1 nd temporary suppression of both Clostridium
coccoides and Clostridium leptum group organisms.
2 tant show a striking morphology of irregular
coccoids and aberrant DNA replication.
3 how cellular clusters of unexpectedly large
coccoids and tubular sheath-like envelopes were trapped
4 ganized biofilm-like community consisting of
coccoid bacteria that ultimately filled most of the cyto
5 In most non-
coccoid bacteria, this shape is also determined by an in
6 Strain 195, a
coccoid bacterium that dechlorinates tetrachloroethene t
7 to as Bacteroidetes), Clostridium leptum, C.
coccoides,
bifidobacteria, Escherichia coli and Archaea
8 Clone libraries targeting Clostridium
coccoides (
C. coccoides) in sewage samples demonstrated
9 , the submucosal microbiota was dominated by
coccoid cells.
10 rized by increased proportion of Clostridium
coccoides (
cluster XIVa), C coccoides-Eubacterium rectal
11 th SS and HC (P = 0.006) and higher fecal C.
coccoides compared to those with SS (P = 0.04).
12 ion resulted in a revised growth model where
coccoid cyanobacteria predominate in mat communities for
13 ommunities develop, which include endolithic
coccoid cyanobacteria.
14 Thus, in common with
coccoids,
Drosophila is capable of generating an imprint
15 n of Clostridium coccoides (cluster XIVa), C
coccoides-
Eubacterium rectale (cluster XIVab), Bacteroid
16 es uniformis, Eggerthella lenta, and Blautia
coccoides-
Eubacterium rectale groups (P < 0.05).
17 against Bacteroides, Prevotella and Blautia
coccoides-
Eubacterium rectale.
18 Here we show that the
coccoid form of H. pylori, in contrast to the spiral for
19 environment transforms into a nonculturable,
coccoid form, which frequently results in the failure to
20 ake and a morphological shift from spiral to
coccoid form.
21 iral form to the nonreplicating, but viable,
coccoid form.
22 The organism has the propensity to become a
coccoid form.
23 nd a nonculturable, but viable, metabolizing
coccoid form.
24 .05) and in an increase in the proportion of
coccoid forms (P <0.0001) relative to baseline.
25 Because only spiral organisms-and not
coccoid forms-are capable of inducing interleukin-8 secr
26 so adopt straight rod, elongated helical and
coccoid forms.
27 the planktic cyanobacterium, Microcystis, a
coccoid genus that at the present-day commonly forms blo
28 otags encompassed the previously reported C.
coccoides group.
29 Coccoid H. pylori, which are thought to be terminally di
30 ibraries targeting Clostridium coccoides (C.
coccoides)
in sewage samples demonstrated that Lachnospi
31 Strain SL100 is a gram-positive
coccoid isolate prototype with an adhesin specific for g
32 These
coccoids modify the sediment, forming thicker lithified
33 demonstrate here that iron depletion induces
coccoid morphology in strains lacking cagA.
34 at the role of this endopeptidase in forming
coccoid morphology may be critical for pathogenesis.
35 nd undergoes a premature transformation to a
coccoid morphology.
36 d the normal transition to a densely packed,
coccoid morphology.
37 res from which the poles disappear, yielding
coccoid or lemon-shaped forms.
38 dult human gut also known as the Clostridium
coccoides or Eubacterium rectale group, contains species
39 s zoonotic disease caused by a Gram-negative
coccoid rod bacterium, Francisella tularensis.
40 ere, in some species, most notably among the
coccoids (
scale insects and allies), the differential ma
41 strains treated with CBR-4830 transition to
coccoid shape, consistent with MreB inhibition or deplet
42 , we hypothesise that most major lineages of
coccoids shifted from gymnosperms onto angiosperms when
43 aled endocarditis with small silver positive
coccoid structures in endothelial cells.
44 The difference in C.
coccoides was no longer significant after adjusting for