Acinetobacter ursingii sp. nov. and Acinetobacter schindleri sp. nov., isolated from human clinical specimens

A Nemec, T De Baere, I Tjernberg, M Vaneechoutte, TJK van der Reijden and L Dijkshoorn National Institute of Public Health, Srobarova 48, 10042 Prague, Czech Republic The taxonomic status of two recently described phenetically distinctive groups within the genus Acinetobacter, designated phenon 1 an...

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Veröffentlicht in:International journal of systematic and evolutionary microbiology 2001-09, Vol.51 (5), p.1891-1899
Hauptverfasser: Nemec, A, De Baere, T, Tjernberg, I, Vaneechoutte, M, van der Reijden, TJK, Dijkshoorn, L
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Sprache:eng
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Zusammenfassung:A Nemec, T De Baere, I Tjernberg, M Vaneechoutte, TJK van der Reijden and L Dijkshoorn National Institute of Public Health, Srobarova 48, 10042 Prague, Czech Republic The taxonomic status of two recently described phenetically distinctive groups within the genus Acinetobacter, designated phenon 1 and phenon 2, was investigated further. The study collection included 51 strains, mainly of clinical origin, from different European countries with properties of either phenon 1 (29 strains) or phenon 2 (22 strains). DNA--DNA hybridization studies and DNA polymorphism analysis by AFLP revealed that these phenons represented two new genomic species. Furthermore, 16S rRNA gene sequence analysis of three representatives of each phenon showed that they formed two distinct lineages within the genus Acinetobacter. The two phenons could be distinguished from each other and from all hitherto-described Acinetobacter (genomic) species by specific phenotypic features and amplified rDNA restriction analysis patterns. The names Acinetobacter ursingii sp. nov. (type strain LUH 3792(T)=NIPH 137(T)=LMG 19575(T)=CNCTC 6735(T)) and Acinetobacter schindleri sp. nov. (type strain LUH 5832(T)=NIPH 1034(T)=LMG 19576(T)=CNCTC 6736(T)) are proposed for phenon 1 and phenon 2, respectively. Clinical and epidemiological data indicate that A. ursingii has the capacity to cause bloodstream infections in hospitalized patients.
ISSN:1466-5026
1466-5034
DOI:10.1099/00207713-51-5-1891