Burkholderia stagnalis sp. nov. and Burkholderia territorii sp. nov., two novel Burkholderia cepacia complex species from environmental and human sources

Author:

De Smet Birgit12,Mayo Mark3,Peeters Charlotte2,Zlosnik James E. A.4,Spilker Theodore5,Hird Trevor J.4,LiPuma John J.5,Kidd Timothy J.6,Kaestli Mirjam3,Ginther Jennifer L.7,Wagner David M.7,Keim Paul7,Bell Scott C.689,Jacobs Jan A.110,Currie Bart J.3,Vandamme Peter2

Affiliation:

1. Department of Clinical Sciences, Institute of Tropical Medicine, Antwerp, Belgium

2. Laboratory of Microbiology, Faculty of Sciences, Ghent University, Ghent, Belgium

3. Global and Tropical Health Division, Menzies School of Health Research, Darwin, Northern Territory, Australia

4. Centre for Understanding and Preventing Infection in Children, Department of Paediatrics, University of British Columbia, Vancouver, BC, Canada

5. Department of Paediatrics and Communicable Diseases, University of Michigan Medical School, Ann Arbor, MI, USA

6. Queensland Children's Medical Research Institute, University of Queensland, Brisbane, Queensland, Australia

7. Center for Microbial Genetics and Genomics, Northern Arizona University, Flagstaff, AZ, USA

8. Department of Thoracic Medicine, The Prince Charles Hospital, Brisbane, Queensland, Australia

9. QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia

10. Department of Microbiology and Immunology, University of Leuven, Belgium

Abstract

Nine Burkholderia cepacia complex (Bcc) bacteria were isolated during environmental surveys for the ecological niche of Burkholderia pseudomallei, the aetiological agent of melioidosis, in the Northern Territory of Australia. They represented two multi-locus sequence analysis-based clusters, referred to as Bcc B and Bcc L. Three additional environmental and clinical Bcc B isolates were identified upon deposition of the sequences in the PubMLST database. Analysis of the concatenated nucleotide sequence divergence levels within both groups (1.4 and 1.9 %, respectively) and towards established Bcc species (4.0 and 3.9 %, respectively) demonstrated that the two taxa represented novel Bcc species. All 12 isolates were further characterized using 16S rRNA and recA gene sequence analysis, RAPD analysis, DNA base content determination, fatty acid methyl ester analysis and biochemical profiling. Analysis of recA gene sequences revealed a remarkable diversity within each of these taxa, but, together, the results supported the affiliation of the two taxa to the Bcc. Bcc B strains can be differentiated from most other Bcc members by the assimilation of maltose. Bcc L strains can be differentiated from other Bcc members by the absence of assimilation of N-acetylglucosamine. The names Burkholderia stagnalis sp. nov. with type strain LMG 28156T ( = CCUG 65686T) and Burkholderia territorii sp. nov. with type strain LMG 28158T ( = CCUG 65687T) are proposed for Bcc B and Bcc L bacteria, respectively.

Publisher

Microbiology Society

Subject

General Medicine,Ecology, Evolution, Behavior and Systematics,Microbiology

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