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1.
Mem. Inst. Oswaldo Cruz ; 109(4): 428-435, 03/07/2014. tab, graf
Article in English | LILACS | ID: lil-716303

ABSTRACT

Viral acute gastroenteritis (AG) is a significant cause of hospitalisation in children younger than five years. Group A rotavirus (RVA) is responsible for 30% of these cases. Following the introduction of RVA immunisation in Brazil in 2006, a decreased circulation of this virus has been observed. However, AG remains an important cause of hospitalisation of paediatric patients and only limited data are available regarding the role of other enteric viruses in these cases. We conducted a prospective study of paediatric patients hospitalised for AG. Stool samples were collected to investigate human adenovirus (HAdV), RVA, norovirus (NoV) and astrovirus (AstV). NoV typing was performed by nucleotide sequencing and phylogenetic analysis. From the 225 samples tested, 60 (26%) were positive for at least one viral agent. HAdV, NoV, RVA and AstV were detected in 16%, 8%, 6% and 0% of the samples, respectively. Mixed infections were found in nine patients: HAdV/RVA (5), HAdV/NoV (3) and HAdV/NoV/RVA (1). The frequency of fever and lymphocytosis was significantly higher in virus-infected patients. Phylogenetic analysis of NoV indicated that all of these viruses belonged to genotype GII.4. The significant frequency of these pathogens in patients with AG highlights the need to routinely implement laboratory investigations.


Subject(s)
Child , Humans , DNA Virus Infections/virology , Feces/virology , Gastroenteritis/virology , Acute Disease , Adenoviruses, Human/genetics , Adenoviruses, Human/isolation & purification , Brazil , Genotype , Hospitalization , Mamastrovirus/genetics , Mamastrovirus/isolation & purification , Norovirus/genetics , Norovirus/isolation & purification , Phylogeny , Prospective Studies , Real-Time Polymerase Chain Reaction , RNA, Viral/genetics , Rotavirus/genetics , Rotavirus/isolation & purification , Seasons
2.
J. pediatr. (Rio J.) ; 89(3): 278-285, maio-jun. 2013. ilus, tab
Article in Portuguese | LILACS | ID: lil-679308

ABSTRACT

OBJETIVO: Descrever a variabilidade genotípica do rotavírus grupo A (RVA) encontrado em pacientes pediátricos imunocompetentes e imunocomprometidos tratados no Hospital de Clínicas/Universidade Federal do Paraná (HC/UFPR), Curitiba, Paraná. MÉTODOS: Foi realizado um estudo transversal com 1.140 amostras de fezes coletadas, de abril de 2001 a dezembro de 2008, em pacientes ambulatoriais e pacientes hospitalizados com gastroenterite aguda encaminhados ao hospital. As técnicas usadas foram o método da aglutinação do látex e imunoensaio enzimático para diagnóstico de RVA. Foi realizada transcrição reversa, seguida por PCR multiplex semi-nested e sequência de nucleotídeos para caracterização do genótipo. Foram relatados dados de combinações de genótipos, clínicos, epidemiológicos, laboratoriais e sobre a presença de infecções hospitalares. RESULTADOS: Foi analisado um total de 80 amostras de fezes positivas para rotavírus. As associações mais frequentes entre os genótipos G e P foram: G4 P[8] (38,9%), G1 P[8] (30,5%), G9 P[8] (13,9%), G2 P[4] (6.9 %) e G3 P[8] 1,4%). O genótipo prevalente foi G2 P[4] depois da implementação da vacina nos anos de 2006 e 2008. Verificou-se que um total de 62,5% das crianças com idade abaixo de 12 meses estavam infectadas. Destas, 55,6% tinham grave desidratação, e 26,7% precisaram de cuidados intensivos. Encontrou-se uma frequência de 12,5% de infecções hospitalares. Não se observou correlação entre o genótipo e a gravidade da infecção nos pacientes estudados. CONCLUSÃO: As infecções por RVA podem associar-se a manifestações clínicas graves e é crucial a vigilância da variabilidade genotípica desse vírus para monitorizar a emergência de novas cepas e o impacto da imunização nesses pacientes.


OBJECTIVE: To describe the genotypic variability of group A rotavirus (RVA) found in immunosuppressed and non-immunosuppressed pediatric patients treated at the Hospital de Clínicas da Universidade Federal do Paraná (HC-UFPR), Curitiba, Paraná. METHODS: A cross-sectional study was conducted with 1,140 stool samples collected from April, 2001 to December, 2008 in outpatients and hospitalized patients with acute gastroenteritis referred to the hospital. RVA diagnosis was performed through the latex agglutination method and enzyme immunoassay. Reverse transcription followed by multiplex hemi-nested polymerase chain reaction (PCR) and nucleotide sequencing were used for genotype characterization. Genotype combinations, clinical data, epidemiological data, laboratory data, and presence of hospital-acquired infections were reported. RESULTS: A total of 80 rotavirus-positive stool samples were analyzed. The most frequent associations between genotypes G and P were: G4 P[8] (38.9%), G1 P[8] (30.5%), G9 P[8] (13.9%), G2 P[4] (6.9%), and G3 P[8] (1.4%). G2 P[4] was the most prevalent genotype after the vaccine implementation in the years 2006 and 2008. A total of 62.5% of children aged less than 12 months were found to be infected. Of these, 55.6% had severe dehydration and 26.7% needed intensive care. A frequency of 12.5% of nosocomial infections was found. No correlation was observed between genotype and severity of infection in the study patients. CONCLUSION: RVA infections can be associated with severe clinical manifestations, and the surveillance of genotypic variability of this virus is crucial to monitor the emergence of new strains and the impact of the immunization in these patients.


Subject(s)
Female , Humans , Infant , Male , Genotype , Gastroenteritis/virology , Immune Tolerance , Immunocompromised Host , Rotavirus Infections/virology , Rotavirus/genetics , Brazil/epidemiology , Cross Infection/epidemiology , Enzyme-Linked Immunosorbent Assay , Epidemiologic Methods , Feces/virology , Gastroenteritis/epidemiology , Gastroenteritis/immunology , Reverse Transcriptase Polymerase Chain Reaction , Rotavirus Infections/epidemiology , Rotavirus Infections/immunology , Rotavirus Vaccines/immunology , Rotavirus/classification , Seasons , Time Factors
3.
Mem. Inst. Oswaldo Cruz ; 105(8): 1010-1018, Dec. 2010. ilus, graf, tab
Article in English | LILACS | ID: lil-570672

ABSTRACT

The human metapneumovirus (hMPV), member of the Paramyxoviridae family, has been reported as an important agent involved with acute respiratory infections (ARIs). The aim of this study is to identify hMPV as the etiological agent of ARIs on in and outpatients in the city of Curitiba, Southern Brazil, and describe clinical data of hMPV subtyping. A retrospective study was performed in 1,572 respiratory samples over a period of three years. hMPV was detected by reverse transcription-polymerase chain reaction and subtyping was performed by nucleotide sequencing. hMPV was present in 61 (3.9 percent) samples and subtypes A1, A2a, B1 and B2 were detected. The incidence of hMPV was higher in outpatients (5.9 percent), whose mean age was 19.7 years (range 6 months-75 years old), than in inpatients (3 percent), whose mean age was 7.6 months (range 1 month-26 years old). The outpatients had upper respiratory tract infections with flu-like symptoms and all hospitalized children had lower respiratory tract infections. A pediatric patient died from complications associated with hMPV A2a infection. hMPV has been reported as a respiratory pathogen in all age groups. No correlation was observed between viral subtype and disease severity in the samples of this study.


Subject(s)
Adolescent , Adult , Aged , Aged, 80 and over , Child , Child, Preschool , Female , Humans , Infant , Male , Middle Aged , Young Adult , Metapneumovirus , Respiratory Tract Infections , Acute Disease , Brazil , Genotype , Hospitalization/statistics & numerical data , Incidence , Outpatients/statistics & numerical data , Phylogeny , Retrospective Studies , Reverse Transcriptase Polymerase Chain Reaction , Respiratory Tract Infections
4.
Rev. Inst. Med. Trop. Säo Paulo ; 52(6): 317-321, Nov.-Dec. 2010. graf, tab
Article in English | LILACS | ID: lil-570730

ABSTRACT

Adenovirus (AdV) respiratory infections are usually described as being associated with high mortality rates. Laboratory diagnosis is essential for the establishment of the appropriate therapy, and for guiding the implementation of preventive measures in order to prevent the spread of the infection. Aiming to analyze the sensitivity and specificity of the laboratorial diagnosis methods available, we compared antigen detection by indirect immunofluorescence assay (IF), and a specific nested polymerase chain reaction (PCR), to detect AdV in respiratory samples collected from patients admitted to hospital with acute respiratory disease. Positive samples were inoculated into a cell culture to confirm the results. We analyzed 381 samples from the nasopharyngeal aspirates collected during the year 2008; of these, 2.6 percent tested were positive for adenovirus through IF and 10 percent through PCR; positive isolation was obtained in 40 percent and 26 percent of these cases, respectively. Most infected patients were children under six months of age, and despite of the fact that a significant number of patients required intensive care, the mortality rate was low (5 percent). In conclusion, molecular methods were found to be useful for rapid diagnosis of adenovirus infections with higher sensitivity than antigen detection; their introduction permitted a significant increase in diagnoses of adenovirus infections.


Infecções respiratórias por Adenovírus (ADV) são geralmente descritas associadas com alta mortalidade. O diagnóstico laboratorial é essencial para o estabelecimento da terapêutica adequada e para orientar a implantação de medidas preventivas evitando a propagação da infecção. Com o objetivo de analisar a sensibilidade e a especificidade dos métodos de avaliação de diagnóstico laboratorial, foi comparada a detecção de antígeno por imunofluorescência indireta (IF) com a reação em cadeia da polimerase específica (PCR) para detectar AdV em amostras respiratórias coletadas de pacientes internados com doença respiratória aguda. As amostras com resultados positivos foram inoculadas em cultura celular. Foram analisadas 381 amostras da secreção nasofaríngea coletadas durante o ano de 2008, das quais 2,6 por cento foram positivas pela IF e 10 por cento pela PCR, isolamento positivo foi obtido em 40 por cento e 26 por cento dos casos positivos pelos testes anteriores, respectivamente. A maioria dos pacientes infectados eram crianças com menos de seis meses de idade, e apesar do fato de que um número significativo de pacientes necessitou de cuidados intensivos, a taxa de mortalidade foi baixa (5 por cento). Em conclusão, os métodos moleculares são úteis para o diagnóstico rápido de infecções por adenovírus com maior sensibilidade do que a detecção do antígeno, a sua introdução na rotina permitiu um aumento significativo no diagnóstico de infecções por adenovírus.


Subject(s)
Child , Child, Preschool , Humans , Infant , Adenoviruses, Human , Adenovirus Infections, Human/diagnosis , Nasopharynx/virology , Respiratory Tract Infections/diagnosis , Respiratory Tract Infections/virology , Adenoviruses, Human/genetics , Adenoviruses, Human/immunology , Adenoviruses, Human/isolation & purification , Cross-Sectional Studies , Fluorescent Antibody Technique, Indirect , Polymerase Chain Reaction , Prospective Studies , Sensitivity and Specificity
5.
Mem. Inst. Oswaldo Cruz ; 103(2): 180-185, Mar. 2008. ilus, graf, tab
Article in English | LILACS | ID: lil-480629

ABSTRACT

Several studies conducted all over the world have reported that the influenza virus is associated with great morbidity and mortality rates. In this study, we analyzed the incidence of the influenza virus between 2000 and 2003 in Curitiba. We studied 1621 samples obtained from outpatients and hospitalized patients of both sexes and all ages. The study was conducted at the local primary care health units (outpatients) and at the tertiary care unit (hospitalized) of the General Hospital of the Federal University in the state of Paraná, Brazil. Nasopharyngeal aspirates and, eventually, bronchoalveolar lavage were assayed for the presence of viral antigens, either by indirect immunofluorescence or cell culture. Of the samples studied, 135 (8.3 percent) were positive for influenza virus, and of those, 103 (76.3 percent) were positive for type A and 32 (23.7 percent) for type B. Additionally, positive samples were analyzed by reverse transcription followed by polymerase chain reaction and subtypes H1 and H3 were identified from this group. A high incidence of positive samples was observed mainly in the months with lower temperatures. Furthermore, outpatients showed a higher incidence of influenza viruses than hospitalized patients.


Subject(s)
Female , Humans , Male , Antigens, Viral/blood , Influenza, Human/epidemiology , Influenzavirus A/immunology , Influenzavirus B/immunology , Brazil/epidemiology , Bronchoalveolar Lavage Fluid/virology , Cell Culture Techniques , Fluorescent Antibody Technique, Indirect , Incidence , Influenza, Human/diagnosis , Influenza, Human/virology , Influenzavirus A/genetics , Influenzavirus B/genetics , Nasal Lavage Fluid/virology , Population Surveillance , Reverse Transcriptase Polymerase Chain Reaction , Seasons
6.
J. bras. patol. med. lab ; 43(1): 31-35, fev. 2007. tab
Article in Portuguese | LILACS | ID: lil-448532

ABSTRACT

INTRODUÇÃO: O papilomavírus humano (HPV) é o principal fator de risco para as neoplasias intra-epiteliais cervicais (NIC) e o câncer cervical. OBJETIVO: O objetivo deste estudo é avaliar se há associação entre a carga viral de HPV oncogênico (alto risco), determinada por meio do teste molecular captura híbrida II (CH II), e o diagnóstico de lesões de alto grau (NIC II/III). MATERIAL E MÉTODOS: Foram analisadas 982 amostras cervicovaginais de exames ginecológicos de rotina, obtidas pelos métodos Papanicolaou convencional e/ou citologia em base líquida (DNA-Citoliq-Digene). Os resultados foram confirmados utilizando-se o método de captura híbrida (CH [Digene]) para detecção de DNA/HPV de alto grau. Os resultados com valor > 1 pg/ml foram considerados positivos, e esses foram divididos em dois grupos: 1. carga viral < 100 pg/ml, e 2. carga viral > 100 pg/ml. RESULTADOS: Dos 210 (21,4 por cento) casos diagnosticados como NIC I, 152 (72,4 por cento) foram positivos para HPV de alto risco por CH II. Desses, 101 (66,4 por cento) apresentaram carga viral > 100 pg/ml. O diagnóstico de NIC II ou III foi confirmado por CH II de alto risco em 86 (43,6 por cento) casos, contudo, entre esses, em 53 (61,6 por cento) a carga viral detectada foi > 100 pg/ml. DISCUSSÃO E CONCLUSÃO: Nossos resultados demonstram que há uma clara associação entre o valor da carga viral determinada pelo método CH II (versão 1) e o grau das lesões precursoras de câncer. Pacientes com carga viral superior a 100 'g/ml devem ser monitoradas periodicamente.


INTRODUCTION: Infection with oncogenic human papilloma virus (HPV) has been established as the main etiologic agent for cervical cancer and of cervical intraepithelial neoplasia (CIN). OBJECTIVE: To determine the association between viral loads of the high risk HPV using the hybrid capture II (HC II) system and CIN lesion stage. MATERIAL AND METHOD: A total of 982 women with diagnosis of negative or of CIN I-III with Pap or liquid-based cytology (DNA-Citoliq-Digene) were included. HC II testing was used to detected HPV DNA. Viral load was measured expressed as relative lights unit (RLU) ratio. RLU ratios were categorized for analysis into three groups: negative (< 1 pg/ml); positive with low viral load (< 100 pg/ml); positive with high viral load (> 100 pg/ml). RESULTS: A total of 152 (72.4 percent) of 210 (21.4 percent) patients with CIN II, 53 (61.6 percent) of 86 (43.6 percent) with CIN II-III were positive for HPV DNA, the higher the viral load (> 100 pg/ml) were observed in 101 (66.4 percent) and 53 (61.6 percent) patients with CIN I or CIN II-III, respectively. DISCUSSION AND CONCLUSIONS: Our results suggest a clear association between viral load HPV DNA determined by HC II (version 1) assay and CIN stage. We concluded that the high viral load has a clinical importance for the management of patients with CIN.


Subject(s)
Humans , Female , Uterine Cervical Dysplasia , Papillomavirus Infections/virology , Uterine Neoplasms/diagnosis , Papilloma/virology , Vaginal Smears , Viral Load
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