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1 lity patterns vary with different species of Nocardia.
2 s; Burkholderia, 1.06 per 100 patient-years; Nocardia, 0.81 per 100 patient-years; Serratia, 0.98 per
3 ess of PCR amplification of a portion of the Nocardia 16S rRNA gene and subsequent restriction endonu
4 tion of N. veterana from the related species Nocardia africana and N. nova because of the very high d
5 r the identification of clinical isolates of Nocardia and for the detection of new or unusual species
7 hiolactone antibiotic produced by species of Nocardia and Streptomyces, is an inhibitor of the beta-k
9 lowed the recognition of many new species of Nocardia and to date have been the most precise methods
11 order Corynebacterineae (e.g., mycobacteria, nocardia, and rhodococci) share a glycolipid-rich cell w
13 tative isolates of the drug pattern types of Nocardia asteroides (except for N. asteroides drug patte
16 dent with the unofficial species designation Nocardia asteroides complex antimicrobial susceptibility
17 or the in vitro susceptibility testing of 26 Nocardia asteroides complex isolates to the following an
18 patterns were seen with Gordona bronchialis, Nocardia asteroides complex type VI, Nocardia otitidisca
20 , DNA-DNA hybridization results confirm that Nocardia asteroides drug pattern type VI, which has long
24 ia thailandica is a rare pathogen related to Nocardia asteroides, Nocardia neocaledoniensis, and Noca
25 xonomic history; this is especially true for Nocardia asteroides, the type species of the genus and p
29 ii pneumonia, infection with Cryptococcus or Nocardia, bacterial pneumonia, viral pneumonia, and Kapo
30 Here we describe the first reported case of Nocardia beijingensis infection in the United States, ma
31 r most transplant-related nocardiosis, while Nocardia brasiliensis rarely causes infection in organ t
32 h microdilution testing on single strains of Nocardia brasiliensis, Nocardia cyriacigeorgica, Nocardi
33 a asteroides, Nocardia neocaledoniensis, and Nocardia caishijiensis that, since its original descript
35 bating purified recombinant Car with CoA and Nocardia cell-free extracts indicated that post-translat
36 retrospective molecular screening of recent Nocardia clinical isolates at our New York City medical
37 The type strains of three Nocardia species, Nocardia concava, Nocardia ignorata, and Nocardia yamana
41 lase system was purified to homogeneity from Nocardia corallina B276, a bacterium phylogenetically un
42 (AMO) from Rhodococcus rhodochrous (formerly Nocardia corallina) B-276 is a three-component enzyme sy
48 on single strains of Nocardia brasiliensis, Nocardia cyriacigeorgica, Nocardia farcinica, Nocardia n
50 tion of 2 isolates, Enterococcus faecium and Nocardia exalbida, all the other 725 (99.7%) gram-positi
52 ochemical and structural characterization of Nocardia farcinica Lys monooxygenase (NbtG), which has s
56 Mycobacterium genomes, Rhodococcus sp. RHA1, Nocardia farcinica, and Saccharopolyspora erythraea.
57 didatus Pelagibacter ubique, actinobacterium Nocardia farcinica, chlorobi species Chloroherpeton thal
58 rdia brasiliensis, Nocardia cyriacigeorgica, Nocardia farcinica, Nocardia nova, and Nocardia wallacei
59 , we report crystal structures of RIFMO from Nocardia farcinica, the determination of the oligomeric
61 ent susceptibilities of clinical isolates of Nocardia from six major laboratories in the United State
63 A gene sequencing and phenotypic analysis as Nocardia higoensis, an opportunistic organism isolated o
64 of three Nocardia species, Nocardia concava, Nocardia ignorata, and Nocardia yamanashiensis, which al
67 this study was to identify risk factors for Nocardia infection after SOT and to describe the present
68 immunocompromised patients with disseminated Nocardia infection, our patient responded favorably to p
70 wise unexplained disseminated/extrapulmonary Nocardia infections, anti-GM-CSF autoantibodies should b
72 ermediates, a carboxylic acid reductase from Nocardia iowensis and an alcohol dehydrogenase from Leif
73 bility testing (AST) of clinical isolates of Nocardia is recommended to detect resistance to commonly
75 all antimicrobial agents tested against all Nocardia isolates by all methods, the BACTEC radiometric
76 describe here a novel method for identifying Nocardia isolates by using sequence analysis of a portio
77 atories have allowed us to define a group of Nocardia isolates from clinical samples which resemble t
80 the importance of accurate identification of Nocardia isolates to the species level by integrated use
85 performed for subgroups of patients with non-Nocardia keratitis and those with no topical antibiotic
86 r 299 cultures submitted to the Mycobacteria/Nocardia Laboratory at the University of Texas Health Ce
87 Reference Laboratories and the Mycobacteria/Nocardia Laboratory at the University of Texas Health Sc
88 ation, and score interpretation, using three Nocardia libraries, the Bruker, National Institutes of H
90 ocol, 150 Nocardia isolates, and NIH and OSU Nocardia MALDI-TOF MS libraries were distributed to thre
92 and may coexist with bacterial (Legionella, Nocardia), mycobacterial, and fungal (Aspergillus, Histo
95 are pathogen related to Nocardia asteroides, Nocardia neocaledoniensis, and Nocardia caishijiensis th
96 nocompromised patients were characterized as Nocardia nova by biochemical and susceptibility testing
104 ulcers that were central, deep or large, non-Nocardia, or classically invasive Pseudomonas aeruginosa
106 hialis, Nocardia asteroides complex type VI, Nocardia otitidiscaviarum, Nocardia transvalensis, and S
109 When incubated with [(3)H]acetyl-CoA and Nocardia PPTase, the labeled acetylphosphopantetheine mo
113 , natural products isolated from a strain of Nocardia, showed growth inhibition against three human t
115 n = 3), Mycobacterium avium complex (n = 2), Nocardia sp. (n = 1), Aspergillus sp. (n = 1), or pulmon
116 lator that was originally misidentified as a Nocardia sp. due, in part, to its partially acid-fast st
119 polymorphism (RFLP) patterns were found for Nocardia sp. type strains (except for the N. asteroides
120 sed as a quality control organism for AST of Nocardia sp., and the use of a disk diffusion test for s
122 hniques for the identification of pathogenic Nocardia species and for the recognition of novel specie
124 orithms for the phenotypic identification of Nocardia species are limited in practice, the true preva
129 evaluation of 297 mycobacteria isolates, 148 Nocardia species isolates, and 61 other aerobic actinomy
130 as sequenced from 40 clinical isolates of 12 Nocardia species previously identified by 16S rRNA gene
131 Molecular methods for identification of Nocardia species provide more accurate and rapid results
134 to devise a method for the identification of Nocardia species that is more technically simple, accura
135 ble with identification of Mycobacterium and Nocardia species using matrix-assisted laser desorption
136 ecA1 gene of 30 type or reference strains of Nocardia species was amplified using secA1-specific prim
139 162 Mycobacterium species and subspecies, 53 Nocardia species, and 13 genera (totaling 43 species) of
141 g isolates, including Mycobacterium species, Nocardia species, and other aerobic actinomycetes) showe
149 rapid identification of clinically relevant Nocardia spp. and to implement MALDI-TOF MS libraries de
152 y for the identification of mycobacteria and Nocardia spp. has also been reported in a limited scope.
153 cal workup of pericardial fluid for possible Nocardia spp. is described in an effort to improve the t
157 including a wound culture that contained two Nocardia taxa that were indistinguishable morphologicall
158 lates that distinguished them from all other Nocardia taxa, but did not differentiate the four taxa w
160 rt a case of pulmonary nocardiosis caused by Nocardia thailandica in a 66-year-old solid organ transp
163 olymorphism (RFLP) identification schema for Nocardia that used an amplified 439-bp segment (amplicon
164 rRNA gene sequences of different species of Nocardia, those laboratories employing molecular methods
172 dentified by treatment for scar size for non-Nocardia ulcers (-0.06 mm, 95% CI, -0.21 to 0.10, P = .4
173 n BSCVA at 12 months among patients with non-Nocardia ulcers (-0.10 logMAR, 95% CI, -0.19 to -0.02, P
174 ifference was observed in 12-month BSCVA for Nocardia ulcers (0.18 logMAR, 95% CI, -0.04 to 0.41, P =
175 provement in visual acuity compared with non-Nocardia ulcers (0.21 logarithm of the minimal angle of
176 ith larger mean scar size at 12 months among Nocardia ulcers (0.47 mm, 95% CI, 0.06-0.88, P = .02) an
177 presentation visual acuity compared with non-Nocardia ulcers (median Snellen visual acuity, 20/45, co
181 verall improvement in visual acuity than non-Nocardia ulcers, but had better presentation acuity.
185 c gene cluster for the nocardicin A producer Nocardia uniformis subsp. tsuyamanensis ATCC 21806 was r
186 tam antibiotics produced by the actinomycete Nocardia uniformis subsp. tsuyamanensis ATCC 21806.
187 c beta-lactam isolated from the actinomycete Nocardia uniformis that shows moderate antibiotic activi
188 c beta-lactam isolated from the actinomycete Nocardia uniformis, which shows moderate activity agains
191 characteristics of the proposed new species Nocardia wallacei (N. asteroides drug pattern IV) and N.
197 rovide background on the current taxonomy of Nocardia, with a focus on clinically relevant species, a
198 es, Nocardia concava, Nocardia ignorata, and Nocardia yamanashiensis, which also showed ambiguous bas
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