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1 om an organoheterotrophic archaeal host to a bacterial symbiont.
2 ansmission mode on an obligate intracellular bacterial symbiont.
3 eals an unexpected toxin-producing defensive bacterial symbiont.
4  an extreme sex-ratio distortion caused by a bacterial symbiont.
5  harbor a maternally inherited intracellular bacterial symbiont.
6 ypes that vary in how strongly they "choose" bacterial symbionts.
7 neages with a diverse panel of Sinorhizobium bacterial symbionts.
8 lonize novel environments by partnering with bacterial symbionts.
9 ic potential Acanthamoeba host infected with bacterial symbionts.
10 gellates are typically colonized by specific bacterial symbionts.
11 bivorous tortoise beetles and their obligate bacterial symbionts.
12 logical functions of colonization factors in bacterial symbionts.
13 unction in interactions with insect hosts or bacterial symbionts.
14  algarvensis, a gutless marine worm, and its bacterial symbionts.
15  cascades to tissues housing light-producing bacterial symbionts.
16 and share the products with sulfate-reducing bacterial symbionts.
17 xonomic groups harbor maternally transmitted bacterial symbionts.
18 ized with a consortium of 15 sequenced human bacterial symbionts, 13 of which harbored one or more pr
19   Wolbachia is a common maternally inherited bacterial symbiont able to induce crossing sterilities k
20                                              Bacterial symbionts and fungal and bacterial pathogens i
21 entral metabolites are utilized by potential bacterial symbionts and opportunists alike, rosmarinic a
22                                        These bacterial symbionts and pathogens each contain a homolog
23       These agents include two broad groups: bacterial symbionts and selfish chromosomes.
24 rrently known about the interactions between bacterial symbionts and their hosts.
25 ome structures and complex associations with bacterial symbionts and viruses, with stark differences
26 y diverse intracellular parasites, including bacterial symbionts and viruses.
27 transmitted micro-organisms, but while their bacterial symbionts are well-studied, little is known ab
28 alysis revealed that a previously overlooked bacterial symbiont belonging to the genus Mycoavidus dwe
29                           In pea aphids, the bacterial symbiont Buchnera is confined to specialized a
30 udy we investigate a mutation in an obligate bacterial symbiont (Buchnera), which has dramatic effect
31 stratified water and can harbor diazotrophic bacterial symbionts, but does not support eutrophication
32 tent algaecidal activity suggesting that the bacterial symbiont can convert algal precursors, tryptop
33  network interaction between hosts and their bacterial symbionts can control host immunological homeo
34  example, in aphids, facultative (secondary) bacterial symbionts can provide protection against natur
35 y invasive species that harbours the primary bacterial symbiont 'Candidatus Pantoea carbekii'.
36  marine symbiosis, in which an intracellular bacterial symbiont ("Candidatus Endobryopsis kahalalidef
37  control groups, the predominant families of bacterial symbionts change with each larval instar despi
38 pp., Borrelia spp., and Rickettsia spp.) and bacterial symbionts (e.g., Cardinium, Rickettsiella, and
39 ri (Hemiptera: Pseudococcidae) contains dual bacterial symbionts existing with an unprecedented organ
40 s at deep-sea hydrothermal vents depend upon bacterial symbionts for nutrition, and thus the mechanis
41 , which are usually associated with specific bacterial symbionts found on their surface or inside the
42                                              Bacterial symbionts frequently provide chemical defenses
43 are cooperatively constructed to deliver the bacterial symbiont from the root surface to cells in the
44           Most insect groups harbor obligate bacterial symbionts from the alpha-proteobacterial genus
45 ts and established pure cultures of isolated bacterial symbionts from toxic newts.
46  a horizontal gene transfer is targeted to a bacterial symbiont, further blurring the distinction bet
47                     The role of symbiosis in bacterial symbiont genome evolution is well understood,
48 grade host-derived NCR peptides and give the bacterial symbionts greater fitness at the expense of ho
49             Upon colonizing juvenile squids, bacterial symbionts grow on host-supplied nutrients, whi
50 e to A. ervi is infection by the facultative bacterial symbiont Hamiltonella defensa.
51 ver, the relationship between bees and their bacterial symbionts has only been explored in a handful
52 between angiosperms and nitrogen-fixing (N2) bacterial symbionts housed in nodules.
53 ng the association between mealybugs and two bacterial symbionts, Husnik et al. (2013) demonstrated t
54 itu hybridization and qPCR, we show that the bacterial symbiont, identified as Parachlamydia acantham
55         New research suggests that secondary bacterial symbionts in insects act as a mechanism for ho
56 nfection with congeners containing different bacterial symbionts in order to exchange metabolites to
57  Anasa tristis, an insect pest that requires bacterial symbionts in the genus Caballeronia(10) for su
58 ilize the squash bug, Anasa tristis, and its bacterial symbionts in the genus Caballeronia.
59                 Animals house a community of bacterial symbionts in their digestive tracts that contr
60            These clams host chemoautotrophic bacterial symbionts in their gills that synthesize organ
61 complex symbioses with at least two obligate bacterial symbionts, inhabiting specialized host cells (
62 se, but the molecular details underlying how bacterial symbionts initially assemble within a host rem
63 cated that the LPS behaves similar to intact bacterial symbionts, interacting with host cells in the
64                 On the contrary, most of the bacterial symbionts lack the essential glycolytic enzyme
65                  Before maternally inherited bacterial symbionts like Wolbachia, which cause cytoplas
66   Animals are typically colonized by diverse bacterial symbionts, many of which are commensal and, in
67 ve consequential associations with microbes: bacterial symbionts may be embedded in different insect
68 esize side-chain alkylated sterols, and that bacterial symbionts may contribute to 24-isopropyl stero
69                                Nevertheless, bacterial symbionts may play an important role in determ
70 ourced from two known mechanisms: protective bacterial symbionts, most commonly Hamiltonella defensa,
71  Sinorhizobium meliloti is a nitrogen-fixing bacterial symbiont of alfalfa and related legumes.
72 o select for strains of Wolbachia wMelPop (a bacterial symbiont of fruit flies) that differed in copy
73 (QS) in Sinorhizobium meliloti, the N-fixing bacterial symbiont of Medicago host plants, involves at
74 ago sativa and Arabidopsis thaliana) and the bacterial symbiont of one of these species (Sinorhizobiu
75 ecies Sin-1, a nitrogen-fixing Gram-negative bacterial symbiont of Sesbania, was determined by compos
76 le bacterium Vibrio fischeri is the specific bacterial symbiont of the Hawaiian squid Euprymna scolop
77  of T6SSs in Snodgrassella alvi wkB2, a core bacterial symbiont of the honey bee gut microbiota.
78                                          The bacterial symbiont of the hydrothermal vent tubeworm fix
79                              We investigated bacterial symbionts of Adelges tsugae, a pest of hemlock
80                      Our study suggests that bacterial symbionts of animals contain antibiotics that
81 hat the previously characterized specialized bacterial symbionts of army ant workers were largely abs
82                         Maternally inherited bacterial symbionts of arthropods are common, yet symbio
83 tive sabotage caused by maternally inherited bacterial symbionts of arthropods.
84 t is hosted by a ciliated protist, Euplotes; bacterial symbionts of ciliates are still poorly known b
85                 Here, we studied the role of bacterial symbionts of free-living amoebae in the establ
86                                              Bacterial symbionts of fungus-growing ants occupy a high
87 y genomes have been discovered from numerous bacterial symbionts of insect hosts.
88 ve been described from nutrient-provisioning bacterial symbionts of several insect lineages [1-5].
89  Exceptions to this rule are found among the bacterial symbionts of surgeonfish; Epulopiscium spp. ar
90           Midichloria spp. are intracellular bacterial symbionts of ticks.
91                                   Engineered bacterial symbionts offer a promising alternative for de
92 n marine invertebrates and their cooperative bacterial symbionts offer access to an understanding of
93 ual secondary metabolites synthesized by the bacterial symbiont Phaeobacter inhibens from precursors
94  nematode Heterorhabditis bacteriophora, its bacterial symbiont Photorhabdus luminescens, and the fru
95                                 Male-killing bacterial symbionts, prevalent in arthropods, skew popul
96 work provides an example of an intracellular bacterial symbiont protecting a protist host against vir
97  abundant and diverse, but their luminescent bacterial symbionts remain enigmatic.
98       This study reveals the potential for a bacterial symbiont's sRNAs not only to control its own a
99 nd energy reserves, it has a unique role for bacterial symbionts-serving as the primary energy storag
100 s (including some thyasirid species) without bacterial symbionts show no comparable foot extension be
101             RaxP and RaxQ are similar to the bacterial symbiont Sinorhizobium meliloti host specifici
102 plants to nodulation factors produced by the bacterial symbiont Sinorhizobium meliloti using a dual-d
103 hota genomes encode gene clusters typical of bacterial symbionts, suggesting host-associated lifestyl
104 ion, the absence of a known obligate partner bacterial symbiont suggests that Uzinura alone can suppl
105  microbiome, a community of host-specialized bacterial symbionts that helps protect hosts against euk
106 ave formed stable associations with pairs of bacterial symbionts that live in specialized cells and p
107 erse genus Nephromyces, as well as the three bacterial symbionts that live within this species comple
108 pods commonly harbour maternally-transmitted bacterial symbionts that manipulate host biology.
109   This study discovers host-species-specific bacterial symbionts that predate hominid diversification
110 Many animals show intimate interactions with bacterial symbionts that provision hosts with limiting n
111        Field releases of mosquitoes carrying bacterial symbionts that reduce vector competence are on
112 rein we highlight metabolic contributions of bacterial symbionts that reside within tsetse flies, bed
113 erived natural products, and the specialized bacterial symbionts that synthesize them, are not shared
114  one strategy used by maternally transmitted bacterial symbionts to boost transmission and spread in
115 ules create an environment for intracellular bacterial symbionts to fix atmospheric nitrogen.
116 rtebrate blood, rely on maternally inherited bacterial symbionts to supply B vitamins.
117 mes that form indeterminate nodules in which bacterial symbionts undergo terminal differentiation.
118 ly stages of the squid-vibrio symbiosis, the bacterial symbiont Vibrio fischeri encounters host-deriv
119  this knowledge gap, we investigated how the bacterial symbiont Vibrio fischeri initially colonizes t
120 he squid Euprymna scolopes and sensed by the bacterial symbiont, Vibrio fischeri, via the NO sensor H
121                       In aphids, facultative bacterial symbionts, which benefit hosts by conferring r
122  other microorganisms, including facultative bacterial symbionts, which occur in a majority of pea ap
123                                 The obligate bacterial symbiont Wigglesworthia glossinidia is critica
124                  We found that introducing a bacterial symbiont with a protective (but not a non-prot
125 oskeleton through the activity of an ancient bacterial symbiont with a tiny genome that serves as a f
126 at these mobile genetic elements can endow a bacterial symbiont with benefits that extend to the anim
127                       Vibrio fischeri is the bacterial symbiont within the light-emitting organ of th
128                                          The bacterial symbiont Wolbachia can cause cytoplasmic incom
129 rnative to traditional control measures, the bacterial symbiont Wolbachia has been transferred from D
130  any maternally inherited factor such as the bacterial symbiont Wolbachia.
131  provide insight into how a parasite and its bacterial symbiont work in concert to regulate host cell

 
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