ライフサイエンスコーパス: infection with

1 ced autophagy and DNA damage repair, whereas infection with 11G5DeltaclbQ did not.

2 cts were studied (7.5% develop gram-negative infection), with 4,768 fecal samples for analysis.

3 e risk reduction in developing postoperative infection, with 6 donors requiring treatment to prevent

4 ecoming increasingly apparent that secondary infection with a closely related flavivirus strain can r

5 iver mechanisms of microbial dysbiosis after infection with a fast-spreading virus.

6 ) may worsen the course of hepatitis C virus infection with a greater risk of liver cirrhosis (LC) an

7 We found that pulmonary but not systemic infection with a high-virulence strain of C. neoformans

8 Infection with a L. monocytogenes mutant impaired in c-d

9 We show that co-infection with a low dose of T. muris that leads to the

10 rnal immune activation (MIA) accomplished by infection with a mouse-adapted influenza virus during pr

11 istent type 2 immune response to respiratory infection with a natural pathogen (Sendai virus).

12 ls within the CNS at defined times following infection with a neuroadapted murine coronavirus using s

13 ine developmental strategies, including that infection with a particular influenza A virus should off

14 In contrast to infection with homologous RV, infection with a STAT1-sensitive heterologous RV strain

15 In this study, we show that infection with a typical neurotropic virus, RABV, can in

16 T(-/-)) mice were highly resistant to lethal infection with a virulent poxvirus strain and that deple

17 Our study demonstrates that infection with a virus that persistently replicates in t

18 lls following GFP-DDDHA infection than after infection with a wild-type (WT) strain.

19 We observed that infection with A/Fort Monmouth/1/1947(H1N1) IAV signific

20 tion of MAL led to a significant decrease in infection, with a drastic reduction in the number of lyt

21 function of human NK cells in chronic HIV-1 infection, with a particular focus on characterizing FcR

22 e report that cats are highly susceptible to infection, with a prolonged period of oral and nasal vir

23 We demonstrate that cervical infections with a greater burden of somatic HPV16 APOBEC

24 We find that systemic infections with a variety of pathogens trigger a hypofer

25 We report the identification of two human infections with A(H1N1)pdm09 viruses originating from sw

26 o estimate daily numbers of vaccinations and infections with A/H1N1, A/H3N2, and B viruses.

27 well-accepted non-human primate model of HIV infection, with adeno-associated virus 9 (AAV9)-CRISPR/C

28 intervals for associations between drugs and infection, with adjustment for confounders, were estimat

29 rotype ayw)-either from a transgene or after infection with an adeno-associated virus that transferre

30 In an infection with an Enterobacter sp. isolate producing Kle

31 We reveal a novel mechanism through which infection with an extracellular pathogen leads to pyropt

32 mpared with typical acute pediatric COVID-19 infection, with an emphasis on thoracic imaging findings

33 ia is a hallmark of arthritogenic alphavirus infections, with an exceptionally higher morbidity obser

34 397 had 881 CT infections and 331 had 861 GC infections, with an incidence of 2.95 and 2.88 per 100 p

35 igators sought to determine the frequency of infection with and without the use of topical antibiotic

36 Corneal infections with antibiotic-resistant microorganisms are

37 ies are surprisingly boosted upon subsequent infections with antigenically distinct influenza A virus

38 n-depth analysis following robust SARS-CoV-2 infection with authentic patient-derived virus in mice o

39 nfect swine; however, only sporadic cases of infection with avian IAVs are reported in domestic swine

40 hat depletion of regulatory T cells prior to infection with B. burgdorferi resulted in sustained swel

41 rucella spp. was the most common bloodstream infection, with B. melitensis isolated from seven partic

42 l transcriptome and translatome during lytic infection with base-pair resolution by computational int

43 Infection with BCG was shown to exert a detrimental effe

44 Infection with BI strains of C. difficile predicted poor

45 expression relevant for the control of viral infection, with both proteins potentially facilitating t

46 n addition, effective treatments for chronic infections with both HBV and HCV should contribute to de

47 centration of secretory IgA (SIgA) following infection with C rodentium.

48 During infection with C. burnetii, both TFEB and TFE3 were acti

49 However, infection with Ca.

50 tion of iron homeostasis in macrophages upon infection with Candida glabrata and exacerbate infection

51 Moreover, p.o. immunization or infection with Chlamydia confers protection against per-

52 mation-follicular (TF) is common, but ocular infection with Chlamydia trachomatis is not.

53 ng childhood following repeated conjunctival infection with Chlamydia trachomatis, which causes a chr

54 WNT4 in colonic crypts at days 6 and 12 post-infection with Citrobacter rodentium (CR) and tended to

55 G(-/-) mice were more susceptible to enteric infection with Citrobacter rodentium compared to wild-ty

56 memory IgA production in the intestines upon infection with Citrobacter rodentium, the percentage of

57 SS, transfer of CD4(+)CD45RB(hi) T cells, or infection with Citrobacter rodentium.

58 ir emergence in Indonesia in 2005, 200 human infections with clade 2.1 highly pathogenic avian influe

59 burden in mice and rescues mice from lethal infections with clinical isolates of Acinetobacter bauma

60 iseases (IBD) are particularly vulnerable to infection with Clostridioides difficile (CDI).

61 influences the severity of colitis caused by infection with Clostridioides difficile, we coinfected m

62 inically silent in this patient until lethal infection with CMV.

63 responses without significant illness after infection with community-acquired RSV.

64 s a broad capacity to neutralize and prevent infection with contemporary H3N2 strains.

65 ere acute respiratory syndrome coronavirus 2 infection, with COVID-19 symptom onset within 7 days and

66 +) helper T (T(H)2) cell bias upon pulmonary infection with Cryptococcus neoformans and other non-T(H

67 rtoire and its affinity during the course of infection with cytomegalovirus, which elicits large T ce

68 compared results from simulated and clinical infections with data from known reference strains and Il

69 tibody response is typical of an acute viral infection, with declining neutralizing antibody titres o

70 can be used in future models to describe co-infection with defective interfering particles, which ar

71 d cellular turnover due to long-standing HIV infection with delayed cART initiation.

72 stimate of the association between H. pylori infection with diabetes was OR = 1.27 (95% CI 1.11 to 1.

73 sing the vulnerability of elephant calves to infection with different EEHVs and evaluating antibody r

74 fic CD4+ T cells longitudinally during acute infection with different infection outcomes.

75 within lesion pathology, and differences in infection with different strains of Mycobacterium tuberc

76 f BN in infants with acute respiratory tract infections with different degrees of disease severity.

77 ologic assay capable of distinguishing among infections with different EEHVs using a luciferase immun

78 correlate antibody kinetics and sequence of infections with disease outcomes.

79 imate the adjusted effect of ASP on rates of infection with drug-resistant organisms.

80 Furthermore, infection with E1B55K-deleted virus resulted in an incre

81 tein abundance and progeny production during infection with E1B55K-deleted virus.

82 Expected frequencies of concurrent infection with each pairwise combination of the vaccine

83 inal model to investigate Pic's roles during infection with EAEC.

84 -catenin transcriptional activity during Ad5 infection, with early viral protein E4orf1 sufficient to

85 roblast-like synoviocytes were permissive to infection with Ebola and Marburg viruses in vitro.

86 T) is a neglected tropical disease caused by infection with either of two subspecies of the parasite

87 lymphoid tissue (iBALT) forms in response to infection with either wild-type cryptococci or the mutan

88 Rocky Mountain spotted fever, are tick-borne infections with frequent neurologic involvement.

89 n treatment-emergent adverse events included infections with grades 3 or 4 neutropenia (n=79, 47%) an

90 romotes NLRP3 inflammasome activation during infection with Gram-negative bacteria.

91 ute lymphoblastic leukemia (ALL) to decrease infections with gram-negative bacteria.

92 In addition, IAV can cause pandemic infections with great consequences when new viruses are

93 After 3 months of infection with H felis, Nlrc5(mo-KO) mice developed gast

94 Infection with H. pylori is the main risk factor for dis

95 PEH were at higher risk of infection with HAV and of severe hepatitis A disease out

96 in patients with alcohol use, older age, and infection with HCV genotype 3.

97 t common cause of cancer death worldwide, is infection with Helicobacter pylori bacterial strains tha

98 and PCs subsequent to primary and secondary infection with helminths.

99 00 persons in the US are living with chronic infection with hepatitis B virus (HBV).

100 lation with poly(I.C) double-stranded RNA or infection with herpes simplex virus 2 (HSV-2).

101 s a common healthcare-associated bloodstream infection with high morbidity and mortality.

102 nes is a foodborne pathogen causing systemic infection with high mortality.

103 nii is a successful pathogen responsible for infections with high mortality rate.

104 irds and poultry and continue to cause human infections with high mortality.

105 s indicated a graded increase in the risk of infection with higher levels of FGF23 (HR, 1.51; 95% CI,

106 enera were identified as associated with HIV infection, with higher abundances of Ruminococcus and Os

107 Infections with Histoplasma can range from asymptomatic

108 In contrast to infection with homologous RV, infection with a STAT1-sen

109 to provide 100% lifetime protection against infections with HPV types 16, 18, 31, 33, 45, 52, and 58

110 we recovered cell populations that survived infection with HSV-1 at high MOI.

111 Infection with human cytomegalovirus (HCMV) remains a si

112 transmitted disease, sex with men (for men), infection with human immunodeficiency virus, and injecti

113 female-to-male (F-M) transmission of genital infection with human papillomavirus (HPV) relative to ma

114 arynx cancers are increasingly attributed to infection with human papillomavirus (HPV), primarily HPV

115 Antiviral drugs for managing infections with human coronaviruses are not yet approved

116 Our results indicate that during infection with IAV, and likely a multitude of other huma

117 piratory syndrome coronavirus 2 (SARS-CoV-2) infection, with incidence rates varying from 8 to 33% de

118 ro-positivity, periodontal disease (Pd), and infections with incident AD and all-cause dementia, amon

119 their trafficking repertoires as a result of infection, with increased expression of CD103 in colon N

120 Clinical features did not distinguish among infection with individual PIV serotypes in patients hosp

121 e and autoreactive immune responses, linking infection with induction of autoimmunity in the human im

122 n in response to other treatments.IMPORTANCE Infection with influenza A virus (IAV) infection is resp

123 e TLR pathways (TLR4, TLR1/2, and TLR7/8) or infection with influenza A virus.

124 Infection with influenza can be aggravated by bacterial

125 We have shown that in mice, prior infection with influenza results in increased inflammati

126 We compared live infection with influenza to an inactivated whole influen

127 Controlled infection with intestinal nematodes has therapeutic pote

128 Infections with intestinal worms, such as Ascaris lumbri

129 Infection with laboratory-adapted Mtb H37Rv resulted in

130 Previous infection with LASV protects from disease after subseque

131 Here, we show that viral infection with LCMV results in type I IFN-dependent Treg

132 e effector Th1 response to an acute systemic infection with Listeria monocytogenes (Lm).

133 ry tract infections and skin and soft tissue infections with local pharmacists.

134 evels of PD-1 during acute, but not chronic, infection with lymphocytic choriomeningitis virus (LCMV)

135 Using murine infection with lymphocytic choriomeningitis virus, we de

136 egulation of CD8(+) T cell fate during acute infection with lymphocytic choriomeningitis virus.

137 the increasing number of reports of primary infection with M tuberculosis or reactivation of latent

138 d in a-nucleated erythrocytes in response to infection with malaria parasites, but the extent of this

139 ts on epitope display at individual sites of infection with MCMV.

140 erwent Ag-driven proliferation during latent infection with MCMV.

141 ry infections, including 14 cases (17.9%) of infections with MDROs, and 13 cases (16.9%) of de novo/r

142 with sepsis and select chronic diseases had infections with methicillin-resistant S. aureus, fungal

143 We further demonstrate that infection with MHV induces a severe attack on host cell

144 mal models, remdesivir was effective against infection with Middle East respiratory syndrome coronavi

145 Human infection with Middle East respiratory syndrome coronavi

146 a case of hydrops fetalis secondary to cCMV infection with minimal sequelae after maternal and subse

147 sceptible to a transient lower genital tract infection with MmuPV1 mouse papillomavirus and display f

148 TV and did not increase in numbers following infection with mouse CMV (MCMV).

149 Notably, in vivo infection with Mtb led to sustained DSBs and ATM activat

150 lantation are vulnerable to colonization and infection with multidrug-resistant organisms, including

151 pment of novel antibacterial drugs to combat infections with multidrug-resistant bacterial pathogens.

152 Infection with multiple CMV genotypes was common during

153 Infection with multiple cytomegalovirus (CMV) strains (m

154 Infection with multiple HPV types was more common among

155 aluated the host transcriptional response to infection with murine coronaviruses encoding independent

156 ust up-regulation of several PARPs following infection with murine hepatitis virus (MHV), a model cor

157 ers in the spleen were observed during acute infection with myeloid-restricted ZIKV that precluded th

158 NV-32, protected ferrets in lethal models of infection with NiV Bangladesh 3 days after exposure.

159 eins VP2/3 that is a potent inhibitor of BKV infection with no observable cellular toxicity.

160 3) between sepsis with organ dysfunction and infection with no organ dysfunction.

161 in vivo antiviral host response 7 days post infection, with no induction of interferon-stimulated ge

162 dy describes the prevalence of SARS-CoV-2 co-infection with noncoronavirus respiratory pathogens in a

163 ; and the difference in mean change in IR of infections with omega-3s vs no omega-3s was -0.13 (99% C

164 lammation, bacterial and viral infection and infection with or without organ dysfunction.

165 their recent expansion across the world, co-infections with other highly prevalent pathogens such as

166 rotect bacteria and archaea from viruses and infections with other mobile genetic elements." There is

167 dual serotypes 1, 2, and 3 and among all PIV infections with other viral, atypical, and bacterial pne

168 immunostimulatory treatments or experimental infections with other viruses.

169 Importantly, polymicrobial infection with P. aeruginosa elicited significantly high

170 is to be contrasted with chronic respiratory infection with P. aeruginosa, suggesting that either the

171 falciparum gametocytes and, on experimental infection with P. falciparum, sporozoites aren't detecte

172 Infection with PAO1 elicited significant increases in pr

173 Early childhood infection with parainfluenza virus or respiratory syncyt

174 owever, a comprehensive understanding of how infections with pathogens that exhibit distinct capabili

175 Infection with Plasmodium falciparum leads to severe mal

176 gitudinal analysis before, during, and after infection with Plasmodium falciparum malaria.

177 Infection with Plasmodium falciparum results in immune d

178 essment of host erythrocyte signaling during infection with Plasmodium falciparum.

179 bs) isolated from a survivor of natural EEEV infection with potent (<20 pM) inhibitory activity of EE

180 ine suspended in 0.9% NaCl prevents cellular infection with pp-SARS-CoV-2 spike.

181 ons of sphingosine prevented adhesion of and infection with pp-VSV-SARS-CoV-2 spike.

182 Infection with protozoa of the genus Cryptosporidium is

183 in VZV infection and least utilized in HSV1 infection, with PRV's usage being closer to HSV1's usage

184 . maltophilia alone and during polymicrobial infection with Pseudomonas aeruginosa Colonization, pers

185 s failure (hazard ratio, 3.39; P = .045) and infections with QR-GNB were independently associated wit

186 ession levels of pro-IL-1beta in response to infection with R. australis, suggesting that rickettsiae

187 ill facilitate differentiation of actual IAV infection with replicating virus versus individuals expo

188 Unexpectedly, infection with respiratory syncytial virus alters Rab11A

189 have been attitudinal changes regarding HIV infection with resultant increases in sexual contact and

190 hypothesized that elevated stool toxins and infection with ribotype 027 associate with severe diseas

191 In response to infection with RNA viruses, host nonself RNA sensors rec

192 les exhibited spontaneous neonatal bacterial infections with robust mucoinflammatory features, includ

193 green monkeys received a primary intranasal infection with RSV and were given a boost with RSV or a

194 ived a primary infection with RSV, a booster infection with RSV ~6 weeks later was completely restric

195 In hamsters that received a primary infection with RSV, a booster infection with RSV ~6 week

196 ts with Staphylococcus aureus Chronic tissue infection with S. aureus was associated with BPI antibod

197 During infection with Salmonella and many other pathogens, flag

198 ficant implications for the establishment of infection with Salmonella.

199 ently been proposed as a strategy to prevent infection with SARS-CoV-2 (CoV-2) to combat the COVID-19

200 Infection with SARS-CoV-2 can lead to excessive producti

201 developed for SARS studies(4), we show that infection with SARS-CoV-2 causes severe disease in the l

202 Finally, we show that infection with SARS-CoV-2 damages the choroid plexus epi

203 Infection with SARS-CoV-2 has become pandemic and the du

204 The COVID-19 pandemic caused by infection with SARS-CoV-2 has led to more than 200,000 d

205 inflammatory syndrome apparently related to infection with SARS-CoV-2 has recently been reported in

206 thics and practicalities of controlled human infection with SARS-CoV-2 have been widely discussed.

207 Although the diagnosis of infection with SARS-CoV-2 is microbiological, imaging te

208 Although infection with SARS-CoV-2 is usually mild in children, s

209 Infection with SARS-CoV-2 occurred in 42 participants re

210 A key unanswered question is whether infection with SARS-CoV-2 results in protective immunity

211 -19, nor are there any vaccines that prevent infection with SARS-CoV-2, and efforts to develop drugs

212 COVID-19, the disease caused by infection with SARS-CoV-2, requires urgent development o

213 ter model(2) and in macaques, YF-S0 prevents infection with SARS-CoV-2.

214 or targeted testing had positive results for infection with SARS-CoV-2.

215 on an X-ray could represent pneumonia due to infection with SARS-CoV-2.

216 reatment of cells with heparinase diminished infection with SBV, confirming that heparan sulfate play

217 but its role in urogenital schistosomiasis, infection with Schistosoma haematobium worms, remains po

218 y tract were associated with the severity of infection with seasonal or avian influenza virus.

219 ross-analyzed chronic lung disease caused by infection with Sendai virus (SeV) or influenza A virus i

220 x5 knockout in mice enhances lethality after infection with several human viruses.

221 the intensive care unit (ICU) with confirmed infection with severe acute respiratory syndrome coronav

222 e vast majority of individuals succumbing to infection with severe acute respiratory syndrome coronav

223 whether immunotherapies increase the risk of infection with severe acute respiratory syndrome coronav

224 Of these, 341 (81%) had laboratory-confirmed infection with severe acute respiratory syndrome coronav

225 durability of the humoral immune response to infection with severe acute respiratory syndrome coronav

226 ltisystem organ involvement, and evidence of infection with severe acute respiratory syndrome coronav

227 Testing of vaccine candidates to prevent infection with severe acute respiratory syndrome coronav

228 Infection with severe acute respiratory syndrome coronav

229 serologic assays for the detection of prior infection with severe acute respiratory syndrome coronav

230 Antibody tests for detecting past infection with severe acute respiratory syndrome coronav

231 al contact carries some risk for exposure to infection with severe acute respiratory syndrome coronav

232 eferral versus risk of death from nosocomial infection with severe acute respiratory syndrome coronav

233 Infection with severe acute respiratory syndrome coronav

234 A total of 6272 case patients in whom infection with severe acute respiratory syndrome coronav

235 nts (57.3%) presented with proven SARS-CoV-2 infection with severe ARDS requiring PP.

236 e frequency and geographical distribution of infections with severe acute respiratory syndrome corona

237 from warmer- to cooler-bodied species caused infections with shorter incubation periods that were ass

238 Infection with sialidase-producing P. timonensis resulte

239 binding to JC polyomavirus VP1 and inhibits infection with similar potency to BKV in a model cell li

240 ming(2), several recent studies suggest that infection with some viruses, including Epstein-Barr viru

241 ied among the H5N6 viruses tested, from mild infection with sporadic virus dissemination beyond the r

242 y T cells promoted bacterial clearance after infection with Staphylococcus aureus and, by licensing e

243 est that genomes entering neurons from HSV-1 infections with strain KOS(M) are more prone to rapid he

244 or PANDAS, describes such a situation after infection with Streptococcus pyogenes.

245 investigate serum N-glycomics changes during infection with T. gondii in BALB/c mice, immunocompetent

246 ve studies, we hypothesized that a prolonged infection with T. gondii may protect against age-associa

247 es clinical and laboratory manifestations of infection with T. pallidum.

248 ver, research into associations of rotavirus infections with T1D development in humans have yielded m

249 ars to reduce the risk of medically attended infection with that subtype throughout life.

250 Chronic infection with the apicomplexan parasite Toxoplasma corr

251 dentify novel host cell factors required for infection with the beta-herpesvirus murine cytomegalovir

252 Symptomatic and asymptomatic infection with the diarrheal pathogen enteroaggregative

253 ally tested the model by inhibiting low dose infection with the drug tenofovir, which interferes with

254 e capacity to produce IgG are protected from infection with the enteric pathogen enterotoxigenic Esch

255 Among the taxa enriched by infection with the fast-spreading virus, Akkermansia muc

256 the metabolic rewiring of macrophages during infection with the fungal pathogen Aspergillus fumigatus

257 Here, we established that infection with the gammaherpesvirus MHV68 leads to a dra

258 Infection with the Gram-negative bacterium Helicobacter

259 Infection with the Gram-negative, microaerophilic bacter

260 Chronic hepatitis B is caused by prolonged infection with the hepatitis B virus (HBV), which can su

261 ide dynamics of protein complexes throughout infection with the herpesvirus, human cytomegalovirus (H

262 Infection with the human CMV associates with phenotypic

263 at increased risk for morbidities related to infection with the human papillomavirus (HPV), yet their

264 esults on age-related changes in response to infection with the influenza virus and on the factors kn

265 the host proteome response during macrophage infection with the intracellular bacterial pathogen Salm

266 that most of those that recovered from acute infection with the LCMV Armstrong (Arm) strain survive.

267 Here we demonstrate that infection with the murine coronavirus mouse hepatitis vi

268 Infection with the novel severe acute respiratory syndro

269 g receptor-blocking antibodies, we show that infection with the PDF2180 spike does not require MERS-C

270 Here, we demonstrate that infection with the periodontal pathogen Porphyromonas gi

271 Infection with the recombinant A4G (rA4G) RSV mutant res

272 del of CM, experimental CM (ECM), induced by infection with the rodent parasite, Plasmodium berghei A

273 ly better response if the host is exposed to infection with the same pathogen.

274 with acute respiratory deterioration during infection with the severe acute respiratory syndrome cor

275 Rationale: Infection with the severe acute respiratory syndrome cor

276 Infection with the severe acute respiratory syndrome nov

277 easurements carried out after murine aerosol infection with the virulent SCHU S4 strain of the bacter

278 lance data in Colombia suggest that maternal infection with the Zika virus during the third trimester

279 For infections with the obligate intracellular bacterium Chl

280 e induced by severe infections, including in infections with the related virus SARS-CoV.

281 fine their unique disease profiles following infection with Theiler's Murine Encephalomyelitis Virus,

282 cted, disease is almost always attributed to infection with these pathogens.

283 response fails to develop following prostate infection with these uropathogens, leading to chronic di

284 o integrate treatment for IDU-associated HIV infections with treatment for drug use disorders.

285 ANCE KS is a prevalent tumor associated with infections with two distinct viruses, KSHV and HIV.

286 s, over a period of 13 months during natural infections with two Theileria spp., pathogenic (T. lesto

287 In children younger than 24 months with MSD, infection with typical enteropathogenic Escherichia coli

288 function that predisposes the host to severe infections with unrelated pathogens.

289 Infection with Ureaplasma species (spp) has been linked

290 g B cells were more resistant to respiratory infection with vaccinia virus than wild-type mice.

291 mune responses are susceptible to persistent infection with variable manifestations of histopathologi

292 Infections with varicella-zoster virus (VZV) are associa

293 reactive PrP(Sc) in experimental and natural infections with various mouse-adapted scrapie strains an

294 Finally, PGAM5 deficient MEFs, upon infection with vesicular stomatitis virus (VSV), reveale

295 Indeed, infection with viruses lacking E7 abrogated most transcr

296 We found that butyrate increases cellular infection with viruses relevant to human and animal heal

297 Surprisingly, similarly to WT, infection with W105A inhibited IFN/ISG expression despit

298 to ineffective control of the pathogen after infection with wild-type cells.

299 Infection with WNV results in febrile illness, which can

300 detects a broad range of pathogens and mixed infections with yeast and Gram-negative organisms from t