ArticlePLoS neglected tropical diseases2014
Influence of household rat infestation on leptospira transmission in the urban slum environment.
Article in PLoS neglected tropical diseases, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers, 3 of them syntheses that pooled it.
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Who cites it
70 citing papers in PubMed, 3 syntheses or guidelines pooled it, 131 citations in OpenAlex.
- Trends and advances inFrontiers in microbiology · 2024Pooled it
- Geoprocessing and spatial analysis for identifying leptospirosis risk areas: a systematic review.Revista do Instituto de Medicina Tropical de Sao Paulo · 2020Pooled it
- Global Morbidity and Mortality of Leptospirosis: A Systematic Review.PLoS neglected tropical diseases · 2015Pooled it
- The Epidemiological Scenario of Human Leptospirosis in Brazil from 2015 to 2024.Epidemiologia (Basel, Switzerland) · 2026Article
- Ecological Niche Modeling of PathogenicPathogens (Basel, Switzerland) · 2026Article
- Leptospirosis in Central Romania: A 17-Year Single-Center Cohort Study of Hospitalized Adults.Microorganisms · 2026Article
- Spatiotemporal dynamics and environmental trends of reported human leptospirosis in Sri Lanka, 2007-2024.Frontiers in public health · 2026Article
- Co-production of informal settlement health: a community based participatory research program for building healthy communities in urban informal settlements of Salvador, Brazil.Frontiers in public health · 2026Article
- Policy Options for Prevention of Leptospirosis Epidemics: A Scoping Review.Iranian journal of public health · 2025Review
- Incorporating Machine Learning Techniques to Enhance Rodent Surveillance in Marginalized Urban Communities.Ecology and evolution · 2025Article
- Epidemiological, temporal, and geographic trends of leptospirosis in the United States, 2014-2020.PLoS neglected tropical diseases · 2025Article
- Hematological and biochemical profiles, infection and habitat quality in an urban rat population.Scientific reports · 2025Article
- Host population dynamics influence Leptospira spp. transmission patterns among Rattus norvegicus in Boston, Massachusetts, US.PLoS neglected tropical diseases · 2025Article
- Genetic Characterization and Zoonotic Potential ofTropical medicine and infectious disease · 2025Article
- Geographical factors and air raid alarms influence leptospirosis epidemiology in Ukraine (2018-2023).One health (Amsterdam, Netherlands) · 2024Article
- Quality of life among residents of informal urban settlements during the COVID-19 pandemic in Salvador, Brazil.BMJ public health · 2024Article
- Factors associated with differential seropositivity to Leptospira interrogans and Leptospira kirschneri in a high transmission urban setting for leptospirosis in Brazil.PLoS neglected tropical diseases · 2024Article
- Systematic surveillance tools to reduce rodent pests in disadvantaged urban areas can empower communities and improve public health.Scientific reports · 2024Article
- Environmental and Occupational Factors Associated with Leptospirosis: A Systematic Review.Heliyon · 2024Article
- Disentangling the influence of reservoir abundance and pathogen shedding on zoonotic spillover of theFrontiers in public health · 2024Article
10 more citing papers are in PubMed but not listed here.
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Authors and funding
12 authors at 6 institutions in 2 countries.
Funding
Abstract
backgroundThe Norway rat (Rattus norvegicus) is the principal reservoir for leptospirosis in many urban settings. Few studies have identified markers for rat infestation in slum environments while none have evaluated the association between household rat infestation and Leptospira infection in humans or the use of infestation markers as a predictive model to stratify risk for leptospirosis. METHODOLOGY/PRINCIPAL
findingsWe enrolled a cohort of 2,003 urban slum residents from Salvador, Brazil in 2004, and followed the cohort during four annual serosurveys to identify serologic evidence for Leptospira infection. In 2007, we performed rodent infestation and environmental surveys of 80 case households, in which resided at least one individual with Leptospira infection, and 109 control households. In the case-control study, signs of rodent infestation were identified in 78% and 42% of the households, respectively. Regression modeling identified the presence of R. norvegicus feces (OR, 4.95; 95% CI, 2.13-11.47), rodent burrows (2.80; 1.06-7.36), access to water (2.79; 1.28-6.09), and un-plastered walls (2.71; 1.21-6.04) as independent risk factors associated with Leptospira infection in a household. We developed a predictive model for infection, based on assigning scores to each of the rodent infestation risk factors. Receiver operating characteristic curve analysis found that the prediction score produced a good/excellent fit based on an area under the curve of 0.78 (0.71-0.84). CONCLUSIONS/SIGNIFICANCE: Our study found that a high proportion of slum households were infested with R. norvegicus and that rat infestation was significantly associated with the risk of Leptospira infection, indicating that high level transmission occurs among slum households. We developed an easily applicable prediction score based on rat infestation markers, which identified households with highest infection risk. The use of the prediction score in community-based screening may therefore be an effective risk stratification strategy for targeting control measures in slum settings of high leptospirosis transmission.
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