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1 ng the rectum may be a reservoir for vaginal lactobacilli.
2 he identification of 97 strains of commensal lactobacilli.
3 edictive of an absence of H(2)O(2)-producing lactobacilli.
4 strains as well as other species of vaginal lactobacilli.
5 unique DNA fingerprint compared to all other lactobacilli.
6 colonized with commensal bacteria, primarily lactobacilli.
7 ilus, are the most common species of vaginal lactobacilli.
8 ift involves organisms other than the MS and lactobacilli.
9 thesis about the natural history and role of lactobacilli.
10 (+) T lymphocytes and vaginal H2O2-producing lactobacilli.
11 pecific traits in the genomes of the vaginal lactobacilli.
12 genes (ISGs) being the most affected by both lactobacilli.
13 teria and levels of Streptococcus mutans and Lactobacilli.
14 or total bacteria, Streptococcus mutans, and Lactobacilli.
15 toxicity, and does not inhibit the growth of lactobacilli.
16 is also highly conserved in streptococci and lactobacilli.
17 the increasing use of probiotics containing lactobacilli.
18 onii is a member of the acidophilus group of lactobacilli.
20 n a pathogen-free facility were colonized by Lactobacilli, a component of the oropharyngeal flora.
27 ted sustained colonization by H2O2-producing lactobacilli among women already colonized (relative ris
29 s: a nucleoside deoxyribosyltransferase from lactobacilli and a 5'-monophosphate-2'-deoxyribonucleosi
30 ant aciduric bacteria from root lesions were lactobacilli and A. israelii, while from sound root surf
31 l women have a relative depletion of vaginal lactobacilli and an increase in vaginal E. coli compared
35 o evidence that a multistrain preparation of lactobacilli and bifidobacteria was effective in prevent
36 ia, while a slight increase on the growth of lactobacilli and bifidobacteria was observed after expos
37 receive either a multistrain preparation of lactobacilli and bifidobacteria, with a total of 6 x 10(
38 nal flora characterized by reduced levels of lactobacilli and concomitant overgrowth of anaerobic bac
39 obial community was found to be dominated by Lactobacilli and Enterobacteria, both typically facultat
40 We conclude that the association between lactobacilli and gonococci is complex and may be subject
41 0) had significantly lower concentrations of lactobacilli and higher concentrations of Gardnerella va
42 g thus allows high efficiency mutagenesis in lactobacilli and lactococci, and may be used to further
44 aginal bacterial flora with disappearance of lactobacilli and overgrowth of Gardnerella vaginalis and
45 aracterized by the replacement of beneficial lactobacilli and the augmentation of anaerobic bacteria.
46 ptide production, which allows overgrowth of Lactobacilli and triggers T regulatory cell expansion in
47 he inverse association between H2O2-positive lactobacilli and vaginal E. coli colonization remained i
48 le to displace pre-coated vaginal protective lactobacilli and we hypothesize this to be a trigger for
49 ensal gut bacteria (e.g., bifidobacteria and lactobacilli) and increase the abundance of enterobacter
50 nderstood, and although mutans streptococci, lactobacilli, and A. naeslundii have been implicated in
51 onserved in streptococci, staphylococci, and lactobacilli, and are required for bacterial biofilm for
52 totoxicity, lack of activity against vaginal lactobacilli, and effectiveness against both HSV-2 and H
53 s, salivary log10 mutans streptococci, log10 lactobacilli, and fluoride level, did not represent stat
54 olved in fatty acid biosynthesis, amounts of lactobacilli, and saturated LCFA were measured in fecal
55 vels of Bifidobacteria, mutans streptococci, lactobacilli, and yeasts were correlated with each other
56 genous microbes that stably colonize a host, lactobacilli appear to be planktonic, opportunistic sett
58 h an associated decrease in caries, if these lactobacilli are fed to rats in an established caries mo
61 en who are colonized with H(2)O(2)-producing lactobacilli are more likely to maintain a normal vagina
65 sufficient data exist to support the use of lactobacilli as candidates for the development of new or
69 lationship between vaginal colonization with lactobacilli, bacterial vaginosis (BV), and acquisition
71 ffect vaginal colonization by H2O2-producing lactobacilli but that such use may promote loss of non-H
72 udies have shown that oral administration of lactobacilli can be an efficient approach to treat lacta
77 ophilus CRL 1014 on microbial metabolism and lactobacilli community composition for improving human h
81 L. monocytogenes infection by treatment with lactobacilli correlates with a decrease in host gene exp
82 obacilli in the vagina, suggest that vaginal lactobacilli could reacidify the vagina at the rate obse
83 ein concentrations were linked to changes in lactobacilli counts (P < 0.05, R(2) = -0.33 for the mode
84 12 months, the proportion with H2O2-positive lactobacilli decreased (n = 32; 53% vs 27%; P = .03).
86 lenged IL-10-deficient murine colitis model, lactobacilli demonstrated probiotic effects by direct mo
87 The proportion positive for H2O2+ or H2O2- lactobacilli did not change significantly with any of th
89 rmal Nugent score at all visits had a stable lactobacilli dominated microbiota with prevailing Lactob
92 Proteinase K treatment of methanol-fixed lactobacilli eliminated the inhibitory effect, suggestin
94 PCRs to detect bifidobacteria, bacteroides, lactobacilli, Escherichia coli, Clostridium difficile, a
95 have shown nonoxynol-9 (N-9) to be toxic to lactobacilli, especially to strains that produce H2O2.
96 ilm community, and successfully compete with lactobacilli for dominance in the vaginal environment.
98 the assertion from other investigators that lactobacilli found in the GI tract originate in the oral
104 ural explanation for the mechanisms in which lactobacilli have adapted to their host niche by maximiz
106 uated the hypothesis that women colonized by lactobacilli have decreased acquisition of vaginal infec
109 sociated with lack of vaginal H2O2-producing lactobacilli (hazard ratio [HR] = 4.0, P < .001) or pres
111 otal levels of LCFA correlated with those of lactobacilli in fecal samples from patients with active
112 are necessary for sustained colonization of lactobacilli in humans: 1) a stagnant, retentive niche t
113 s emphasize a potentially important role for lactobacilli in modulating immunological functions of DC
114 tobacillus after using probiotics containing lactobacilli in the course of her treatment of Clostridi
115 foundation for further exploring the role of lactobacilli in the ecological dynamics of vaginal micro
116 and Lactobacillus jensenii, the most common lactobacilli in the female genital tract, inhibit gonoco
120 to reflect on the health implications of the lactobacilli in the mouth and downstream GI and to ponde
121 iginate in the oral cavity by proposing that lactobacilli in the oral cavity arise from caries lesion
122 ined with an estimate of the total number of lactobacilli in the vagina, suggest that vaginal lactoba
124 terial counts (G. vaginalis, M. hominis, and lactobacilli) in our model improved the sensitivity and
125 ict failure to become colonized by probiotic lactobacilli include exposure to semen, vaginal intercou
126 heir selective effects on bifidobacteria and lactobacilli, influence many aspects of bowel function t
128 capacity for biotransformations catalysed by lactobacilli is an untapped biotechnology resource.
129 differentiation of group B streptococci from lactobacilli is not possible, but lactobacillus cells al
130 cterial microbiome of the stomach, including lactobacilli, is vital in promoting colonization resista
136 een suggested that vaginal colonization with lactobacilli may reduce the risk of vulvovaginal candidi
137 at predict sustained colonization by vaginal lactobacilli, microbiologic, behavioral, and demographic
138 ed Atopobium vaginae, Gardnerella vaginalis, lactobacilli, Mycoplasma hominis, and the human albumin
142 ection was adapted to examine the effects of lactobacilli on gonococcal interactions with endometrial
143 onectin and casein, as did CbpG expressed on lactobacilli or as a purified full-length or truncated r
145 ngs the colonization rates at age 5 weeks of lactobacilli (P < .001) and bacteroides (P = .02) increa
147 increased the bifidobacterial (P < 0.01) and lactobacilli (P < 0.001) populations but significantly d
148 loss of colonization with H(2)O(2)-producing lactobacilli (P=.018), as was antibiotic use (P< or =.00
151 into 2 groups: those with H(2)O(2)-producing lactobacilli present (n=191; 20.2%) and those with H(2)O
154 guished CTV-05 from other endogenous vaginal lactobacilli prior to and after vaginal capsule use.
157 t the hypothesis that H2O2-producing vaginal lactobacilli protect against acquisition of BV but do no
159 estinal colonization by TNF-alpha-inhibitory lactobacilli reduced intestinal inflammation in H. hepat
161 itially colonized only by non-H2O2-producing lactobacilli resulted in loss of vaginal lactobacilli (R
162 OS promoted the growth of bifidobacteria and lactobacilli, resulting in high levels of short chain fa
164 V and promotion of vaginal colonization with lactobacilli should be evaluated as potential interventi
166 vable microbes, including oral streptococci, lactobacilli, Streptococcus mutans, and Candida, in sali
168 udies indicate that probiotics, particularly lactobacilli, suppressCandidagrowth and biofilm developm
169 detection of H(2)O(2) by a broader range of lactobacilli than a published, widely used agar formulat
170 P < .001) and in women without H2O2-positive lactobacilli than in women with (odds ratio [OR], 4.0; P
173 esence of novel CRISPR-Cas immune systems in lactobacilli that may be exploited for genome editing.
179 the vagina and rectum by H(2)O(2)-producing lactobacilli was associated with the lowest prevalence o
180 s can naturally or therapeutically encounter lactobacilli, we investigated the effects of several wel
186 Salivary levels of mutans streptococci and lactobacilli were enumerated at baseline, 3, 6, and 12 m
187 ariable fragment Abs secreted by transformed lactobacilli were evaluated for their protective efficac
197 alis and M. hominis and decreasing levels of lactobacilli were significantly associated with BV by Nu
201 biotics, or by endogenous bifidobacteria and lactobacilli, whose metabolic activity and growth may al
203 which is indicative of DC maturation, those lactobacilli with greatest capacity to induce IL-12 were
204 tobacillus acidophilus BG2FO4 is a strain of lactobacilli with properties of marked intestinal adhere
205 t juice appeared to support the viability of lactobacilli, with higher microorganism numbers observed
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