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      Phylogenomic Analysis Reveals an Asian Origin for African Burkholderia pseudomallei and Further Supports Melioidosis Endemicity in Africa

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          Abstract

          Sporadic melioidosis cases have been reported in the African mainland and Indian Ocean islands, but until recently, these regions were not considered areas where B. pseudomallei is endemic. Given the high mortality rate of melioidosis, it is crucial that this disease be recognized and suspected in all regions of endemicity. Previous work has shown that B. pseudomallei originated in Australia, with subsequent introduction into Asia; however, the precise origin of B. pseudomallei in other tropical regions remains poorly understood. Using whole-genome sequencing, we characterized B. pseudomallei isolates from Madagascar and Burkina Faso. Next, we compared these strains to a global collection of B. pseudomallei isolates to identify their evolutionary origins. We found that African B. pseudomallei strains likely originated from Asia and were closely related to South American strains, reflecting a relatively recent shared evolutionary history. We also identified substantial genetic diversity among African strains, suggesting long-term B. pseudomallei endemicity in this region.

          ABSTRACT

          Burkholderia pseudomallei, an environmental bacterium that causes the deadly disease melioidosis, is endemic in northern Australia and Southeast Asia. An increasing number of melioidosis cases are being reported in other tropical regions, including Africa and the Indian Ocean islands. B. pseudomallei first emerged in Australia, with subsequent rare dissemination event(s) to Southeast Asia; however, its dispersal to other regions is not yet well understood. We used large-scale comparative genomics to investigate the origins of three B. pseudomallei isolates from Madagascar and two from Burkina Faso. Phylogenomic reconstruction demonstrates that these African B. pseudomallei isolates group into a single novel clade that resides within the more ancestral Asian clade. Intriguingly, South American strains reside within the African clade, suggesting more recent dissemination from West Africa to the Americas. Anthropogenic factors likely assisted in B. pseudomallei dissemination to Africa, possibly during migration of the Austronesian peoples from Indonesian Borneo to Madagascar ~2,000 years ago, with subsequent genetic diversity driven by mutation and recombination. Our study provides new insights into global patterns of B. pseudomallei dissemination and adds to the growing body of evidence of melioidosis endemicity in Africa. Our findings have important implications for melioidosis diagnosis and management in Africa.

          IMPORTANCE Sporadic melioidosis cases have been reported in the African mainland and Indian Ocean islands, but until recently, these regions were not considered areas where B. pseudomallei is endemic. Given the high mortality rate of melioidosis, it is crucial that this disease be recognized and suspected in all regions of endemicity. Previous work has shown that B. pseudomallei originated in Australia, with subsequent introduction into Asia; however, the precise origin of B. pseudomallei in other tropical regions remains poorly understood. Using whole-genome sequencing, we characterized B. pseudomallei isolates from Madagascar and Burkina Faso. Next, we compared these strains to a global collection of B. pseudomallei isolates to identify their evolutionary origins. We found that African B. pseudomallei strains likely originated from Asia and were closely related to South American strains, reflecting a relatively recent shared evolutionary history. We also identified substantial genetic diversity among African strains, suggesting long-term B. pseudomallei endemicity in this region.

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          ART: a next-generation sequencing read simulator.

          ART is a set of simulation tools that generate synthetic next-generation sequencing reads. This functionality is essential for testing and benchmarking tools for next-generation sequencing data analysis including read alignment, de novo assembly and genetic variation discovery. ART generates simulated sequencing reads by emulating the sequencing process with built-in, technology-specific read error models and base quality value profiles parameterized empirically in large sequencing datasets. We currently support all three major commercial next-generation sequencing platforms: Roche's 454, Illumina's Solexa and Applied Biosystems' SOLiD. ART also allows the flexibility to use customized read error model parameters and quality profiles. Both source and binary software packages are available at http://www.niehs.nih.gov/research/resources/software/art.
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            Multilocus sequence typing and evolutionary relationships among the causative agents of melioidosis and glanders, Burkholderia pseudomallei and Burkholderia mallei.

            A collection of 147 isolates of Burkholderia pseudomallei, B. mallei, and B. thailandensis was characterized by multilocus sequence typing (MLST). The 128 isolates of B. pseudomallei, the causative agent of melioidosis, were obtained from diverse geographic locations, from humans and animals with disease, and from the environment and were resolved into 71 sequence types. The utility of the MLST scheme for epidemiological investigations was established by analyzing isolates from captive marine mammals and birds and from humans in Hong Kong with melioidosis. MLST gave a level of resolution similar to that given by pulsed-field gel electrophoresis and identified the same three clones causing disease in animals, each of which was also associated with disease in humans. The average divergence between the alleles of B. thailandensis and B. pseudomallei was 3.2%, and there was no sharing of alleles between these species. Trees constructed from differences in the allelic profiles of the isolates and from the concatenated sequences of the seven loci showed that the B. pseudomallei isolates formed a cluster of closely related lineages that were fully resolved from the cluster of B. thailandensis isolates, confirming their separate species status. However, isolates of B. mallei, the causative agent of glanders, recovered from three continents over a 30-year period had identical allelic profiles, and the B. mallei isolates clustered within the B. pseudomallei group of isolates. Alleles at six of the seven loci in B. mallei were also present within B. pseudomallei isolates, and B. mallei is a clone of B. pseudomallei that, on population genetics grounds, should not be given separate species status.
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              The global distribution of Burkholderia pseudomallei and melioidosis: an update.

              While Southeast Asia and northern Australia are well recognized as the major endemic regions for melioidosis, recent reports have expanded the endemic zone. Severe weather events and environmental disasters such as the 2004 Asian tsunami have unmasked locations of sporadic cases and have reconfirmed endemicity in Indonesia. The endemic region now includes the majority of the Indian subcontinent, southern China, Hong Kong and Taiwan. Sporadic cases have occurred in Brazil and elsewhere in the Americas and in island communities such as New Caledonia, in the Pacific Ocean, and Mauritius in the Indian Ocean. Some of the factors that are critical to further elucidating the global distribution of Burkholderia pseudomallei and melioidosis include improved access to diagnostic laboratory facilities and formal confirmation of the identity of bacterial isolates from suspected cases.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                mSphere
                mSphere
                msph
                msph
                mSphere
                mSphere
                American Society for Microbiology (1752 N St., N.W., Washington, DC )
                2379-5042
                9 March 2016
                Mar-Apr 2016
                : 1
                : 2
                : e00089-15
                Affiliations
                [a ]Global and Tropical Health Division, Menzies School of Health Research, Darwin, Australia
                [b ]Bacteriological Unit, Institut Pasteur de Madagascar, Antananarivo, Madagascar
                [c ]Department of Clinical Sciences, Institute of Tropical Medicine, Antwerp, Belgium
                [d ]Faculty of Sciences, Laboratory of Microbiology, Ghent University, Ghent, Belgium
                [e ]Department of Microbiology and Immunology, University of Leuven, Leuven, Belgium
                [f ]Clinical Research Unit of Nanoro (IRSS-CRUN), Nanoro, Burkina Faso
                [g ]Androva University Hospital, Mahajanga, Madagascar
                University of Wisconsin—Madison
                Author notes
                Address correspondence to Derek S. Sarovich, derek.sarovich@ 123456menzies.edu.au .
                [*]

                Present address: Benoit Garin, Molecular Prevention and Therapy of Human Diseases, Whooping Cough and Other Bordetelloses Reference Center, and Corynebacteriae of the Diphtheriae Complex Reference Center, Institut Pasteur, Paris, France

                Citation Sarovich DS, Garin B, De Smet B, Kaestli M, Mayo M, Vandamme P, Jacobs J, Lompo P, Tahita MC, Tinto H, Djaomalaza I, Currie BJ, Price EP. 2016. Phylogenomic analysis reveals an Asian origin for African Burkholderia pseudomallei and further supports melioidosis endemicity in Africa. mSphere 1(2):e00089-15. doi:10.1128/mSphere.00089-15.

                Author information
                http://orcid.org/0000-0002-6944-3980
                http://orcid.org/0000-0002-1079-4882
                Article
                mSphere00089-15
                10.1128/mSphere.00089-15
                4863585
                27303718
                a988f0f5-3a86-4b8b-bc09-0acc45f8f47f
                Copyright © 2016 Sarovich et al.

                This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license.

                History
                : 8 December 2015
                : 5 February 2016
                Page count
                Figures: 3, Tables: 1, Equations: 0, References: 74, Pages: 12, Words: 8831
                Funding
                Funded by: Department of Health | National Health and Medical Research Council (NHMRC) http://dx.doi.org/10.13039/501100000925
                Award ID: 1098337
                Award ID: 1046812
                Award Recipient : Derek S. Sarovich Award Recipient : Mirjam Kaestli Award Recipient : Mark Mayo Award Recipient : Bart J. Currie Award Recipient : Erin P. Price
                Funded by: Institut Pasteur http://dx.doi.org/10.13039/501100003762
                Award ID: ACIP A11_2011
                Award Recipient : Benoit Garin Award Recipient : Innocente Djaomalaza
                Categories
                Research Article
                Clinical Science and Epidemiology
                Custom metadata
                March/April 2016

                burkholderia,epidemiology,infectious disease,melioidosis,phylogeography,population genetics

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