» Articles » PMID: 28620680

Landscape, Climate and Hantavirus Cardiopulmonary Syndrome Outbreaks

Overview
Journal Ecohealth
Publisher Springer
Date 2017 Jun 17
PMID 28620680
Citations 19
Authors
Affiliations
Soon will be listed here.
Abstract

We performed a literature review in order to improve our understanding of how landscape and climate drivers affect HCPS outbreaks. Anthropogenic landscape changes such as forest loss, fragmentation and agricultural land uses are related with a boost in hantavirus reservoir species abundance and hantavirus prevalence in tropical areas, increasing HCPS risk. Additionally, higher precipitation, especially in arid regions, favors an increase in vegetational biomass, which augments the resources for reservoir rodents, also increasing HCPS risk. Although these relationships were observed, few studies described it so far, and the ones that did it are concentrated in few places. To guide future research on this issue, we build a conceptual model relating landscape and climate variables with HCPS outbreaks and identified research opportunities. We point out the need for studies addressing the effects of landscape configuration, temperature and the interaction between climate and landscape variables. Critical landscape thresholds are also highly relevant, once HCPS risk transmission can increase rapidly above a certain degree of landscape degradation. These studies could be relevant to implement preventive measures, creating landscapes that can mitigate disease spread risk.

Citing Articles

Anthropogenic land consolidation intensifies zoonotic host diversity loss and disease transmission in human habitats.

Pei S, Yu P, Raghwani J, Wang Y, Liu Z, Li Y Nat Ecol Evol. 2024; 9(1):99-110.

PMID: 39558089 DOI: 10.1038/s41559-024-02570-x.


Orthohantavirus Infection in Two Rodent Species that Inhabit Wetlands in Argentina.

Maroli M, Bellomo C, Coelho R, Martinez V, Pina C, Gomez Villafane I Ecohealth. 2023; 20(4):402-415.

PMID: 38091181 DOI: 10.1007/s10393-023-01661-8.


Viral diversity in wild and urban rodents of Yunnan Province, China.

Kane Y, Tendu A, Li R, Chen Y, Mastriani E, Lan J Emerg Microbes Infect. 2023; 13(1):2290842.

PMID: 38047395 PMC: 10829829. DOI: 10.1080/22221751.2023.2290842.


Seroprevalence of Hantavirus among Manual Cane Cutters and Epidemiological Aspects of HPS in Central Brazil.

Maia R, Fernandes J, de Mattos L, Camacho L, Caetano K, Carneiro M Viruses. 2023; 15(11).

PMID: 38005915 PMC: 10674252. DOI: 10.3390/v15112238.


Land-cover, land-use and human hantavirus infection risk: a systematic review.

Moirano G, Botta A, Yang M, Mangeruga M, Murray K, Vineis P Pathog Glob Health. 2023; 118(5):361-375.

PMID: 37876214 PMC: 11338209. DOI: 10.1080/20477724.2023.2272097.


References
1.
Oliveira R, Gentile R, Guterres A, Fernandes J, Teixeira B, Vaz V . Ecological study of hantavirus infection in wild rodents in an endemic area in Brazil. Acta Trop. 2013; 131:1-10. DOI: 10.1016/j.actatropica.2013.11.016. View

2.
Keesing F, Holt R, Ostfeld R . Effects of species diversity on disease risk. Ecol Lett. 2006; 9(4):485-98. DOI: 10.1111/j.1461-0248.2006.00885.x. View

3.
Schmaljohn C, Hjelle B . Hantaviruses: a global disease problem. Emerg Infect Dis. 1997; 3(2):95-104. PMC: 2627612. DOI: 10.3201/eid0302.970202. View

4.
Palma R, Polop J, Owen R, Mills J . Ecology of rodent-associated hantaviruses in the Southern Cone of South America: Argentina, Chile, Paraguay, and Uruguay. J Wildl Dis. 2012; 48(2):267-81. DOI: 10.7589/0090-3558-48.2.267. View

5.
Oliveira R, Guterres A, Fernandes J, DAndrea P, Bonvicino C, de Lemos E . Hantavirus reservoirs: current status with an emphasis on data from Brazil. Viruses. 2014; 6(5):1929-73. PMC: 4036540. DOI: 10.3390/v6051929. View