ライフサイエンスコーパス: Listeria monocytogenes

1 d by two other pathogens (vaccinia virus and Listeria monocytogenes).

2 immunoassay for ultrasensitive detection of Listeria monocytogenes.

3 ection by the inflammasome-evasive bacterium Listeria monocytogenes.

4 -positive facultative intracellular pathogen Listeria monocytogenes.

5 ffector responses with improved clearance of Listeria monocytogenes.

6 ysaccharide (EPS) in the food-borne pathogen Listeria monocytogenes.

7 idomas with lipid extracts from the pathogen Listeria monocytogenes.

8 ginosa but not in the Gram-positive pathogen Listeria monocytogenes.

9 ce that were subsequently infected i.v. with Listeria monocytogenes.

10 n pathogens such as Enterococcus faecium and Listeria monocytogenes.

11 red for the growth of the bacterial pathogen Listeria monocytogenes.

12 ansgenic granulysin are better able to clear Listeria monocytogenes.

13 e protected from lethal infection induced by Listeria monocytogenes.

14 ation of 100S ribosomes by an HPF homolog in Listeria monocytogenes.

15 responses to immunization or infection with Listeria monocytogenes.

16 n of epithelial and macrophage-like cells by Listeria monocytogenes.

17 , including Bacillus cereus and the pathogen Listeria monocytogenes.

18 ed by the facultative intracellular pathogen Listeria monocytogenes.

19 ion properties of the intracellular pathogen Listeria monocytogenes.

20 in of internalins of the food borne pathogen Listeria monocytogenes.

21 was created by intraperitoneal injection of Listeria monocytogenes.

22 icidal activity against Escherichia coli and Listeria monocytogenes.

23 lethal infection with the bacterial pathogen Listeria monocytogenes.

24 ice infected with the intracellular pathogen Listeria monocytogenes.

25 t proteins expressed from vaccinia virus and Listeria monocytogenes.

26 gainst a subsequent challenge infection with Listeria monocytogenes.

27 at the peak of the CD8(+) T cell response to Listeria monocytogenes.

28 Salmonella enterica serovar Typhimurium and Listeria monocytogenes.

29 ingitis virus and the intracellular bacteria Listeria monocytogenes.

30 cell response to the intracellular bacterium Listeria monocytogenes.

31 AM and ZinABC, in the intracellular pathogen Listeria monocytogenes.

32 avior upon primary and secondary exposure to Listeria monocytogenes.

33 cells that supported protective immunity to Listeria monocytogenes.

34 Ns promote macrophage death postinfection by Listeria monocytogenes.

35 ts of the facultative intracellular pathogen Listeria monocytogenes.

36 ellipsoidal beads resembling the geometry of Listeria monocytogenes.

37 rulence factor of the intracellular pathogen Listeria monocytogenes.

38 y (ELISA) to detect the food-borne pathogen -Listeria monocytogenes.

39 hages and thus of innate immune responses to Listeria monocytogenes.

40 tic pathogens, such as influenza viruses and Listeria monocytogenes.

41 sensitive against Staphylococcus aureus and Listeria monocytogenes.

42 ted osmotic stress in the bacterial pathogen Listeria monocytogenes.

43 to infection with the intracellular bacteria Listeria monocytogenes.

44 We present the genome sequence of Listeria monocytogenes 07PF0776, a serovar 4b isolate fr

45 thogens such as Salmonella Typhimurium, (7%) Listeria monocytogenes (3%) and Escherichia coli (0%).

46 anscriptional regulators to the virulence of Listeria monocytogenes, a Gram-positive facultative intr

47 e viral infection localized to the lung, and Listeria monocytogenes, a systemic bacterial infection.

48 In Listeria monocytogenes, a vitamin B12-binding (B12) ribo

49 ular pathogens such as Shigella flexneri and Listeria monocytogenes achieve dissemination in the inte

50 as a factor that stimulates the formation of Listeria monocytogenes actin comet tails, thereby implic

51 Here we show that attenuated recombinant Listeria monocytogenes, administered orally utilizing it

52 galovirus and DNA, and the infectious agents Listeria monocytogenes and Aspergillus fumigatus.

53 resentative of CsoRs from pathogenic bacilli Listeria monocytogenes and Bacillus anthracis.

54 s (Salmonella enteritidis, Escherichia coli, Listeria monocytogenes and Bacillus cereus) was evaluate

55 , as well as for the intracellular pathogens Listeria monocytogenes and Chlamydia trachomatis.

56 neity in manifestations of disease caused by Listeria monocytogenes and demonstrate that a previously

57 llin-resistant Staphylococcus aureus (MRSA), Listeria monocytogenes and Enterococcus faecalis, and ag

58 es for Salmonella spp. and other pathogens ( Listeria monocytogenes and Escherichia coli ) are compar

59 multaneous detection of Salmonella enterica, Listeria monocytogenes and Escherichia coli based on tri

60 the survival of common food borne pathogens, Listeria monocytogenes and Escherichia coli O157:H7.

61 stored resistance to the perinatal pathogens Listeria monocytogenes and Escherichia coli.

62 rn of trafficking confers protection against Listeria monocytogenes and is regulated by the repressiv

63 this question with the facultative pathogen Listeria monocytogenes and its PrfA virulence regulon.

64 showed potent antibacterial activity against Listeria monocytogenes and methicillin-resistant Staphyl

65 tructures of ClpP1 and ClpP2 from pathogenic Listeria monocytogenes and observe an unprecedented regu

66 g infection with the Th1-associated pathogen Listeria monocytogenes and observed that IS001 enhanced

67 Listeria monocytogenes and other pathogenic bacteria mod

68 ry mechanisms employed by two intracellular [Listeria monocytogenes and Salmonella enterica serovar T

69 splays antibacterial activities against both Listeria monocytogenes and Salmonella enterica sv. Enter

70 food-borne pathogens Staphylococcus aureus, Listeria monocytogenes and Salmonella spp. were not dete

71 ew recent advances in the field showing that Listeria monocytogenes and Shigella flexneri have evolve

72 ting the growth of Staphylococcus aureus and Listeria monocytogenes and showed high inhibitory capaci

73 hylogenetically related human pathogens like Listeria monocytogenes and Staphylococcus aureus possess

74 Toll-like receptor 5 ligand flagellin A from Listeria monocytogenes and the birch pollen allergen Bet

75 receptor agonists, as well as in response to Listeria monocytogenes and Toxoplasma gondii infection.

76 memory phase and provided optimal control of Listeria monocytogenes and vaccinia virus, despite weak

77 n in vivo T-cell priming during infection by Listeria monocytogenes and vesicular stomatitis virus.

78 ity of 24p3(-/-) mice to both intracellular (Listeria monocytogenes) and extracellular (Candida albic

79 ere promoted by the TLR2 ligand (heat killed Listeria monocytogenes) and the TLR4 ligand (lipopolysac

80 sed by diverse pathogens (Trypanosoma cruzi, Listeria monocytogenes, and adenovirus) to promote their

81 gainst Gram-positive (Staphylococcus aureus, Listeria monocytogenes, and Bacillus cereus) and Gram-ne

82 aped pathogens including Bacillus anthracis, Listeria monocytogenes, and Clostridium difficile.

83 three unrelated bacteria: Escherichia coli, Listeria monocytogenes, and Mycobacteria tuberculosis.

84 e intracellular pathogens Toxoplasma gondii, Listeria monocytogenes, and Mycobacterium tuberculosis H

85 Escherichia coli O157:H7, non-O157 E. coli, Listeria monocytogenes, and Salmonella spp.) was modeled

86 Cutaneous infections due to Listeria monocytogenes are rare.

87 ection against intracellular bacteria, using Listeria monocytogenes as a model organism.

88 The emergence of Listeria monocytogenes as a promising immunotherapeutic

89 this study, we used an attenuated strain of Listeria monocytogenes as a vaccine expression system fo

90 high-affinity Fe(2+) efflux transporter from Listeria monocytogenes, as an inducible genetic tool to

91 so required for rapid activation of NLRP3 by Listeria monocytogenes, as deletion of IRAK1 or IRAK4 le

92 the in situ detection and discrimination of Listeria monocytogenes at a concentration of single cell

93 particular Staphylococcus aureus ATCC 6538, Listeria monocytogenes ATCC 13932 and methicillin-resist

94 oximately 300 nM) had activity against MRSA, Listeria monocytogenes, Bacillus anthracis, and a vancom

95 y against Gram positive foodborne pathogens (Listeria monocytogenes, Bacillus cereus and Staphylococc

96 tificially inoculated with Escherichia coli, Listeria monocytogenes, Bacillus cereus, Staphylococcus

97 om Escherichia coli, Pseudomonas aeruginosa, Listeria monocytogenes, Bacillus subtilis, and Staphyloc

98 trophil superoxide anion production, and for Listeria monocytogenes bacterial clearance in vivo.

99 PGRN-deficient mice are sensitive to Listeria monocytogenes because of deficits in xenophagy,

100 Listeria monocytogenes binds to the epithelial host cell

101 The formation of Listeria monocytogenes biofilms contributes to persisten

102 ng of the MOLF strain in response to HSV and Listeria monocytogenes both in vitro and in vivo.

103 ctivities compared to free LAE in inhibiting Listeria monocytogenes, but was less effective against E

104 that the expression of CD8 T-cell epitope of Listeria monocytogenes by a recombinant mouse CMV (MCMV)

105 hat c-di-AMP regulates central metabolism in Listeria monocytogenes by inhibiting its pyruvate carbox

106 owth of the foodborne intracellular pathogen Listeria monocytogenes by promoting mechanisms that damp

107 iated with the functional transitions in the Listeria monocytogenes Ca(2+)-ATPase (LMCA1), an ortholo

108 Although Listeria monocytogenes can induce systemic infection cau

109 Here we show that a bacterial pathogen, Listeria monocytogenes, can exploit efferocytosis to pro

110 lococcus epidermidis, Staphylococcus aureus, Listeria monocytogenes, Candida albicans, and Candida pa

111 The bacterial pathogen Listeria monocytogenes causes food-borne illnesses resul

112 The bacterial pathogen Listeria monocytogenes causes foodborne systemic disease

113 The facultative intracellular pathogen Listeria monocytogenes causes listeriosis, a rare but li

114 We recently showed that infection by Listeria monocytogenes causes mitochondrial network frag

115 Listeria monocytogenes causes often-fatal infections aff

116 The bacterial pathogen Listeria monocytogenes causes spontaneous abortion, stil

117 In the human pathogen Listeria monocytogenes, cdiA is an essential molecule th

118 Listeria monocytogenes cells were grown at 37 degrees C

119 iled to protect against a lethal recombinant Listeria monocytogenes challenge.

120 vaccination increasing protection against a Listeria monocytogenes challenge.

121 s showed high antibacterial activity against Listeria monocytogenes: cIsf pool had a minimum inhibito

122 EPS had the largest inhibition zone against Listeria monocytogenes CMCC 54001.

123 w that a diverse microbiota markedly reduces Listeria monocytogenes colonization of the gut lumen and

124 increased resistance in mice to infection of Listeria monocytogenes compared with CpG-ODN treatment a

125 The food-borne pathogen Listeria monocytogenes contains mostly saturated branche

126 The pathogenesis of Listeria monocytogenes depends on the ability of this ba

127 Indeed, following infection with Listeria monocytogenes, DNA-PKcs-deficient murine macrop

128 s of Escherichia coli , Salmonella spp., and Listeria monocytogenes , due to the severity and frequen

129 ed by the Gram-positive facultative pathogen Listeria monocytogenes during an in vivo infection.

130 es of the facultative intracellular pathogen Listeria monocytogenes encode two functional enoyl-acyl

131 Immunization of KPC mice with Listeria monocytogenes engineered to express Kras(G12D),

132 enically express a TCR specific for the same Listeria monocytogenes epitope, elicited distinct interl

133 18 and LLO56, specific for an immunodominant Listeria monocytogenes epitope, with dramatically differ

134 icidal effect against Staphylococcus aureus, Listeria monocytogenes, Escherichia coli and Salmonella

135 -2S4B6-treated HSCT recipients infected with Listeria monocytogenes exhibited decreased bacterial lev

136 ed contraction in response to infection with Listeria monocytogenes expressing a cognate Ag.

137 D8 cell adoptive transfer and challenge with Listeria monocytogenes expressing a cognate antigen, we

138 ely can be expanded by secondary exposure to Listeria monocytogenes expressing recombinant Plasmodium

139 vaccine and rLm/iglC (recombinant attenuated Listeria monocytogenes expressing the F. tularensis immu

140 lymphocytic choriomeningitis virus (LCMV) or Listeria monocytogenes expressing the LCMV gp61-80 pepti

141 ine, DMOT4039A, BMS-986148), live attenuated Listeria monocytogenes-expressing mesothelin (CRS-207, J

142 CRS-207, live-attenuated Listeria monocytogenes-expressing mesothelin, induces in

143 d sheep erythrocytes, zymosan particles, and Listeria monocytogenes failed to show any significant di

144 the highest on tyramine production (55%) by Listeria monocytogenes, following Lc. lactis subsp. lact

145 prevents the human gastrointestinal pathogen Listeria monocytogenes from invading cultured mammalian

146 The peptide sensor also selectively detected Listeria monocytogenes from other Gram-positive strains

147 Diagnosis is made by culturing Listeria monocytogenes from sterile body fluids or from

148 Listeria monocytogenes FrvA (Lmo0641) is critical for vi

149 ive (Bacillus cereus, Staphylococcus aureus, Listeria monocytogenes, Geobacillus stearothermophilus)

150 Indeed, following systemic infection with Listeria monocytogenes, germ-free and oral-antibiotic-tr

151 rin alone had antimicrobial activity against Listeria monocytogenes, however, films incorporating cit

152 crobial properties of SAMN@TA were tested on Listeria monocytogenes in comparison with free TA, showi

153 We show that clearance of Listeria monocytogenes in macrophages requires IRF8-depe

154 the antibacterial activity observed against Listeria monocytogenes in vitro, in cell culture, and in

155 ia coli O157:H7, Salmonella typhimurium, and Listeria monocytogenes) in buffer.

156 ce also harboured a strong TH1 cell inducer, Listeria monocytogenes, in their intestine.

157 A fruit extract matrix was selected and Listeria monocytogenes inactivation was followed from th

158 We found that oral infection with Listeria monocytogenes induced a robust intestinal CD8 T

159 Importantly, Listeria monocytogenes induces NLRP3-dependent rapid cas

160 Listeria monocytogenes infected CD8alpha(+) DCs in the s

161 MHC class II-specific GC-Tfh cells following Listeria monocytogenes infection and a 2-fold decrease f

162 defensive role of the gut microbiota against Listeria monocytogenes infection and identify intestinal

163 tegrins, we examined CD8 T cell responses to Listeria monocytogenes infection in CD11a-, CD11b-, and

164 (+) T cell formation and their function upon Listeria monocytogenes infection in mice.

165 cells conferred increased protection against Listeria monocytogenes infection in susceptible IFN-gamm

166 a T cells are important for the clearance of Listeria monocytogenes infection in the intestinal mucos

167 ticulate antigen in vitro and to recombinant Listeria monocytogenes infection in vivo.

168 ate that fetal wastage triggered by prenatal Listeria monocytogenes infection is driven by placental

169 ainst microbial infections, we have used the Listeria monocytogenes infection model to explore the im

170 f cardiac transplantation, we show that when Listeria monocytogenes infection precipitates acute reje

171 l uptake and were more susceptible to lethal Listeria monocytogenes infection than were DT-treated CL

172 CD8(+) T cell responses to Listeria monocytogenes infection that are restricted by

173 tion of B cells at different times following Listeria monocytogenes infection to show that B cells ar

174 t expansion of CD8(+) T cell response during Listeria monocytogenes infection, but plays a key role i

175 Upon acute Listeria monocytogenes infection, deleting miR-23a in T

176 LT have been uncovered: as a host factor for Listeria monocytogenes infection, in the maintenance of

177 tantly, VM cells showed efficient control of Listeria monocytogenes infection, indicating memory-like

178 ough IFN-gamma is required for resolution of Listeria monocytogenes infection, the identities of the

179 cing CD4(+) and CD8(+) T cells responding to Listeria monocytogenes infection.

180 tion of memory CD8(+) T cells in response to Listeria monocytogenes infection.

181 Tim-3 affects CD8 T cell responses to acute Listeria monocytogenes infection.

182 and conferred protection against recombinant Listeria monocytogenes infection.

183 survival of CD8(+) T cells in vivo following Listeria monocytogenes infection.

184 n the innate immune response of mice against Listeria monocytogenes infection.

185 increased bacterial burden in the liver upon Listeria monocytogenes infection.

186 ive secondary, but not primary, responses to Listeria monocytogenes infection.

187 ector CD8+ T cell populations in response to Listeria monocytogenes infection.

188 and dampened innate immune responses against Listeria monocytogenes infection.

189 ophils in the spleen than did WT mice during Listeria monocytogenes infection.

190 uced tolerance and more effective control of Listeria monocytogenes infection.

191 Listeria monocytogenes is a bacterial parasite that uses

192 Listeria monocytogenes is a bacterial pathogen that indu

193 Listeria monocytogenes is a facultative intracellular pa

194 The Gram-positive bacterium Listeria monocytogenes is a facultative intracellular pa

195 The Gram-positive bacterium Listeria monocytogenes is a facultative intracellular pa

196 Listeria monocytogenes is a food-borne pathogen that can

197 Listeria monocytogenes is a foodborne pathogen capable o

198 Listeria monocytogenes is a foodborne pathogen responsib

199 Listeria monocytogenes is a foodborne pathogen that caus

200 Listeria monocytogenes is a foodborne pathogen that caus

201 Listeria monocytogenes is a foodborne pathogen that cros

202 Listeria monocytogenes is a Gram-positive bacterium that

203 Listeria monocytogenes is a Gram-positive facultative in

204 Listeria monocytogenes is a gram-positive facultative in

205 Listeria monocytogenes is a Gram-positive intracellular

206 Listeria monocytogenes is a Gram-positive intracellular

207 Listeria monocytogenes is a Gram-positive, facultative i

208 Listeria monocytogenes is a highly adaptive bacterium th

209 Listeria monocytogenes is a major cause of mortality res

210 Listeria monocytogenes is a major intracellular human fo

211 Listeria monocytogenes is a serious cause of human foodb

212 Listeria monocytogenes is an intracellular food-borne pa

213 Listeria monocytogenes is an intracellular Gram-positive

214 Listeria monocytogenes is an intracellular pathogen that

215 The intracellular bacterial pathogen Listeria monocytogenes is capable of remodelling the act

216 Infection by the human bacterial pathogen Listeria monocytogenes is mainly controlled by the posit

217 Listeria monocytogenes is responsible for gastroenteriti

218 Listeria monocytogenes is responsible for the life-threa

219 Listeriosis, caused by Listeria monocytogenes, is an important foodborne diseas

220 ith any of five outbreak-related subtypes of Listeria monocytogenes isolated during the period from A

221 We performed WGS on Listeria monocytogenes isolates from patients and availa

222 LST) each identified a diverse population of Listeria monocytogenes isolates, and within that, both m

223 ell transfers in the well-established murine Listeria monocytogenes (L.m.) infection model.

224 ular pathogens, such as Bartonella henselae, Listeria monocytogenes, Legionella pneumophila, or adeno

225 atitis and in models of bacterial infection (Listeria monocytogenes, lipopolysaccharide).

226 pe, (188)Rhenium, to an attenuated (at) live Listeria monocytogenes (Listeria(at)) using Listeria-bin

227 Remarkably Hfq from Gram-positive Listeria monocytogenes (Lm) binds (GU)3G on its proximal

228 Yet, the intracellular bacterium Listeria monocytogenes (Lm) causes lethal infections in

229 Listeria monocytogenes (Lm) causes severe foodborne illn

230 ed a novel approach utilizing infection with Listeria monocytogenes (LM) encoding proteolipid protein

231 (MSKO) vs wild-type mice were infected with Listeria monocytogenes (Lm) for 36 hours or 72 hours bef

232 ta T cells mounts an immune response to oral Listeria monocytogenes (Lm) infection and leads to the d

233 Listeria monocytogenes (Lm) is a major human foodborne p

234 Listeria monocytogenes (Lm) is both a life-threatening p

235 nonphagocytic cells, a critical property of Listeria monocytogenes (Lm) that enables it to cross hos

236 Listeria monocytogenes (LM), an important food-borne pat

237 th Mycobacterium tuberculosis (Mtb), but not Listeria monocytogenes (Lm), induced robust lymph node e

238 -type mice when challenged by infection with Listeria monocytogenes (Lm), whereas p47(phox)-deficient

239 at ~10(2)-10(3) cells of foodborne pathogen, Listeria monocytogenes (LM).

240 tabolic pathway from the food-borne pathogen Listeria monocytogenes (Lm).

241 hemokine production following infection with Listeria monocytogenes (Lm).

242 tic diversity, and outcome of 92 adults with Listeria monocytogenes meningitis included in 2 prospect

243 To address this question, we used the Listeria monocytogenes model of infection and followed C

244 (Leishmania major), and infectious disease (Listeria monocytogenes) models, we establish ibrutinib a

245 facultative intracellular bacterial pathogen Listeria monocytogenes, most of the bacterial burden in

246 In Listeria monocytogenes, mutations that prevent addition

247 SARM(-/-) mice show normal responses to Listeria monocytogenes, Mycobacterium tuberculosis, and

248 tococcus pyogenes, Streptococcus pneumoniae, Listeria monocytogenes, Neisseria meningitidis serogroup

249 Escherichia coli K1, Haemophilus influenzae, Listeria monocytogenes, Neisseria meningitidis, Streptoc

250 ith the Gram-positive intracellular pathogen Listeria monocytogenes, neutrophils are recruited from t

251 Escherichia coli (STEC) O157, STEC non-O157, Listeria monocytogenes, nontyphoidal Salmonella species,

252 Both compounds appeared effective against Listeria monocytogenes, one of the most important foodbo

253 ages and is induced following infection with Listeria monocytogenes or stimulation with TLR ligands (

254 s mediated protection against Gag-expressing Listeria monocytogenes or vaccinia viral infections.

255 ibited a modest expansion defect early after Listeria monocytogenes or vesicular stomatitis virus inf

256 Listeria monocytogenes PdxR is a member of the poorly ch

257 itive bacteria, including the human pathogen Listeria monocytogenes, possess an additional nonessenti

258 -A CRISPR-Cas9 inhibitor proteins encoded by Listeria monocytogenes prophages.

259 Using chemical proteomics, we identified the Listeria monocytogenes protein PgpH as a molecular targe

260 facultative intracellular bacterial pathogen Listeria monocytogenes remodels its transcriptional prog

261 Pathogenic Listeria monocytogenes replicates within the host cytoso

262 nvestigate novel live attenuated recombinant Listeria monocytogenes (rLm) vaccines expressing the Myc

263 coli (ETEC), enteropathogenic E.coli (EPEC), Listeria monocytogenes, Salmonella entericaserovartyphi,

264 ood pathogens, namely Staphylococcus aureus, Listeria monocytogenes, Salmonella enteritidis and Esche

265 omposition and volatile molecule profiles of Listeria monocytogenes, Salmonella enteritidis, Escheric

266 Escherichia coli, Listeria monocytogenes, Salmonella sp. and Staphylococcu

267 nt to infection with the bacterial pathogens Listeria monocytogenes, Salmonella typhimurium and Esche

268 e to apoptotic immune cells and live or dead Listeria monocytogenes scavenger receptor BI (SR-BI), an

269 analyzed for antimicrobial activity against Listeria monocytogenes Scott A and Escherichia coli K12.

270 Listeria monocytogenes serotype 4b was more common in pr

271 Since Listeria monocytogenes, Shigella flexneri, and Vaccinia

272 DeltagpsB mutants of the human pathogen Listeria monocytogenes show severe lysis, division and g

273 packaged leafy green salad contaminated with Listeria monocytogenes singleton sequence type 382 (ST38

274 the spoilage food bacteria Escherichia coli, Listeria monocytogenes, Staphylococcus aureus and Salmon

275 om the report that DCs are more resistant to Listeria monocytogenes than macrophages.

276 of DNA from the gram-positive test organism (Listeria monocytogenes) than from the gram-negative orga

277 roduction after infection with the bacterium Listeria monocytogenes that was correlated with elevated

278 In Listeria monocytogenes, the sole diadenylate cyclase, Da

279 estinal pathogens Salmonella typhimurium and Listeria monocytogenes to induce the expression of IL-8.

280 Using recombinant Listeria monocytogenes to prime stably differentiated Th

281 how that NO helps the intracellular bacteria Listeria monocytogenes to spread.

282 he sensitivity of the intracellular pathogen Listeria monocytogenes to various beta-lactams by inhibi

283 l-molecule inhibitor of sigma(B) activity in Listeria monocytogenes, to inhibit sigma(B) activity in

284 The Gram-positive bacterium Listeria monocytogenes transitions from an environmental

285 ogens such as Zika virus, Toxoplasma gondii, Listeria monocytogenes, Treponema pallidium, parvovirus,

286 facultative intracellular bacterial pathogen Listeria monocytogenes Two days after foodborne infectio

287 In Listeria monocytogenes, two enzymes are required for the

288 tinase, as well as unrelated chitinases from Listeria monocytogenes using the fluorescently labeled s

289 Listeria monocytogenes V7 and Salmonella enterica serova

290 e tested this hypothesis using a recombinant Listeria monocytogenes vaccine platform that targets CD1

291 this function upon secondary challenges with Listeria monocytogenes, vesicular stomatitis virus, or V

292 inhibition against Staphylococcus aureus and Listeria monocytogenes was >89% when fPEM extracts were

293 ed by the facultative intracellular pathogen Listeria monocytogenes, was posttranslationally modified

294 -di-AMP-interacting proteins in the pathogen Listeria monocytogenes, we identified several broadly co

295 ine kinase Src upon incubation of cells with Listeria monocytogenes, we searched for novel host prote

296 opy of the bloodstream of mice infected with Listeria monocytogenes, we show that bacterial clearance

297 ed Drosophila melanogaster with the pathogen Listeria monocytogenes, we tested this framework, findin

298 Pdx-1-Cre mice with attenuated intracellular Listeria monocytogenes (which induces CD4(+) and CD8(+)

299 from vacuoles by the intracellular pathogen Listeria monocytogenes, which suggested a role for this

300 proliferation of the intracytosolic pathogen Listeria monocytogenes Within a few hours of systemic in