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. 2018 May 1:9:816.
doi: 10.3389/fmicb.2018.00816. eCollection 2018.

Biodiversity of Environmental Leptospira: Improving Identification and Revisiting the Diagnosis

Affiliations

Biodiversity of Environmental Leptospira: Improving Identification and Revisiting the Diagnosis

Roman Thibeaux et al. Front Microbiol. .

Abstract

Leptospirosis is an important environmental disease and a major threat to human health causing at least 1 million clinical infections annually. There has recently been a growing interest in understanding the environmental lifestyle of Leptospira. However, Leptospira isolation from complex environmental samples is difficult and time-consuming and few tools are available to identify Leptospira isolates at the species level. Here, we propose a polyphasic isolation and identification scheme, which might prove useful to recover and identify environmental isolates and select those to be submitted to whole-genome sequencing. Using this approach, we recently described 12 novel Leptospira species for which we propose names. We also show that MALDI-ToF MS allows rapid and reliable identification and provide an extensive database of Leptospira MALDI-ToF mass spectra, which will be valuable to researchers in the leptospirosis community for species identification. Lastly, we also re-evaluate some of the current techniques for the molecular diagnosis of leptospirosis taking into account the extensive and recently revealed biodiversity of Leptospira in the environment. In conclusion, we describe our method for isolating Leptospira from the environment, confirm the usefulness of mass spectrometry for species identification and propose names for 12 novel species. This also offers the opportunity to refine current molecular diagnostic tools.

Keywords: MALDI-TOF MS; WGS comparisons; isolation; novel species; soil microbiology.

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Figures

Figure 1
Figure 1
Leptospira isolation on EMJH agar plates. (A) Global isolation strategy. (B) Macroscopic aspect of colonies. (C) Closer view from (A) showing colonies of different sizes. (D) Opaque (yellow arrow) and transparent (red arrow) colonies. (E) Translucent colonies.
Figure 2
Figure 2
Melting peaks and melting temperatures (Tm) of a 16S rRNA PCR product for representative strains from all 23 validly described Leptospira species, evidencing the clustering of Tm values with the notable exception of Leptospira weilii.
Figure 3
Figure 3
Dendrogram based on the comparison of MALDI-ToF mass spectra of the 35 Leptospira species. Novel species are indicated in bold.
Figure 4
Figure 4
SEM morphology of representative cells of novel Leptospira species. L, length; W, width.
Figure 5
Figure 5
Real-time PCR amplification curves and Ct gains using the original (Merien et al., 2005) and a modified qPCR using degenerate primers (d) described in this paper targeting lipL32 to detect pathogenic Leptospira.

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