Mem Inst Oswaldo Cruz, Rio de Janeiro, 113(5) May 2018
Genome announcements and highlights

Genomic characterisation of Leptospira inadai serogroup Genomic characterisation of Leptospira inadai serogroup Lyme isolated from captured rat in Brazil and comparative analysis with human reference strain

Luisa Z Moreno1, Fabiana Miraglia2, Ana P Loureiro2, Frederico S Kremer3, Luisa Z Moreno1, Fabiana Miraglia2, Ana P Loureiro2, Frederico S Kremer3, Marcus R Eslabao3, Odir A Dellagostin3, Walter Lilenbaum2, Silvio A Vasconcellos1, Marcos B Heinemann1, Andrea M Moreno1,+

1Universidade de São Paulo, Faculdade de Medicina Veterinária e Zootecnia, Laboratório de Epidemiologia Molecular e Resistência a Antimicrobianos, São Paulo, SP, Brasil
2Universidade Federal Fluminense, Departamento de Microbiologia e Parasitologia, Laboratório de Bacteriologia Veterinária, Niterói, RJ, Brasil
3Universidade Federal de Pelotas, Centro de Desenvolvimento Tecnológico, Pelotas, RS, Brasil

DOI: 10.1590/0074-02760170444
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ABSTRACT

Leptospira inadai is classified as a species of the Leptospira intermediate group that has been poorly studied due to its apparent insignificance to human and animal health. Nevertheless, over the last two decades the species has been described in human cases in India and in carrier animals in Ecuador. Here, we present the first identification and genomic characterisation of L. inadai serogroup Lyme isolated from captured rodent in Brazil. Even though the M34/99 strain was not pathogenic for hamsters, it was able to establish renal colonisation. The M34/99 strain presented high similarity with L. inadai serogroup Lyme human reference indicating that animal strain could also infect humans, although it does not represent high risk of severe disease. An extrachromosomal sequence was also identified in M34/99 strain and presented high identity with previously described L. inadai phage LinZ 10, suggesting that phage-like extrachromosomal sequence may be another feature of this understudied species.

Leptospirosis is a worldwide zoonosis, with higher incidence in tropical climates, caused by bacteria of the Leptospira genus (Levett 2001 12 , Evangelista and Coburn 2010 7 ). To date, the genus comprises 10 pathogenic species, seven non-pathogenic species, and an intermediate group containing five species (Bourhy et al. 2014 3 ). The intermediate clade includes Leptospira inadai, L. broomii, L. fainei, L. wolffii and L. licerasiae, of which L. wolffii and L. licerasiae have been associated with mild leptospirosis (Matthias et al. 2008 13 , Slack et al. 2008 16 , Zakeri et al. 2010 20 ), while L. broomii and L. fainei have been reported from severe cases of the disease (Arzouni et al. 2002 2 , Levett et al. 2006 11 ).

L. inadai was first isolated from a skin biopsy of a patient with Lyme disease, in 1981 (Schmid et al. 1986 15 ). Even though the strain was classified as pathogenic to laboratory animals, it was also considered only a concurrent infection in the patient. The isolated strain (strain 10) is considered the species type strain that was only formally described by Yasuda et al. (1987) 19 . Over the last two decades, L. inadai was only reported in two fatal human cases in India (Gangadhar et al. 2008 9 ) and in carrier animals in Ecuador (Chiriboga et al. 2015 5 ). Here, we present the identification, genomic characterisation and comparative analysis of L. inadai serogroup Lyme isolated from captured rodent in Brazil.

The M34/99 strain was isolated in 1999 from the kidney of a captured urban brown rat (Rattus norvegicus) in São Paulo city. The strain was included in the Leptospira collection of the Laboratory of Bacterial Zoonosis - University of São Paulo, with inconclusive results for identification, and stored in Fletcher's medium (DIFCO/USA), enriched with 15% rabbit serum and maintained in EMJH broth (DIFCO/USA) at 30ºC.

Serogrouping was performed at the Laboratory of Veterinary Bacteriology -Fluminense Federal University. The isolate was subjected to microscopic agglutination test (MAT) using a panel of polyclonal rabbit antisera of 32 reference serovars representing the 24 known serogroups (provided by Royal Tropical Institute - KIT, Amsterdam). The M34/99 strain presented high agglutination rates with serogroup Lyme antisera (25,600).

Virulence assessment was performed with five Golden Syrian hamsters (Mesocricetus auratus); animals were infected with M34/99 strain (108 leptospires) through intraperitoneal route. The animal experiment was conducted with the approval of the Ethics Committee from the School of Veterinary Medicine and Animal Science - University of São Paulo (2244/2011). Clinical symptoms were checked daily for 21 consecutive days. All animals survived the challenge and were euthanised and necropsied to assess renal infection. Kidney samples were aseptically collected, homogenised in 50 mL of Sorensen saline and 100 µL aliquots of 10-1 to 10-3 dilutions were inoculated in Fletcher medium and incubated at 30ºC for six weeks. Even though the M34/99 strain was not pathogenic for hamsters, it could establish renal colonisation as the hamsters kidney samples enabled recovery of the M34/99 strain.

For species identification and complete genetic characterisation, the M34/99 strain was submitted to whole-genome sequencing. Genomic DNA was purified with illustra bacteria genomicPrep Mini Spin Kit (GE Healthcare do Brasil Ltda, São Paulo, Brazil) and used for paired-end library preparation with Nextera DNA Sample Prep Kit (Illumina®) and sequencing through Illumina® Miseq platform. The de novo assembly was performed with Geneious R10 (Biomatters Ltd, Auckland, New Zealand) and resulted in 59 scaffolds with a N50 of 163,176 bp. Automatic genome annotation was performed with NCBI Prokaryotic Genome Annotation Pipeline (Tatusova et al. 2016 18 ).

The species identification was confirmed by phylogenetic analysis of 16S rRNA and rpoB sequences performed with Mega 5.10 software (Tamura et al. 2011 17 ) with maximum-likelihood method and Tamura-Nei model, using reference sequences from GenBank. Strain identification was also confirmed by pairwise comparison of average nucleotide identity (ANIb) trough JSpeciesWS (Richter et al. 2016 14 ). The phylogenetic analysis resulted in the L. inadai identification for both genes (Supplementary data). The ANIb results (Table) also confirmed the species identification (> 99% of nucleotide identity with L. inadai serovar Lyme strain 10 genome) and differentiation from the remaining species of the Leptospira intermediate group.

The obtained scaffolds were ordered according to L. inadai serovar Lyme strain 10 (NZ_AHMM00000000.2) using Mauve Multiple Genome Aligner (Darling et al. 2010 6 ). Due to the unavailability of a complete L. inadai reference genome, the chromosomes of the studied genome were not individualised. The M34/99 draft genome (MCRM00000000.2) comprises ~4.56 Mb and only one scaffold (scaffold 22, ~87 kb) did not align with the reference strain 10. BLASTn against non-redundant NCBI database was applied for the extrachromosomal sequence and resulted in high identity (>99%) with L. inadai strain 10 phage LinZ_10 (KF114880).

The L. inadai drafts genomes (strains 10 and M34/99) were compared to the closely related species L. broomii serovar Hurstbridge (NZ_AHMO00000000) and L. fainei serovar Hurstbridge (NZ_AKWZ00000000) through Artemis Comparison Tool (ACT) (Carver et al. 2005 4 ) and BLAST Ring Image Generator (BRIG) (Alikhan et al. 2011 1 ). L. inadai chromosomal content presented high synteny and 99% identity at DNA level among studied strains (Fig. 1). It is also worth noting a few deletion regions in L. broomii and L. fainei compared to L. inadai; although the species present some similarity of content (> 80% genetic similarity) (Fig. 1A), the sequences also present arrangement variation (blocks of inverted sequences among the genomes) (Fig. 1B).

With regard to the virulence genes, M34/99 strain presents only a few genes encoding lipoproteins (lipA) and flagellar proteins (fliG/F), as expected. In addition, resistance genes were identified, including antimicrobial resistance genes (tetA), efflux pumps (mdtC, norM), and heavy metal and antiseptic resistance genes (merR, sugE, qacA). Fouts et al. (2016) 8 had already demonstrated that L. inadai serovar Lyme strain 10 lacked some of Leptospira major virulence factors, such as LipL32 and LipL41, which are markers of pathogenic Leptospira and, therefore, could explain L. inadai isolation from asymptomatic hosts. Considering that fatal L. inadai infection has only been reported in India (Gangadhar et al. 2008 9 ), these strains require further study to ensure the species and genetic mechanisms of virulence identification.

Regarding the L. inadai extrachromosomal content, M34/99 phage-like sequence was deposited in GenBank as Lin_34 under the accession number KX656785. The sequence, of 87,3 kb, only differs from the reference L. inadai serovar Lyme strain 10 LinZ_10 bacteriophage by ~2,3 kb due to the absence of IS66 family proteins in strain M34/99. Both sequences are mostly composed of hypothetical proteins and although the gene content is very similar, Mauve and ACT analyses demonstrate that there are blocks of inverted sequences (Fig. 2) that appear to be related to the presence of insertion sequences in LinZ_10 bacteriophage.

This is the first report of L. inadai in Brazil and the second of this species in South America; it is an important epidemiological data of the Leptospira species circulating in the country. L. inadai has been described as highly adapted to rodents in India (Gangadhar et al. 2000 10 ) and in Ecuador the species has also been recovered from dogs, pigs, bovines and rats (Chiriboga et al. 2015 5 ). The identification of a Brazilian L. inadai strain isolated from urban rat corroborates that the species is adapted to rodents as a reservoir and it also suggests that L. inadai presents a wider dissemination that probably goes unnoticed because it is not part of the routine antigen battery of diagnostics laboratories.

The high similarity of L. inadai serogroup Lyme rodent stain with the genome of the human strain indicates that the species could able to infect humans even though it does not represent a high risk of severe disease. Considering the geographical and chronological distance and the high genomic similarity observed between strains, this may suggest a possibility of a similar lineage of L. inadai serogroup Lyme in the Americas. The phage identification in the Brazilian L. inadai serogroup Lyme strain, as well as in strain 10 original description (LinZ_10), also suggests that phage-like extrachromosomal sequence may be another common feature of this understudied species.

 

ACKNOWLEDGEMENTS

To Dr Margareth Genovez for kindly sending her isolate to the Leptospira collection.

 

AUTHORS' CONTRIBUTION

LZM, SAV, OAD, WL and AMM - Conceived and designed the experiments; LZM, FM and APL - performed the experiments; LZM and AMM - analysed the data; FSK and MRE - contributed reagents/materials/analysis tools; SAV and MBH - samples collection and strains isolation; LZM, AMM, MBH, WL and OAD - wrote the paper. All authors reviewed the manuscript.

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Financial support: CNPq, CAPES, FAPESP (2011/18290-0, 2013/17136-2).
+ Corresponding author: morenoam@usp.br
Received 17 October 2017
Accepted 6 February 2018

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