Multi‑locus sequence analyses reveal a clonal L. borgpetersenii genotype in a heterogeneous invasive Rattus spp. community across the City of Johannesburg, South Africa

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Authors

Moseley, Mark
Naidoo, Kovashnee
Bastos, Armanda D.S.
Retief, Liezl
Frean, John
Telfer, Sandra
Rossouw, Jennifer

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BioMed Central

Abstract

BACKGROUND : Rattus spp. are frequently implicated as key reservoir hosts for leptospirosis, one of the most common, but neglected, bacterial zoonoses in the world. Although leptospirosis is predicted to be a significant public health threat in Africa, studies from the continent are limited. METHODS : Rattus spp. (n = 171) were sampled (January–May 2016) across the City of Johannesburg, South Africa’s largest inland metropole. Rattus spp. genetic diversity was evaluated by full length (1140 bp) cyt b sequencing of 42 samples. For comparison, a further 12 Rattus norvegicus samples collected in Cape Town, South Africa’s largest coastal metropole, were also genotyped. Leptospira infections were identified and genotyped using real-time PCR and multilocus (lfb1, secY and lipL41) DNA sequencing. RESULTS : Five R. norvegicus haplotypes were identified across Johannesburg, four of which have not previously been detected in South Africa, and one in Cape Town. Across Johannesburg we identified a Leptospira spp. infection prevalence of 44% (75/171) and noted significant differences in the prevalence between administrative regions within the metropole. Multi-locus sequence analyses identified a clonal genotype consistent with L. borgpetersenii serogroup Javanica (serovar Ceylonica). DISCUSSION : The prevalence of infection identified in this study is amongst the highest detected in Rattus spp. in similar contexts across Africa. Despite the complex invasion history suggested by the heterogeneity in R. norvegicus haplotypes identified in Johannesburg, a single L. borgpetersenii genotype was identified in all infected rodents. The lack of L. interrogans in a rodent community dominated by R. norvegicus is notable, given the widely recognised hostpathogen association between these species and evidence for L. interrogans infection in R. norvegicus in Cape Town. It is likely that environmental conditions (cold, dry winters) in Johannesburg may limit the transmission of L. interrogans. Spatial heterogeneity in prevalence suggest that local factors, such as land use, influence disease risk in the metropole. CONCLUSIONS : In South Africa, as in other African countries, leptospirosis is likely underdiagnosed. The high prevalence of infection in urban rodents in Johannesburg suggest that further work is urgently needed to understand the potential public health risk posed by this neglected zoonotic pathogen.

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Additional file 1: Figure S1. The Köppen-Geiger climate classification zones for South Africa at 0.0083° resolution. Johannesburg falls within the Cwb bioclimatic zone, characterised by dry, cold winters and warm, wet summers and Cape Town falls within the Csb zone, characterised by wet winters and warm summers.
Additional file 2: Table S1. The prevalence of Leptospira infection in Rattus spp. in the seven administrative regions of the City of Johannesburg and in R. norvegicus tested during a leptospirosis outbreak investigation in the City of Cape Town. Figure S2. The spatial distribution of regional prevalence across the seven administrative regions of the City of Johannesburg. Region F, where only three animals were tested is excluded from the analysis
Additional file 3: Figure S3. Maximum clade credibility tree based on L. borgpetersenii lfb1 sequences (167 bp) implemented using the Jukes- Cantor evolutionary model. Figure S4. Maximum clade credibility tree based on L. borgpetersenii secY sequences (433bp) implemented using the Jukes-Cantor evolutionary model. Figure S5. Maximum clade credibility tree based on L. borgpetersenii lipL41 sequences (594 bp) implemented using the Jukes-Cantor evolutionary model. Figure S6. Maximum clade credibility tree based on L. interrogans lfb1 sequences (261 bp) implemented using the Jukes-Cantor substitution model. Figure S7. Maximum clade credibility tree based on L. interrogans secY sequences (433 bp) implemented using the Hasegawa-Kishino-Yano evolutionary model (4) substitution model. Figure S8. Maximum clade credibility tree based on L. interrogans MST1 sequences (174 bp) implemented using the Hasegawa- Kishino-Yano evolutionary model (4) substitution model. Figure S9. Maximum clade credibility tree based on L. interrogans MST3 sequences (220 bp) implemented using the Hasegawa-Kishino-Yano evolutionary model (4) with a gamma distribution (4 categories). Figure S10. Maximum clade credibility tree based on L. interrogans MST9 sequences (204 bp) implemented using the Jukes-Cantor evolutionary model.

Keywords

Leptospirosis, Zoonosis, Urbanisation, Rats, Public health, Molecular epidemiology, Disease ecology, Multilocus DNA sequencing, Real-time PCR

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Citation

Moseley, M., Naidoo, K., Bastos, A. et al. 2020, 'Multi‑locus sequence analyses reveal a clonal L. borgpetersenii genotype in a heterogeneous invasive Rattus spp. community across the City of Johannesburg, South Africa', Parasites Vectors, vol. 13, art. 570, pp. 1-9.