Abstract
Buruli ulcer (BU) disease caused by Mycobacterium ulcerans is the third most common mycobacterial disease of public health importance. Decades of molecular studies aimed at improving our understanding of the epidemiology of BU have proven difficult to achieve in part due to the use of genotyping methods with insufficient discriminatory power to crack the highly clonal population structure of M. ulcerans to allow tracking the spread and transmission route of the pathogen in communities.
Comparative whole genome analysis showed for the first time that M. ulcerans focal distribution pattern breakdown and multiple M. ulcerans genotypes circulate within a local setting. This offers new perspectives on the nature of the reservoir and mode of transmission of M. ulcerans. The possibility of the bacteria or a reservoir spreading it to be widely distributed across a region and infections being acquired locally seems to be consistent with whole genome sequence data. Potential reservoirs of M. ulcerans thus might include humans or perhaps M. ulcerans-infected animals such as livestock that move regularly between countries.
Comparative whole genome analysis is illuminating our understanding of the nature of M. ulcerans niche environment to enable us to make accurate predictions about its possible reservoir and for the development of targeted and appropriate measures for the primary prevention of BU disease.
Beyond this, comparative genomics can potentially lead to the identification of new targets for development of rapid diagnostic tests to augment early detection and treatment of cases, which is the current strategy for BU control.
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References
Portaels F, Johnson P, Meyers WM, editors. Buruli ulcer: diagnosis of Mycobacterium ulcerans disease. A manual for health care providers. Geneva: World Health Organization; 2001. WHO/CDS/CPE/GBUI/2001.4
MacCallum P, Tolhurst JC, Buckle G, Sissons HA. A new mycobacterial infection in man. J Pathol Bacteriol. 1948;60(1):93–122.
Portaels F, Meyers WM, Ablordey A, Castro A, Chemlal K, De Rijk P, et al. First cultivation and characterization of Mycobacterium ulcerans from the environment. PLoS Negl Trop Dis. 2008;2(3):e178. https://doi.org/10.1371/journal.pntd.0000178.
Stinear TP, Seemann T, Pidot S, Frigui W, Reysset G, Garnier T, et al. Reductive evolution and niche adaptation inferred from the genome of Mycobacterium ulcerans, the causative agent of Buruli ulcer. Genome Res. 2007;17(2):192–200.
Stinear TP, Seemann T, Harrison PF, Jenkin GA, Davies JK, Johnson PDR, et al. Insights from the complete genome sequence of Mycobacterium marinum on the evolution of Mycobacterium tuberculosis. Genome Res. 2008;18(5):729–41. https://doi.org/10.1101/gr.075069.107.
Stinear T, Ross BC, Davies JK, Marino L, Robins-Browne RM, Oppedisano F, et al. Identification and characterization of IS2404 and IS2606: two distinct repeated sequences for detection of Mycobacterium ulcerans by PCR. J Clin Microbiol. 1999;37(4):1018–23.
Demangel C, Stinear T, Cole S. Buruli ulcer: reductive evolution enhances pathogenicity of Mycobacterium ulcerans. Nat Rev Microbiol. 2009;7:50–60. https://doi.org/10.1038/nrmicro2077.
Doig KD, Holt KE, Fyfe JA, Lavender CJ, Eddyani M, Portaels F, et al. On the origin of Mycobacterium ulcerans, the causative agent of Buruli ulcer. BMC Genomics. 2012;13:258. https://doi.org/10.1186/1471-2164-13-258.
Käser M, Rondini S, Naegeli M, Stinear T, Portaels F, Certa U, et al. Evolution of two distinct phylogenetic lineages of the emerging human pathogen Mycobacterium ulcerans. BMC Evol Biol. 2007;7:177. https://doi.org/10.1186/1471-2148-7-177.
Abdallah AM, Gey van Pittius NC, Champion PA, Cox J, Luirink J, Vandenbroucke-Grauls CM, et al. Type VII secretion—mycobacteria show the way. Nat Rev Microbiol. 2007;5(11):883–91. https://doi.org/10.1038/nrmicro1773.
Huber CA, Ruf MT, Pluschke G, Kaser M. Independent loss of immunogenic proteins in Mycobacterium ulcerans suggests immune evasion. Clin Vaccine Immunol. 2008;15(4):598–606.
Daffe M, Varnerot A, Levy-Frebault VV. The phenolic mycoside of Mycobacterium ulcerans: structure and taxonomic implications. J Gen Microbiol. 1992;138:131–7.
Ramakrishnan L, Tran HT, Federspiel NA, Falkow S. A crtB homolog essential for photochromogenicity in Mycobacterium marinum: isolation, characterization, and gene disruption via homologous recombination. J. Bacteriol. 1997;179(18):5862–8.
Stinear TP, Jenkins GA, Johnson PDR, Davis JK. Comparative genetic analysis of Mycobacterium ulcerans and Mycobacterium marinum reveals evidence of recent divergence. J Bacteriol. 2000;182(22):6322–30.
Parkhill J, Sebaihia M, Preston A, Murphy LD, Thomson N, Harris DE, et al. Comparative analysis of the genome sequences of Bordetella pertussis, Bordetella parapertussis and Bordetella bronchiseptica. Nat Genet. 2003;35(1):32–40.
Cole ST, Eiglmeier K, Parkhill J, James KD, Thomson NR, Wheeler PR, et al. Massive gene decay in the leprosy bacillus. Nature. 2001;409(6823):1007–11.
Ablordey A, Swings J, Hubans C, Chemlal K, Locht C, Portaels F. Multilocus variable-number tandem repeat typing of Mycobacterium ulcerans. J Clin Microbiol. 2005;43(4):1546–51.
Stragier P, Ablordey A, Meyers WM, Portaels F. Genotyping Mycobacterium ulcerans and M. marinum by using mycobacterial interspersed repetitive units. J Bacteriol. 2005;187(5):1639–47.
Hilty M, Yeboah-Manu D, Boakye D, Mensah-Quainoo E, Rondini S, Schelling E, et al. Genetic diversity in Mycobacterium ulcerans isolates from Ghana revealed by a newly identified locus containing a variable number of tandem repeats. J Bacteriol. 2006;188(4):1462–5.
Chemlal K, De Ridder K, Fonteyne PA, Meyers WM, Swings J, Portaels F. The use of IS2404 restriction fragment length polymorphisms suggests the diversity of Mycobacterium ulcerans from different geographical areas. Am J Trop Med Hyg. 2001;64(5–6):270–3.
Ablordey A, Kotlowski R, Swings J, Portaels F. PCR amplification with primers based on IS2404 and GC-rich repeated sequence reveals polymorphism in Mycobacterium ulcerans. J Clin Microbiol. 2005;43(1):448–51.
Stinear T, Davies JK, Jenkin GA, Portaels F, Ross BC, Oppidesano F, et al. A simple PCR method for rapid genotype analysis of Mycobacterium ulcerans. J Clin Microbiol. 2000;38(4):1482–7.
Roltgen K, Qi W, Ruf MT, Mensah-Quainoo E, Pidot SJ, et al. Single nucleotide polymorphism typing of Mycobacterium ulcerans reveals focal transmission of Buruli ulcer in a highly endemic region of Ghana. PLoS Negl Trop Dis. 2010;4(7):e751. https://doi.org/10.1371/journal.pntd.0000751.
Pearson T, Busch JD, Ravel J, Read TD, Rhoton SD, et al. Phylogenetic discovery bias in Bacillus anthracis using single nucleotide polymorphisms from whole-genome sequencing. Proc Natl Acad Sci USA. 2004;101(37):13536–41.
Bolz M, Bratschi MW, Kerber S, Minyem JC, Um Boock A, Vogel M, et al. Locally confined clonal complexes of Mycobacterium ulcerans in two buruli ulcer endemic regions of cameroon. PLoS Negl Trop Dis. 2015;9(6):e0003802. https://doi.org/10.1371/journal.pntd.0003802.
Ablordey AS, Vandelannoote K, Frimpong IA, Ahortor EK, Amissah NA, Eddyani M, et al. Whole genome comparisons suggest random distribution of Mycobacterium ulcerans genotypes in a buruli ulcer endemic region of Ghana. PLoS Negl Trop Dis. 2015;9(3):e0003681. https://doi.org/10.1371/journal.pntd.0003681.
Buultjens AH, Vandelannoote K, Meehan CJ, Eddyani M, de Jong BC, Fyfe JAM, et al. Comparative genomics shows that Mycobacterium ulcerans migration and expansion preceded the rise of buruli ulcer in southeastern Australia. Appl Environ Microbiol. 2018;84(8):e02612–7. https://doi.org/10.1128/AEM.02612-17.28.
Ross BC, Marino L, Oppedisano F, Edwards R, Robins-Browne RM, Johnson PD. Development of a PCR assay for rapid diagnosis of Mycobacterium ulcerans infection. J Clin Microbiol. 1997;35(7):1696–700.
Tortoli E, Meehan CJ, Grottola A, Fregni Serpini G, Fabio A, Trovato A, Pecorari M, et al. Genome-based taxonomic revision detects a number of synonymous taxa in the genus Mycobacterium. Infect Genet Evol. 2019;75:103983. https://doi.org/10.1016/j.meegid.2019.
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Ablordey, A., Portaels, F. (2022). Microbiology of Mycobacterium Ulcerans. In: Nunzi, E., Massone, C., Portaels, F. (eds) Leprosy and Buruli Ulcer. Springer, Cham. https://doi.org/10.1007/978-3-030-89704-8_40
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DOI: https://doi.org/10.1007/978-3-030-89704-8_40
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