36 t supplemented with Bifidobacterium animalis subsp. lactis DN-173010 versus a placebo yogurt, followe

37 stigate the role of Bifidobacterium animalis subsp. lactis in preventing nosocomial infections in the

38 two fully sequenced Bifidobacterium animalis subsp. lactis strains, BL-04 and DSM 10140, to hydrogen

39 ial virulence in vivo, since fewer S. aureus subsp. aureus NCTC8325-4 DeltasdrD bacteria than bacteri

40 Deletion of sdrD from S. aureus subsp. aureus strain NCTC8325-4 attenuated bacterial sur

41 ethicillin-susceptible Staphylococcus aureus subsp. aureus in a patient who was concomitantly coloniz

42 : a fruit blotch bacterium Acidovorax avenae subsp. citrulli (Aac), chilli vein-banding mottle virus

43 ial fruit blotch bacterium Acidovorax avenae subsp. citrulli (Aac), Chilli veinal mottle virus (ChiVM

44 ease in cattle caused by Mycobacterium avian subsp. paratuberculosis (MAP).

45 ommon (n = 238, 92.6%), followed by M. avium subsp. avium serotype 1 (n = 12, 4.7%) and serotype 2, 3

46 minissuis; the bird type, including M. avium subsp. avium serotype 1 and serotype 2, 3 (also M. avium

47 hich have been shown to induce anti-M. avium subsp. hominissuis activity when added to THP-1 cells in

48 t MBP-1 expression is important for M. avium subsp. hominissuis adherence to the host cell.

49 gocytes cocultured with established M. avium subsp. hominissuis biofilm and surveyed various aspects

50 Our data collectively indicate that M. avium subsp. hominissuis biofilm induces TNF-alpha-driven hype

51 The reasoning behind how M. avium subsp. hominissuis biofilm is allowed to establish and p

52 ay determined that contact with the M. avium subsp. hominissuis biofilm led to early, widespread onse

53 M. avium subsp. hominissuis biofilm triggered robust tumor necros

54 nitial colonization of the airways, M. avium subsp. hominissuis forms microaggregates composed of 3 t

55 icient approach to prevent or treat M. avium subsp. hominissuis infection in the lungs.

56 mmune serum significantly inhibited M. avium subsp. hominissuis infection throughout the respiratory

57 seen until much later in planktonic M. avium subsp. hominissuis infection.

58 We therefore conclude that M. avium subsp. hominissuis is the dominant M. avium subspecies c

59 Results showed M. avium subsp. hominissuis to be most common (n = 238, 92.6%), f

60 a pathogenic mechanism utilized by M. avium subsp. hominissuis to bind and invade the host respirato

61 HP-1 cells infected with planktonic M. avium subsp. hominissuis).

62 Of the 238 patients with M. avium subsp. hominissuis, 65 (27.3%) showed evidence of defini

63 but did not lead to elimination of M. avium subsp. hominissuis.

64 exposed at the bacterial surface of M. avium subsp. hominissuis.

65 e types: the human or porcine type, M. avium subsp. hominissuis; the bird type, including M. avium su

66 Total lipids from an M. avium subsp. paratuberculosis (Map) ovine strain (S-type) cont

67 We now know that M. avium subsp. paratuberculosis activates the epithelial layer a

68 itoring cellular markers, only live M. avium subsp. paratuberculosis bacilli were able to prevent pha

69 sease, allowing the transmission of M. avium subsp. paratuberculosis between animals.

70 o ensure that low concentrations of M. avium subsp. paratuberculosis can be detected.

71 ted in a greater recovery of viable M. avium subsp. paratuberculosis cells from milk than from sample

72 nt decreased the recovery of viable M. avium subsp. paratuberculosis cells more than treatment with N

73 We interrogated an M. avium subsp. paratuberculosis DeltasigL mutant against a selec

74 d with transcriptional responses of M. avium subsp. paratuberculosis during macrophage infection.

75 hree evaluated for the isolation of M. avium subsp. paratuberculosis from milk, as it achieved the lo

76 the transcriptional level, over 300 M. avium subsp. paratuberculosis genes were significantly and dif

77 We hypothesized that M. avium subsp. paratuberculosis harnesses host responses to recr

78 mized protocol for the isolation of M. avium subsp. paratuberculosis in milk.

79 We show that M. avium subsp. paratuberculosis infection led to phagosome acidi

80 in the pathogenesis and immunity of M. avium subsp. paratuberculosis infection, a potential role that

81 n of immune responses occurs during M. avium subsp. paratuberculosis infection, with these responses

82 to further elucidate the process of M. avium subsp. paratuberculosis invasion.

83 Thus, M. avium subsp. paratuberculosis is an opportunist that takes adv

84 Once inside the cell, M. avium subsp. paratuberculosis is known to survive harsh microe

85 with 10(2) to 10(8) CFU/ml of live M. avium subsp. paratuberculosis organisms.

86 To improve our understanding of M. avium subsp. paratuberculosis pathogenesis, we examined phagos

87 cipher the role of sigma factors in M. avium subsp. paratuberculosis pathogenesis, we targeted a key

88 significance of such regulators in M. avium subsp. paratuberculosis rremains elusive.

89 that was shown to be important for M. avium subsp. paratuberculosis survival inside gamma interferon

90 sted a substantial role for sigL in M. avium subsp. paratuberculosis virulence, as indicated by the s

91 rain, suggesting a role for sigH in M. avium subsp. paratuberculosis virulence.

92 No strains of M. avium subsp. paratuberculosis were found.

93 f the cell communication pathway by M. avium subsp. paratuberculosis, which loosens the integrity of

94 reactivity against M. kansasii- and M. avium subsp. paratuberculosis-infected animals.

95 silvaticum); and the ruminant type, M. avium subsp. paratuberculosis.

96 .0% did not affect the viability of M. avium subsp. paratuberculosis.

97 serotype 1 and serotype 2, 3 (also M. avium subsp. silvaticum); and the ruminant type, M. avium subs

98 Mycobacterium avium subsp hominissuis is associated with infection of immuno

99 disease (JD), caused by Mycobacterium avium subsp paratuberculosis (MAP), occurs worldwide as chroni

100 Mycobacterium avium subsp. hominissuis (MAH) is increasingly recognized as a

101 Mycobacterium avium subsp. hominissuis is an opportunistic human pathogen th

102 "Mycobacterium avium subsp. hominissuis" is an opportunistic environmental pa

103 zed for the isolation of Mycobacterium avium subsp. paratuberculosis (MAP) from milk and colostrum, w

104 le diagnostic assays for Mycobacterium avium subsp. paratuberculosis (MAP) have poor sensitivities an

105 matory disease caused by Mycobacterium avium subsp. paratuberculosis (MAP) in cattle and other rumina

106 sms of host responses to Mycobacterium avium subsp. paratuberculosis (MAP) infection during the early

107 m kansasii (n = 10), and Mycobacterium avium subsp. paratuberculosis (n = 10), cases exposed to M. bo

108 Mycobacterium avium subsp. paratuberculosis causes Johne's disease in rumina

109 Mycobacterium avium subsp. paratuberculosis causes Johne's disease, an enter

110 The infection biology of Mycobacterium avium subsp. paratuberculosis has recently crystallized, with

111 Mycobacterium avium subsp. paratuberculosis is shed into the milk and feces

112 fection of the host with Mycobacterium avium subsp. paratuberculosis results in chronic and progressi

113 Biological pesticides Bt subsp. Kurstaki is one of the most important biological

114 fficacy of this formulation in protecting Bt subsp. Kurstaki against deactivation by UV-A irradiation

115 GALV infection in the Indonesian M. burtoni subsp. was consistent with the susceptibility of the spe

116 aculeastrum root bark and Sesamum calycinum subsp. angustifolium leaves exhibited strong quorum sens

117 ly distributed tree Eucalyptus camaldulensis subsp. camaldulensis to partition intraspecific variatio

118 DNA and bacterial culture from M. capricolum subsp. capripneumoniae strain ILRI181, while no amplific

119 a specific target sequence in M. capricolum subsp. capripneumoniae, as found in the genome sequence

120 ion (RPA) for the detection of M. capricolum subsp. capripneumoniae.

121 subsp. capri (Mmc) and Mycoplasma capricolum subsp. capricolum (Mcap), and the main factors driving t

122 ious disease caused by Mycoplasma capricolum subsp. capripneumoniae that affects goats in Africa and

123 s lactis BCMC(R) 12,451, Lactobacillus casei subsp BCMC(R) 12,313, Bifidobacterium longum BCMC(R) 021

124 he trisaccharide of Pseudomonas chlororaphis subsp. aureofaciens strain M71.

125 ), Ralstonia solanacearum, Xanthomonas citri subsp. citri (X. citri), and Xanthomonas euvesicatoria.

126 nonhost resistance against Xanthomonas citri subsp. citri (Xcc) and Pseudomonas syringae pv. phaseoli

127 omology with the avrBs2 of Xanthomonas citri subsp. citri (Xcc), the causal agent of citrus canker di

128 -like (TAL) effectors from Xanthomonas citri subsp. malvacearum (Xcm) are essential for bacterial bli

129 ocky Mountain lodgepole pine (Pinus contorta subsp. latifolia), a conifer that dominates millions of

130 subsp. cremoris, Lactobacillus coryniformis subsp. coryniformis, Lactobacillus paraplantarum were al

131 actis subsp. lactis and Lactococcus cremoris subsp.

132 actis subsp. lactis and Lactococcus cremoris subsp. cremoris.

133 ude, pre-hydrolysis of BLG by L. delbrueckii subsp. bulgaricus CRL 454 has a positive effect on BLG d

134 Pre-hydrolysis of BLG by L. delbrueckii subsp. bulgaricus CRL 454 increases digestion of BLG ass

135 ive of the group b Lactobacillus delbrueckii subsp. bulgaricus (Ldb)-infecting bacteriophages, was sh

136 he contribution of Lactobacillus delbrueckii subsp. bulgaricus CRL 454 to BLG digestion and to analys

137 s helveticus and 6 Lactobacillus delbrueckii subsp. bulgaricus) were then selected and further evalua

138 C Streptococcus), Streptococcus dysgalactiae subsp. equisimilis (Group G Streptococcus), or Streptoco

139 ly found in human Streptococcus dysgalactiae subsp. equisimilis.

140 S. enterica subsp. salamae, and S. enterica subsp. arizonae share features of the infection strategy

141 wildlife including turtles, but S. enterica subsp. enterica serovar Typhimurium or lesions associate

142 n 3588/07 against the genomes of S. enterica subsp. enterica serovar Typhimurium strain LT2 and Salmo

143 Among the methods, S. enterica subsp. enterica serovars 4,5,12:i:-, Typhimurium, and Ty

144 S. enterica subsp. salamae encodes the Salmonella pathogenicity isla

145 Concurrently, S. enterica subsp. salamae infection of J774.A1 macrophages inhibite

146 ng (e.g., avrA, sopB, and sseL), S. enterica subsp. salamae invades HeLa cells and contains homologue

147 se results show that S. bongori, S. enterica subsp. salamae, and S. enterica subsp. arizonae share fe

148 d EspJ homologues in S. bongori, S. enterica subsp. salamae, and Salmonella enterica subsp. arizonae

149 rica subsp. salamae, and Salmonella enterica subsp. arizonae The beta-lactamase TEM-1 reporter system

150 h a nuclease domain from Salmonella enterica subsp. arizonae This modified V. cholerae strain was abl

151 Here, we recovered eight Salmonella enterica subsp. enterica genomes from human skeletons of transiti

152 hromosome and plasmid of Salmonella enterica subsp. enterica serovar Bareilly and Escherichia coli O1

153 Salmonella enterica subsp. enterica serovar Newport (S. Newport) is the thir

154 We report here that Salmonella enterica subsp. enterica serovar Typhimurium (S. Typhimurium) use

155 posable immunosensor for Salmonella enterica subsp. enterica serovar Typhimurium LT2 (S) detection us

156 e (LrS) on TNF-alpha and Salmonella enterica subsp. enterica serovar Typhimurium secretome (STS)-indu

157 te to the persistence of Salmonella enterica subsp. enterica serovar Typhimurium through liver-reside

158 taphylococcus aureus and Salmonella enterica subsp. enterica serovar Typhimurium, were exposed to 25

159 Salmonella enterica subsp. enterica serovars Typhimurium and its four closes

160 draft genome assembly of Salmonella enterica subsp. salamae strain 3588/07 against the genomes of S.

161 differences between Yersinia enterocolitica subsp. enterocolitica and Yersinia enterocolitica subsp.

162 . enterocolitica and Yersinia enterocolitica subsp. palearctica.

163 nogen is a common phenotype of human S. equi subsp. zooepidemicus isolates but much less so in equine

164 S. equi subsp. zooepidemicus isolates of equine and human origin

165 isolates but much less so in equine S. equi subsp. zooepidemicus isolates.

166 tant virulence mechanism of zoonotic S. equi subsp. zooepidemicus isolates.

167 the zoonotic potential varies among S. equi subsp. zooepidemicus strains in association with differe

168 eletion mutagenesis of two different S. equi subsp. zooepidemicus strains that the M-like protein SzM

169 (Group B Streptococcus), Streptococcus equi subsp. zooepidemicus (Group C Streptococcus), Streptococ

170 Streptococcus equi subsp. zooepidemicus is an important pathogen in horses

171 rent bacteremia caused by Streptococcus equi subsp. zooepidemicus, likely transmitted from mother to

172 to originate from its ancestor, M. esculenta subsp. flabellifolia.

173 three of the phenotypically defined C. fetus subsp. fetus strains to C. fetus subsp. venerealis strai

174 ed C. fetus subsp. fetus strains to C. fetus subsp. venerealis strains, when considering the core gen

175 extracts of Propionibacterium freudenreichii subsp. shermanii and after immunoaffinity purification i

176 ort the first known cases of S. gallolyticus subsp. pasteurianus infection in twin infants.

177 Colonization by Streptococcus gallolyticus subsp. gallolyticus (SGG) is strongly associated with th

178 Streptococcus gallolyticus subsp. pasteurianus, previously known as Streptococcus b

179 human isolates and Streptococcus halichoeri subsp. halichoeri is proposed for the gray seal isolates

180 a novel subspecies, Streptococcus halichoeri subsp. hominis, is proposed for the human isolates and S

181 nominations S. pseudoporcinus subsp. hominis subsp. nov. for the human isolates and S. pseudoporcinus

182 y matched the 16S rRNA of C. hyointestinalis subsp. lawsonii (56%), C. troglodytis (33%), C. upsalien

183 vided into four distinct clusters, including subsp. animalis, nucleatum, polymorphum, and fusiforme/v

184 PDB:3KZT], Cj0202c from Campylobacter jejuni subsp. jejuni serotype O:2 (strain NCTC 11168) [PDB:3K7C

185 h 1 x 10(9) colony-forming units of L lactis subsp cremoris ATCC 19257 or Lactobacillus rhamnosus GG

186 Mice fed the L lactis subsp cremoris had increased glucose tolerance while on

187 Dietary supplementation with L lactis subsp cremoris in female mice on a high-fat, high-carboh

188 L lactis subsp cremoris is safe for oral ingestion and might be d

189 Mice fed L lactis subsp cremoris while on the Western-style diet gained le

190 Hepatic lipid profiles of L lactis subsp cremoris-supplemented mice were characterized by l

191 ctococcus lactis subsp. lactis and L. lactis subsp. cremoris (R704); QLA - with Lactobacillus acidoph

192 obacillus bulgaricus, and Lactococcus lactis subsp Lactis.

193 of two starter strains of Lactococcus lactis subsp. cremoris (strains from the Culture Collection of

194 subsp. jonggajibkimchii, Lactococcus lactis subsp. cremoris, Lactobacillus coryniformis subsp. coryn

195 o inhibited by 50% CFS of Lactococcus lactis subsp. lactis and 25% CFS of Leuconostoc lactis. subsp.

196 ulture Start, composed by Lactococcus lactis subsp. lactis and L. lactis subsp. cremoris (R704); QLA

197 utanol were identified in Lactococcus lactis subsp. lactis and Lactococcus cremoris subsp.

198 utanol were identified in Lactococcus lactis subsp. lactis and Lactococcus cremoris subsp. cremoris.

199 of phage 340, a 936-type Lactococcus lactis subsp. lactis bacteriophage.

200 Recombinant HPP from Lactococcus lactis subsp. lactis that was expressed in Escherichia coli con

201 Listeria monocytogenes, following Lc. lactis subsp. lactis and Leuconostoc mesenteroides subsp. cremo

202 of Leu. mes. subsp. cremoris and Lc. lactis subsp. lactis showed stimulator effects (160%).

203 of 50% CFS of S. thermophilus and Lc. lactis subsp. lactis were more than 70% by Staphylococcus aureu

204 isolates and S. pseudoporcinus subsp. lactis subsp. nov. for the dairy isolates.

205 p. lactis and 25% CFS of Leuconostoc lactis. subsp. cremoris.

206 However, Lactococcus latics subsp. lactis strain X and Lactobacillus casei strain B

207 MO utilization for the type strain B. longum subsp. infantis ATCC 15697 (type strain) have been well

208 of 2'FL, 3FL and DFL (FLs) between B. longum subsp. infantis Bi-26 (Bi-26) and the type strain.

209 B. longum subsp. infantis is a prevalent species in the breast-fed

210 nfant-gut isolates of Bifidobacterium longum subsp. infantis and Bifidobacterium bifidum using indivi

211 -1,3-galactosidase in Bifidobacterium longum subsp. infantis ATCC 15697 (B. infantis).

212 syllactose (2'-FL) in Bifidobacterium longum subsp. infantis Bi-26.

213 2'-FL utilization by Bifidobacterium longum subsp. infantis Bi-26.

214 ish infants harboured Bifidobacterium longum subsp. infantis, a subspecies specialized in human milk

215 by two subspecies of Bifidobacterium longum: subsp. infantis (B. infantis) and subsp. longum (B. long

216 etic diversity in natural Arabidopsis lyrata subsp. petraea populations that differ in demographic hi

217 ified, which corresponded to 32 A. marginale subsp. centrale genotypes detected in cattle, buffalo, a

218 ts indicated high occurrence of A. marginale subsp. centrale infections, ranging from 25 to 100% in n

219 sp1aS as a genotypic marker for A. marginale subsp. centrale strain diversity.

220 ults demonstrate a diversity of A. marginale subsp. centrale strains from cattle and wildlife hosts f

221 Samples positive for A. marginale subsp. centrale were further characterized using the msp

222 interest in the epidemiology of A. marginale subsp. centrale, and, as a result, there are few reports

223 neously detect A. marginale and A. marginale subsp. centrale.

224 Anaplasma marginale subsp. centrale was the first vaccine used to protect ag

225 . cremoris (20%) whilst 25% CFS of Leu. mes. subsp. cremoris and Lc. lactis subsp. lactis showed stim

226 subsp. lactis and Leuconostoc mesenteroides subsp. cremoris (20%) whilst 25% CFS of Leu. mes. subsp.

227 were dominant, but Leuconostoc mesenteroides subsp. jonggajibkimchii, Lactococcus lactis subsp. cremo

228 eriophages against Clavibacter michiganensis subsp. nebraskensis (Cmn), the causal agent of Goss's wi

229 s that can protect Clavibacter michiganensis subsp. nebraskensis (CN8) bacteriophages against dehydra

230 roteome profiling to compare the M. mycoides subsp. capri wild type with a mutant lacking the proteol

231 brane lipoprotein Q (LppQ-N') of M. mycoides subsp. mycoides as the major antigen and a possible viru

232 ltered phenotypes reminiscent of M. mycoides subsp. mycoides SC and had significant impacts on the pr

233 djuvant and challenged them with M. mycoides subsp. mycoides.

234 losely related bacteria, Mycoplasma mycoides subsp. capri (Mmc) and Mycoplasma capricolum subsp. capr

235 Mycoplasma mycoides subsp. capri (Mmc) and subsp. mycoides (Mmm) are importa

236 proteolytic phenotype in Mycoplasma mycoides subsp. capri GM12.

237 ith the caprine pathogen Mycoplasma mycoides subsp. capri or an engineered mutant lacking the capsula

238 ease of cattle caused by Mycoplasma mycoides subsp. mycoides.

239 itudes utilises oilseed rape (Brassica napus subsp. oleifera) and turnip rape (B. rapa subsp. oleifer

240 Fusobacterium nucleatum subsp. polymorphum was the most significantly overrepres

241 infective endocarditis Streptococcus oralis subsp. dentisani displays a striking monolateral distrib

242 s H. ducreyi (23% of specimens), T. pallidum subsp pertenue (16%), Streptococcus dysgalactiae (12%),

243 ed for real-time PCR testing for T. pallidum subsp pertenue and H. ducreyi.

244 When the T. pallidum subsp. pallidum Nichols strain genome was initially anno

245 Treponema pallidum subsp pertenue and Haemophilus ducreyi are causative age

246 ce of ulcers negative for Treponema pallidum subsp pertenue on PCR, and active yaws was defined as ul

247 ction, which is caused by Treponema pallidum subsp. pallidum (TPA), has been re-emerging globally in

248 us to map the circulating Treponema pallidum subsp. pallidum allelic profiles in this geographic regi

249 In silico analyses of Treponema pallidum subsp. pallidum genomes and predicted proteomes to searc

250 The spirochete Treponema pallidum subsp. pallidum is the causative agent of syphilis, a ch

251 In Treponema pallidum subsp. pallidum, the agent of syphilis, the TP0092 gene

252 -exposed proteins, and in Treponema pallidum subsp. pallidum, the syphilis agent, it was reported to

253 tobacillus casei and Lactobacillus paracasei subsp.

254 ei (ATCC(R) 393) and Lactobacillus paracasei subsp. paracasei (ATCC(R) BAA52) in yogurt.

255 s (LA-5); QLP - with Lactobacillus paracasei subsp. paracasei (L. casei 01); QB - with Bifidobacteriu

256 the probiotic strain Lactobacillus paracasei subsp. paracasei, L. casei 431 (Chr. Hansen A/S) (hereaf

257 tobacillus casei and Lactobacillus paracasei subsp. paracasei.

258 and polar extracts of Lavandula pedunculata subsp. lusitanica (Chaytor) Franco collected in south Po

259 obacillus plantarum, Lactobacillus plantarum subsp. argentoratensis and Oenococcus oeni strains along

260 sp. pneumophila, 3 strains of L. pneumophila subsp. fraseri or L. pneumophila subsp. pascullei, 4 str

261 pneumophila subsp. fraseri or L. pneumophila subsp. pascullei, 4 strains of "L. donaldsonii," 3 strai

262 or subspecies: 15 strains of L. pneumophila subsp. pneumophila, 3 strains of L. pneumophila subsp. f

263 e subspecies denominations S. pseudoporcinus subsp. hominis subsp. nov. for the human isolates and S.

264 for the human isolates and S. pseudoporcinus subsp. lactis subsp. nov. for the dairy isolates.

265 us subsp. oleifera) and turnip rape (B. rapa subsp. oleifera), having similar oil compositions.

266 greens or leaves) of pak choi (Brassica rapa subsp. chinensis) and kale (Brassica oleracea var. sabel

267 ished in the fine fescue grass Festuca rubra subsp. rubra (strong creeping red fescue) infected with

268 dobacterium spp and Streptococcus salivarius subsp thermophilus, might produce the largest reduction

269 Lactococcus garvieae, Aeromonas salmonicida subsp. salmonicida, and Yersinia ruckeri and a parasitic

270 explain the genetic structure of P. sativum subsp. elatius in its westward expansion from its center

271 cies, while the diversity of wild P. sativum subsp. elatius was structured into 5 partly geographical

272 he effects of Lactococcus lactis subspecies (subsp) cremoris on weight gain, liver fat, serum cholest

273 roasted) wattle, Acacia saligna subspecies (subsp.) saligna, pruinescens, stolonifera and lindleyi,

274 PGA and PGAs from nonpathogenic B. subtilis subsp. chungkookjang and B. licheniformis Monocytes and

275 it shares more orthologues with B. subtilis subsp. subtilis NCIB 3610(T) (ANIm values, 85.4-86.7%) t

276 from the leaves of the plant Acer tataricum subsp. ginnala that has been consumed in some regions of

277 Bt152 gene is expressed in B. thuringiensis subsp. israelensis, we disrupted its function and showed

278 squitocidal bacteria, Bacillus thuringiensis subsp. israelensis (Bti) and Lysinibacillus sphaericus (

279 Bacillus thuringiensis subsp. israelensis produces crystal inclusions composed

280 zania infection with Treponema pallidum (TP) subsp. pertenue (TPE) is present in four different monke

281 ubsp. tularensis subtype A.II, F. tularensis subsp. holarctica (also referred to as type B), and F. t

282 t challenge with two different F. tularensis subsp. holarctica (type B) live vaccine strains, thereby

283 subsp. tularensis (type A) and F. tularensis subsp. holarctica (type B).

284 ibuting to the survival of the F. tularensis subsp. holarctica live vaccine strain (LVS) in macrophag

285 so referred to as type B), and F. tularensis subsp. mediasiatica, as well as opportunistic F. tularen

286 tica, as well as opportunistic F. tularensis subsp. novicida from each other and near neighbors, such

287 aerobe Francisella tularensis: F. tularensis subsp. tularensis (type A) and F. tularensis subsp. hola

288 and identify the hypervirulent F. tularensis subsp. tularensis subtype A.I, the virulent F. tularensi

289 nsis subtype A.I, the virulent F. tularensis subsp. tularensis subtype A.II, F. tularensis subsp. hol

290 TPR-like proteins in Francisella tularensis subsp. holarctica FSC200.

291 s spectrometry on the Francisella tularensis subsp. holarctica LVS defined three protein biomarkers t

292 opportunistic microbe Francisella tularensis subsp. novicida, there are considerable differences in g

293 m the highly virulent Francisella tularensis subsp. tularensis (type A) strain Schu S4 in hypervesicu

294 gia ATCC 25015 and on Francisella tularensis subsp. tularensis CCUG 2112, the most virulent Francisel

295 pies of iglE rendered Francisella tularensis subsp. tularensis Schu S4 avirulent and incapable of int

296 d characterization of Francisella tularensis subsp. tularensis strain Schu S4 mutants that lack funct

297 her with chlorogenic acid, and V. uliginosum subsp. gaultherioides dominated by malvidin derivatives

298 TMA, RSA and FRAP values than V. uliginosum subsp. gaultherioides fruits.

299 two magnitude orders higher in V. uliginosum subsp. gaultherioides than in V. myrtillus berries.

300 "false bilberry" (i.e. Vaccinium uliginosum subsp. gaultherioides Bigelow).