Genetic variability of hepatitis A virus isolates in Rio de Janeiro: implications for the vaccination of school children

The epidemiology of hepatitis A virus (HAV) infection is shifting from high to intermediate endemicity in Brazil, resulting in increased numbers of susceptible individuals and a greater potential for the emergence of outbreaks. Universal vaccination against HAV has been recommended for children, but updated sero-epidemiological data are necessary to analyze the level of natural immunity and to identify candidates for preventive measures. In addition, more molecular studies are necessary to characterize the genotypes involved in HAV infections and outbreaks. Sera from 299 school children (5-15 years old) and 25 school staff members, collected during an outbreak of HAV at a rural public school in June 2000, were tested for IgM and total anti-HAV antibodies (ELISA). Viral RNA was amplified by RT-PCR from anti-HAV IgM-positive sera and from 19 fecal samples. Direct nucleotide sequencing of the VP1/2A region was carried out on 18 PCR-positive samples. Acute HAV infection was detected by anti-HAV IgM in 93/299 children and in 3/25 adult staff members. The prevalence of total anti-HAV antibodies in IgM-negative children under 5 years of age was only 10.5%. HAV-RNA was detected in 46% IgM-positive serum samples and in 16% stool samples. Sequence analysis showed that half the isolates belonged to subgenotype IA and the other half to IB. On the basis of these data, mass vaccination against HAV is recommended without prevaccination screening, especially for children before they enter school, since nearly 90% of the children under 5 years were susceptible. Molecular characterization indicated the endemic circulation of specific HAV strains belonging to subgenotypes IA and IB.

CYP2A6 and CYP2E1 polymorphisms in a Brazilian population living in Rio de Janeiro

Cytochrome P450 (CYP) is a superfamily of enzymes involved in the metabolism of endogenous compounds and xenobiotics. CYP2A6 catalyzes the oxidation of nicotine and the activation of carcinogens such as aflatoxin B1 and nitrosamines. CYP2E1 metabolizes ethanol and other low-molecular weight compounds and can also activate nitrosamines. The CYP2A6 and CYP2E1 genes are polymorphic, altering their catalytic activities and susceptibility to cancer and other diseases. A number of polymorphisms described are ethnic-dependent. In the present study, we determined the genotype and allele frequencies of the main CYP2A6 and CYP2E1 polymorphisms in a group of 289 volunteers recruited at the Central Laboratory of Hospital Universit��rio Pedro Ernesto. They had been residing in the city of Rio de Janeiro for at least 6 months and were divided into two groups according to skin color (white and non-white). The alleles were determined by allele specific PCR (CYP2A6) or by PCR-RFLP (CYP2E1). The frequencies of the CYP2A6*1B and CYP2A6*2 alleles were 0.29 and 0.02 for white individuals and 0.24 and 0.01 for non-white individuals, respectively. The CYP2A6*5 allele was not found in the population studied. Regarding the CYP2E1*5B allele, we found a frequency of 0.07 in white individuals, which was statistically different (P < 0.05) from that present in non-white individuals (0.03). CYP2E1*6 allele frequency was the same (0.08) in both groups. The frequencies of CYP2A6*1B, CYP2A6*2 and CYP2E1*6 alleles in Brazilians are similar to those found in Caucasians and African-Americans, but the frequency of the CYP2E1*5B allele is higher in Brazilians.

The association of ACE gene D/I polymorphism with cardiovascular risk factors in a population from Rio de Janeiro

Our aim was to determine the frequencies of the angiotensin-converting enzyme (ACE) gene alleles D and I and any associations to cardiovascular risk factors in a population sample from Rio de Janeiro, Brazil. Eighty-four adults were selected consecutively during a 6-month period from a cohort subgroup of a previous large cross-sectional survey in Rio de Janeiro. Anthropometric data and blood pressure measurements, echocardiogram, albuminuria, glycemia, lipid profile, and ACE genotype and serum enzyme activity were determined. The frequency of the ACE*D and I alleles in the population under study, determined by PCR, was 0.59 and 0.41, respectively, and the frequencies of the DD, DI, and II genotypes were 0.33, 0.51, and 0.16, respectively. No association between hypertension and genotype was detected using the Kruskal-Wallis method. Mean plasma ACE activity (U/mL) in the DD (N = 28), DI (N = 45) and II (N = 13) groups was 43 (in males) and 52 (in females), 37 and 39, and 22 and 27, respectively; mean microalbuminuria (mg/dL) was 1.41 and 1.6, 0.85 and 0.9, and 0.6 and 0.63, respectively; mean HDL cholesterol (mg/dL) was 40 and 43, 37 and 45, and 41 and 49, respectively, and mean glucose (mg/dL) was 93 and 108, 107 and 98, and 85 and 124, respectively. A high level of ACE activity and albuminuria, and a low level of HDL cholesterol and glucose, were found to be associated with the DD genotype. Finally, the II genotype was found to be associated with variables related to glucose intolerance.

Phenotypic and genotypic variant of MDR-Mycobacterium tuberculosis multiple isolates in the same tuberculosis episode, Rio de Janeiro, Brazil

Assuming that the IS6110-restriction fragment length polymorphism (RFLP) changes at a constant rate of 3.2 years, this methodology was applied to demonstrate, for the first time, variant patterns of Mycobacterium tuberculosis (MTB) in multiple isolates obtained at short time intervals from sputum and blood of an HIV+ patient with multiple admissions to the Emergency Room and to the multidrug-resistant tuberculosis (MDR-TB) Reference Center of a secondary-care hospital in Rio de Janeiro, Brazil. In sputum, the IS6110-RFLP appeared in isolates with two variant patterns with 10 and 13 IS6110 copies. However, blood presented only the pattern corresponding to 10 copies, suggesting compartmentalization. With regard to the exact match of 10 of 13 bands, this may be a subpopulation with the same clonal origin and this may be related to the IS6110 transposition. A susceptibility test demonstrated an MDR profile (INH R, RIF R, SM R, and EMB R), with the sputum isolate also exhibiting EMB S (R = resistant; S = sensitive). A gene mutation confirmed resistance only to streptomycin. There was agreement between the results of the phenotypic test and the clinical response to MDR-TB treatment, suggesting serious implications with regard to treatment administration based exclusively on molecular methods, and calling attention to the fact that more effective control strategies against the emergence of MDR strains must be implemented by the TB control program to prevent transmission of MDR-MTB strains at health facilities in areas highly endemic for TB.

Diphtheria toxin IgG levels in military and civilian blood donors in Rio de Janeiro, Brazil

Serologic data on diseases that are preventable by vaccines are necessary to evaluate the success of immunization programs and to identify susceptible subgroups. In the present study, we determined serum IgG levels against diphtheria toxin of military and civilian blood donors (N = 75; 69.3% males and 30.7% females) aged 18-64 years, from the Brazilian Army Biology Institute, Rio de Janeiro, using a commercial diphtheria kit (Diphtheria IgG ELISA; IBL, Germany). Most (63%) unprotected military donors were from the older age group of 41 to 64 years. In contrast, the majority (71%) of young military donors (18 to 30 years) were fully protected. About half of the military donors aged 31 to 40 years were protected against diphtheria. Among the civilians, about 50% of persons aged 18 to 30 years and 31 to 40 years had protective antibody levels against diphtheria as also did 64% of individuals aged 41 to 64 years. All civilians had a similar antibody response (geometric mean = 0.55 IU/mL) independent of age group. Military donors aged 18-30 years had higher IgG levels (geometric mean = 0.82 IU/mL) than military donors of 41-64 years (geometric mean = 0.51 IU/mL; P > 0.05). In conclusion, the existence of a considerable proportion of susceptible adults supports the position that reliable data on the immune status of the population should be maintained routinely and emphasizes the importance of adequate immunization during adulthood.

Human papillomavirus infection among sexual partners attending a Sexually Transmitted Disease Clinic in Rio de Janeiro, Brazil

Cervical cancer is a major source of illness and death among women worldwide and genital infection with oncogenic human papillomavirus (HPV) its principal cause. There is evidence of the influence of the male factor in the development of cervical neoplasia. Nevertheless, the pathogenic processes of HPV in men are still poorly understood. It has been observed that different HPV types can be found among couples. The objective of the present study was to investigate HPV infections in female patients (n = 60 females/group) as well as in their sexual partners and to identify the concordance of HPV genotypes among them. By using the polymerase chain reaction, we detected a 95% prevalence of HPV DNA in women with cervical intraepithelial neoplasia (CIN) compared to 18.3% in women with normal cervical epithelium, with a statistically significant difference (P < 0.001). The HPV DNA prevalence was 50% in male partners of women with CIN and 16.6% in partners of healthy women. In the control group (healthy women), only 9 couples were simultaneously infected with HPV, and only 22.2% of them had the same virus type, showing a weak agreement rate (kappa index = 0.2). Finally, we observed that HPV DNA was present in both partners in 30 couples if the women had CIN, and among them, 53.3% shared the same HPV type, showing moderate agreement, with a kappa index of 0.5. This finding supports the idea of circulation and recirculation of HPV among couples, perpetuating HPV in the sexually active population, rather than true recurrences of latent infections.

N��veis de merc��rio em atum s��lido enlatado comercializado na cidade do Rio de Janeiro

No presente trabalho, estudou-se o n��vel de merc��rio em atum s��lido enlatado, comercializado na cidade do Rio de Janeiro. Foram analisadas 39 amostras, pertencente a 5 marcas e lotes distintos, utilizando-se a espectrometria de absor����o at��mica pela t��cnica de vapor-frio. Os resultados obtidos demonstraram que 53% das amostras apresentaram um teor acima do m��ximo recomendado, sendo que somente uma entre as cinco marcas estudadas apresentou todas as amostras com n��veis dentro dos limites tolerados. Tais resultados demonstram a necessidade de um maior controle da qualidade destes produtos.

Aeromonas spp. e Plesiomonas shigelloides isoladas a partir de mexilh��es (Perna perna) in natura e pr��-cozidos no Rio de Janeiro, RJ

O ecossistema aqu��tico �� o habitat de mexilh��es (Perna perna), animais filtradores que refletem a qualidade ambiental atrav��s de an��lise microbiol��gica de sua carne. No presente trabalho avaliou-se a presen��a de pat��genos emergentes (Aeromonas hydrophila e Plesiomonas shigelloides), em mexilh��es in natura e pr��-cozidos coletados por pescadores da Esta����o Experimental de Cultivo de Mexilh��es situada em Jurujuba, Niter��i, Rio de Janeiro. Foram analisadas 86 amostras de mexilh��es (43 in natura e 43 pr��-cozidos) as quais foram submetidas a enriquecimento em ��gua Peptonada Alcalina (APA) acrescida de 1 e 3% de Cloreto de S��dio (NaCl) e em solu����o Salina de Butterfield, incubadas a 37��C por 24 horas. Em seguida, foram semeadas em ��gar Seletivo para Pseudomonas-Aeromonas (GSP), ��gar Tiossulfato Citrato Bile Sacarose (TCBS) e ��gar Inositol Bile Verde Brilhante (IBB). A an��lise geral dos resultados permitiu a identifica����o de Areomonas spp e Plesiomonas shigelloides em 86% das amostras de mexilh��es in natura e pr��-cozidas avaliadas. A posterior caracteriza����o bioqu��mica permitiu a identifica����o das esp��cies Aeromonas media (37,10%), A. hydrophila (15,50%), A. caviae (14,80%), A. veronii biogrupo veronii (11,60%), Aeromonas sp. (7,36%), A. sobria (4,20%), A. trota (4,20%), A. schubertii (1,31%), A. jandaei (1,31%), A. veronii biogrupo sobria (0,52%) e Plesiomonas shigelloides (2,10%). A relev��ncia epidemiol��gica desses microrganismos em casos de gastrenterite humana, ap��s consumo de mexilh��es crus ou parcialmente cozidos, revela a import��ncia de alertar as autoridades de Sa��de P��blica no Brasil, sobre a presen��a desses pat��genos na cadeia alimentar e seus riscos para a sa��de humana.

Vibrio spp. isolados a partir de mexilh��es (Perna perna) in natura e pr��-cozidos de Esta����o Experimental de Cultivo, Rio de Janeiro, RJ, Brasil

A an��lise microbiol��gica dos mexilh��es reflete a qualidade do habitat aqu��tico, pois estes animais podem reter em seus organismos diversos pat��genos, dentre os quais aqueles pertencentes �� fam��lia Vibrionaceae. No presente estudo foi avaliada a presen��a de Vibrio spp. em mexilh��es (in natura e pr��-cozidos), comercializados na Esta����o Experimental de Cultivo de Mexilh��es, situada em Jurujuba, Niter��i, Rio de Janeiro. Foram avaliadas 86 amostras, tomando como procedimento, o enriquecimento em ��gua Peptonada Alcalina (APA) adicionada de 1 e 3% de NaCl, isolamento em Agar Tiossulfato Citrato Bile Sacarose (TCBS) e confirma����o das col��nias t��picas por an��lise bioqu��mica. Dentre as 12 esp��cies de Vibrio identificadas destacaram-se como de maior preval��ncia as esp��cies Vibrio alginolyticus, V. cholerae n��o-O1, V. parahaemolyticus, V. carchariae e Vibrio vulnificus. A relev��ncia epidemiol��gica destes pat��genos associada a casos de gastrenterite humana ap��s consumo de mexilh��es crus ou parcialmente cozidos, refor��a a import��ncia de alertar as autoridades de Vigil��ncia Sanit��ria sobre sua presen��a na cadeia alimentar e seus riscos para a Sa��de P��blica.