1 vity was variable against diverse strains of
Xenorhabdus and Photorhabdus and was not correlated with
2 Xenorhabdus and Photorhabdus species dedicate a large am
3 Xenorhabdus and Photorhabdus spp. are gram negative gamm
4 Toxin complexes from
Xenorhabdus and Photorhabdus spp. bacteria represent nov
5 Molecular biological studies suggest that
Xenorhabdus and Photorhabdus spp. may serve as valuable
6 Photorhabdus and
Xenorhabdus appear very similar at the DNA sequence leve
7 hogenicity and mutualism in Photorhabdus and
Xenorhabdus are very different.
8 Photorhabdus and
Xenorhabdus bacteria colonize the intestines of the infe
9 Photorhabdus and
Xenorhabdus bacteria therefore engage in both pathogenic
10 Xenorhabdus bovienii (SS-2004) bacteria reside in the in
11 Xenorhabdus bovienii exhibits phenotypic variation betwe
12 Xenorhabdus bovienii primary and secondary form isolates
13 e pixA gene was not present in the genome of
Xenorhabdus bovienii, which also produces proteinaceous
14 colonized mutualistically by members of the
Xenorhabdus genus of bacteria.
15 symbiotic interaction between the bacterium
Xenorhabdus nematophila and its nematode host, Steinerne
16 Two gram-negative insect pathogens,
Xenorhabdus nematophila and Photorhabdus luminescens, pr
17 The association between the bacterium
Xenorhabdus nematophila and the nematode Steinernema car
18 matodes are always found in association with
Xenorhabdus nematophila bacteria.
19 The bacterial mutualist
Xenorhabdus nematophila colonizes a specific region of i
20 Xenorhabdus nematophila colonizes the intestinal tract o
21 The gammaproteobacterium
Xenorhabdus nematophila engages in a mutualistic associa
22 Xenorhabdus nematophila is a gamma-proteobacterial mutua
23 The bacterium
Xenorhabdus nematophila is a mutualist of entomopathogen
24 The bacterium
Xenorhabdus nematophila is a mutualist of the entomopath
25 The gammaproteobacterium
Xenorhabdus nematophila is a mutualistic symbiont that c
26 Xenorhabdus nematophila is an emerging model for both mu
27 An insertion between iscA and hscB of the
Xenorhabdus nematophila iscRSUA-hscBA-fdx locus, predict
28 virulence, suggesting that X. bovienii, like
Xenorhabdus nematophila may undergo virulence modulation
29 of one of the toxin components, XptA1, from
Xenorhabdus nematophila PMFI296 to a resolution of 23 A.
30 The gram-negative insect pathogen
Xenorhabdus nematophila possesses potential virulence fa
31 The symbiotic pathogenic bacterium
Xenorhabdus nematophila produces two distinct intracellu
32 ofiling in Photorhabdus luminescens TT01 and
Xenorhabdus nematophila revealed that L-proline in the i
33 We identified
Xenorhabdus nematophila transposon mutants with defects
34 iation in the symbiotic-pathogenic bacterium
Xenorhabdus nematophila was examined in this study.
35 a symbiotic relationship with the bacterium
Xenorhabdus nematophila, and is emerging as a genetic mo
36 carpocapsae is associated with the bacterium
Xenorhabdus nematophila, and we show that X. nematophila
37 Xenorhabdus nematophila, the mutualistic bacterium of th
38 he major antimicrobial compounds produced by
Xenorhabdus nematophila.
39 monella enterica, Streptococcus pyogenes and
Xenorhabdus nematophila.
40 Xenorhabdus nematophilus, a gram-negative bacterium, is
41 native toxin complex (toxin complex 1) from
Xenorhabdus nematophilus.
42 om the bacteria Photorhabdus luminescens and
Xenorhabdus nematophilus.
43 ria belonging to the genera Photorhabdus and
Xenorhabdus participate in a trilateral symbiosis in whi
44 nificus, Yersinia sp., Photorhabdus sp., and
Xenorhabdus sp.; and a filamentous/hemagglutinin-like pr
45 of the nilA, nilB, and nilC genes into other
Xenorhabdus species enables them to colonize the same S.
46 In this work, we showed that of all the
Xenorhabdus species examined, only X. nematophila has th
47 X. nematophila, but not other
Xenorhabdus species, colonize a discrete region of a spe
48 by nilA and nilC, it confers upon noncognate
Xenorhabdus spp. the ability to colonize S. carpocapsae
49 By exposing S. carpocapsae to other
Xenorhabdus spp., we established that only X. nematophil
50 ular mechanisms utilized by Photorhabdus and
Xenorhabdus to control their host-dependent interactions
51 h the same 4:1:1 stoichiometry as the native
Xenorhabdus toxin complex 1.
52 e entomopathogenic bacteria Photorhabdus and
Xenorhabdus were analyzed by MALDI-MS(2), and a database
53 roteins from Photorhabdus luminescens to the
Xenorhabdus XptA2 protein resulted in formation of a hyb