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 tic pathogens, such as influenza viruses and Listeria monocytogenes.

3 sensitive against Staphylococcus aureus and Listeria monocytogenes.

4 ted osmotic stress in the bacterial pathogen Listeria monocytogenes.

5 to infection with the intracellular bacteria Listeria monocytogenes.

6 immunoassay for ultrasensitive detection of Listeria monocytogenes.

7 ection by the inflammasome-evasive bacterium Listeria monocytogenes.

8 -positive facultative intracellular pathogen Listeria monocytogenes.

9 ffector responses with improved clearance of Listeria monocytogenes.

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

11 idomas with lipid extracts from the pathogen Listeria monocytogenes.

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

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

14 n pathogens such as Enterococcus faecium and Listeria monocytogenes.

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

16 ansgenic granulysin are better able to clear Listeria monocytogenes.

17 e protected from lethal infection induced by Listeria monocytogenes.

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

19 responses to immunization or infection with Listeria monocytogenes.

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

21 , including Bacillus cereus and the pathogen Listeria monocytogenes.

22 ed by the facultative intracellular pathogen Listeria monocytogenes.

23 ion properties of the intracellular pathogen Listeria monocytogenes.

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

25 was created by intraperitoneal injection of Listeria monocytogenes.

26 icidal activity against Escherichia coli and Listeria monocytogenes.

27 lethal infection with the bacterial pathogen Listeria monocytogenes.

28 expression of dozens of genes and operons in Listeria monocytogenes.

29 eSTK substrate in the Gram-positive pathogen Listeria monocytogenes.

30 lar peptidoglycans and host defenses against Listeria monocytogenes.

31 obial activities, except P#4 (AAGGV) against Listeria monocytogenes.

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

33 monella enterica serovar Typhimurium (7.8%), Listeria monocytogenes (3.88%) and Escherichia coli (1.5

34 We found that orally inoculated Listeria monocytogenes, a bacterial foodborne pathogen,

35 In contrast to damage caused by Listeria monocytogenes, a Gram-positive bacterium, BCV r

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

37 Listeria monocytogenes, a Gram-positive, facultative int

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

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

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

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

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

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

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

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

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

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

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

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

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

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

52 fection using two important human pathogens: Listeria monocytogenes and Mycobacterium tuberculosis.

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

54 Listeria monocytogenes and other pathogenic bacteria mod

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

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

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

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

59 enables L-form growth in Bacillus subtilis, Listeria monocytogenes and Staphylococcus aureus.

60 three bacterial species (Bacillus subtilis, Listeria monocytogenes and Streptococcus pneumoniae) and

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

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

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

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

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

66 t Lactococcus lactis, Staphylococcus aureus, Listeria monocytogenes, and Bacillus cereus, using the w

67 e Legionella pneumophila, Coxiella burnetii, Listeria monocytogenes, and Chlamydia trachomatis have d

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

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

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

71 The emergence of Listeria monocytogenes as a promising immunotherapeutic

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

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

74 em that is present in the foodborne pathogen Listeria monocytogenes, as well as many other Gram-posit

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

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

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

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

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

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

81 Here we report a sensing method for Listeria monocytogenes based on the agglutination of all

82 e vaccination effect of radiation, we used a Listeria monocytogenes based vaccine to generate a large

83 5a receptor 1 synergized with antiangiogenic Listeria monocytogenes-based vaccines to decrease the lu

84 CD8(+) T cells in isolation, we engineered a Listeria monocytogenes-based vector to express a single

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

86 Listeria monocytogenes binds to the epithelial host cell

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

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

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

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

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

92 of defense, yet foodborne pathogens such as Listeria monocytogenes can overcome this barrier; howeve

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

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

95 The bacterial pathogen Listeria monocytogenes causes foodborne systemic disease

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

97 Listeria monocytogenes causes often-fatal infections aff

98 The bacterial pathogen Listeria monocytogenes causes spontaneous abortion, stil

99 bacteria, including pathogenic bacteria like Listeria monocytogenes CdaA is the sole diadenylate cycl

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

101 Listeria monocytogenes cells were grown at 37 degrees C

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

103 vaccination increasing protection against a Listeria monocytogenes challenge.

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

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

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

107 w that perforin-2 is critical for inhibiting Listeria monocytogenes colonization of the placenta and

108 pathogens such as Staphylococcus aureus and Listeria monocytogenes, DacA in S. pyogenes was not esse

109 and for an efficient immune defense against Listeria monocytogenes Deletion of TYK2 in NK cells did

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

111 igen-specific CD4(+)CD8alphaalpha(+) IELs by Listeria monocytogenes did not alter their state but cor

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

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

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

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

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

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

118 pneumonia induced by Staphylococcus aureus, Listeria monocytogenes, Escherichia coli, Citrobacter ro

119 pneumonia induced by Staphylococcus aureus, Listeria monocytogenes, Escherichia coli, Citrobacter ro

120 -2S4B6-treated HSCT recipients infected with Listeria monocytogenes exhibited decreased bacterial lev

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

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

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

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

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

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

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

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

129 e cholesterol to elucidate how 25HC prevents Listeria monocytogenes from traversing the plasma membra

130 Listeria monocytogenes FrvA (Lmo0641) is critical for vi

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

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

133 coli (E. coli), Group B Streptococcus (GBS), Listeria monocytogenes, Haemophilus influenzae, S. aureu

134 Live-attenuated Listeria monocytogenes has shown encouraging potential a

135 Listeria monocytogenes hijacks host actin to promote its

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

137 the effect of R848 on host susceptibility to Listeria monocytogenes in a murine challenge model and d

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

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

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

141 of either BALB/cByJ or C57BL/6J mice to kill Listeria monocytogenes in vitro.

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

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

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

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

146 Importantly, Listeria monocytogenes induces NLRP3-dependent rapid cas

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

148 y signaling leading to cytokine secretion in Listeria monocytogenes-infected macrophages.

149 show that heterogeneity in susceptibility to Listeria monocytogenes infection among primary human vas

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

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

152 ate that VPA increases the susceptibility to Listeria monocytogenes infection and suggest that NK cel

153 ixture enhances both host resistance against Listeria monocytogenes infection and the therapeutic eff

154 nous in vivo ISGylome in the liver following Listeria monocytogenes infection by combining murine mod

155 tion and profilin (PRF) confer resistance to Listeria monocytogenes infection in a CCR2-dependent man

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

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

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

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

160 and resident memory T cells after foodborne Listeria monocytogenes infection of mice.

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

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

163 P2X5 is a protective immune regulator during Listeria monocytogenes infection, as P2X5-deficient mice

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

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

166 and conferred protection against recombinant Listeria monocytogenes infection.

167 and dampened innate immune responses against Listeria monocytogenes infection.

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

169 -lived effector cells in vivo in response to Listeria monocytogenes infection.

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

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

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

173 ntaneous immune activation and resistance to Listeria monocytogenes infection.

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

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

176 priming but, paradoxically, promote splenic Listeria monocytogenes infection.

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

178 Listeria monocytogenes is a bacterial parasite that uses

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

180 Listeria monocytogenes is a facultative intracellular pa

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

182 Listeria monocytogenes is a facultative intracellular pa

183 Listeria monocytogenes is a food-borne pathogen that can

184 Listeria monocytogenes is a foodborne pathogen capable o

185 Listeria monocytogenes is a foodborne pathogen causing s

186 Listeria monocytogenes is a foodborne pathogen responsib

187 Listeria monocytogenes is a foodborne pathogen that caus

188 Listeria monocytogenes is a foodborne pathogen that caus

189 Listeria monocytogenes is a foodborne, facultative intra

190 Listeria monocytogenes is a Gram-positive bacterium that

191 Listeria monocytogenes is a Gram-positive facultative in

192 Listeria monocytogenes is a gram-positive facultative in

193 Listeria monocytogenes is a Gram-positive intracellular

194 Listeria monocytogenes is a Gram-positive intracellular

195 Listeria monocytogenes is a Gram-positive, intracellular

196 Listeria monocytogenes is a highly adaptive bacterium th

197 Listeria monocytogenes is a human bacterial pathogen tha

198 Listeria monocytogenes is a major cause of mortality res

199 Listeria monocytogenes is a major intracellular human fo

200 Listeria monocytogenes is a serious cause of human foodb

201 However, we previously showed that Listeria monocytogenes is able to avoid the NOX2 activit

202 Infection with Listeria monocytogenes is acquired through ingestion of

203 Listeria monocytogenes is an intracellular Gram-positive

204 Listeria monocytogenes is an intracellular pathogen resp

205 Listeria monocytogenes is an intracellular pathogen that

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

207 Listeria monocytogenes is responsible for gastroenteriti

208 Listeria monocytogenes is responsible for the life-threa

209 positive, facultative intracellular pathogen Listeria monocytogenes is unusual because it carries all

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

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

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

213 ons and used whole-genome sequencing to type Listeria monocytogenes isolates.

214 udy aimed to evaluate the role of VPA during Listeria monocytogenes (L.m) infection, and whether NK c

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

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

217 Attenuated Listeria monocytogenes (Lm(at)-LLO) represents a valuabl

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

219 Listeria monocytogenes (Lm) causes severe foodborne illn

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

221 epidemiology of the major foodborne pathogen Listeria monocytogenes (Lm) in Europe and North America,

222 The bacterial pathogen Listeria monocytogenes (Lm) invades host cells, ruptures

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

224 reviously shown that systemic infection with Listeria monocytogenes (Lm) months after transplantation

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

226 ravillous trophoblasts to kill intracellular Listeria monocytogenes (Lm) without killing the trophobl

227 eventing fatal infection caused by foodborne Listeria monocytogenes (Lm), is inconsistent.

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

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

230 response to an acute systemic infection with Listeria monocytogenes (Lm).

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

232 in Firmicutes, including the human pathogen Listeria monocytogenes, making it essential for growth.

233 s observed during the CD8 T cell response to Listeria monocytogenes Memory cells mounted larger secon

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

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

236 In Listeria monocytogenes, mutations that prevent addition

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

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

239 allow the presence of the foodborne pathogen Listeria monocytogenes) on equipment and environment sur

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

241 Mice were subsequently infected with Listeria monocytogenes or Clostridioides difficile, foll

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

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

244 Listeria monocytogenes PdxR is a member of the poorly ch

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

246 olysin O (LLO) of the intracellular pathogen Listeria monocytogenes promotes egress of the bacteria f

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

248 In Listeria monocytogenes, prophages encode two to three di

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

250 profile diverse microbial species including Listeria monocytogenes, Proteus mirabilis, and Escherich

251 facultative intracellular bacterial pathogen Listeria monocytogenes remodels its transcriptional prog

252 Pathogenic Listeria monocytogenes replicates within the host cytoso

253 Studies on the roles of phospholipases in Listeria monocytogenes revealed distinctions between its

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

255 al activity of CAR against Escherichia coli, Listeria monocytogenes, Salmonella enterica and Staphylo

256 By developing and analyzing 720 Listeria monocytogenes, Salmonella enterica, and Escheri

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

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

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

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

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

262 Listeria monocytogenes serotype 4b was more common in pr

263 Since Listeria monocytogenes, Shigella flexneri, and Vaccinia

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

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

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

267 ion to high densities of an orally-delivered Listeria monocytogenes strain carrying an antigen of cho

268 NDH-2 from Caldalkalibacillus thermarum and Listeria monocytogenes strain EGD-e while bound to nativ

269 ival of outbreak-associated and non-outbreak Listeria monocytogenes strains on Red Delicious, Granny

270 , Staphylococcus lugdunensis, Listeria spp., Listeria monocytogenes, Streptococcus spp., Streptococcu

271 we determined the atomic organization of the Listeria monocytogenes stressosome at 3.38 angstrom reso

272 Listeria monocytogenes temperate phages encode up to thr

273 ily orthologue in the intracellular pathogen Listeria monocytogenes that is essential for aerobic gro

274 ion studies were conducted using a strain of Listeria monocytogenes that served as a robust xenophagi

275 In Listeria monocytogenes, the sole diadenylate cyclase, Da

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

277 Using recombinant Listeria monocytogenes to prime stably differentiated Th

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

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

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

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

282 In Listeria monocytogenes, two enzymes are required for the

283 The facultative intracellular pathogen Listeria monocytogenes uses an actin-based motility proc

284 rly immune response in the intestine against Listeria monocytogenes Using a modified strain of L. mon

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

286 Listeria monocytogenes V7 and Salmonella enterica serova

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

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

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

290 in" with growth-suppressive activity against Listeria monocytogenes was characterized.

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

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

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

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

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

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

297 CRISPR-Cas systems from Escherichia coli and Listeria monocytogenes, which target DNA via a multi-com

298 lin-susceptible S. aureus (MSSA), S. aureus, Listeria monocytogenes, whilst the FE acted as a moderat

299 C films enriched with 2% (w/w) RE against to Listeria monocytogenes with 20.3 +/- 2.5 mm zone diamete

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