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Article

Malaria and Hantavirus Pulmonary Syndrome in Gold Mining in the Amazon Region, Brazil

by
Ana Cláudia Pereira Terças-Trettel
1,2,*,
Elaine Cristina de Oliveira
3,
Cor Jesus Fernandes Fontes
2,
Alba Valéria Gomes de Melo
3,
Renata Carvalho de Oliveira
4,
Alexandro Guterres
4,
Jorlan Fernandes
4,
Raphael Gomes da Silva
4,
Marina Atanaka
2,
Mariano Martinez Espinosa
2 and
Elba Regina Sampaio de Lemos
4
1
Nursing Department, Mato Grosso State University Campus Tangará da Serra, Tangara da Serra (MT) 78300-000, Brazil
2
Department, Mato Grosso Federal University, Cuiaba (MT) 78000-000, Brazil
3
Epidemiology Department, Health Secretary of State of Mato Grosso, Cuiaba (MT) 78000-000, Brazil
4
Hantaviruses and Rickettsiosis Laboratory, Oswaldo Cruz—FIOCRUZ Institute, Rio de Janeiro (RJ) 21000-000, Brazil
*
Author to whom correspondence should be addressed.
Int. J. Environ. Res. Public Health 2019, 16(10), 1852; https://doi.org/10.3390/ijerph16101852
Submission received: 18 March 2019 / Revised: 11 April 2019 / Accepted: 18 April 2019 / Published: 25 May 2019
(This article belongs to the Special Issue Emerging and Reemerging Infectious Diseases)

Abstract

:
People living in mining regions are exposed to numerous biological agents by several specific types of transmission mechanisms. This study is designed to describe fatal hantavirus pulmonary syndrome (HPS) cases confirmed by serology and molecular analysis, where a seroprevalence survey was conducted in the gold mining regions of the state of Mato Grosso, in the official Amazon region, Brazil. Two fatal cases of HPS were confirmed in a mining area in the Legal Amazon, where malaria is one of the most important public health problems. A molecular analysis detected the presence of the genome of the Castelo dos Sonhos virus. Out of the 112 blood samples analyzed, five were positive for Plasmodium infection (four P. falciparum and one P. vivax), and four were seropositive for hantavirus, showing a seroprevalence of 3.57%. One of the four miners who was seroreactive for hantavirus concomitantly had P. falciparum infection, which was confirmed by thick blood smear. This manuscript highlights the importance of considering hantavirus pulmonary syndrome as a diagnostic possibility in febrile infection associated with pulmonary manifestations in mining areas where malaria cases are often identified.

1. Introduction

People living in mining areas are subject to adverse conditions that are often dangerous, painful and unhealthy. The miners’ job is one of the most precarious and intense existing occupations [1]. This vulnerability exposes them to different risks, such as hearing impairment, disc herniation, repetitive stress injury, skin and urinary problems, respiratory system diseases, febrile illnesses, malaria, and long-term cancer [2,3].
The occurrence of malaria cases in gold mining regions has been reported in the countries of Africa, Asia [4,5,6], and South America (Brazil, Colombia, Guyana, Peru, Suriname and Venezuela) [7,8,9,10,11,12]. These occurrences are related to the profound environmental changes that mining activities cause, disrupting the existing ecological balance in areas that were previously preserved.
In Brazil, most malaria cases come from rural areas associated with gold mining [12,13]. The gold mining areas of northern Mato Grosso greatly contribute to the numbers of malaria cases, and these populations are exposed to numerous vulnerabilities, such as poor housing quality due to physical proximity to the workplaces, poor access to health services, and a modified environment that favors the presence of vectors and wild animals [14,15,16].
Because of both close contact with a wild environment that has undergone extensive modification and the unspecific health problems identified in this population, it is likely that emerging diseases are occurring and not diagnosed, possibly because of the difficulty of access to health services.
Hantavirus pulmonary syndrome (HPS), also known as hantavirus cardiopulmonary syndrome (HCPS), is an emerging, acute, severe, and highly lethal disease caused by several genotypes of hantavirus and transmitted by wild rodents in the American continent. Since the first evidence of hantavirus circulation in the Brazilian official Amazon region in 1991, 124 confirmed cases have been identified, associated with the genotypes of the Anajatuba, Castelo dos Sonhos and Rio Mamore viruses. Cases of HPS have been reported in the legal Amazon region as a consequence of, among other factors, major changes in the environment and close contact between humans and wild animals, mainly rodents [17,18,19,20,21,22].
In South America, the hantavirus rodent reservoirs that cause HPS belong to the subfamily Sigmodontinae, and in Brazil, where there is a wide diversity of wild rodents distributed in different biomes, six hantavirus genotypes associated with SPH have been described: Juquitiba (also identified as Araucaria), Araraquara, Castelo dos Sonhos, Laguna Negra-like, Anajatuba, and Rio Mamoré [21,22]. In the state of Mato Grosso, where the study was conducted, two genotypes of hantavirus are associated with HPS: (i) Castelo dos Sonhos, responsible for the miners’ cases, maintained in the rodent reservoir Oligoryzomys utiairitensis previously identified in this region [23,24] and (ii) the Laguna Negra, also described in the regions close to the mining of Mato Grosso, for which the reservoir is the wild rodent Calomys callidus [25].
It is noteworthy that the characteristic signs and symptoms of the prodromal phase of HPS are nonspecific, including fever, myalgia, malaise, headache, chills, nausea, and vomiting; thus, the differential diagnosis method is essential to distinguish HPS from other diseases that have similar initial characteristics [26,27,28,29,30]. In fact, although infrequent, the appearance of respiratory complications related to malaria can simulate HPS in the cardiopulmonary stage when the patient has dry cough, accompanied by tachycardia, dyspnea, and hypoxemia, followed by rapid progression to pulmonary edema, hypotension, and circulatory collapse [29,31,32,33,34,35].
In this context, the objective of this study is to describe the occurrence of hantavirus in the gold-mining regions of Mato Grosso state, Brazil, emphasizing the importance of differential diagnosis.

2. Cases

2.1. Case Presentation

This study reports two cases of HPS in the gold mining region of the União do Norte district, Peixoto de Azevedo in northern Mato Grosso (Figure 1), and a study of seroprevalence in the population of a region located to the west of the occurrence of confirmed cases.

2.2. Case Report

In this study, HPS was confirmed, by serology and molecular analysis, in two miners who worked in the far northern part of Mato Grosso, in the União do Norte district, city of Peixoto de Azevedo, a malaria transmission area. The epidemiological investigation of HPS cases revealed that the patients were exposed to aerosolized dust while cleaning the accommodations where they lived and worked one week before the occurrence of the first symptoms. In addition, they also had a history of consuming fruits collected from the ground in rodent-infested areas. The lack of previous notifications about HPS cases among miners and the frequent occurrence of malaria and arboviruses in the population of the mining areas were determinants in the fatal evolution of the two clinical cases.
Patient 1 (gold mining region of the União do Norte district, Peixoto de Azevedo in northern Mato Grosso):
In June 2015, a 37-year-old male patient presented to a public hospital with a history of fever, headache, and myalgia; he was treated and released with suspected dengue. Four days later, the patient presented with dyspnea, acute respiratory failure, blurred vision, and chest pain, and was referred to the intensive care unit (ICU), where treatment included the use of antibiotics and a mechanical respirator. His nonspecific tests showed increased urea and creatinine (127.40 mg/dL and 2.42 mg/dL, respectively), thrombocytopenia (58,000/mm3), and leukocytosis (20,040/mm3). A chest radiograph confirmed a pulmonary diffuse interstitial infiltrate (Figure 2). On the sixth day of the disease, with suspected HPS, a blood sample was collected, of which the serological analysis confirmed the presence of anti-hantavirus IgM antibodies with negative IgG [36]. Hantavirus genome was detected in a blood sample using reverse transcription polymerase chain reaction (RT-PCR), and the genotype identified was Castelo dos Sonhos virus [37]. Despite the measures imposed in the intensive care unit, the patient progressed to death three weeks after the onset of illness. The patient was a machine operator in a gold mine and lived in Sinop, a municipality in the Legal Amazon region in Mato Grosso state.
Patient 2 (gold mining region of the União do Norte district, Peixoto de Azevedo in northern Mato Grosso):
A 47-year-old man with fever, headache, myalgia, chest pain, dry cough, dizziness, asthenia, dyspnea, acute respiratory failure, and back pain was admitted to the same public hospital as Patient 1 in June 2015. The laboratory test revealed hemoconcentration (47.1%), thrombocytopenia (37,000/mm3), leukocytosis (22,180/mm3), increased urea and creatinine (72.56 mg/dL and 1.87 mg/dL, respectively), aspartate aminotransferase (102.4 IU), and alanine aminotransferase (57.14 IU). Chest X-ray was not performed. The analysis of the serum sample collected on the seventh day of the disease showed the presence of anti-hantavirus IgM antibodies, with negative IgG, but detected hantavirus Castelo dos Sonhos by RT-PCR. Although a therapeutic strategy based on antibiotics associated with hemodynamic and respiratory support was followed, the patient died nine days after the onset of the illness.
After the first occurrence of HPS in miners, a study was carried out to estimate the prevalence of anti-hantavirus antibodies in 112 samples previously collected from a population living in a mining area in the Três Fronteiras district in the city of Colniza, Mato Grosso (Figure 1). These serum samples, which were stored in the Malaria Biorepository of the University Hospital Júlio Muller following a malaria survey conducted in 2012, were used due to the physiogeographical and population similarities between this gold mining area and the area where the two fatal HPS cases were identified. These two mining areas, even if geographically distant, are comparable because they are located in the Amazon biome, have the same environmental modifications from the garimpo and the populations have similar income, housing and access to health.
The data were collected in July 2012 from 112 Igarapé Grande gold mining and São Francisco gold mining, municipality of Colniza, this number represents all inhabitants of the mining areas mentioned above. This data included collection of blood samples using the finger prick and thick smear technique, completion of the SIVEP-Malaria notification form, and completion of an interview to obtain demographic and socioeconomic information and information about exposure to malaria transmission.
The serum samples from human cases of HPS and cohort were tested by anti-hantavirus IgG and IgM antibodies screening, using the recombinant N protein of Araraquara virus, provided by the University of São Paulo/Ribeirão Preto [38], following the protocols of enzyme immunoassays ELISA. This antigen is representative for all genotypes isolated in Brazil.
The malaria incidence in the population of miners in Colniza in 2012 was 4.46% (4 cases of Plasmodium falciparum and one of P. vivax), whereas the hantavirus seroprevalence was 3.57%, with four reactive IgG samples, all negative for IgM antibodies. One of the four hantavirus seropositive patients, in addition to mentioning an unspecific fever history on the day of data collection, also presented positive results in a thick blood smear for malaria with the identification of P. falciparum.
For demographic data, among the 112 study participants, 56.25% were men. Nevertheless, when evaluating the four hantavirus seroreactive patients, three were women. The age of the study population ranged from six months to 65 years, with an average of 29 years. It is noteworthy that one of the 48 women was pregnant. The predominant color was pardo in 68.8% of the general population and 50% of the seroreactive population, while 41.1% of the study population were married and another 41.1% single, see Table 1.
Regarding educational attainment, Table 1 shows that all seropositive patients and 75% of the total attended school. Vegetal exploration (18.75%), which include professional activities that involve explorations of the environment, and housewife (12.5%) were the most common occupations, but 64.4% of the respondents mentioned other types of employment related to mining activity. The most common housing type was wooden houses, in addition to seven houses built from canvas. Eight interviewees reported information collected on clinical aspects, and one hantavirus seroreactive individual reported fever, headache, and body pain, see Table 2.

3. Discussion

The clinical manifestations of acute febrile diseases are nonspecific and may hinder diagnosis and clinical management, especially in relation to infectious diseases such as HPS and malaria that can often coexist in endemic areas, as well as dengue, chikungunya, zika, and leptospirosis, among others. Both malaria and HPS, in the prodromal phase, have fever, myalgia, malaise, headache, abdominal discomfort, chills, nausea, and vomiting as clinical manifestations, which reinforces the need to consider differential diagnosis in areas with eco-epidemiological conditions suitable for vector and rodent transmissions as in the mining areas of this study [26,29,39].
In HPS, hemoconcentration, leukocytosis, atypical lymphocytes and thrombocytopenia, and elevated serum levels of liver enzymes are generally observed [27,40,41,42,43]; laboratory findings are similar to those observed in malaria and dengue [44,45,46,47,48]. In relation to chest radiographs in HPS, frequently observed findings include bilateral diffuse interstitial infiltrates, pulmonary edema, and pleural effusion during the cardiorespiratory phase [29,49]. Respiratory involvements in malaria are rare, but well-documented; they can be confused, however, with the severe phase of HPS [31,32,34,35]. In this context, the occurrence of HPS must be considered in patients with acute febrile illness associated with respiratory failure in areas where environmental changes can facilitate hantaviral transmission.
According to the National Department of Mineral Production, there are 185,832 workers in mineral extraction and 8368 mining regions officially registered in Brazil, although these numbers may be underestimates due to the informality of this professional activity [44]. Thousands of people living in the mining areas of the Brazilian Amazon are subject to numerous risks that can influence their health condition and quality of life.
In our study of seroprevalence, the most frequent housing type was wooden houses, but there were also canvas houses, demonstrating the social fragility to which the miners are exposed and the resulting risk of contact with animals that transmit the different diseases described herein. These existing housing conditions facilitate the transmission of causative agents of both malaria and HPS since the cracks in the walls of these residences facilitate the entry of the malaria mosquito and wild rodents searching for food and shelter [15,17,45]. Environmental changes resulting from mining activities have continuously influenced the habitat and species composition of wild rodents with consequent impacts on the health conditions of the people living there. These influences are already observable in the high number of cases of malaria in these regions [12,13] and can also be observed in the transmission of hantavirus, since the predators and competitors of rodents are usually exterminated in the habitats altered by human activities, an event that favors, in due course, the increased density of rodents and the establishment of new species. Thus, environmental changes caused in nature by the exploitation of mining activities favor the emergence of new diseases such as HPS [19,46,47].
Studies conducted to clarify doubts in the diagnosis of febrile disease of unknown etiology point to the need for immediate laboratory confirmation during outbreak/epidemic situations, as the many clinical manifestations may not characterize the diseases [48,49]. Serologic evidence of hantavirus has been identified in patients with clinical suspicion of dengue, malaria, influenza, chikungunya, rickettsial infections, leptospirosis, and HIV [50,51,52,53,54,55,56,57,58,59]. Thus, the results of this study in which the initial diagnosis was malaria and dengue, reinforce the need for an alert to health professionals working in endemic areas of malaria regarding the importance to investigate the hantavirus infection, as here performed with the population from Colniza.
One of the 112 participants of the malaria survey, who was P. falciparum positive, showed immunoserological evidence of hantavirus infection. Concomitant hantavirus infection with other agents, such as Leptospira, Mammarenavirus, Dengue virus, hepatitis B virus, and Mycobacterium, have been reported rarely as pulmonary malaria and HPS, the two important and fatal infectious diseases that are clinically indistinguishable and may exist in endemic areas; this coinfection, however, is rarely investigated. Thus, although the possible false reactivity should be considered in interpreting this result, the identification of two fatal HPS cases and serological evidence of infection in another three malaria negative miners (one of them with history of fever, headache, and body pain), reinforce the possibility of concomitant malaria–hantavirus infection in patients living in this Brazilian malaria-endemic area. A positive IgG assay with IgM negative serology indicates past infection because IgM antibodies appear early after infection and can remain, on average, for 30 days after the onset of infection [60,61,62,63]. However, it is important to recognize that at the onset of hantavirus infection, IgG antibodies are also detectable concomitantly with IgM antibodies. In this context, there may be a possibility of dual infection of malaria and HPS in the miner from Colniza in 2012, given that he had unspecific febrile illness.
Lastly, although there are no other studies that describe the presence of HPS in mines, it is possible to compare this finding with hantavirus seroprevalence studies conducted in populations from different regions of Brazil, where rates have ranged from 0.52% to 13.2% [64,65,66,67,68,69,70]. It is noteworthy that in cluster situations as described by Terças et al. [71] in the indigenous community in far northern Mato Grosso, the seroprevalence can be high and reach 51.1%.
In Brazil, the Amazon region accounts for 99% of malaria cases, and the incidence of malaria in gold mining regions is proportional to deforestation, being present in 39 cities of this biome [72,73]. Although the incidence rates may be even higher (31.3 to 94%), there has been a reduction in recent years in response to control programs implemented by public health services, which can be seen in the gold mining region in Colniza, where there was a seroprevalence of 4.5% [14,15,16,44,74,75].

4. Conclusions

This study presents two fatal cases of HPS confirmed by serological and molecular analysis in miners in the União do Norte district of Peixoto de Azevedo, Mato Grosso and shows that the genotype Castelo dos Sonhos virus infected the patients. Malaria and HPS may have the same level of seroprevalence in the study area of Mato Grosso.
Considering the absence of previous serological surveys for hantavirus in vulnerable populations residing in the mining area, the detection of hantavirus antibodies in the mining region in the city of Colniza, Mato Grosso reinforces the need for vigilance in preventing this rodent-borne disease in the Brazilian gold mining regions.
The confirmation of hantavirus cases in the mining region of far northern Mato Grosso prompts reflection in relation to emerging diseases in vulnerable and more susceptible populations due to their constantly changing environments. In this scenario, the investigation of other infectious agents, particularly zoonotic pathogens such as hantavirus, should be encouraged by health services because the correct diagnosis will direct proper and effective assistance.
Finally, this study highlights the importance of including HPS in a differential diagnosis and performing hantavirus screening among patients with febrile illness living in malaria-endemic areas, particularly in individuals with pulmonary failure.

Author Contributions

A.C.P.T.-T., E.C.d.O. and A.V.G.d.M. assisted with data and sample collection, completed data cleaning and all statistical, and drafted the manuscript; C.J.F.F. and M.A. contributed to the design and execution of the study, as well as providing critical review of the manuscript; M.M.E. managed the database for the study as well as ensuring quality control of the data; R.G.d.S., J.F., A.G., and R.C.d.O. performed the molecular testing, drafted the laboratory methods section, and provided critical review of the manuscript; E.R.S.d.L. assisted with conception of study hypotheses, statistical analyses, and interpretations, and provided critical review of the manuscript. All authors read and approved the final manuscript.

Funding

This research was funded by Fundação de amparo à pesquisa do Estado de Mato Grosso (FAPEMAT). Check carefully that the details given are accurate and use the standard spelling of funding agency names at http://www.fapemat.mt.gov.br, any errors may affect your future funding.

Acknowledgments

The authors thank the many Mato Grosso families who allowed us to disrupt their lives to study them and their households.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Nobrega, J.; Menezes, M. Homens “subterrâneos”: O trabalho informal e precário nos garimpos de junco do Seridó. Raízes 2010, 30, 140–152. [Google Scholar]
  2. Santos, E. Garimpagem e saúde. In Conseqüências da Garimpagem no Âmbito Social e Ambiental da Amazônia; Mathis, A., Rehaag, R., Eds.; Buntstift: Manaus, Brazil, 1993; pp. 36–72. [Google Scholar]
  3. Lima, E. Doenças Respiratórias Associadas à Atividade de Mineração no Municipio de PARELHAS, Região do Sérido Norte-Riograndense, Dissertação em Meio Ambiente; Universidade Federal do Rio Grande do Norte: Natal, Brazil, 2009. [Google Scholar]
  4. Asante, K.P.; Zandoh, C.; Dery, D.B.; Brown, C.; Adjei, G.; Antwi-Dadzie, Y.; Ajuik, M.; Tchum, K.; Dosso, D.; Amenga-Etego, S.; et al. Malaria epidemiology in the Ahafo area of Ghana. Malar. J. 2011, 10, 211. [Google Scholar] [CrossRef] [PubMed]
  5. Knoblauch, A.M.; Winkler, M.S.; Archer, C.; Divall, M.J.; Owuor, M.; Yapo, R.M.; Yao, P.A.; Utzinger, J. The epidemiology of malaria and anaemia in the Bonikro mining area, central Cote d’Ivoire. Malar. J. 2014, 13, 194. [Google Scholar] [CrossRef]
  6. Mitjà, O.; Paru, R.; Selve, B.; Betuela, I.; Siba, P.; De Lazzari, E.; Bassat, Q. Malaria epidemiology in Lihir Island, Papua New Guinea. Malar. J. 2013, 12, 98. [Google Scholar] [CrossRef]
  7. Adhin, M.R.; Labadie-Bracho, M.; Vreden, S. Gold mining areas in Suriname: Reservoirs of malaria resistance? Infect. Drug Resist. 2014, 7, 111–116. [Google Scholar] [CrossRef]
  8. Moreno, J.E.; Rubio-Palis, Y.; Páez, E.; Pérez, E.; Sánchez, V.; Vaccari, E. Malaria entomological inoculation rates in gold mining areas of Southern Venezuela. Mem. Inst. Oswaldo Cruz 2009, 104, 764–768. [Google Scholar] [CrossRef]
  9. De Santi, V.P.; Dia, A.; Adde, A.; Hyvert, G.; Galant, J.; Mazevet, M.; Nguyen, C.; Vezenegho, S.B.; Dusfour, I.; Girod, R.; et al. Malaria in French guiana linked to illegal gold mining. Emerg. Infect. Dis. 2016, 22, 344–346. [Google Scholar] [CrossRef] [PubMed]
  10. Castellanos, A.; Chaparro-Narváez, P.; Morales-Plaza, C.D.; Alzate, A.; Padilla, J.; Arévalo, M.; Herrera, S. Malaria in gold-mining areas in Colombia. Mem. Inst. Oswaldo Cruz 2016, 111, 59–66. [Google Scholar] [CrossRef]
  11. Parker, B.S.; Olortegui, M.P.; Yori, P.P.; Escobedo, K.; Florin, D.; Pinedo, S.R.; Cardenas Greffa, R.; Capcha Veja, L.; Rodriguez Ferrucci, H.; Pan, W.K.; et al. Hyperendemic malaria transmission in areas of occupation-related travel in the Peruvian Amazon. Malar. J. 2013, 12, 178. [Google Scholar] [CrossRef] [PubMed]
  12. Oliveira, E.C.; dos Santos, E.S.; Zeilhofer, P.; Souza-Santos, R.; Atanaka-Santos, M. Geographic information systems and logistic regression for high-resolution malaria risk mapping in a rural settlement of the southern Brazilian Amazon. Malar. J. 2013, 12, 420. [Google Scholar] [CrossRef]
  13. Duarte, E.C.; Fontes, C.J.F. Associação entre a produção anual de ouro em garimpos e incidência de malária em Mato Grosso—Brasil, 1985-1996. Rev. Soc. Bras. Med. Trop. 2002, 35, 665–668. [Google Scholar] [CrossRef] [PubMed]
  14. Atanaka-Santos, M.; Czeresnia, D.; Souza-Santos, R.; Oliveira, R.M. Comportamento epidemiológico da malária no Estado de Mato Grosso, 1980–2003. Rev. Soc. Bras. Med. Trop. 2006, 39, 187–192. [Google Scholar] [CrossRef] [PubMed]
  15. Barbieri, A.F.; Sawyer, D.O. Heterogeneity of malaria prevalence in alluvial gold mining areas in Northern Mato Grosso State, Brazil. Cad. Saude Publica 2007, 23, 2878–2886. [Google Scholar] [CrossRef] [Green Version]
  16. Oliveira, E.C.; dos Santos, E.S.; Zeilhofer, P.; Souza-Santos, R.; Atanaka-Santos, M. Spatial patterns of malaria in a land reform colonization project, Juruena municipality, Mato Grosso, Brazil. Malar. J. 2011, 10, 177. [Google Scholar] [CrossRef] [PubMed]
  17. Prist, P.R.; Uriarte, M.; Fernandes, K.; Metzger, J.P. Climate change and sugarcane expansion increase Hantavirus infection risk. PLoS Negl. Trop. Dis. 2017, 11, e0005705. [Google Scholar] [CrossRef] [PubMed]
  18. Schatzmayr, H.G. Viroses emergentes e reemergentes. Cad. Saude Publica 2001, 17, 209–213. [Google Scholar] [CrossRef] [PubMed]
  19. Guterres, A.; Lemos, E.R.S. Hantaviruses and a neglected environmental determinant. One Health 2018, 5, 27–33. [Google Scholar] [CrossRef]
  20. Ayres, J.; Calazans, G.; Saletti Filho, H.C.; França Junior, I. Risco, vulnerabilidade e práticas de prevenção e promoção da saúde. In Tratado de Saúde Coletiva; Campos, G., Minayo, M., Akerman, M., Drumond, J.M., Carvalho, Y., Eds.; Hucitec: São Paulo, Brazil, 2006. [Google Scholar]
  21. Jonsson, C.B.; Figueiredo, L.T.; Vapalahti, O. A global perspective on hantavirus ecology, epidemiology, and disease. Clin. Microbiol. Rev. 2010, 23, 412–441. [Google Scholar] [CrossRef]
  22. Oliveira, R.C.; Guterres, A.; Fernandes, J.; D’Andrea, P.S.; Bonvicino, C.R.; de Lemos, E.R.S. Hantavirus reservoirs: Current status with an emphasis on data from Brazil. Viruses 2014, 6, 1929–1973. [Google Scholar] [CrossRef]
  23. Medeiros, D.B.; da Rosa, E.S.; Marques, A.; Simith, D.B.; Carneiro, A.R.; Chiang, J.O.; Prazeres, I.T.E.; Vasconcelos, P.F.C.; Nunes, M.R.T. Circulation of hantaviruses in the influence area of the Cuiaba-Santarem Highway. Mem. Inst. Oswaldo Cruz 2010, 105, 665–671. [Google Scholar] [CrossRef]
  24. Da Rosa, E.S.T.; Medeiros, D.B.; Nunes, M.R.; Simith, D.B.; de Souza Pereira, A.; Elkhoury, M.R. Pygmy rice rat as potential host of Castelo dos Sonhos Hantavirus. Emerg. Infect. Dis. 2011, 17, 1527–1530. [Google Scholar] [CrossRef] [PubMed]
  25. Rosa, E.S.T.; Medeiros, D.B.; Nunes, M.R.; Simith, D.B.; Pereira, A.S.; Elkhoury, M.R. Molecular epidemiology of Laguna Negra Virus, Mato Grosso State, Brazil. Emerg. Infect. Dis. 2012, 18, 982–985. [Google Scholar] [CrossRef]
  26. Amaral, C.N.D.; Albuquerque, Y.D.D.; Pinto, A.Y.D.N.; Souza, J.M.D. A importância do perfil clínico-laboratorial no diagnóstico diferencial entre malária e hepatite aguda viral. J. Pediatr. 2003, 79, 429–434. [Google Scholar] [CrossRef]
  27. Ferreira, M.S. Hantaviroses. Rev. Soc. Bras. Med. Trop. 2003, 36, 81–96. [Google Scholar] [CrossRef]
  28. Enria, D. Epidemiología de las infecciones por hantavirus. Acta Bioquím. Clín. Latinoam. 2004, 38, 537–544. [Google Scholar]
  29. Oliveira, R.C.; Guterres, A.; Teixeira, B.R.; Fernandes, J.; Junior, J.M.P.; de Jesus Oliveira, J.R.; Pereira, L.S.; Junior, J.B.; Meneguete, P.S.; Dias, C.M.G.; et al. A fatal hantavirus pulmonary syndrome misdiagnosed as dengue: An investigation into the first reported case in Rio de Janeiro state, Brazil. Am. J. Trop. Med. Hyg. 2017, 97, 125–129. [Google Scholar] [CrossRef] [PubMed]
  30. Vial, P.A.; Valdivieso, F.; Ferres, M.; Riquelme, R.; Rioseco, M.L.; Calvo, M. High-dose intravenous methylprednisolone for hantavirus cardiopulmonar syndrome in chile: A double-blind, randomized controlled clinical trial. Clin. Infect. Dis. 2013, 57, 943–951. [Google Scholar] [CrossRef]
  31. Anstey, N.M.; Jacups, S.P.; Cain, T.; Pearson, T.; Ziesing, P.J.; Fisher, D.A. Pulmonary manifestations of uncomplicated falciparum and vivax malaria: Cough, small airways obstruction, impaired gas transfer, and increased pulmonary phagocytic activity. J. Infect. Dis. 2002, 185, 1326–1334. [Google Scholar] [CrossRef] [PubMed]
  32. Lomar, A.V.; Vidal, J.E.; Lomar, F.P.; Barbas, C.V.; de Matos, G.J.; Boulos, M. Acute respiratory distress syndrome due to vivax malaria: Case report and literature review. Braz. J. Infect. Dis. 2005, 9, 425–430. [Google Scholar] [CrossRef] [PubMed]
  33. Campos, G.M.; Borges, A.A.; Badra, S.J.; Figueiredo, G.G.; Souza, R.L.; Moreli, M.L. Pulmonary and cardiovascular syndrome due to hantavirus: Clinical aspects of an emerging disease in southeastern Brazil. Rev. Soc. Bras. Med. Trop. 2009, 42, 282–289. [Google Scholar] [CrossRef]
  34. Lau, Y.L.; Lee, W.C.; Tan, L.H.; Kamarulzaman, A.; Omar, S.F.S.; Fong, M.Y.; Cheong, F.W.; Mahmud, R. Acute respiratory distress syndrome and acute renal failure from Plasmodium ovale infection with fatal outcome. Malar. J. 2013, 12, 389. [Google Scholar] [CrossRef]
  35. Rahman, A.K.; Sulaiman, F.N. Plasmodium vivax malaria presenting as acute respiratory distress syndrome: A case report. Trop. Doct. 2013, 43, 83–85. [Google Scholar] [CrossRef]
  36. Raboni, S.M.; Levis, S.; Rosa, E.S.; Bisordi, I.; Delfraro, A.; Lemos, E.; Correia, D.C.; Duarte dos Santos, C.C. Hantavirus infection in Brazil: Development and evaluation of an enzyme immunoassay and immunoblotting based on N recombinant protein. Diagn. Microbiol. Infect. Dis. 2007, 58, 89–97. [Google Scholar] [CrossRef]
  37. Guterres, A.; Oliveira, R.C.; Fernandes, J.; Schrago, C.G.; Lemos, E.R. Detection of different South American hantaviruses. Virus Res. 2015, 2, 106–113. [Google Scholar] [CrossRef]
  38. Figueiredo, L.T.; Moreli, M.L.; Borges, A.A.; de Figueiredo, G.G.; Badra, S.J.; Bisordi, I.; Suzuki, A.; Capria, S.; Padula, P. Evaluation of an enzyme-linked immunosorbent assay based on Araraquara virus recombinant nucleocapsid protein. Am. J. Trop. Med. Hyg. 2009, 81, 273–276. [Google Scholar] [CrossRef] [PubMed]
  39. Fauci, A.; Braunwald, E.; Kasper, D.; Hauser, S.; Longo, D.; Jameson, J. Harrison’s Principles of Internal Medicine, 17th ed.; Mcgraw-Hill: New York, NY, USA, 2008. [Google Scholar]
  40. Hutchinson, K.L.; Rollin, P.E.; Peters, C.J. Pathogenesis of a North American hantavirus, Black Creek Canal virus, in experimentally infected Sigmodon hispidus. Am. J. Trop. Med. Hyg. 1998, 59, 58–65. [Google Scholar] [CrossRef]
  41. Brasil. Ministério da Saúde. Secretaria de Vigilância em Saúde. Guia de Vigilância em Saúde; Ministério da Saúde: Brasília, Brzail, 2014. [Google Scholar]
  42. Nolte, K.B.; Feddersen, R.M.; Foucar, K.; Zaki, S.R.; Koster, F.T.; Madar, D.; Merlin, T.L.; Mcfeeley, P.J.; Umland, E.T.; Zumwalt, R.E. Hantavirus Pulmonary Syndrome in the United-States—A Pathological Description of a Disease Caused by a New Agent. Hum. Pathol. 1995, 26, 110–120. [Google Scholar] [CrossRef]
  43. Peters, C.J. Hantavirus pulmonary syndrome in the Americas. In Emerging Infections; Scheld, W.M., Craig, W.A., Hughes, J.M., Eds.; ASM Press: Washington, DC, USA, 1998; pp. 15–50. [Google Scholar]
  44. Brasil. Departamento Nacional de Produção Mineral. Informe Mineral Julho a Dezembro de 2015; Departamento Nacional de Produção Mineral: Brasília, Brzail, 2015. [Google Scholar]
  45. Santos, E.D.O.; Loureiro, E.C.B.; Jesus, I.M.D.; Brabo, E.; Silva, R.D.S.U.D.; Soares, M.D.C.P. Diagnóstico das condições de saúde de uma comunidade garimpeira na região do Rio Tapajós, Itaituba, Pará, Brasil, 1992. Cad. Saúde Pública 1995, 11, 212–225. [Google Scholar] [CrossRef] [PubMed]
  46. Pignatti, M.G. Saúde e ambiente: As doenças emergentes no Brasil. Ambiente Soc. 2004, 7, 133–147. [Google Scholar] [CrossRef]
  47. Schmidt, R. A questão ambiental na promoção da saúde: Uma oportunidade de ação multiprofissional sobre doenças emergentes. Physis 2007, 17, 373–392. [Google Scholar] [CrossRef]
  48. Dahanayaka, N.J.; Agampodi, S.B.; Bandaranayaka, A.K.; Priyankara, S.; Vinetz, J.M. Hantavirus infection mimicking leptospirosis: How long are we going to rely on clinical suspicion? J. Infect. Dev. Ctries. 2014, 8, 1072–1075. [Google Scholar] [CrossRef] [PubMed]
  49. Kasper, M.R.; Blair, P.J.; Touch, S.; Sokhal, B.; Yasuda, C.Y.; Williams, M.; Richards, A.L.; Burgess, T.H.; Wierzba, T.F.; Putnam, S.D. Infectious etiologies of acute febrile illness among patients seeking health care in south-central Cambodia. Am. J. Trop. Med. Hyg. 2012, 86, 246–253. [Google Scholar] [CrossRef] [PubMed]
  50. Figueiredo, L.T.M. Febres hemorrágicas por vírus no Brasil. Rev. Soc. Bras. Med. Trop. 2006, 39, 203–210. [Google Scholar] [CrossRef]
  51. Lima, D.M.; Sabino-Santos Junior, G.; Oliveira, A.C.; Fontes, R.M.; Colares, J.K.; Araujo, F.M. Hantavirus infection in suspected dengue cases from State of Ceara, Brazil. Rev. Soc. Bras. Med. Trop. 2011, 44, 795–796. [Google Scholar] [CrossRef] [PubMed]
  52. Suharti, C.; van Gorp, E.C.; Dolmans, W.M.; Groen, J.; Hadisaputro, S.; Djokomoeljanto, R.J. Hantavirus infection during dengue virus infection outbreak in Indonesia. Acta Med. Indones. 2009, 41, 75–80. [Google Scholar] [PubMed]
  53. Lamas, C.; Oliveira, R.; Bóia, M.; Silva, A.; Vicente, L.H.B.; Almeida, E.B.; Lemos, E.R.S.; Bóia, M.N. Hantavirus infection in HIV positive individuals in Rio de. Janeiro, Brazil: A seroprevalence study. Braz. J. Infect. Dis. 2013, 17, 120–121. [Google Scholar] [CrossRef]
  54. Lemos, E.; Alves-Correa, A.; Oliveira, R.; Rozental, T.; Pereira, M.; Schatzmayr, Y. Serologic evidence of hantavirus infection in patients from Rio de Janeiro with suspected leptospirosis. Virus Rev. Res. Soc. Bras. Virol. 2003, 8, 96–97. [Google Scholar]
  55. Goeijenbier, M.; Hartskeerl, R.A.; Reimerink, J.; Verner-Carlsson, J.; Wagenaar, J.F.; Goris, M.G.; Martina, B.E.; Ludkvist, A.; Koopmans, M.; Osterhaus, A.D.; et al. The hanta hunting study: Underdiagnosis of Puumala hantavirus infections in symptomatic non-travelling leptospirosis-suspected patients in the Netherlands, in 2010 and April to November 2011. EuroSurveillance 2014, 19, 20878. [Google Scholar] [CrossRef]
  56. Mattar, S.; Garzon, D.; Tadeu, L.; Faccini-Martinez, A.A.; Mills, J.N. Serological diagnosis of hantavirus pulmonary syndrome in a febrile patient in Colombia. Int. J. Infect. Dis. 2014, 25, 201–203. [Google Scholar] [CrossRef] [Green Version]
  57. Silva, A.D.; Evangelista, M.D.O.S. Syndromic surveillance: Etiologic study of acute febrile illness in dengue suspicious cases with negative serology. Brazil, Federal District, 2008. Rev. Inst. Med. Trop. Sao Paulo 2010, 52, 237–242. [Google Scholar] [CrossRef]
  58. Bostik, P.; Winter, J.; Ksiazek, T.G.; Rollin, P.E.; Villinger, F.; Zaki, S.R. Sin Nombre virus (SNV) Ig isotype antibody response during acute and convalescent phases of hantavirus pulmonary syndrome. Emerg. Infect. Dis. 2000, 6, 184–187. [Google Scholar] [CrossRef] [PubMed]
  59. Carneiro, K.; Carneiro, C. Abordagem clínico imunológico da infecção por hantavírus. Rev. Patol. Trop. 2004, 33, 183–191. [Google Scholar]
  60. MacNeil, A.; Comer, J.A.; Ksiazek, T.G.; Rollin, P.E. Sin Nombre virus-specific immunoglobulin M and G kinetics in hantavirus pulmonary syndrome and the role played by serologic responses in predicting disease outcome. J. Infect. Dis. 2010, 202, 242–246. [Google Scholar] [CrossRef] [PubMed]
  61. Hindrichsen, S.; de Andrade, A.M.; Clement, J.; Leirs, H.; McKenna, P.; Matthys, P. Hantavirus infection in Brazilian patients from Recife with suspected leptospirosis. Lancet 1993, 341, 50. [Google Scholar] [CrossRef]
  62. Mascarenhas-Batista, A.V.; da Rosa, E.S.; Ksiazek, T.G.; da Rosa, A.P.; Leduc, J.W.; Pinheiro, F. Anti-Hantavirus antibodies in school children in Salvador, Bahia. Rev. Soc. Bras. Med. Trop. 1998, 31, 433–440. [Google Scholar] [CrossRef] [PubMed]
  63. Figueiredo, L.T.M.; Moreli, M.L.; de Sousa, R.L.M.; Borges, A.A.; de Figueiredo, G.G.; Machado, A.M. Hantavirus pulmonary syndrome, Central Plateau, Southeastern, and Southern Brazil. Emerg. Infect. Dis. 2009, 15, 561–567. [Google Scholar] [CrossRef] [PubMed]
  64. Mendes, W.S.; da Silva, A.A.; Neiva, R.F.; Costa, N.M.; de Assis, M.S.; Vidigal, P.M. Serologic survey of hantavirus infection, Brazilian Amazon. Emerg. Infect. Dis. 2010, 16, 889–891. [Google Scholar] [CrossRef] [PubMed]
  65. Badra, S.J.; Maia, F.G.; Figueiredo, G.G.; Dos Santos Junior, G.S.; Campos, G.M.; Figueiredo, L.T. A retrospective serologic survey of hantavirus infections in the county of Cassia dos Coqueiros, State of Sao Paulo, Brazil. Rev. Soc. Bras. Med. Trop. 2012, 45, 468–470. [Google Scholar] [CrossRef]
  66. Souza, W.M.D.; Machado, A.M.; Figueiredo, L.T.M.; Boff, E. Serosurvey of hantavirus infection in humans in the border region between Brazil and Argentina. Rev. Soc. Bras. Med. Trop. 2011, 44, 131–135. [Google Scholar] [CrossRef] [Green Version]
  67. Pereira, G.W.; Teixeira, A.M.; Souza, M.S.; Braga, A.D.; Santos, G.S., Jr.; Figueiredo, G.G. Prevalence of serum antibodies to hantavirus in a rural population from the Southern State of Santa Catarina, Brazil. Rev. Soc. Bras. Med. Trop. 2012, 45, 117–119. [Google Scholar] [CrossRef]
  68. Gimaque, J.B.; Bastos, M.D.E.S.; Braga, W.S.; Oliveira, C.M.; Castilho, M.D.A.C.; Figueiredo, R.M. Serological evidence of hantavirus infection in rural and urban regions in the state of Amazonas, Brazil. Mem. Inst. Oswaldo Cruz 2012, 107, 135–137. [Google Scholar] [CrossRef]
  69. Santos, I.O.; Figueiredo, G.G.; Figueiredo, L.T.; Azevedo, M.R.; Novo, N.F.; Vaz, C.A. Serologic survey of hantavirus in a rural population from the northern State of Mato Grosso, Brazil. Rev. Soc. Bras. Med. Trop. 2013, 46, 30–33. [Google Scholar] [CrossRef] [PubMed]
  70. Pereira, L. Avaliação da Infecção por Hantavirus em as Mostras Humanas e de Roedores Silvestres e Sinantrópicos no Estado do Rio de Janeiro; Mestrado em Medicina Tropical; Fiocruz: Rio de Janeiro, Brazil, 2014. [Google Scholar]
  71. Terças, A.C.P.; Atanaka-Santos, M.; Pignatti, M.G.; Espinosa, M.M.; de Melo Via, A.V.G.; Menegatti, J.A. Hantavirus pulmonary syndrome outbreak, Brazil, December 2009–January 2010. Emerg. Infect. Dis. 2013, 19, 1824–1827. [Google Scholar] [CrossRef] [PubMed]
  72. Confalonieri, U.E.C. Saúde na Amazônia: Um modelo conceitual para a análise de paisagens e doenças. Estud. Av. 2005, 19, 221–236. [Google Scholar] [CrossRef]
  73. Guimarães, R.M.; Valente, B.C.; Faria, P.A.; Stephanelli, L.L.; Chaiblich, J.V.; Arjona, F.B.S. Deforestation and malaria incidence in the legal Amazon Region between 1996 and 2012. Cad. Saude Colet 2016, 24, 3–8. [Google Scholar] [CrossRef] [Green Version]
  74. Camacho, L.H.; Gordeuk, V.R.; Wilairatana, P.; Pootrakul, P.; Brittenham, G.M.; Looareesuwan, S. The course of anaemia after the treatment of acute, falciparum malaria. Ann. Trop. Med. Parasitol. 1998, 92, 525–537. [Google Scholar] [CrossRef]
  75. Maciel, G.B.M.L.; Oliveira, E.C.D. Perfil entomológico e epidemiológico da malária em região garimpeira no norte do Mato Grosso, 2011. Epidemiol. Serv. Saude 2014, 23, 355–360. [Google Scholar] [CrossRef]
Figure 1. The geographic location of the study areas, gold mining regions of Mato Grosso, Brazil 2016.
Figure 1. The geographic location of the study areas, gold mining regions of Mato Grosso, Brazil 2016.
Ijerph 16 01852 g001
Figure 2. An X-ray of Patient 1 at the time of admission to the intensive care unit (ICU), Mato Grosso, Brazil, 2015
Figure 2. An X-ray of Patient 1 at the time of admission to the intensive care unit (ICU), Mato Grosso, Brazil, 2015
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Table 1. The socio-demographic characteristics of 112 residents of Três Fronterias, state of Mato Grosso, Brazil, 2012.
Table 1. The socio-demographic characteristics of 112 residents of Três Fronterias, state of Mato Grosso, Brazil, 2012.
Independent VariablesAnti-hantavirus IgG + PatientsTotal
N%N%
GenderMale1256356.25
Female3754943.75
Total4100112100
Educational AttainmentNo education--1311.6
Elementary School41008475
High School--1412.5
Higher Education--10.9
Race ColorWhite1252017.8
Black1251513.4
Pardo2507768.8
OccupationLivestock activity--21.7
Agricultural activity--32.7
Housewife--1412.5
Vegetal exploration1252118.75
Other mining activity3757364.4
Marital StatusSingle1254641.1
Married2504641.1
Divorced--43.5
Widower--10.9
Consensual Union1251513.4
Housing TypeWood410010492.8
Canvas--76.3
Other--10.9
Table 2. The clinical characteristics of 112 residents of Três Fronterias, state of Mato Grosso, Brazil, 2012.
Table 2. The clinical characteristics of 112 residents of Três Fronterias, state of Mato Grosso, Brazil, 2012.
Independent VariablesAnti-hantavirus IgG + PatientsTotal
N%N%
Signs and symptoms during data collectionYes12587.2
No37510492.8
Total4100112100
Thick Blood SmearNegative37510795.5
Positive for P. falciparum12543.6
Positive for P. falciparum + Falciparum gametocity (FG)----
Positive for P. vivax--10.9
Reported co-morbidityYes125108.9
No37510291.1

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MDPI and ACS Style

Terças-Trettel, A.C.P.; Oliveira, E.C.d.; Fontes, C.J.F.; Melo, A.V.G.d.; Oliveira, R.C.d.; Guterres, A.; Fernandes, J.; Silva, R.G.d.; Atanaka, M.; Espinosa, M.M.; et al. Malaria and Hantavirus Pulmonary Syndrome in Gold Mining in the Amazon Region, Brazil. Int. J. Environ. Res. Public Health 2019, 16, 1852. https://doi.org/10.3390/ijerph16101852

AMA Style

Terças-Trettel ACP, Oliveira ECd, Fontes CJF, Melo AVGd, Oliveira RCd, Guterres A, Fernandes J, Silva RGd, Atanaka M, Espinosa MM, et al. Malaria and Hantavirus Pulmonary Syndrome in Gold Mining in the Amazon Region, Brazil. International Journal of Environmental Research and Public Health. 2019; 16(10):1852. https://doi.org/10.3390/ijerph16101852

Chicago/Turabian Style

Terças-Trettel, Ana Cláudia Pereira, Elaine Cristina de Oliveira, Cor Jesus Fernandes Fontes, Alba Valéria Gomes de Melo, Renata Carvalho de Oliveira, Alexandro Guterres, Jorlan Fernandes, Raphael Gomes da Silva, Marina Atanaka, Mariano Martinez Espinosa, and et al. 2019. "Malaria and Hantavirus Pulmonary Syndrome in Gold Mining in the Amazon Region, Brazil" International Journal of Environmental Research and Public Health 16, no. 10: 1852. https://doi.org/10.3390/ijerph16101852

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