Mycobacterium sherrisii sp. nov., a slow-growing non-chromogenic species

Author:

van Ingen Jakko12,Tortoli Enrico3,Selvarangan Rangaraj4,Coyle Marie B.5,Crump John A.6789,Morrissey Anne B.9,Dekhuijzen P. N. Richard2,Boeree Martin J.2,van Soolingen Dick1

Affiliation:

1. National Mycobacteria Reference Laboratory, National Institute for Public Health and the Environment (RIVM), Bilthoven, The Netherlands

2. Department of Pulmonary Diseases, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands

3. Regional Reference Centre for Mycobacteria, Microbiology and Virology Laboratory, Careggi Hospital, Florence, Italy

4. Department of Pathology and Laboratory Medicine, Children’s Mercy Hospital, Kansas City, Missouri, USA

5. Department of Microbiology, University of Washington, Seattle, Washington, USA

6. Kilimanjaro Christian Medical Centre, Moshi, Tanzania

7. Duke Global Health Institute, Duke University, Durham, North Carolina, USA

8. Kilimanjaro Christian Medical College, Tumaini University, Moshi, Tanzania

9. Division of Infectious Diseases and International Health, Duke University Medical Center, Durham, North Carolina, USA

Abstract

Mycobacterium sherrisii’ is an undescribed species that appears to be emerging, in particular, among HIV-positive patients originating from Africa. To describe ‘M. sherrisii’, to ensure that the species name is validly published and to define its phylogenetic position, we collected 11 of these strains reported in five previous studies, and subjected them to biochemical identification, cell-wall mycolic acid analysis and sequencing of multiple housekeeping genes. The bacteria formed smooth and generally non-chromogenic colonies after 2–3 weeks of subculture at 24–37 °C; photochromogenic and scotochromogenic pigmentation were exhibited by three and two strains, respectively. The strains were positive for the heat-stable catalase test, but negative in tests for hydrolysis of Tween 80, nitrate reduction, β-glucosidase and 3-day arylsulfatase. Mycolic acid patterns, obtained by HPLC, resembled a trimodal profile similar to those of type strains of Mycobacterium simiae, Mycobacterium lentiflavum, Mycobacterium triplex and Mycobacterium genavense. The 16S rRNA gene sequences of the 11 strains differed by 4 bp (99.7 % similarity) from that of the type strain of the closest related species, M. simiae ATCC 25275T. Levels of internal transcribed spacer (ITS) and partial hsp65 and rpoB gene sequence similarity between the two taxa were 95.8 % (271/283 bp), 97.5 % (391/401 bp) and 95.2 % (700/735 bp), respectively. On the basis of these results, we propose the formal recognition of Mycobacterium sherrisii sp. nov. The type strain is 4773T ( = ATCC BAA-832T = DSM 45441T).

Funder

NIH Fogarty International Center AIDS International Training and Research Program

ISAAC

Duke University Center for AIDS Research

US NIH awards Duke Clinical Trials Unit and Clinical Research Sites

US National Institutes of Health (NIH) International Studies on AIDS Associated Coinfections award

Publisher

Microbiology Society

Subject

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

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