Literature DB >> 27881537

Complete Genome Sequence of Mycobacterium chimaera Strain AH16.

Nabeeh A Hasan1, Jennifer R Honda2,3, Rebecca M Davidson4, L Elaine Epperson4, Matthew J Bankowski5,6, Edward D Chan2,7,8, Michael Strong4,7.   

Abstract

Mycobacterium chimaera is a nontuberculous mycobacterial species that causes cardiovascular, pulmonary, and postsurgical infections. Here, we report the first complete genome sequence of M. chimaera This genome is 6.33 Mbp, with a G+C content of 67.56%, and encodes 4,926 protein-coding genes, as well as 74 tRNAs, one ncRNA, and three rRNA genes.
Copyright © 2016 Hasan et al.

Entities:  

Year:  2016        PMID: 27881537      PMCID: PMC5122679          DOI: 10.1128/genomeA.01276-16

Source DB:  PubMed          Journal:  Genome Announc


GENOME ANNOUNCEMENT

Mycobacterium chimaera is a nontuberculous mycobacterial species within the Mycobacterium avium complex (MAC). The use of single genes such as the 16s rRNA or rpoB for species identification often misidentifies M. chimaera as the closely related MAC species M. intracellulare (1, 2). M. chimaera is an opportunistic environmental pathogen implicated in cardiovascular and pulmonary infections (1, 3). In health-care settings, the occurrence and spread of M. chimaera infections have increased in prevalence in recent years, including recent outbreaks that have been attributed to contaminated medical equipment (4–6). Despite the public health relevance of M. chimaera, only three draft genomes are publicly available, none of which is a complete genome (7). To improve our understanding of this emerging pathogen, we sequenced and report here the first complete genome of M. chimaera. M. chimaera strain AH16, isolated from an 87-year-old male with suspected mycobacterial lung disease in O’ahu, Hawai’i, was identified using partial rpoB sequencing. The genome of M. chimaera AH16 was sequenced using Pacific Biosciences (PacBio) RSII single-molecule real-time (SMRT) technology. PacBio sequencing produced 243,370 reads (mean: 6,808 bp; min: 50 bp; max: 45,065 bp; ~262× genome coverage). The de novo genome assembly was performed using the Hierarchical Genome Assembly Process (8). The assembly was compared to other MAC genomes using Mauve version 2.3.1 (9). Genomic features were identified and annotated using the NCBI Prokaryotic Genome Annotation Pipeline (10). The genome of M. chimaera AH16 consists of 4 scaffolds equaling 6,328,534 bp (5,851,561-bp chromosome; 437,456-bp plasmid; 25,007-bp plasmid; 14,510-bp plasmid) and a G+C content of 67.56%. A total of 4,926 coding sequences (CDSs) were predicted, including 3,161 CDSs (64.17%) with functional annotations and 1,765 CDSs (35.83%) annotated as hypothetical proteins. Our genome assembly contains 74 tRNAs, one ncRNA, and one rRNA cistron consisting of the 16S, 23S, and 5S rRNA genes. Whole-genome alignments of M. chimaera AH16 and six MAC genomes revealed 511,189 variable single nucleotide polymorphisms (SNPs), including: 459,672 SNPs compared to M. avium subsp. hominis suis TH135; 64,709 SNPs compared to M. intracellulare ATCC 13950; 50,875 SNPs compared to Mycobacterium sp. MOTT 36Y; 49,805 SNPs compared to M. yongonense 05-0390T; and 49,524 SNPs compared to Mycobacterium sp. H4Y. Comparing the M. chimaera AH16 genome against the M. avium subsp. hominis suis TH135, M. intracellulare ATCC 13950, M. yongonense 05-0390T, Mycobacterium sp. MOTT 36Y, and Mycobacterium sp. H4Y genomes, the average nucleotide identities (ANIs) were 85.55%, 96.87%, 97.14%, 97.16%, and 97.22%, respectively. The limited SNP variation (0.78 to 7.26% of the M. chimaera AH16 genome) and ANI values observed between M. chimaera AH16 and MAC species suggests that the non–M. avium MAC species have limited genomic variation. Furthermore, intraspecies genome comparisons of M. chimaera AH16 to M. chimaera MCIMRL6, MCIMRL4, and MCIMRL2 (accession nos. LJHN00000000, LJHM00000000, and LJHL00000000) have 99.14%, 99.11%, and 99.18% ANIs, respectively, which are within the 95 to 96% cutoff for species boundaries (11).

Accession number(s).

The genome sequence of M. chimaera AH16 is deposited in NCBI GenBank under the accession numbers CP012885 to CP012888.
  10 in total

1.  Nonhybrid, finished microbial genome assemblies from long-read SMRT sequencing data.

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Journal:  Nat Methods       Date:  2013-05-05       Impact factor: 28.547

2.  Healthcare-associated prosthetic heart valve, aortic vascular graft, and disseminated Mycobacterium chimaera infections subsequent to open heart surgery.

Authors:  Philipp Kohler; Stefan P Kuster; Guido Bloemberg; Bettina Schulthess; Michelle Frank; Felix C Tanner; Matthias Rössle; Christian Böni; Volkmar Falk; Markus J Wilhelm; Rami Sommerstein; Yvonne Achermann; Jaap Ten Oever; Sylvia B Debast; Maurice J H M Wolfhagen; George J Brandon Bravo Bruinsma; Margreet C Vos; Ad Bogers; Annerose Serr; Friedhelm Beyersdorf; Hugo Sax; Erik C Böttger; Rainer Weber; Jakko van Ingen; Dirk Wagner; Barbara Hasse
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3.  Prolonged Outbreak of Mycobacterium chimaera Infection After Open-Chest Heart Surgery.

Authors:  Hugo Sax; Guido Bloemberg; Barbara Hasse; Rami Sommerstein; Philipp Kohler; Yvonne Achermann; Matthias Rössle; Volkmar Falk; Stefan P Kuster; Erik C Böttger; Rainer Weber
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4.  Absence of Mycobacterium intracellulare and presence of Mycobacterium chimaera in household water and biofilm samples of patients in the United States with Mycobacterium avium complex respiratory disease.

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5.  progressiveMauve: multiple genome alignment with gene gain, loss and rearrangement.

Authors:  Aaron E Darling; Bob Mau; Nicole T Perna
Journal:  PLoS One       Date:  2010-06-25       Impact factor: 3.240

6.  Proposal to elevate the genetic variant MAC-A, included in the Mycobacterium avium complex, to species rank as Mycobacterium chimaera sp. nov.

Authors:  Enrico Tortoli; Laura Rindi; Maria J Garcia; Patrizia Chiaradonna; Rosanna Dei; Carlo Garzelli; Reiner M Kroppenstedt; Nicoletta Lari; Romano Mattei; Alessandro Mariottini; Gianna Mazzarelli; Martha I Murcia; Anna Nanetti; Paola Piccoli; Claudio Scarparo
Journal:  Int J Syst Evol Microbiol       Date:  2004-07       Impact factor: 2.747

7.  Shifting the genomic gold standard for the prokaryotic species definition.

Authors:  Michael Richter; Ramon Rosselló-Móra
Journal:  Proc Natl Acad Sci U S A       Date:  2009-10-23       Impact factor: 11.205

8.  Occurrence and clinical relevance of Mycobacterium chimaera sp. nov., Germany.

Authors:  Birgitta Schweickert; Oliver Goldenberg; Elvira Richter; Ulf B Göbel; Annette Petrich; Petra Buchholz; Annette Moter
Journal:  Emerg Infect Dis       Date:  2008-09       Impact factor: 6.883

9.  Draft Genome Sequences of Three Mycobacterium chimaera Respiratory Isolates.

Authors:  Micheál Mac Aogáin; Emma Roycroft; Philomena Raftery; Simone Mok; Margaret Fitzgibbon; Thomas R Rogers
Journal:  Genome Announc       Date:  2015-12-03

10.  Transmission of Mycobacterium chimaera from Heater-Cooler Units during Cardiac Surgery despite an Ultraclean Air Ventilation System.

Authors:  Rami Sommerstein; Christian Rüegg; Philipp Kohler; Guido Bloemberg; Stefan P Kuster; Hugo Sax
Journal:  Emerg Infect Dis       Date:  2016-06-15       Impact factor: 6.883

  10 in total
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1.  Complete Genome Sequence of Mycobacteriumchimaera Strain CDC2015-22-71.

Authors:  Nabeeh A Hasan; Adrian Lawsin; K Allison Perry; Efe Alyanak; Nadege C Toney; Allyson Malecha; Lori A Rowe; Dhwani Batra; Heather Moulton-Meissner; Jeffrey R Miller; Michael Strong; Alison Laufer Halpin
Journal:  Genome Announc       Date:  2017-08-03

2.  Complete Genome Sequence of Mycobacterium chimaera SJ42, a Nonoutbreak Strain from an Immunocompromised Patient with Pulmonary Disease.

Authors:  Nabeeh A Hasan; René L Warren; L Elaine Epperson; Allyson Malecha; David C Alexander; Christine Y Turenne; Daniel MacMillan; Inanc Birol; Stephen Pleasance; Robin Coope; Steven J M Jones; Marc G Romney; Monica Ng; Tracy Chan; Mabel Rodrigues; Patrick Tang; Jennifer L Gardy; Michael Strong
Journal:  Genome Announc       Date:  2017-09-14

3.  Physical Measures to Reduce Exposure to Tap Water-Associated Nontuberculous Mycobacteria.

Authors:  Grant J Norton; Myra Williams; Joseph O Falkinham; Jennifer R Honda
Journal:  Front Public Health       Date:  2020-06-12

4.  A scalable, efficient, and safe method to prepare high quality DNA from mycobacteria and other challenging cells.

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  4 in total

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