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Tom Coenye - One of the best experts on this subject based on the ideXlab platform.
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Use of PCR Analyses To Define the Distribution of Ralstonia Species Recovered from Patients with Cystic Fibrosis
Journal of clinical microbiology, 2005Co-Authors: Tom Coenye, Theodore Spilker, Rebecca Reik, Peter Vandamme, John J. LipumaAbstract:Two new PCR assays (for Ralstonia species and Ralstonia respiraculi), together with previously published PCR assays, were used to assess Ralstonia isolates recovered from 111 cystic fibrosis patients. Ralstonia mannitolilytica accounted for 46% of isolates, while R. respiraculi and Ralstonia pickettii accounted for 19% and 18%, respectively. Ralstonia basilensis and Ralstonia metallidurans, species not previously recovered from human samples, were also identified.
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Classification of Ralstonia pickettii-like isolates from the environment and clinical samples as Ralstonia insidiosa sp. nov.
International Journal of Systematic and Evolutionary Microbiology, 2003Co-Authors: Tom Coenye, Johan Goris, Paul De Vos, Peter Vandamme, John J. LipumaAbstract:Thirteen Ralstonia pickettii-like isolates from the environment (water, soil and activated sludge) and human clinical samples (including respiratory secretions of cystic fibrosis patients) were investigated in a polyphasic taxonomic study that employed 16S rDNA sequence analysis, DNA–DNA hybridization, determination of DNA base composition, whole-cell protein analysis, biochemical characterization and PCR-based assays. All isolates were classified as a novel Ralstonia species, for which the name Ralstonia insidiosa sp. nov. is proposed. The type strain, LMG 21421T (=CCUG 46789T), was isolated from the sputum of a patient with acute lymphoblastic leukaemia. R. insidiosa can be differentiated from other species of the genus Ralstonia and phenotypically similar species (including the Burkholderia cepacia complex and Achromobacter xylosoxidans) by a variety of biochemical tests, whole-cell protein analysis and several PCR-based assays. Some outstanding issues in the taxonomy of the genus Ralstonia are also discussed.
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Ralstonia respiraculi sp. nov., isolated from the respiratory tract of cystic fibrosis patients.
International journal of systematic and evolutionary microbiology, 2003Co-Authors: Tom Coenye, Peter Vandamme, John J. LipumaAbstract:Five isolates recovered from the respiratory tract of cystic fibrosis patients were included in a polyphasic taxonomic study that employed 16S rDNA sequence analysis, cellular protein and fatty acid analysis and biochemical characterization. Four isolates were classified as a novel Ralstonia species, for which the name Ralstonia respiraculi sp. nov. is proposed; the other isolate was phylogenetically closely related to R. respiraculi, but is likely to represent another novel Ralstonia species. The type strain of R. respiraculi is AU3313(T) (=LMG 21510(T)=CCUG 46809(T)).
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infection by Ralstonia species in cystic fibrosis patients identification of r pickettii and r mannitolilytica by polymerase chain reaction
Emerging Infectious Diseases, 2002Co-Authors: Tom Coenye, Peter Vandamme, John J. LipumaAbstract:The frequency of respiratory tract infections caused by Ralstonia species in persons with cystic fibrosis (CF) and the role of these species in CF pulmonary disease are not well documented. In part, this lack of documentation may be attributed to the difficulty in accurately identifying Ralstonia species; R. mannitolilytica and R. pickettii in particular may be misidentified as other closely related species, particularly those of the Burkholderia cepacia complex. We used polyphasic analyses to identify 42 Ralstonia isolates from sputum cultures from 38 CF patients. Several isolates that could not be identified to the species level may belong to novel Ralstonia species. We demonstrated chronic colonization by using genotyping of serial isolates recovered from the same patient. To facilitate identification of R. mannitolilytica and R. pickettii, we developed 16S ribosomal DNA-based polymerase chain reaction assays that allow sensitive and specific identification of these species.
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Classification of metal-resistant bacteria from industrial biotopes as Ralstonia campinensis sp. nov., Ralstonia metallidurans sp. nov. and Ralstonia basilensis Steinle et al. 1998 emend.
International Journal of Systematic and Evolutionary Microbiology, 2001Co-Authors: Johan Goris, P De Vos, Tom Coenye, B Hoste, D Janssens, K Kersters, H Brim, L Diels, Max Mergeay, Peter VandammeAbstract:Thirty-one heavy-metal-resistant bacteria isolated from industrial biotopes were subjected to polyphasic characterization, including 16S rDNA sequence analysis, DNA-DNA hybridizations, biochemical tests, whole-cell protein and fatty-acid analyses. All strains were shown to belong to the Ralstonia branch of the beta-Proteobacteria. Whole-cell protein profiles and DNA-DNA hybridizations revealed two clearly distinct groups, showing low similarity to known Ralstonia species. These two groups, of 8 and 17 isolates, were assigned to two new species, for which the names Ralstonia campinensis sp. nov. and Ralstonia metallidurans sp. nov. are proposed. The type strains are WS2T (= LMG 19282T = CCUG 44526T) and CH34T (= LMG 1195T = DSM 2839T), respectively. Six isolates were allocated to Ralstonia basilensis, which presently contains only the type strain; an emendation of the latter species description is therefore proposed.
Peter Vandamme - One of the best experts on this subject based on the ideXlab platform.
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Use of PCR Analyses To Define the Distribution of Ralstonia Species Recovered from Patients with Cystic Fibrosis
Journal of clinical microbiology, 2005Co-Authors: Tom Coenye, Theodore Spilker, Rebecca Reik, Peter Vandamme, John J. LipumaAbstract:Two new PCR assays (for Ralstonia species and Ralstonia respiraculi), together with previously published PCR assays, were used to assess Ralstonia isolates recovered from 111 cystic fibrosis patients. Ralstonia mannitolilytica accounted for 46% of isolates, while R. respiraculi and Ralstonia pickettii accounted for 19% and 18%, respectively. Ralstonia basilensis and Ralstonia metallidurans, species not previously recovered from human samples, were also identified.
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Classification of Ralstonia pickettii-like isolates from the environment and clinical samples as Ralstonia insidiosa sp. nov.
International Journal of Systematic and Evolutionary Microbiology, 2003Co-Authors: Tom Coenye, Johan Goris, Paul De Vos, Peter Vandamme, John J. LipumaAbstract:Thirteen Ralstonia pickettii-like isolates from the environment (water, soil and activated sludge) and human clinical samples (including respiratory secretions of cystic fibrosis patients) were investigated in a polyphasic taxonomic study that employed 16S rDNA sequence analysis, DNA–DNA hybridization, determination of DNA base composition, whole-cell protein analysis, biochemical characterization and PCR-based assays. All isolates were classified as a novel Ralstonia species, for which the name Ralstonia insidiosa sp. nov. is proposed. The type strain, LMG 21421T (=CCUG 46789T), was isolated from the sputum of a patient with acute lymphoblastic leukaemia. R. insidiosa can be differentiated from other species of the genus Ralstonia and phenotypically similar species (including the Burkholderia cepacia complex and Achromobacter xylosoxidans) by a variety of biochemical tests, whole-cell protein analysis and several PCR-based assays. Some outstanding issues in the taxonomy of the genus Ralstonia are also discussed.
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Ralstonia respiraculi sp. nov., isolated from the respiratory tract of cystic fibrosis patients.
International journal of systematic and evolutionary microbiology, 2003Co-Authors: Tom Coenye, Peter Vandamme, John J. LipumaAbstract:Five isolates recovered from the respiratory tract of cystic fibrosis patients were included in a polyphasic taxonomic study that employed 16S rDNA sequence analysis, cellular protein and fatty acid analysis and biochemical characterization. Four isolates were classified as a novel Ralstonia species, for which the name Ralstonia respiraculi sp. nov. is proposed; the other isolate was phylogenetically closely related to R. respiraculi, but is likely to represent another novel Ralstonia species. The type strain of R. respiraculi is AU3313(T) (=LMG 21510(T)=CCUG 46809(T)).
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infection by Ralstonia species in cystic fibrosis patients identification of r pickettii and r mannitolilytica by polymerase chain reaction
Emerging Infectious Diseases, 2002Co-Authors: Tom Coenye, Peter Vandamme, John J. LipumaAbstract:The frequency of respiratory tract infections caused by Ralstonia species in persons with cystic fibrosis (CF) and the role of these species in CF pulmonary disease are not well documented. In part, this lack of documentation may be attributed to the difficulty in accurately identifying Ralstonia species; R. mannitolilytica and R. pickettii in particular may be misidentified as other closely related species, particularly those of the Burkholderia cepacia complex. We used polyphasic analyses to identify 42 Ralstonia isolates from sputum cultures from 38 CF patients. Several isolates that could not be identified to the species level may belong to novel Ralstonia species. We demonstrated chronic colonization by using genotyping of serial isolates recovered from the same patient. To facilitate identification of R. mannitolilytica and R. pickettii, we developed 16S ribosomal DNA-based polymerase chain reaction assays that allow sensitive and specific identification of these species.
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Classification of metal-resistant bacteria from industrial biotopes as Ralstonia campinensis sp. nov., Ralstonia metallidurans sp. nov. and Ralstonia basilensis Steinle et al. 1998 emend.
International Journal of Systematic and Evolutionary Microbiology, 2001Co-Authors: Johan Goris, P De Vos, Tom Coenye, B Hoste, D Janssens, K Kersters, H Brim, L Diels, Max Mergeay, Peter VandammeAbstract:Thirty-one heavy-metal-resistant bacteria isolated from industrial biotopes were subjected to polyphasic characterization, including 16S rDNA sequence analysis, DNA-DNA hybridizations, biochemical tests, whole-cell protein and fatty-acid analyses. All strains were shown to belong to the Ralstonia branch of the beta-Proteobacteria. Whole-cell protein profiles and DNA-DNA hybridizations revealed two clearly distinct groups, showing low similarity to known Ralstonia species. These two groups, of 8 and 17 isolates, were assigned to two new species, for which the names Ralstonia campinensis sp. nov. and Ralstonia metallidurans sp. nov. are proposed. The type strains are WS2T (= LMG 19282T = CCUG 44526T) and CH34T (= LMG 1195T = DSM 2839T), respectively. Six isolates were allocated to Ralstonia basilensis, which presently contains only the type strain; an emendation of the latter species description is therefore proposed.
Gerda Verschraegen - One of the best experts on this subject based on the ideXlab platform.
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Wautersia gen. nov., a novel genus accommodating the phylogenetic lineage including Ralstonia eutropha and related species, and proposal of Ralstonia [Pseudomonas] syzygii (Roberts et al. 1990) comb. nov.
International Journal of Systematic and Evolutionary Microbiology, 2004Co-Authors: Mario Vaneechoutte, Peter Kämpfer, Thierry De Baere, Enevold Falsen, Gerda VerschraegenAbstract:Comparative 16S rDNA sequence analysis indicates that two distinct sublineages, with a sequence dissimilarity of >4 % (bootstrap value, 100 %), exist within the genus Ralstonia: the Ralstonia eutropha lineage, which comprises Ralstonia basilensis, Ralstonia campinensis, R. eutropha, Ralstonia gilardii, Ralstonia metallidurans, Ralstonia oxalatica, Ralstonia paucula, Ralstonia respiraculi and Ralstonia taiwanensis; and the Ralstonia pickettii lineage, which comprises Ralstonia insidiosa, Ralstonia mannitolilytica, R. pickettii, Ralstonia solanacearum and Ralstonia syzygii comb. nov. (previously Pseudomonas syzygii). This phylogenetic discrimination is supported by phenotypic differences. Members of the R. eutropha lineage have peritrichous flagella, do not produce acids from glucose and are susceptible to colistin, in contrast to members of the R. pickettii lineage, which have one or more polar flagella, produce acid from several carbohydrates and are colistin-resistant. Members of the R. pickettii lineage are viable for up to 6 days on tryptic soy agar at 25 °C, whereas members of the R. eutropha lineage are viable for longer than 9 days. It is proposed that species of the R. eutropha lineage should be classified in a novel genus, Wautersia gen. nov. Finally, based on the literature and new DNA–DNA hybridization data, it is proposed that Pseudomonas syzygii should be renamed Ralstonia syzygii comb. nov.
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Wautersia gen. nov., a novel genus accommodating the phylogenetic lineage including Ralstonia eutropha and related species, and proposal of Ralstonia [Pseudomonas] syzygii (Roberts et al. 1990) comb. nov.
International journal of systematic and evolutionary microbiology, 2004Co-Authors: Mario Vaneechoutte, Peter Kämpfer, Thierry De Baere, Enevold Falsen, Gerda VerschraegenAbstract:Comparative 16S rDNA sequence analysis indicates that two distinct sublineages, with a sequence dissimilarity of >4 % (bootstrap value, 100 %), exist within the genus Ralstonia: the Ralstonia eutropha lineage, which comprises Ralstonia basilensis, Ralstonia campinensis, R. eutropha, Ralstonia gilardii, Ralstonia metallidurans, Ralstonia oxalatica, Ralstonia paucula, Ralstonia respiraculi and Ralstonia taiwanensis; and the Ralstonia pickettii lineage, which comprises Ralstonia insidiosa, Ralstonia mannitolilytica, R. pickettii, Ralstonia solanacearum and Ralstonia syzygii comb. nov. (previously Pseudomonas syzygii). This phylogenetic discrimination is supported by phenotypic differences. Members of the R. eutropha lineage have peritrichous flagella, do not produce acids from glucose and are susceptible to colistin, in contrast to members of the R. pickettii lineage, which have one or more polar flagella, produce acid from several carbohydrates and are colistin-resistant. Members of the R. pickettii lineage are viable for up to 6 days on tryptic soy agar at 25 degrees C, whereas members of the R. eutropha lineage are viable for longer than 9 days. It is proposed that species of the R. eutropha lineage should be classified in a novel genus, Wautersia gen. nov. Finally, based on the literature and new DNA-DNA hybridization data, it is proposed that Pseudomonas syzygii should be renamed Ralstonia syzygii comb. nov.
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classification of Ralstonia pickettii biovar 3 thomasii strains pickett 1994 and of new isolates related to nosocomial recurrent meningitis as Ralstonia mannitolytica sp nov
International Journal of Systematic and Evolutionary Microbiology, 2001Co-Authors: T De Baere, Sophia Steyaert, Georges Wauters, P De Vos, Johan Goris, Tom Coenye, Teruaki Suyama, Gerda Verschraegen, Mario VaneechoutteAbstract:Strains isolated independently from two patients could be recognized as Ralstonia pickettii biovar 3/'thomasii'. The 16S rDNA sequences of these strains and two other strains of R. pickettii biovar 3/'thomasii' clustered at less than 98% similarity versus all other described Ralstonia species and at less than 97 % versus the two other R. pickettii biovars. The separate species status of R. pickettii biovar 3/'thomasii' was confirmed by DNA-DNA hybridization, indicating less than 60% DNA homology with the R. pickettii biovars Va-1 and Va-2 and with two as-yet unclassified but biochemically similar Ralstonia strains. Phenotypically, this Ralstonia species can be distinguished from all described Ralstonia species by its acidification of D-arabitol and mannitol and by its lack of nitrate reduction and of alkalinization of tartrate and from two as-yet unclassified Ralstonia strains only by its lack of nitrate reduction. The name Ralstonia mannitolytica sp. nov. is proposed, reflecting the characteristic acidification of mannitol. Resistance to desferrioxamine is another difference from R. pickettii and Ralstonia solanacearum. Although several nosocomial outbreaks have been associated with R. mannitolytica, life-threatening infections have not yet been reported, possibly due to misidentification as Pseudomonas fluorescens or Burkholderia cepacia. In at least one of the two cases reported here, the R. mannitolytica isolate was found to be clinically relevant, causing recurrent nosocomial meningitis, with an infected implanted catheter as the source. The type strain of R. mannitolytica is NCIMB 10805T (= LMG 6866T), which was isolated during the first described outbreak as 'Pseudomonas thomasii' at St Thomas' Hospital, London, UK, in 1971.
Philippe Prior - One of the best experts on this subject based on the ideXlab platform.
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TALE-Like Effectors Are an Ancestral Feature of the Ralstonia solanacearum Species Complex and Converge in DNA Targeting Specificity
Frontiers in Plant Science, 2016Co-Authors: Niklas Schandry, Philippe Prior, Orlando De Lange, Thomas LahayeAbstract:Raistonia solanacearum, a species complex of bacterial plant pathogens divided into four monophyletic phylotypes, causes plant diseases in tropical climates around the world. Some strains exhibit a broad host range on solanaceous hosts, while others are highly host-specific as for example some banana-pathogenic strains. Previous studies showed that transcription activator-like (TAL) effectors from Raistonia, termed RipTALs, are capable of activating reporter genes in planta, if these are preceded by a matching effector binding element (EBE). RipTALs target DNA via their central repeat domain (CRD), where one repeat pairs with one DNA-base of the given EBE. The repeat variable diresidue dictates base repeat specificity in a predictable fashion, known as the TALE code. In this work, we analyze RipTALs across all phylotypes of the Ralstonia solanacearum species complex. We find that RipTALs are prevalent in phylotypes I and IV but absent from most phylotype III and II strains (10/12, 8/14, 1/24, and 1/5 strains contained a RipTAL, respectively). RipTALs originating from strains of the same phylotype show high levels of sequence similarity (>98%) in the N-terminal and C-terminal regions, while RipTALs isolated from different phylotypes show 47-91% sequence similarity in those regions, giving rise to four RipTAL classes. We show that, despite sequence divergence, the base preference for guanine, mediated by the N-terminal region, is conserved across RipTALs of all classes. Using the number and order of repeats found in the CRD, we functionally sub-classify RipTALs, introduce a new simple nomenclature, and predict matching EBEs for all seven distinct RipTALs identified. We experimentally study RipTAL EBEs and uncover that some RipTALs are able to target the EBEs of other RipTALs, referred to as cross-reactivity. In particular, RipTALs from strains with a broad host range on solanaceous hosts cross-react on each other's EBEs. Investigation of sequence divergence between RipTAL repeats allows for a reconstruction of repeat array biogenesis, for example through slipped strand mispairing or gene conversion. Using these studies we show how RipTALs of broad host range strains evolved convergently toward a shared target sequence. Finally, we discuss the differences between TALE-likes of plant pathogens in the context of disease ecology.
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First Report of Ralstonia pseudosolanacearum Phylotype I Causing Bacterial Wilt on Rodrigues Island, Indian Ocean
Plant Disease, 2016Co-Authors: Noura Yahiaoui, Philippe Prior, Jean-jacques Chéron, R. Jeetah, S. Benimadhu, J. Félicité, Gilles Cellier, Fabien Guérin, Stephane PoussierAbstract:First Report of Ralstonia pseudosolanacearum Phylotype I Causing Bacterial Wilt on Rodrigues Island, Indian Ocean
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Horizontal gene transfer between Ralstonia solanacearum strains detected by comparative genomic hybridization on microarrays.
The ISME Journal, 2009Co-Authors: Alice Guidot, Bénédicte Coupat, Saliou Fall, Philippe Prior, Franck BertollaAbstract:Horizontal gene transfer between Ralstonia solanacearum strains detected by comparative genomic hybridization on microarrays
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bacterial wilt disease and the Ralstonia solanacearum species complex
Bacterial wilt disease and the Ralstonia solanacearum species complex., 2005Co-Authors: Caitilyn Allen, Philippe Prior, A C HaywardAbstract:Contents: Preface. Introductory overviews: Research on bacterial wilt: a perspective on international linkages and access to the literature; the current bacterial wilt situation: a global overview - Epidemiology of Ralstonia solanacearum: introduction and prospectus on the survival of introduction and prospectus on the survival; Fate of Ralstonia solanacearum Biovar 2 as affected by conditions and soil treatments in temperate climate zones; Mechanization has contributed to the spread of bacterial wilt on flue-cured tobacco in the Southeastern USA; Processes in the development of a biocontrol agent against bacterial wilt; Colonization capacity of Ralstonia solanacearum; Tomato strains differing in aggressiveness on tomatoes and weeds; Introduction to Europe of Ralstonia solanacearum Biovar 2, Race 3 in Pelargonium zonale cuttings from Kenya; Seeds from infected tomato plants appear to be free from contamination by Ralstonia solanacearum when tested by PCR or microbiological assays; The viable but non-culturable state in Ralstonia solanacearum: is there a realistic threat to our strategic concepts? - Bacterial wilt disease management: Management of bacterial wilt disease; Management of bacterial wilt in tomato with essential oils and systemic acquired resistance inducers; Monitoring of bacterial wilt in potato propagation material: a success story; Integrated control of potato bacterial wilt in Eastern Africa: the experience of African highlands initiative; Using Brassica spp. as biofumigants to reduce the population of Ralstonia solanacearum; Seed-plot technique: empowerment of farmers in production of bacterial wilt-free seed potato in Kenya and Uganda; Primary bacterial wilt study on tomato in vegetable areas of Ho Chi Minh City, Vietnam; Rhizome solarization and microwave treatment: ecofriendly methods for disinfecting ginger seed rhizomes; Management of bacterial wilt of potato using one-season rotation crops in South-Western Uganda; Potato bacterial wilt management: new prospects for an old problem - Breeding and deployment of wilt-resistant crops: A broad review and perspective on breeding for resistance to bacterial wilt; Progress on genetic enhancement for resistance to groundnut bacterial wilt in China; Search for resistance to bacterial wilt in a Brazilian Capsicum germplasm collection; Solanum phureja and S. stenotomum are sources of resistance to Ralstonia solanacearum for somatic hybrids of potato; Assessment of resistance to bacterial wilt in CIP advanced potato clones; Screening long pepper (Piper spp.) resistance to bacterial wilt caused by Ralstonia solanacearum - Host plant response and disease development: Host resistance to Ralstonia solanacearum; Microscopic studies of root infection in resistant tomato cv. Hawaii 7996; Development of bacterial wilt resistant varieties and basis of resistance in eggplant (Solanum melongena); QTL mapping for bacterial wilt resistance in Hawaii 7996 using AFLP, RGA, and SSR markers; Genetic basis of resistance to bacterial wilt in Arabidopsi thaliana; Roles of the Hrp-secreted PopA protein in Ralstonia solanacearum interactions with plants - Pathogen genetics: A short history of the biochemical and genetic research on Ralstonia solanacearum pathogenesis; The Ralstonia solanacearum complete genome sequence: outputs and prospects; Genes involved in early bacterial wilt pathogenesis; Phase reversion from phenotype conversion mutants to wild type may be induced in Ralstonia solanacearum by a susceptible host-plant; Insertions in the avirulence gene AvrA alter the virulence of Ralstonia solanacearum on Nicotiana tabacum; Ralstonia solanacearum requires type-4 Pili for twitching motility, adherence, natural transformation and virulence; Understanding the molecular basis of bacterial wilt disease: a view from the inside out - R. solanacearum in banana and plantains: Bacterial wilt diseases of banana: evolution and ecology; Comparative genome plasticity of tomato and banana strains o
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partial sequencing of the hrpb and endoglucanase genes confirms and expands the known diversity within the Ralstonia solanacearum species complex
Systematic and Applied Microbiology, 2000Co-Authors: Stephane Poussier, Jacques Luisetti, Chris Hayward, Philippe Prior, Michael FeganAbstract:We determined partial hrpB and endoglucanase genes sequences for 30 strains of Ralstonia solanacearum and one strain of the blood disease bacterium (BDB), a close relative of Ralstonia solanacearum. Sequence comparisons showed high levels of variability within these two regions of the genome involved in pathogenicity. Phylogenetic analysis based upon sequence comparisons of these two regions revealed three major clusters comprising all Ralstonia solanacearium isolates, the BDB strain constituted a phylogenetically distinct entity. Cluster 1 and cluster 2 corresponded to the previously defined divisions 1 and 2 of Ralstonia solanacearum. Moreover, two subclusters could be identified within cluster 2. The last cluster, designated cluster 3 in this study, included biovar 1 and N2 strains originating from Africa. This recently described group of strains was confirmed to be clearly different from the other strains suggesting a separate evolution from those of both divisions 1 and 2.
Mario Vaneechoutte - One of the best experts on this subject based on the ideXlab platform.
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Wautersia gen. nov., a novel genus accommodating the phylogenetic lineage including Ralstonia eutropha and related species, and proposal of Ralstonia [Pseudomonas] syzygii (Roberts et al. 1990) comb. nov.
International Journal of Systematic and Evolutionary Microbiology, 2004Co-Authors: Mario Vaneechoutte, Peter Kämpfer, Thierry De Baere, Enevold Falsen, Gerda VerschraegenAbstract:Comparative 16S rDNA sequence analysis indicates that two distinct sublineages, with a sequence dissimilarity of >4 % (bootstrap value, 100 %), exist within the genus Ralstonia: the Ralstonia eutropha lineage, which comprises Ralstonia basilensis, Ralstonia campinensis, R. eutropha, Ralstonia gilardii, Ralstonia metallidurans, Ralstonia oxalatica, Ralstonia paucula, Ralstonia respiraculi and Ralstonia taiwanensis; and the Ralstonia pickettii lineage, which comprises Ralstonia insidiosa, Ralstonia mannitolilytica, R. pickettii, Ralstonia solanacearum and Ralstonia syzygii comb. nov. (previously Pseudomonas syzygii). This phylogenetic discrimination is supported by phenotypic differences. Members of the R. eutropha lineage have peritrichous flagella, do not produce acids from glucose and are susceptible to colistin, in contrast to members of the R. pickettii lineage, which have one or more polar flagella, produce acid from several carbohydrates and are colistin-resistant. Members of the R. pickettii lineage are viable for up to 6 days on tryptic soy agar at 25 °C, whereas members of the R. eutropha lineage are viable for longer than 9 days. It is proposed that species of the R. eutropha lineage should be classified in a novel genus, Wautersia gen. nov. Finally, based on the literature and new DNA–DNA hybridization data, it is proposed that Pseudomonas syzygii should be renamed Ralstonia syzygii comb. nov.
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Wautersia gen. nov., a novel genus accommodating the phylogenetic lineage including Ralstonia eutropha and related species, and proposal of Ralstonia [Pseudomonas] syzygii (Roberts et al. 1990) comb. nov.
International journal of systematic and evolutionary microbiology, 2004Co-Authors: Mario Vaneechoutte, Peter Kämpfer, Thierry De Baere, Enevold Falsen, Gerda VerschraegenAbstract:Comparative 16S rDNA sequence analysis indicates that two distinct sublineages, with a sequence dissimilarity of >4 % (bootstrap value, 100 %), exist within the genus Ralstonia: the Ralstonia eutropha lineage, which comprises Ralstonia basilensis, Ralstonia campinensis, R. eutropha, Ralstonia gilardii, Ralstonia metallidurans, Ralstonia oxalatica, Ralstonia paucula, Ralstonia respiraculi and Ralstonia taiwanensis; and the Ralstonia pickettii lineage, which comprises Ralstonia insidiosa, Ralstonia mannitolilytica, R. pickettii, Ralstonia solanacearum and Ralstonia syzygii comb. nov. (previously Pseudomonas syzygii). This phylogenetic discrimination is supported by phenotypic differences. Members of the R. eutropha lineage have peritrichous flagella, do not produce acids from glucose and are susceptible to colistin, in contrast to members of the R. pickettii lineage, which have one or more polar flagella, produce acid from several carbohydrates and are colistin-resistant. Members of the R. pickettii lineage are viable for up to 6 days on tryptic soy agar at 25 degrees C, whereas members of the R. eutropha lineage are viable for longer than 9 days. It is proposed that species of the R. eutropha lineage should be classified in a novel genus, Wautersia gen. nov. Finally, based on the literature and new DNA-DNA hybridization data, it is proposed that Pseudomonas syzygii should be renamed Ralstonia syzygii comb. nov.
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classification of Ralstonia pickettii biovar 3 thomasii strains pickett 1994 and of new isolates related to nosocomial recurrent meningitis as Ralstonia mannitolytica sp nov
International Journal of Systematic and Evolutionary Microbiology, 2001Co-Authors: T De Baere, Sophia Steyaert, Georges Wauters, P De Vos, Johan Goris, Tom Coenye, Teruaki Suyama, Gerda Verschraegen, Mario VaneechoutteAbstract:Strains isolated independently from two patients could be recognized as Ralstonia pickettii biovar 3/'thomasii'. The 16S rDNA sequences of these strains and two other strains of R. pickettii biovar 3/'thomasii' clustered at less than 98% similarity versus all other described Ralstonia species and at less than 97 % versus the two other R. pickettii biovars. The separate species status of R. pickettii biovar 3/'thomasii' was confirmed by DNA-DNA hybridization, indicating less than 60% DNA homology with the R. pickettii biovars Va-1 and Va-2 and with two as-yet unclassified but biochemically similar Ralstonia strains. Phenotypically, this Ralstonia species can be distinguished from all described Ralstonia species by its acidification of D-arabitol and mannitol and by its lack of nitrate reduction and of alkalinization of tartrate and from two as-yet unclassified Ralstonia strains only by its lack of nitrate reduction. The name Ralstonia mannitolytica sp. nov. is proposed, reflecting the characteristic acidification of mannitol. Resistance to desferrioxamine is another difference from R. pickettii and Ralstonia solanacearum. Although several nosocomial outbreaks have been associated with R. mannitolytica, life-threatening infections have not yet been reported, possibly due to misidentification as Pseudomonas fluorescens or Burkholderia cepacia. In at least one of the two cases reported here, the R. mannitolytica isolate was found to be clinically relevant, causing recurrent nosocomial meningitis, with an infected implanted catheter as the source. The type strain of R. mannitolytica is NCIMB 10805T (= LMG 6866T), which was isolated during the first described outbreak as 'Pseudomonas thomasii' at St Thomas' Hospital, London, UK, in 1971.
