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1 genes (ISGs) being the most affected by both lactobacilli.
2 teria and levels of Streptococcus mutans and Lactobacilli.
3 or total bacteria, Streptococcus mutans, and Lactobacilli.
4 toxicity, and does not inhibit the growth of lactobacilli.
5 is also highly conserved in streptococci and lactobacilli.
6 onii is a member of the acidophilus group of lactobacilli.
7 ng the rectum may be a reservoir for vaginal lactobacilli.
8 he identification of 97 strains of commensal lactobacilli.
9 edictive of an absence of H(2)O(2)-producing lactobacilli.
10 strains as well as other species of vaginal lactobacilli.
11 unique DNA fingerprint compared to all other lactobacilli.
12 colonized with commensal bacteria, primarily lactobacilli.
13 ilus, are the most common species of vaginal lactobacilli.
14 nowledge about the action mode of antifungal lactobacilli.
15 ift involves organisms other than the MS and lactobacilli.
16 the anti-inflammatory effects of beneficial lactobacilli.
17 en have microbiota that are not dominated by lactobacilli.
18 lly digested patterns of previous reports on lactobacilli.
19 ven rennet was assessed for the existence of lactobacilli.
20 the increasing use of probiotics containing lactobacilli.
21 thesis about the natural history and role of lactobacilli.
22 hibit growth of vaginal protective commensal lactobacilli.
23 (+) T lymphocytes and vaginal H2O2-producing lactobacilli.
24 pecific traits in the genomes of the vaginal lactobacilli.
26 n a pathogen-free facility were colonized by Lactobacilli, a component of the oropharyngeal flora.
30 resent (community type L) and those in which lactobacilli accounted for less than 50% of the species
31 seudoalteromonas, Burkholderia, Bacteroides, Lactobacillis, Acetobacter, Allobaculum, Ruminococcus, a
33 lactobacilli were inversely associated with lactobacilli adhesion to epithelial cells and D-lactate
34 rations, and decreased relative abundance of lactobacilli after one and six months of use, relative t
40 ted sustained colonization by H2O2-producing lactobacilli among women already colonized (relative ris
42 s: a nucleoside deoxyribosyltransferase from lactobacilli and a 5'-monophosphate-2'-deoxyribonucleosi
43 ant aciduric bacteria from root lesions were lactobacilli and A. israelii, while from sound root surf
46 l women have a relative depletion of vaginal lactobacilli and an increase in vaginal E. coli compared
49 daily dose of the Lab4P probiotic comprising lactobacilli and bifidobacteria (50 billion cfu/day).
51 o evidence that a multistrain preparation of lactobacilli and bifidobacteria was effective in prevent
52 ia, while a slight increase on the growth of lactobacilli and bifidobacteria was observed after expos
53 monkeys differ in the relative abundances of Lactobacilli and Bifidobacteria, two taxa predominant in
54 receive either a multistrain preparation of lactobacilli and bifidobacteria, with a total of 6 x 10(
55 nal flora characterized by reduced levels of lactobacilli and concomitant overgrowth of anaerobic bac
56 obial community was found to be dominated by Lactobacilli and Enterobacteria, both typically facultat
57 ired microflora in mayonnaise preserved with lactobacilli and essential oils decreased significantly
58 We conclude that the association between lactobacilli and gonococci is complex and may be subject
59 0) had significantly lower concentrations of lactobacilli and higher concentrations of Gardnerella va
61 g thus allows high efficiency mutagenesis in lactobacilli and lactococci, and may be used to further
63 sers demonstrated an increased prevalence of lactobacilli and non-albicans yeast, while dapivirine ri
64 aginal bacterial flora with disappearance of lactobacilli and overgrowth of Gardnerella vaginalis and
65 nosis (BV) is characterized by low levels of lactobacilli and overgrowth of potential pathogens in th
66 aracterized by the replacement of beneficial lactobacilli and the augmentation of anaerobic bacteria.
67 aginal microbiota is frequently dominated by lactobacilli and transition to a more diverse community
68 ptide production, which allows overgrowth of Lactobacilli and triggers T regulatory cell expansion in
69 he inverse association between H2O2-positive lactobacilli and vaginal E. coli colonization remained i
70 le to displace pre-coated vaginal protective lactobacilli and we hypothesize this to be a trigger for
71 ensal gut bacteria (e.g., bifidobacteria and lactobacilli) and increase the abundance of enterobacter
72 aginal probiotic (G3, oral placebo + vaginal lactobacilli), and probiotic combination (oral lactic ac
73 nderstood, and although mutans streptococci, lactobacilli, and A. naeslundii have been implicated in
74 onserved in streptococci, staphylococci, and lactobacilli, and are required for bacterial biofilm for
75 totoxicity, lack of activity against vaginal lactobacilli, and effectiveness against both HSV-2 and H
76 s, salivary log10 mutans streptococci, log10 lactobacilli, and fluoride level, did not represent stat
77 olved in fatty acid biosynthesis, amounts of lactobacilli, and saturated LCFA were measured in fecal
78 vels of Bifidobacteria, mutans streptococci, lactobacilli, and yeasts were correlated with each other
79 genous microbes that stably colonize a host, lactobacilli appear to be planktonic, opportunistic sett
81 h an associated decrease in caries, if these lactobacilli are fed to rats in an established caries mo
84 en who are colonized with H(2)O(2)-producing lactobacilli are more likely to maintain a normal vagina
92 hat reduced levels of core bacteria, such as lactobacilli, are associated with conditions like bacter
93 sufficient data exist to support the use of lactobacilli as candidates for the development of new or
94 was altered tryptophan metabolism in airway lactobacilli associated with reduced indole-3-acetic aci
99 lationship between vaginal colonization with lactobacilli, bacterial vaginosis (BV), and acquisition
102 S DP (1-4) derived from LBG supported better Lactobacilli biofilm formation as compared to KG hydroly
103 genetic and biochemical characterization of lactobacilli BSHs lend to a model of Lactobacillus adapt
104 ffect vaginal colonization by H2O2-producing lactobacilli but that such use may promote loss of non-H
105 udies have shown that oral administration of lactobacilli can be an efficient approach to treat lacta
107 y infectious HIV-1 particles, the engineered lactobacilli can potentially capture HIV-1 of different
111 0%), and L. gasseri (10%) were the prevalent lactobacilli colonizing the rectums of 290 females.
112 ophilus CRL 1014 on microbial metabolism and lactobacilli community composition for improving human h
113 The DGGE obtained showed changes in the lactobacilli community from the colon compartments of th
118 L. monocytogenes infection by treatment with lactobacilli correlates with a decrease in host gene exp
119 obacilli in the vagina, suggest that vaginal lactobacilli could reacidify the vagina at the rate obse
120 ein concentrations were linked to changes in lactobacilli counts (P < 0.05, R(2) = -0.33 for the mode
121 c ablation of the glands markedly suppressed Lactobacilli counts and heightened vulnerability to infe
123 12 months, the proportion with H2O2-positive lactobacilli decreased (n = 32; 53% vs 27%; P = .03).
125 lenged IL-10-deficient murine colitis model, lactobacilli demonstrated probiotic effects by direct mo
126 The proportion positive for H2O2+ or H2O2- lactobacilli did not change significantly with any of th
128 rmal Nugent score at all visits had a stable lactobacilli dominated microbiota with prevailing Lactob
130 nd vaginal microbiomes has demonstrated that lactobacilli drive epithelial and immune cell responses,
133 asmid-borne genes mediate the persistence of lactobacilli during olive fermentation and enhance their
135 Proteinase K treatment of methanol-fixed lactobacilli eliminated the inhibitory effect, suggestin
138 PCRs to detect bifidobacteria, bacteroides, lactobacilli, Escherichia coli, Clostridium difficile, a
139 have shown nonoxynol-9 (N-9) to be toxic to lactobacilli, especially to strains that produce H2O2.
140 with the ultimate goal of restoring vaginal lactobacilli following microbiological disturbances.
141 ilm community, and successfully compete with lactobacilli for dominance in the vaginal environment.
144 the assertion from other investigators that lactobacilli found in the GI tract originate in the oral
154 ural explanation for the mechanisms in which lactobacilli have adapted to their host niche by maximiz
156 uated the hypothesis that women colonized by lactobacilli have decreased acquisition of vaginal infec
160 sociated with lack of vaginal H2O2-producing lactobacilli (hazard ratio [HR] = 4.0, P < .001) or pres
162 of vaginal epithelial cells with any of the lactobacilli immediately following exposure to douching
163 otal levels of LCFA correlated with those of lactobacilli in fecal samples from patients with active
164 are necessary for sustained colonization of lactobacilli in humans: 1) a stagnant, retentive niche t
165 s emphasize a potentially important role for lactobacilli in modulating immunological functions of DC
166 tobacillus after using probiotics containing lactobacilli in the course of her treatment of Clostridi
167 foundation for further exploring the role of lactobacilli in the ecological dynamics of vaginal micro
168 and Lactobacillus jensenii, the most common lactobacilli in the female genital tract, inhibit gonoco
172 to reflect on the health implications of the lactobacilli in the mouth and downstream GI and to ponde
173 iginate in the oral cavity by proposing that lactobacilli in the oral cavity arise from caries lesion
174 n by vaginal epithelial cells in response to lactobacilli in the presence and absence of Gardnerella
175 ined with an estimate of the total number of lactobacilli in the vagina, suggest that vaginal lactoba
177 terial counts (G. vaginalis, M. hominis, and lactobacilli) in our model improved the sensitivity and
178 ict failure to become colonized by probiotic lactobacilli include exposure to semen, vaginal intercou
179 cantly more among subjects with NC-LC, while Lactobacilli (including L. fermentum) were more among su
180 genes conserved in L. crispatus and related lactobacilli, including an oleate hydratase (ohyA) and p
182 CncC-dependent fashion, and may function in lactobacilli-induced AMP proliferation and intestinal ti
184 heir selective effects on bifidobacteria and lactobacilli, influence many aspects of bowel function t
186 capacity for biotransformations catalysed by lactobacilli is an untapped biotechnology resource.
187 e investigate whether the anti-HIV effect of lactobacilli is mediated by extracellular vesicles (EVs)
188 differentiation of group B streptococci from lactobacilli is not possible, but lactobacillus cells al
189 amples produced under laboratory conditions, lactobacilli is one of the dominant groups in all the re
190 tic dogma that the mere absence of "healthy" lactobacilli is the sole mechanism that creates a permis
191 cterial microbiome of the stomach, including lactobacilli, is vital in promoting colonization resista
193 blood were phylogenetically inseparable from Lactobacilli isolated from the associated probiotic prod
194 Whole-genome-based phylogeny showed that Lactobacilli isolated from treated patients' blood were
195 with HIV-1 and treated with EVs released by lactobacilli isolated from vaginas of healthy women.
197 on of "controlled" inflammation by probiotic lactobacilli may be beneficial to improve neutrophil fun
201 een suggested that vaginal colonization with lactobacilli may reduce the risk of vulvovaginal candidi
202 ifies a family of compounds by which vaginal lactobacilli mediate host immune homeostasis and highlig
203 at predict sustained colonization by vaginal lactobacilli, microbiologic, behavioral, and demographic
204 nges in pH, concentration of viable cells of lactobacilli, microbiological, and organoleptic characte
205 ed Atopobium vaginae, Gardnerella vaginalis, lactobacilli, Mycoplasma hominis, and the human albumin
209 ection was adapted to examine the effects of lactobacilli on gonococcal interactions with endometrial
211 onectin and casein, as did CbpG expressed on lactobacilli or as a purified full-length or truncated r
213 ngs the colonization rates at age 5 weeks of lactobacilli (P < .001) and bacteroides (P = .02) increa
215 increased the bifidobacterial (P < 0.01) and lactobacilli (P < 0.001) populations but significantly d
216 loss of colonization with H(2)O(2)-producing lactobacilli (P=.018), as was antibiotic use (P< or =.00
219 into 2 groups: those with H(2)O(2)-producing lactobacilli present (n=191; 20.2%) and those with H(2)O
222 guished CTV-05 from other endogenous vaginal lactobacilli prior to and after vaginal capsule use.
226 t the hypothesis that H2O2-producing vaginal lactobacilli protect against acquisition of BV but do no
228 s that although most of the tested probiotic lactobacilli reduced C. albicans-induced vaginal epithel
229 estinal colonization by TNF-alpha-inhibitory lactobacilli reduced intestinal inflammation in H. hepat
233 itially colonized only by non-H2O2-producing lactobacilli resulted in loss of vaginal lactobacilli (R
234 OS promoted the growth of bifidobacteria and lactobacilli, resulting in high levels of short chain fa
236 V and promotion of vaginal colonization with lactobacilli should be evaluated as potential interventi
237 each sample, we calculated the proportion of lactobacilli species (ie, Lactobacillus crispatus, Lacto
239 Fourteen postbiotics derived from various lactobacilli species were screened, and Latilactobacillu
244 ARDRA and RAPD data showed three distinct lactobacilli strains, including L. acidophilus, L. plane
246 vable microbes, including oral streptococci, lactobacilli, Streptococcus mutans, and Candida, in sali
248 udies indicate that probiotics, particularly lactobacilli, suppressCandidagrowth and biofilm developm
250 detection of H(2)O(2) by a broader range of lactobacilli than a published, widely used agar formulat
251 P < .001) and in women without H2O2-positive lactobacilli than in women with (odds ratio [OR], 4.0; P
254 esence of novel CRISPR-Cas immune systems in lactobacilli that may be exploited for genome editing.
260 The goal of this study was to employ these lactobacilli to combat human immunodeficiency virus type
261 teria-free postbiotics, bioactive lysates of lactobacilli, to reduce intracellular S. aureus coloniza
264 the vagina and rectum by H(2)O(2)-producing lactobacilli was associated with the lowest prevalence o
265 s can naturally or therapeutically encounter lactobacilli, we investigated the effects of several wel
272 Salivary levels of mutans streptococci and lactobacilli were enumerated at baseline, 3, 6, and 12 m
273 ariable fragment Abs secreted by transformed lactobacilli were evaluated for their protective efficac
274 cecal crypt communities is diverse and that Lactobacilli were found closer to the lumen than Bactero
282 o-cultivation with C. albicans and probiotic lactobacilli were mostly driven by specific bacterial sp
288 alis and M. hominis and decreasing levels of lactobacilli were significantly associated with BV by Nu
293 biotics, or by endogenous bifidobacteria and lactobacilli, whose metabolic activity and growth may al
295 which is indicative of DC maturation, those lactobacilli with greatest capacity to induce IL-12 were
296 ome axis and provide a framework to engineer lactobacilli with improved bile resistance and use probi
297 tobacillus acidophilus BG2FO4 is a strain of lactobacilli with properties of marked intestinal adhere
298 t juice appeared to support the viability of lactobacilli, with higher microorganism numbers observed
299 ample, vaginal suppositories containing live lactobacilli, would alter the microbiomial composition h