Bat-transmitted human rabies outbreaks, Brazilian Amazon.
Rabies virus, the prototype species in the family Rhabdoviridae, is a single-stranded, RNA, negative-sense, nonsegmented virus of the genus Lyssavirus; it is the causal agent of rabies, a disease that has been poorly studied in most developing countries (1,2). Nonetheless, Brazil has implemented rabies control measures, and urban human rabies, transmitted by dogs and cats, has decreased from 73 cases in 1990 to 17 cases in 2003 (3). Carnivores and bats are the primary reservoirs of rabies virus in all continents, and bat-transmitted rabies is relatively commonly diagnosed in Latin American and Caribbean countries (1,4-6). In Brazil, a small number of human cases have been confirmed as having been transmitted by vampire bat bites (7,8), but because surveillance has improved in the last few years, the occurrence of sporadic episodes suggests a situation similar to that observed in other American countries (5,9,10). Indeed, [approximate equal to] 39 cases of human rabies have been reported in the United States since the 1950s, and cases of rabies transmitted by vampire bat bites are commonly reported in Mexico, Chile, Colombia, Peru, Venezuela, and other New World countries (1,5,6,9,11,12).
Although rabies control measures have improved in many South American countries, the transmission of the disease by bats has increased and has become a public health concern, and several human cases have been detected. Outbreaks of bat-transmitted rabies have occurred in several remote areas in Peru (5,13), Venezuela (9), and more recently in Brazil (7). This article reports the results of an epidemiologic investigation and the antigenic and genetic characterization of rabies virus isolated during outbreaks of the bat-transmitted disease that occurred in March and May 2004 in remote areas of Portel and Viseu municipalities, respectively, in Para State, Brazilian Amazon region.
Material and Methods
All patients reported receiving vampire bat bites several weeks or months before manifesting encephalitic symptoms. All were poor persons who lived in primitive conditions in the Acuty-Perera River communities in Portel or in the Curupati community in the municipality of Viseu, both in Para State, Brazilian Amazon region (Figure 1). All patients exhibited a similar disease pattern, characterized by acute ascendant paralytic encephalitis. Twelve patients were hospitalized and after their deaths, an autopsy was performed and central nervous system (CNS) specimens were obtained for laboratory diagnostic procedures. Patient ages ranged from 2 to 58 years. Detailed information concerning the patients is shown in the Table.
[FIGURE 1 OMITTED]
Areas of Occurrence
Many persons live in poor conditions in both municipalities where cases were reported. The municipality of Portel (50[degrees]57"W, 1[degrees]59'S), is situated in the Marajo Island region, state of Para, and is [approximately equal to] 278 km distant from Belem, the state capital; access to Belem is by the Amazon River. Portel has [approximately equal to] 41,500 inhabitants (1.6 inhabitants/[km.sup.2]); [approximately equal to] 55% of them live in rural areas. The principal economic activities are wood extraction agriculture (especially cultivation of manioc), and hook-and-line fishing; cattle grazing is uncommon. In the Acuty-Perera River area, where cases were reported, the infected persons were from the following 3 communities: Ajara, Laranjal (Aparecida), and Tauacu.
The municipality of Viseu, (50[degrees]49'W, 1[degrees]56'S) is in the Bragantina region of the state of Para, 320 km distant from Belem, with access by highways. It has [approximately equal to] 52,893 inhabitants (10.2 inhabitants/[km.sup.2]); 68% live in rural areas. Rabies cases were reported in the Curupati community where [approximately equal to] 77 families lived. Economic activities include cultivation of manioc and hook-and-line fishing.
All laboratory analyses were performed under pressurized containment cabinets, class II B2. From all patient specimens, homogenates were obtained as previously described (14). Briefly, 0.02 mL of each suspension in phosphate-buffered saline (pH 7.4) containing fraction V bovine albumin solution (0.75%), penicillin (100 IU/mL), and streptomycin (100 [micro]/mL), was injected intracerebrally into 12 newborn mice. After injection, the mice were observed daily for 3 weeks or until the animals became sick, when their brains were removed and used for immunofluorescence assay (IFA) or stored at -70[degrees]C for further molecular biology procedures.
Detection and Characterization of Isolates
All human CNS samples and suckling mouse brains were used to prepare impression smears, which were examined by direct IFA with a fluorescent antirabies conjugate, as described elsewhere (15). All rabies virus strains isolated were antigenically typed by indirect IFA by using a panel of 8 monoclonal antibodies prepared against the viral nucleoprotein (Centers for Disease Control and Prevention, Atlanta, GA, USA) (9,16). Six original CNS samples (3066M, 3067M, 3068M, 3072M, and 3522M from Portel and 5214 from Viseu) were tested in a reverse transcription--PCR that amplifies a 1,352-bp fragment of the nucleoprotein gene with sense primer N1 5'-ATGGATGCCGACAAGATT 3' and anti-sense primer N2 5'-TTATGAGTCACTCGAATA 3' as described by Carnieli et al. (17) by using Superscript II Reverse Transcriptase (Invitrogen Ltd., Sao Paulo, Brazil) and Taq DNA Polymerase (Invitrogen, Carlsbad, CA, USA), according to the manufacturer's instructions.
PCR products were excised from agarose gel, purified with QIA quick gel extraction kit (Qiagen Inc., Valencia, CA, USA), and sequenced reaction with anti-sense primer and DYEnamic ET Dye Terminator (Amersham Biosciences, Piscataway, NJ, USA), according to the manufacturer's instructions, in 4 replicates. The sequences were resolved in a MegaBACE DNA sequencer (Amersham Biosciences).
The final sequence of each strain was aligned by the Clustal method with Bioedit (18) (http://www.mbio. ncsu.edu/BioEdit/bioedit.html) and MEGA 2.1 (www. megasoftware.net), with homologous sequences derived from GenBank (accession numbers shown in Figure 2). The alignment was used to build a neighbor-joining distance tree with the Kimura 2-parameter model and 1,000 bootstrap replicates with MEGA 2.1 (19).
[FIGURE 2 OMITTED]
Twenty-one cases of bat-transmitted rabies were reported (15 from Portel and 6 from Viseu). Twelve were confirmed by laboratory diagnostic procedures, and 9 cases (5 of Portel and 4 of Viseu) were confirmed by clinical and epidemiologic linkage. Of the laboratory-confirmed cases, 2 from Portel were diagnosed by histopathologic examination and 10 (8 from Portel and 2 from Viseu) were diagnosed by IFA or by virus isolation in suckling mice. Antigenic characterization showed variant 3 (AgV3), the primary reservoir of which is the vampire bat Desmodus rotundus. One additional rabies virus isolate obtained from a D. rotundus was also typed as AgV3 (E.S.T. da Rosa and P.F.C. Vasconcelos, unpub. data).
The nucleotide identity among the 6 sequences from the human rabies strains of this study was 99.3%; identity among the 5 strains from Portel was 100%, and identity among these and the strain from Viseu was 97.2%. These same 6 strains had an identity of 97% when compared to AgV3 D. rotundus strains and 82.8% when compared to AgV2 Brazilian dog strains. Furthermore, the nucleotide identity among the 6 human strains and strains related to raccoons was 85.2%; it was 84.5% when compared to fixed strains CVS and AV01 (GenBank accession nos. D42112.1 and X 13357.1, respectively). The phylogenetic tree (Figure 2) shows a clustering pattern that is in accordance with each specific host or variant of the rabies virus, each cluster supported by a bootstrap value of at least 98%.
The 6 human isolates were genetically grouped in the D. rotundus cluster, supported by a bootstrap value as high as 1,000. The 5 strains from Portel grouped together in an exclusive polytomic subcluster, supported by a bootstrap value of 97%, while strain 5214M from Viseu grouped in a paraphyletic and more resolved subcluster among samples detected in D. rotundus and Artibeus spp. from Brazil and an AgV3 strain detected in a Brazilian cat (AY563517.1).
This is the first outbreak of vampire bat--transmitted rabies reported in Brazil in which rabies virus was isolated from humans and bats and in which the isolated strains were antigenically and genetically characterized. Previous reports of bat-transmitted outbreaks were based only on clinical and epidemiologic linkage, and in all of these outbreaks, infected persons were living in small, remote areas with difficult access in the Amazon region, including isolated Indian villages and clandestine gold mining areas in the states of central and northern Brazil. In these episodes, deaths were reported several weeks after the patients had died and therefore, no clinical specimens could be examined (7,20).
In contrast, although the outbreaks of Portel and Viseu occurred in isolated remote areas, access to them was facilitated by rivers (Portel) and highways (Viseu) and also by the fact that both areas were considerably closer to Belem, the capital of Para State.
Moreover, in the last few years, improvement in the surveillance for rabies and several other less-studied infectious diseases by the Brazilian Ministry of Health and Secretary of Health for Para State has resulted in a more sensitive system for detecting and investigating all relevant and unusual episodes suspected to be bat-transmitted rabies. The number of cases of bat-transmitted human rabies is, therefore, expected to increase: not only because of the improved epidemiologic surveillance system but also because of the reduction in opportunities for the bat's life cycle to be maintained in urban areas (1,5,7-9,12). An epidemiologic investigation of cases in humans in Portel and Viseu areas showed that vampire bat bites are common. Indeed, all victims had a history of bat bites, but bites were not considered a risk for acquiring rabies. Moreover, 1,558 persons in Portel (Acuty Perera River communities) reported [greater than or equal to] 1 episode of vampire bat aggression, and many inhabitants reported several bat bites in the 12 months before the outbreak. All these persons received postexposure treatment (antirabies serum and 5 doses of diploid human cells vaccine). Persons reporting bat bites for >1 year (838 persons in the Acuty Perera River communities) received pre-exposure treatment (3 doses of diploid human cells vaccine). After treatment measures, cases of rabies by bat aggression were no longer reported. Moreover, in Portel County, 4,504 dogs and 1,789 cats were also vaccinated (3).
Nonetheless, the lack of clinicians to diagnose the first cases at local hospitals has contributed to the increased number of noninvestigated cases and for the delay in recognizing them as rabies. In Peru, the country with the highest prevalence of bat-transmitted rabies in the Americas, several epidemics have been recognized. Delay in recognizing the disease was associated with several outbreaks (5,13). In Portel and Viseu, all clinical cases were characterized as ascendant paralytic rabies. Patients exhibited paresis, paralysis, dyspnea and difficulties of speech, soreness or lethargy, photophobia, aerophobia, hydrophobia, and coma, symptoms similar to those previously reported in other vampire bat-transmitted rabies outbreaks (1,5,7,21-24). The topology of the neighbor-joining tree, shown in Figure 2, grouped all rabies strains according to each respective host and variant, which validates the sequenced region and the tree-building method; in addition, the nucleotide identity among AgV3 strains and the human strains studied here (97%) match the thresholds described for different variant-host associations (25). The distance-based phylogenetic analysis of the N gene, based on full-length (1,350 nt) or partial (200-300 nt) sequencing, allows highly statistically supported clusterings for each rabies virus variant or each host-specific variant; the method is the most efficient in rabies molecular epidemiology (26).
These results lead to the conclusion that all strains of rabies virus isolated from humans during the rabies outbreak in northern Brazil in 2004 are related to the D. rotundus variant commonly found in Brazil, which supports the data generated by antigenic typing. Nevertheless, since all 5 sequenced strains from Portel grouped in different subclusters when compared with the sequenced strain from Viseu, this finding might be a sign that regional patterns of lineages of AgV3 rabies virus exist. Because the 2 municipalities are 530 km apart and in different ecologic and geographic regions, the Portel subclusters represent a unique and exclusive lineage. Whether the strain involved in the Viseu outbreak is in fact, monophyletic with all D. rotundus strains used in the phylogenetic analysis or could give rise to other paraphyletic subclusters still remains to be answered by analysis of more samples from the same area.
The complete identity among the 5 Portel strains might be due to the high attack rates reported in this specific outbreak, because the same virus lineage or subclusters would be rapidly transmitted by a homogeneously infected population of vampire bats sharing an exclusive lineage of rabies virus. Subclusters in AgV3 from D. rotundus are not an uncommon binding, and strains from the same area are likely to cluster together (27). In Latin America, area-specific clusterings have been described for AgV3 in Argentina, Venezuela, and Mexico, where clusterings divergent from those in Brazil are known to occur (6,9,12,28).
The genetic data obtained from the human strains studied here might be used to follow in a more accurate way, the population of D. rotundus involved in transmission when the rabies virus strains detected in these bats and regional ecologic information about these become available. This information might provide a powerful tool to help understand the factors that facilitated the outbreak and prevent others in the future.
The isolation of a strain from the vampire bat D. rotundus in Breves, a municipality bordering Portel (Figure 1) and close to where human infections were reported, is definitively incriminates this species in the transmission of rabies virus in Pardi State (E.S.T. da Rosa and P.F.C. Vasconcelos, unpub. data).
Previous reports showed a rabid infection frequency ranging from 0% to 3% for D. rotundus, which is associated with high or low endemicity (29). In the outbreaks described in this article, rabies virus was only isolated near the Portel area (Breves municipality) from a single D. rotundus among 23 of 132 bats studied. The aggression of vampire bats in these remote areas may be because persons live in unprotected dwellings (houses either without walls or without windows and doors) as shown in Figure 3, and the number of wild animals, cattle or equines, is small.
[FIGURE 3 OMITTED]
Moreover, in June 2005, 9 other vampire bat-transmitted rabies cases in humans were reported in communities of Augusto Correa Municipality (Figure 1), which borders Viseu (E.S. Travassos da Rosa and P.F.C. Vasconcelos, unpub. data).
Finally, public health campaigns should carried out to alert inhabitants of remote, small communities in the Amazon region to the risk of bat bites in transmitting rabies, and the need for all persons who report attacks of bats to undergo postexposure treatment to prevent other cases of vampire bat-transmitted rabies. Also, ecologic studies should be initiated to clarify the dynamics of rabies infection between populations of D. rotundus in affected areas.
We thank Armando S. Pereira, Carlos A. Vieira, Helio A. C. Saraiva, Orlando Vaz da Silva, , and all personnel of Instituto Brasileiro do Meio Ambiente e Recursos Naturais Renovaveis, Secretaria de Estado de Saude do Para, and the municipal health departments in Portel and Viseu for technical assistance in the field and the laboratory. Thanks are also due Ralph Lainson for critically reviewing this manuscript.
This work had financial support of Instituto Evandro Chagas/Secretaria de Vigilancia em Saude, Secretaria de Saude do Estado do Para, and Instituto Pasteur, Sao Paulo.
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Elizabeth S.T. da Rosa, * Ivanete Kotait, ([dagger]) Taciana F.S. Barbosa, * Maria L. Carrieri, ([dagger]) Paulo E. Brandao, ([dagger]) Amiraldo S. Pinheiro, ([double dagger]) Alberto L. Begot, ([double dagger]) Marcelo Y. Wada, ([section] Rosely C. de Oliveira, ([section]) Edmundo C. Grisard, ([paragraph]) Marcia Ferreira, ([section]) Reynaldo J. da Silva Lima, ([double dagger]) Lucia Montebello, ([section]) Daniele B.A. Medeiros, * Rita C.M. Sousa, # Gilberta Bensabath, * Eduardo H. Carmo, ([paragraph]) and Pedro F.C. Vasconcelos *
* Instituto Evandro Chagas, Belem, Brazil; ([dagger]) Instituto Pasteur, Sao Paulo, Brazil; ([double dagger]) Secretaria de Saude do Estado do Para, Belem, Brazil; ([section]) Ministerio da Saude, Brasilia, Brazil; ([paragraph]) Universidade Federal de Santa Catarina, Florianopolis, Brazil; and # Universidade Federal do Para, Belem, Brazil
Dr da Rosa is the principal investigator of the rabies and hantavirus laboratories at Instituto Evandro Chagas. Her interest is focused on laboratory diagnosis, epidemiology, and molecular biology of rabies and New World hantavirus infections.
Address for correspondence: Pedro F.C. Vasconcelos, Departamento de Arbovirologia e Febres Hemorragicas, Institute Evandro Chagas, Ministry of Health, Av Almirante Barroso 492, 66093-020, Belem, Para, Brazil; email: email@example.com
Table. Generic information regarding 12 patients with diagnosis of paralytic rabies from Portel and Viseu municipalities, Para State Patient Age (y), Place Municipality Virus sex isolation 1 11, F Tauacu Portel Yes 2 22, F Ajara Portel Yes 3 42, M Ajara Portel Yes 4 30, M Ajara Portel Yes 5 12, M Ajara Portel Yes 6 26, F Ajara Portel Yes 7 30, F Laranjal Portel Yes 8 2, M Laranjal Portel Yes 9 22, M Laranjal Portel No ([dagger]) 10 2, M Laranjal Portel No ([dagger]) 11 58, M Curupati Viseu Yes 12 22, M Curupati Viseu Yes Patient Onset Death Place of GenBank bite(s) accession no. * 1 19 Mar 28 Mar Feet NA 2 9 Mar 24 Mar Feet DQ097077 3 10 Mar 31 Mar Feet NA 4 19 Mar 30 Mar Feet NA 5 9 mar 30 Mar Feet DQ097076 6 19 Mar 1 Apr Feet DQ097080 7 23 Mar 3 Apr Feet DQ097078 8 1 Apr 6 Apr Head DQ097079 9 15 Mar 28 Mar Feet NA 10 16 Mar 30 Mar Head/feet NA 11 30 Apr 17 May NA DQ097075 12 5 May 14 May NA NA * NA, not available or unknown. ([dagger]) Diagnosis by histopathologic examination.
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|Author:||Vasconcelos, Pedro F.C.|
|Publication:||Emerging Infectious Diseases|
|Date:||Aug 1, 2006|
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