Literature DB >> 30533730

Complete Genome Sequences of Three Leptospira mayottensis Strains from Tenrecs That Are Endemic in the Malagasy Region.

Colette Cordonin1, Céline Toty2, Patrick Mavingui1, Pablo Tortosa1.   

Abstract

Leptospirosis is a zoonosis caused by Leptospira, a diversified genus containing more than 10 pathogenic species. Tenrecs are small terrestrial mammals endemic in the Malagasy region and are known to be reservoirs of the recently described species Leptospira mayottensis. We report the complete genome sequences of three L. mayottensis strains isolated from two tenrec species.

Entities:  

Year:  2018        PMID: 30533730      PMCID: PMC6256437          DOI: 10.1128/MRA.01188-18

Source DB:  PubMed          Journal:  Microbiol Resour Announc        ISSN: 2576-098X


ANNOUNCEMENT

Leptospirosis is an environmental infectious disease caused by spirochetal bacteria belonging to the genus Leptospira. Humans usually get infected during recreational or work-related outdoor activities through contact with urine excreted by animal reservoirs. This zoonosis is estimated to cause more than one million human cases and 58,900 deaths each year (1). Disease incidence is highest on tropical islands, notably in the southwestern Indian Ocean, where investigations carried out under a One Health framework have revealed distinct transmission chains in the different islands (2–5), including the occurrence of Leptospira mayottensis, a pathogenic Leptospira species recently recognized as new to science (6). Representatives of L. mayottensis (formerly known as Leptospira borgpetersenii group B) were originally isolated from human acute cases (7) and later identified in tenrecs (2, 5, 8), a diversified family of mammals endemic to Madagascar (9, 10). Three L. mayottensis strains were isolated in the field from two tenrec species, namely, Tenrec ecaudatus on Mayotte (MDI222 and MDI272) (2) and Microgale dobsoni on Madagascar (VS2413) (5). Frozen isolates were thawed in liquid Ellinghausen-McCullough-Johnson-Harris (EMJH) medium containing albumin fatty acid supplements (AFAS) (3), and they were further subcultured in EMJH supplemented with AFAS, 1% fetal calf serum, and 8% rabbit serum. DNA was extracted with the EZ1 virus minikit v.2.0 (Qiagen, Germany), and sequencing was performed on PacBio platforms. The sequence for VS2413 was assembled de novo with SMRT Analysis HGAP.2, those for MDI222 and MDI272 were assembled de novo using Canu 1.6, and contigs were circularized using AMOS v.3.1 (11). Overall, genome sizes and structures (see Table 1) are close to those of previously published ones, with comparably low (≤40%) GC contents, two chromosomes, and, in the case of T. ecaudatus-borne strains, an additional plasmid (12).
TABLE 1

Genome architecture of L. mayottensis isolates

IsolateSource hostSampling locationChromosome length (bp)
Plasmid length (bp)No. of readsN50 length (bp)
III
MDI222Tenrec ecaudatusMayotte3,934,331 (not circularized)330,241111,32844,97620,779
MDI272Tenrec ecaudatusMayotte3,861,885332,64752,50952,10117,832
VS2413Microgale dobsoniMadagascar3,787,562300,21955,59521,656

All but one replicon were successfully circularized.

Genome architecture of L. mayottensis isolates All but one replicon were successfully circularized. Automatic annotation was performed with the NCBI Prokaryotic Genome Annotation Pipeline (13), which revealed that the VS2413, MDI272, and MDI222 genomes are composed of 3,893, 3,917, and 4,136 coding sequences, respectively. Human leptospirosis on Mayotte is peculiar because it is associated with four distinct bacterial species, including L. mayottensis (14), and characterized by a relatively low fatality rate (0.9%) (15). The epidemiology is clearly distinct in the neighboring Seychelles and on Reunion Island, where L. interrogans is overwhelmingly dominant and fatality rates are higher (11.8% in the Seychelles and 3 to 5% on Reunion Island) (3, 4, 16). An attenuated virulence of Leptospira species prevailing on Mayotte, including L. mayottensis, may be at least in part responsible for this contrasted regional epidemiology. The genomes presented herein will accelerate comparative genomic approaches aimed at delineating the main genomic features involved in Leptospira virulence.

Data availability.

Genome sequences were deposited in DDBJ/EMBL/GenBank under the accession numbers CP030142 and CP030143, CP030144 to CP030146, and CP030147 to CP030149 for strains VS2413, MDI222, and MDI272, respectively, as well as BioProject number PRJNA477299. Raw sequence data are available from the NCBI Sequence Read Archive (accession number SRP154442).
  15 in total

1.  Human leptospira isolates circulating in Mayotte (Indian Ocean) have unique serological and molecular features.

Authors:  P Bourhy; L Collet; T Lernout; F Zinini; R A Hartskeerl; Hans van der Linden; J M Thiberge; L Diancourt; S Brisse; C Giry; F Pettinelli; M Picardeau
Journal:  J Clin Microbiol       Date:  2011-12-07       Impact factor: 5.948

2.  Tenrecs.

Authors:  Link E Olson
Journal:  Curr Biol       Date:  2013-01-07       Impact factor: 10.834

3.  Diversification of an emerging pathogen in a biodiversity hotspot: Leptospira in endemic small mammals of Madagascar.

Authors:  Muriel Dietrich; David A Wilkinson; Voahangy Soarimalala; Steven M Goodman; Koussay Dellagi; Pablo Tortosa
Journal:  Mol Ecol       Date:  2014-05-17       Impact factor: 6.185

4.  Next generation sequence assembly with AMOS.

Authors:  Todd J Treangen; Dan D Sommer; Florent E Angly; Sergey Koren; Mihai Pop
Journal:  Curr Protoc Bioinformatics       Date:  2011-03

5.  Human leptospirosis in Seychelles: A prospective study confirms the heavy burden of the disease but suggests that rats are not the main reservoir.

Authors:  Leon Biscornet; Koussay Dellagi; Frédéric Pagès; Jastin Bibi; Jeanine de Comarmond; Julien Mélade; Graham Govinden; Maria Tirant; Yann Gomard; Vanina Guernier; Erwan Lagadec; Jimmy Mélanie; Gérard Rocamora; Gildas Le Minter; Julien Jaubert; Patrick Mavingui; Pablo Tortosa
Journal:  PLoS Negl Trop Dis       Date:  2017-08-28

6.  Distribution of Plasmids in Distinct Leptospira Pathogenic Species.

Authors:  Yanzhuo Wang; Xuran Zhuang; Yi Zhong; Cuicai Zhang; Yan Zhang; Lingbing Zeng; Yongzhang Zhu; Ping He; Ke Dong; Utpal Pal; Xiaokui Guo; Jinhong Qin
Journal:  PLoS Negl Trop Dis       Date:  2015-11-10

7.  Human leptospirosis on Reunion Island: past and current burden.

Authors:  Frédéric Pagès; Dominique Polycarpe; Jean-Sébastien Dehecq; Mathieu Picardeau; Nadège Caillère; Marie-Christine Jaffar-Bandjee; Alain Michault; Laurent Filleul
Journal:  Int J Environ Res Public Health       Date:  2014-01-10       Impact factor: 3.390

8.  Human Leptospirosis on Reunion Island, Indian Ocean: Are Rodents the (Only) Ones to Blame?

Authors:  Vanina Guernier; Erwan Lagadec; Colette Cordonin; Gildas Le Minter; Yann Gomard; Frédéric Pagès; Marie-Christine Jaffar-Bandjee; Alain Michault; Pablo Tortosa; Koussay Dellagi
Journal:  PLoS Negl Trop Dis       Date:  2016-06-13

9.  NCBI prokaryotic genome annotation pipeline.

Authors:  Tatiana Tatusova; Michael DiCuccio; Azat Badretdin; Vyacheslav Chetvernin; Eric P Nawrocki; Leonid Zaslavsky; Alexandre Lomsadze; Kim D Pruitt; Mark Borodovsky; James Ostell
Journal:  Nucleic Acids Res       Date:  2016-06-24       Impact factor: 16.971

10.  Identification of Tenrec ecaudatus, a Wild Mammal Introduced to Mayotte Island, as a Reservoir of the Newly Identified Human Pathogenic Leptospira mayottensis.

Authors:  Erwan Lagadec; Yann Gomard; Gildas Le Minter; Colette Cordonin; Eric Cardinale; Beza Ramasindrazana; Muriel Dietrich; Steven M Goodman; Pablo Tortosa; Koussay Dellagi
Journal:  PLoS Negl Trop Dis       Date:  2016-08-30
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