Volume 23, Number 1—January 2017
Meningitis Associated with Simultaneous Infection by Multiple Dengue Virus Serotypes in Children, Brazil
Dengue is a disease of high incidence and a major public health problem worldwide (1). Approximately 2.5 billion persons live in dengue transmission risk areas, and 50 million dengue virus (DENV) infections occur annually. This disease is endemic in Brazil, with 4 DENV serotypes circulating; > 1.6 million clinical cases were reported in 2015 (2).
DENV belongs to the family Flaviviridae, genus Flavivirus, and has 4 serotypes (DENV-1–4). These viruses are usually associated with a systemic and dynamic disease; the clinical conditions range from a nonspecific viral syndrome to severe disease. The most common symptoms are fever, rash, headache, nausea, vomiting, retro-orbital pain, and weakness (3). Neurologic manifestations have been increasingly reported; DENV could be considered an emergent etiologic agent of central nervous system (CNS) infection that causes encephalopathy, encephalitis, and meningitis (1). DENV infections of the CNS may or may not be associated with the classical systemic manifestations of dengue (4).
In dengue-endemic areas, co-circulation of different serotypes has been reported (5). Co-infection by different DENV serotypes has already been reported in patients and arthropods, but the effects on the disease and on the virus cycle has not been well established (6,7). The molecular diversity of DENV serotypes has been linked to different patterns of virulence. DENV-3 genotypes I and III, which circulate in Brazil, demonstrate distinct biological characteristics in mouse models (8). In 2014, the number of suspected dengue cases in Brazil was 589,107, with 58,177 in the state of Minas Gerais; in 2015, the number of cases increased to 1,649,008 in Brazil and 189,378 in Minas Gerais, with DENV-1 being the most frequently detected serotype (2). We report the detection of DENV-1, -2, and -3 co-infections in the CNS by reverse transcription PCR (RT-PCR) from cerebrospinal fluid (CSF) samples that tested negative for other classic neurotropic pathogens.
During the 2014–15 DENV epidemic in Minas Gerais, 22 CSF samples were collected from children suspected of having viral CNS infection who were hospitalized at the Hospital Infantil João Paulo II, Belo Horizonte, Minas Gerais, a reference children’s hospital for all counties of the state. A presumptive diagnosis of CNS viral infection was given when the CSF of patients with clinical signs and symptoms of CNS infection had normal or slightly altered cytochemical parameters and tested negative for bacterial pathogens (9). The protocol for this study was approved by the hospital’s scientific and ethical committee (no. 132/2009), and consent was obtained from parents or accompanying relatives.
The CSF samples tested negative for typical neurotropic viruses such as enteroviruses and human herpesviruses 1, 2, and 3. For DENV detection, RNA isolation and RT-PCR from 140 µL of CSF targeting the NS5 region was performed as described (10). The analyses showed that 7 samples (32%) were DENV positive. DENV-1 was detected in 1 sample (14.2% of positive samples); DENV-2 was detected in 3 samples (42.9%); DENV-3 was detected in 1 sample (14.2%); and DENV-4 was not detected in any samples. Co-infection with > 1 DENV serotype was found in 2 CSF samples (28.6%); 1 sample was co-infected with DENV-2 and DENV-3 (sample from patient 571), and the other sample was triple infected with DENV-1, -2, and -3 (sample from patient 557) (Table).
Retrospective analysis of medical records provided us with information on evolution of the clinical condition of the 7 DENV-positive patients (Table). Patients 575 and 572 received a presumptive diagnosis of meningitis on the basis of clinical signs and symptoms, but they did not show the classical symptoms and signs of dengue fever. Thus, serologic testing for dengue was not requested by clinicians. Patients 100, 557, 571, and 577 were admitted to the hospital with suspected dengue fever. In addition, they demonstrated some neurologic alterations such as seizures; among those patients, only patient 571 showed signs of meningitis. Patient 571 had a predominance of polymorphonuclear neutrophils in the CSF. However, the leukocyte count was < 400 cells/mm3, and the bacterial culture was negative (3).
To confirm DENV as the etiologic agent of CNS infection, we used a 3730 DNA Analyzer (Applied Biosystems, Foster City, CA, USA) to directly sequence the amplified DNA. The nucleotide sequences were aligned and used to construct phylogenetic trees by using the neighbor-joining method (Figure). The Tamura-Nei statistical model implemented in MEGA 6.0 software (Arizona State University, Tempe, AZ, USA) was used with 1,000 bootstrap replicates. These sequences were deposited in GenBank (sequence and accession nos.: 557 CNS DENV-1, KU615569; 557 CNS DENV-2, KU726002; 557 CNS DENV-3, KU948725; 571 CNS DENV-2, KU948727; and 571 CNS DENV-3, KU948726).
The 3 DENV serotypes found in CSF co-infection have been classified into genotypes, as described (11). Phylogenetic analysis of the NS5 gene sequences demonstrated that isolate 557 CNS DENV-1 grouped with isolates of American/African genotype V (Figure, panel A), which has been reported in Southeast Asia (Singapore), South America, and Africa and is the genotype that circulates in Brazil (12).
The DENV-2 isolates from samples from patients 557 and 571 grouped with isolates of Asian II, which is a genotype that consists of viruses circulating in China, the Philippines, Sri Lanka, Taiwan, and Vietnam (13). The American/Asian genotype has been the only genotype previously identified in Brazil, although some variations have occurred within this genotype (12) (Figure, panel B). Singh et al. demonstrated that the Asian II and Cosmopolitan DENV-2 genotypes co-circulated in Nepal, with no differences in their replication rate in mosquito cells (14,15).
The DENV-3 nucleotide sequences of samples from patients 577 and 571 showed a close phylogenetic relationship with genotype III when compared with the nonstructural-5 gene sequences of other DENV-3 viruses circulating in different parts of the world (Figure, panel C). Previous studies have reported circulation of DENV-3 genotypes I and III in Brazil, and differences in the course of the infection between these 2 genotypes in a mouse model have been described. This study relates DENV-3 genotype III to CNS infection (8). DENV serotype co-infection has already been described in the literature from human blood samples and in Aedes mosquitoes (5–7). However, to our knowledge, DENV serotype co-infections have not previously been detected in the CNS.
DENV co-infection with other flaviviruses has been described, but not in relation to the different DENV serotypes involved in CNS infection. We identified 2 patients with meningitis: 1 was infected with 2 DENV serotypes and the other with 3 DENV serotypes. We also report the circulation of the DENV-2 genotype Asian II in Brazil, where the DENV-2 genotype American/Asian has been the most prevalent genotype since 1990 (13). When and where genotype Asian II started to circulate in Brazil is unclear.
Our results also suggest that CNS DENV infection can be preceded by classic dengue fever symptoms or can occur without any classic symptoms. Because the evolution of DENV infection and DENV serotype co-infection into a CNS infection is underreported, attempts to identify the serotypes and genotypes involved in this severe clinical manifestation should be undertaken to clarify the clinical relevance of cases of DENV serotype co-infections.
Ms. Marinho is a biologist and PhD student, and Dr. Oliveira is a postdoctoral resident, at the Laboratório de Vírus, Microbiology Department, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil. Their research focuses on the monitoring and control of emerging viruses.
We thank colleagues from the Laboratório de Vírus for their excellent technical support.
Financial support was provided by the Conselho Nacional de Desenvolvimento Científico e Tecnológico (to D.B.O. and E.G.K.), Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (to P.E.S.M.), and Fundação de Amparo à Pesquisa do Estado de Minas Gerais.
- Solomon T, Dung NM, Vaughn DW, Kneen R, Thao LT, Raengsakulrach B, et al. Neurological manifestations of dengue infection. Lancet. 2000;355:1053–9. DOIPubMed
- Secretaria de Vigilância em Saúde−Ministério da Saúde. Boletim Epidemiológico. Brasil, Brasília, 2015 [cited 2015 Dec 2]. http://portalsaude.saude.gov.br/images/pdf/2015/novembro/24/2015-040.pdf
- National Institute of Health. Cerebral spinal fluid (CSF) collection. Bethesda, Maryland, United States of America, 2013 May 28 [cited 2015 Nov 17]. https://www.nlm.nih.gov/medlineplus/ency/article/003428.htm
- Garg RK, Malhotra HS, Gupta A, Kumar N, Jain A. Concurrent dengue virus and Japanese encephalitis virus infection of the brain: is it co-infection or co-detection? Infection. 2012;40:589–93. DOIPubMed
- Mondini A, Bronzoni RVM, Cardeal ILS, dos Santos TMIL, Lázaro E, Nunes SHP, et al. Simultaneous infection by DENV-3 and SLEV in Brazil. J Clin Virol. 2007;40:84–6. DOIPubMed
- Figueiredo RM, Naveca FG, Oliveira CM, Bastos MS, Mourão MP, Viana SS, et al. Co-infection of Dengue virus by serotypes 3 and 4 in patients from Amazonas, Brazil. Rev Inst Med Trop Sao Paulo. 2011;53:321–3.PubMed
- Thavara U, Siriyasatien P, Tawatsin A, Asavadachanukorn P, Anantapreecha S, Wongwanich R, et al. Double infection of heteroserotypes of dengue viruses in field populations of Aedes aegypti and Aedes albopictus (Diptera: Culicidae) and serological features of dengue viruses found in patients in southern Thailand. Southeast Asian J Trop Med Public Health. 2006;37:468–76.PubMed
- Ferreira GP, Figueiredo LB, Coelho LFL, S PA Jr, Cecilio AB, Ferreira PCP, et al. Dengue virus 3 clinical isolates show different patterns of virulence in experimental mice infection. Microbes Infect. 2010;12:546–54. DOIPubMed
- Somand D, Meurer W. Central nervous system infections. Emerg Med Clin North Am. 2009;27:89–100, ix. DOIPubMed
- de Morais Bronzoni RV, Baleotti FG, Ribeiro Nogueira RM, Nunes M, Moraes Figueiredo LT. Duplex reverse transcription-PCR followed by nested PCR assays for detection and identification of Brazilian alphaviruses and flaviviruses. J Clin Microbiol. 2005;43:696–702. DOIPubMed
- Chen R, Vasilakis N. Dengue—quo tu et quo vadis? Viruses. 2011;3:1562–608. DOIPubMed
- Martins VC, Bastos MS, Ramasawmy R, de Figueiredo RP, Gimaque JB, Braga WS, et al. Clinical and virological descriptive study in the 2011 outbreak of dengue in the Amazonas, Brazil. PLoS One. 2014;9:e100535. DOIPubMed
- Chakravarti A, Chauhan MS, Kumar S, Ashraf A. Genotypic characterization of dengue virus strains circulating during 2007-2009 in New Delhi. Arch Virol. 2013;158:571–81. DOIPubMed
- Singh S, Gupta BP, Manakkadan A, Das Manandhar K, Sreekumar E. Phylogenetic study reveals co-circulation of Asian II and Cosmopolitan genotypes of Dengue virus serotype 2 in Nepal during 2013. Infect Genet Evol. 2015;34:402–9. DOIPubMed
- Barcelos Figueiredo L, Sakamoto T, Leomil Coelho LF, de Oliveira Rocha ES, Gomes Cota MM, Ferreira GP, et al. Dengue virus 2 American-Asian genotype identified during the 2006/2007 outbreak in Piauí, Brazil reveals a Caribbean route of introduction and dissemination of dengue virus in Brazil. PLoS One. 2014;9:e104516. DOIPubMed
TableCite This Article
1These authors contributed equally to this article.
No hay comentarios:
Publicar un comentario