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Revista da Sociedade Brasileira de Medicina Tropical

Print version ISSN 0037-8682

Rev. Soc. Bras. Med. Trop. vol.46 no.1 Uberaba Jan./Feb. 2013

http://dx.doi.org/10.1590/S0037-86822012005000002 

Major Article

Serologic survey of hantavirus in a rural population from the northern State of Mato Grosso, Brazil

Ioni Oliveira SantosI, Glauciane Garcia de FigueiredoII, Luiz Tadeu Moraes FigueiredoII, Maria Regina Andrade de AzevedoIII, Neil Ferreira NovoIII, Celidéia Aparecida Coppi VazIII

ISecretaria Estadual de Saúde de Mato Grosso, Escritório Regional de Saúde de Colíder, Colider, MT

IIUniversidade de São Paulo, Faculdade de Medicina de Ribeirão Preto, Centro de Pesquisa em Virologia, São Paulo, SP

IIIUniversidade de Santo Amaro, Departamento de Pós Graduação, Santo Amaro, SP

ABSTRACT

INTRODUCTION:

Hantavirus is a genus of ribonucleic acid (RNA) viruses included in the family Bunyaviridae. Hantaviruses are rodent-borne zoonoses that, in the last 18 years, became an emergent public health problem in the Americas, causing a severe cardiopulmonary syndrome. This disease has no specific treatment and has a high case fatality. The transmission of hantavirus to man occurs by inhaling aerosols of rodent excreta. The aim of this study was to determine the prevalence of antibodies to hantavirus in the population of the rural settlement of Tupã in the county of Marcelândia, state of Mato Grosso, Brazil.

METHODS:

The participants of the serologic survey were visited at their homes and selected randomly among the settlement population. Blood samples of the participants were collected by venopuncture. The serum samples were tested by an IgG-ELISA using an N recombinant protein of Araraquara hantavirus as antigen, using the protocol previously established by Figueiredo et al.

RESULTS:

IgG antibodies to hantavirus were detected in 7 (13%) of the 54 participants. The positivity was higher among men. It was observed that there was an association of seropositivity to hantavirus within the participants born in the south of Brazil.

CONCLUSIONS:

The results suggest that, in this rural area, everyone is exposed to the same risk of becoming infected with hantavirus, and, therefore, there is a need to intensify surveillance activities and education of the local people to prevent this viral infection.

Key words: Hantavirus; Hantavirosis; Bunyaviridae

INTRODUCTION

The north of the state of Mato Grosso, Brazil, has suffered an extensive deforestation in order to use the land for farming soybeans and corn. This area also received a large migration of agricultural workers from other parts of the country. Thus, in recent years, the north of the state of Mato Grosso became a setting for the spread of various health disorders directly related to vectors and wild hosts. These health disorders, such as malaria, leishmaniasis, and yellow fever, are considered as endemic. However, in the last decade, hantaviruses emerged in the area and took the lives of many people, mainly farm workers1.

Hantaviruses are worldwide zoonoses from wild rodents belonging to different species. These are ribonucleic acid (RNA) viruses of the family Bunyaviridae that, currently, includes more than 300 distinct viral species distributed in 5 genera: Orthobunyavirus, Phlebovirus, Nairovirus, Hantavirus, and Tospovirus 2 . The Hantavirus genus includes at least 45 virus species and half of them were reported as causing human disease3. Different from other Bunyaviridae, which are arboviruses, hantaviruses are maintained in nature-infecting wild rodents. Hantavirus transmission to humans occurs when these pathogens are primarily inhaled through the aerosolization of rodent excreta and contaminated secretions4,5. The American hantaviruses, when infecting man, cause a severe hantavirus cardiopulmonary syndrome (HCPS). In Brazil, HCPS has been reported in 1,335 patients until August 2010, and 525 of these died (39% case fatality ratio). Hantavirus cardiopulmonary syndrome has been reported in all Brazilian regions, predominating in the south, southeast, and midwest (91.2% of the cases)6. From 1999 to August 2010, 206 HCPS cases including 86 (43%) fatalities were reported in the Brazilian midwestern state of Mato Grosso6. From 2007, 12 of these cases occurred in the county of Marcelândia, the place where this study was performed to investigate the circulation of hantavirus. Recently, it was described that evidence of the circulation of hantavirus in four counties were influenced by the BR-163, also known as Cuiabá-Santarém. The county of Marcelândia was contemplated in this research and presented a prevalence of 9.4% of the specific antibodies against hantavirus7.

METHODS

Participants of the serologic survey

In this serologic survey, 54 individuals participated, mostly migrants living in Tupã, a 540-inhabitants rural settlement in the county of Marcelândia, located in the north of the state of Mato Grosso, Brazil, at 11° 05' 22 latitude and 54° 27' 02 longitude ( Figure 1 ).

FIGURE 1  Map of the state of Mato Grosso, Brazil, showing (in red) the county of Marcelândia. 

The participants were visited at their homes and selected randomly among the settlement population after giving a signed authorization. The group of participants included 61.1% males and 38.9% females. All participants answered a questionnaire, which includes personal information, education, professional activities, previous diseases, and contact with rodents. The vegetation surrounding the homes of the participants and their sources of drinking water were also analyzed.

Serum samples

Blood samples of the participants were collected by venopuncture. The sera were separated and stored at -20°C in the Laboratory of Clinical Analysis of the county of Marcelândia. These samples were latterly transported, at 4°C and following biosafety regulations, to the Virology Research Center, School of Medicine of the University of São Paulo in Ribeirão Preto City, Brazil (VRC-SMUSP-RP).

IgG-ELISA to hantavirus

The serum samples were tested by an immunoglobulin G-enzyme linked immuno-assay (IgG-ELISA) using an N recombinant protein of Araraquara hantavirus as antigen in the VRC-SMUSP-RP8.

The ELISA, using the N recombinant protein of Araraquara hantavirus produced in Escherichia coli, was standardized using the protocol previously established by Figueiredo and collaborators8.

Statistical analysis

The chi-square test was applied to the results shown in contingency tables, and the Fisher's exact test was used to look for an association between qualitative variables of the participants and seropositivity to hantavirus. The level of significance was 5% (p=0.05) for both tests9.

Ethical considerations

This study was approved by the National Ethics Committee of the Ministry of Health (CONEP/MS), as well as by the Ethics Committee in Research of the University of Santo Amaro/SP (144/09, May 2010).

RESULTS

All 54 participants of this study were agricultural workers referring elementary school education, doing subsistence agriculture, and living in the Tupã settlement (for 6.5 years in average). Twenty-five participants were born in the south, 12 in the midwest, 10 in the southeast, 5 in the northeast, and 2 in the north of Brazil. Most of the participants referred a previous working activity in other regions of the state of Mato Grosso, following fronts of agricultural expansion and trying to receive agriculture lands from the government.

Based on the serologic test, 7 participants had IgG antibodies to hantavirus (positivity of 13%), as shown in Table 1. There was no association of the gender of the participants with the seropositivity to hantavirus. Six of the 7 seropositive participants were born in the south of Brazil and 1 in the northern state of Pará, Brazil. The seropositivity among southern participants was significantly higher than in those from other regions (p=0.031), as shown in Table 2.

TABLE 1  Seropositivity to hantavirus associated to gender of the participants of the study (n=54). 

Fisher's exact test (p=0.436).

TABLE 2  Seropositivity to hantavirus associated to the birthplace of the participants. 

The Fisher's exact test was significant (p=0.031).

Regarding the occurrence of diseases in the participants 60 days preceding the collection of serum, fever, dry cough, headache, myalgia, and asthenia were reported by 6 participants. Three other participants referred gastrointestinal symptoms (diarrhea and vomiting). Chronic diseases, such as hypertension and diabetes, were referred by 24% of the participants. However, the occurrence of any of these signs, symptoms, or diseases was not associated to seropositivity to hantavirus.

It was observed that all participants had a basic knowledge about hantavirus. They knew about the natural reservoir, forms of contamination, severity of the hantavirus disease, and measures to prevent infection. A proportion of the participants (59.3%) referred a previous direct contact with rodents and their excreta while 40.7% reported they do not remember or have not had such contact, as shown in Table 3. However, rodent contact was not associated with hantavirus in the previous infection. Therefore, 46.3% of the participants referred to store grains in the peridomiciliary environment and 33.3% inside of their residences, without association with seropositivity to hantavirus.

TABLE 3  Seropositivity to hantavirus associated to reference of contact with rodents by the participants. 

Fisher's exact test (p=0.1315).

The predominant environment surrounding the homes of the participants was pasture, in 38.9%, followed by poultry, in 27.8%. Other vegetation surroundings were forest, manioc plantation, pineapple plantation, primary forest, and fruit orchard and the sum of these 5 environments accounted for 33.3% of the houses of the participants. There was no association of any of these environments with seropositivity to hantavirus.

Regarding the source of water used in houses by the participants, 83.3% used underground water treated with sodium hypochlorite while 16.7% used river water. It was not observed if there was an association between the type and source of water used in houses by the participants and the seropositivity to hantavirus.

DISCUSSION

It is important to understand the distinct epidemiologic aspects related to hantavirus striking populations at risk in different regions of Brazil. This study is the first work of this nature conducted in the state of Mato Grosso, and the results could help to better understand the epidemiology of this disease in the region, helping on decision-making and implementation of appropriate public health policies for emerging diseases in the region.

The first report of HCPS in the Americas occurred in the United States of America in 1993, and this disease was also reported in Brazil of the same year10-13. These were severe HCPS cases with fatalities that occurred in Juquitiba, state of São Paulo12. Presently, about one thousand and a half HCPS cases were reported in Brazil, and some hantaviruses and their probable rodent-reservoirs were also known. The area of ​​Atlantic rainforest predominates the Juquitiba virus (JUQV), and its reservoir is Oligoryzomys nigripes 14 . The cerrado (savannah) of the southeastern countryside and of the central plateau predominates Araraquara virus (ARAV), having Necromys lasiurus as reservoir14,15. Anajatuba virus (ANAJV) causes HCPS in the swamp areas in the northeast of Brazil (state of Maranhão) and is associated to Oligoryzomys fornesii. Castelo dos Sonhos virus (CASV) and Laguna Negra virus (LNV) are both associated with cases of HCPS in Amazonian and Pantanal (swamp) ecosystems of Pará and Mato Grosso states, and associated to Oligoryzomys moojeni and Calomys callosus, respectively16. Based on the known geographic distribution, CASV could be the causative of hantavirus infections we detected in Tupã. This randomized serologic survey included 10% of the population of Tupã settlement as participants and showed that 13% of them were previously infected with hantavirus. This seroprevalence to hantavirus is almost 3 times higher than that observed in another Amazonic biome region at the state of Maranhão, 4.7% and similar to that observed in the Jardinópolis county at the state of São Paulo17,18. This high seroprevalence to hantavirus also shows that most of these infections, especially those causing mild forms of disease, may remain undiagnosed.

It was also observed that there was a slightly higher seropositivity to hantavirus among men when compared to females as previously observed in other Brazilian hantavirus serologic surveys17. The participants of the serologic survey were mostly migrant agricultural workers from all regions of Brazil, mostly from the south, especially from the state of Paraná. It was found that seropositivity to hantavirus was significantly higher in southern participants when compared to those from other regions. Thus, seropositives could become infected by hantavirus when lived in the south, where most of the Brazilian HCPS cases occurred. However, 12 hantavirus-confirmed cases occurred in the county of Marcelândia from 2007 to 2009, which shows that local infections could also have occurred1.

In this study, it was not possible to detect any personal, morbid, or labor-related antecedent referred by the participants that could be associated to hantavirus infection. Curiously, it also included the contact with rodents and their excreta. Similar results were also observed in the previous hantavirus serologic survey in Jardinópolis county18.

No environment surrounding the homes of the participants, especially pastures that have grass seeds and food attractive of large populations of wild rodents, was associated with hantavirus infection in this study19. The source of water used in houses by the participants was also not associated with hantavirus infection20.

Briefly, we presented that there is a high prevalence of individuals infected with hantavirus in the population of a rural settlement in the north of the state of Mato Grosso. It was also suggested that all inhabitants of the settlement are exposed to the same risk of becoming infected with hantavirus. Therefore, there is a need to intensify surveillance activities and education of the local people to prevent this viral infection.

ACKNOWLEDGMENTS

The authors would like to thank the Secretariat of Health of the state of Mato Grosso and the Team of the Regional Office of Health of Colíder.

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Received: July19, , 2011; Accepted: December09, , 2011

Address to: Dr. Ioni Oliveira Santos. ERSCOL/SES/MT. Av. Costa e Silva 125, Setor Norte, 78500-000 Colíder, MT, Brasil. Phone/Fax: 55 66 3541-2757 e-mail: ionibiologo1@hotmail.com

CONFLICT OF INTEREST The authors declare that there is no conflict of interest.

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.