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2.
J Med Virol ; 85(1): 144-8, 2013 Jan.
Article in English | MEDLINE | ID: mdl-23154878

ABSTRACT

The aim of this study was to investigate and compare the frequency of BKV, JCV, WUV, and KIV in the saliva of healthy individuals. Samples were analyzed for the presence of polyomaviruses (BKV, JCV, WUV, and KIV) DNA by real-time PCR. Of the 291 samples tested, 71 (24.3%) were positive for at least one of the screened polyomaviruses. Specifically, 12.7% (37/291) were positive for WUV, 7.2% (21/291) positive for BKV, 2.4% (7/291) positive for KIV, and 0.3% (1/291) positive for JCV. BKV and WUV co-infections were detected in 1.7% (5/291) of individuals. No other co-infection combinations were found. The mean number of DNA copies was high, particularly for WUV and BKV, indicating active replication of these viruses. Polyomavirus detection was higher among individuals 15-19 years of age (46.0%; 23/50) and ≥50 years of age (33.3%; 9/27). However, the detection rate in the first group was almost 1.7× greater than the latter. WUV infections were more frequent in individuals between the ages of 15 and 19 years and the incidence decreased with age. By contrast, BKV excretion peaked and persisted during the third decade of life and KIV infections were detected more commonly in subjects ≥50 years old. These findings reinforced the previous hypotheses that saliva may be a route for BKV transmission, and that the oral cavity could be a site of virus replication. These data also demonstrated that JCV, WUV, and KIV may be transmitted in a similar fashion.


Subject(s)
Polyomavirus Infections/virology , Polyomavirus/isolation & purification , Saliva/virology , Virus Shedding , Adolescent , Adult , Age Factors , Aged , Carrier State/epidemiology , Carrier State/virology , Coinfection/epidemiology , Coinfection/virology , DNA, Viral/genetics , DNA, Viral/isolation & purification , Female , Humans , Incidence , Male , Middle Aged , Polyomavirus/genetics , Polyomavirus Infections/epidemiology , Prevalence , Viral Load , Young Adult
3.
Infect Genet Evol ; 12(7): 1397-404, 2012 Oct.
Article in English | MEDLINE | ID: mdl-22579479

ABSTRACT

The polymorphism of species A rotavirus genotype G1 strains (RVA-G1) circulating in Rio de Janeiro between 1996 and 2004 was evaluated. The VP7 encoding gene of 36 G1 isolates was sequenced and compared to references strains. The deduced amino acid sequences were used as basis for in silico analysis of the VP7 protein. We observed the circulation of two major G1 lineages and five sublineages during the studied period. Comparison between the VP7 trimeric structures of a rotavirus vaccine strain and Brazilian G1 strains showed mutations at amino acid residues located at the calcium binding site and at several neutralizing antibody recognition sites. Although the rotavirus vaccine program has clearly been successful in Brazil, these results suggest the possibility of the emergence of G1 strains that could evade the immune response elicited by a RVA vaccine and cause a vaccine breakthrough. Consequently, continuous monitoring of rotavirus intragenotypes diversity is critical to understand how it could affect vaccine effectiveness.


Subject(s)
Diarrhea/virology , Polymorphism, Genetic , Rotavirus Infections/virology , Rotavirus/genetics , Amino Acid Sequence , Antigens, Viral/chemistry , Antigens, Viral/genetics , Brazil , Capsid Proteins/chemistry , Capsid Proteins/genetics , Child, Preschool , Computer Simulation , Diarrhea/prevention & control , Evolution, Molecular , Humans , Mass Vaccination , Models, Genetic , Models, Molecular , Molecular Sequence Data , Phylogeny , Protein Structure, Quaternary , Protein Structure, Tertiary , Reference Values , Rotavirus Infections/prevention & control , Sequence Analysis, DNA
4.
J Oral Pathol Med ; 40(8): 610-5, 2011 Sep.
Article in English | MEDLINE | ID: mdl-21501230

ABSTRACT

The aim of this investigation was to identify the prevalence of herpesvirus types 1-8 in the oral cavity of subjects with chronic renal failure (CRF) and healthy subjects and compare the two groups, and also correlate the presence of the virus with some characteristics of CRF disease (the type of treatment, drugs administered for CRF and the presence of oral manifestations). The sample was made up of 60 subjects (aged 4-20) divided into the renal group (RG) and healthy group. Anamnesis, intraoral examination and collection of clinical specimens (swab smears) were carried out. The nested-PCR technique was used to identify the viral species. The results showed a higher prevalence of HSV-1 (20%), human herpes virus (HHV)-6B (83%), CMV (13.3%) in RG group than in healthy group (HSV-1: 3.3%; HHV-6B: 20%) (P ≤ 0.05). There was no difference in the prevalence of HHV-7 between the two groups (P > 0.05). HSV-2, EBV, VZV, HHV-6A, and HHV-8 were not identified in either group. The most common symptoms in RG were dry-mouth sensation (60%), changes in taste (33.3%), and uremic odor (26.7%). There was a correlation between HHV-7 and the use of anticoagulants and HHV-6B with dry-mouth sensation (P ≤ 0.05). Based on the results, the prevalence of herpesvirus types (HSV-1, HHV-6B and CMV) were shown to be higher in subjects with CRF as well as in healthy children, but only the HHV-6B and HHV-7 were correlated with some of the disease characteristics. So, more attention should be paid to the oral health of these individuals in order to prevent infection by opportunistic pathogens.


Subject(s)
Herpesviridae/isolation & purification , Kidney Failure, Chronic/virology , Mouth Diseases/virology , Mouth/virology , Virus Diseases/virology , Adolescent , Case-Control Studies , Child , Child, Preschool , Cross-Sectional Studies , DNA, Viral/analysis , Female , Herpesviridae/classification , Herpesviridae/genetics , Humans , Kidney Failure, Chronic/complications , Male , Mouth Diseases/complications , Polymerase Chain Reaction , Reference Values , Virus Diseases/complications , Young Adult
5.
Braz. j. infect. dis ; 14(6): 549-552, Nov.-Dec. 2010. tab
Article in English | LILACS | ID: lil-578428

ABSTRACT

BACKGROUND: Diarrhea is a major cause of morbidity and mortality among HIV-infected patients worldwide. OBJECTIVE: We sought to determine the frequency of viral gastrointestinal infections among Brazilian HIV-infected patients with diarrhea. METHODS: A collection of 90 fecal specimens from HIV-infected individuals with diarrhea, previously tested for the presence of bacteria and parasite was analyzed by polymerase chain reaction and sequence analysis for the presence of enteric viruses such as astrovirus, norovirus, rotavirus groups A, B and C, adenovirus, herpes simplex virus, Epstein-Barr virus, cytomegalovirus, and human bocavirus. RESULTS: Twenty patients (22.2 percent; n = 90) were infected with parasites (11 single infections and nine coinfected with virus). Enteropathogenic bacteria were not found. Virus infections were detected in 28.9 percent (26/90) of the specimens. Cytomegalovirus was the most common virus detected (24.4 percent; 22/90). Coinfections with viruses and/or parasite were observed in 10 (11.1 percent) samples. CONCLUSION: Gastrointestinal virus infections were more frequent than parasitic or bacterial infections in this patient population.


Subject(s)
Adolescent , Adult , Female , Humans , Male , Middle Aged , Young Adult , AIDS-Related Opportunistic Infections/virology , Diarrhea/virology , Gastroenteritis/virology , AIDS-Related Opportunistic Infections/parasitology , Diarrhea/parasitology , Feces/parasitology , Feces/virology , Gastroenteritis/parasitology , Polymerase Chain Reaction
6.
Braz. j. infect. dis ; 14(6): 553-557, Nov.-Dec. 2010. tab
Article in English | LILACS | ID: lil-578429

ABSTRACT

Acute diarrheal disease is still one of the major public health problems worldwide. Rotaviruses (RV) are the most important viral etiologic agents and children under five years of age are the target population. OBJECTIVE: To investigate the rate of RV infection in hospitalized patients due to acute diarrhea in the cities of Ponta Grossa, Londrina and Assai - Paraná. METHODS: Latex agglutination (LA); immunochromatography (ICG); polyacrylamide gel electrophoresis (PAGE) and negative staining electron microscopy (ME) tests were used to detect the virus. For the genotyping, RT-PCR and RT-PCR-ELISA were used, respectively, for NSP4 and VP4/VP7. RESULT: Out of 124 samples there were 69 positive stool samples for RV, for at least one of the used tests, 67 of them being RV group A (RV-A). Overall, most of the RV positive stool samples came from children under thirteen years of age. However, 12 positive cases occurred in patients aged 13 years or above, including an 81-year old patient. CONCLUSION: The data showed similar electropherotypes and genotypes G, P and NSP4 of the inland wild circulating strains of RV.


Subject(s)
Adolescent , Adult , Aged, 80 and over , Child , Child, Preschool , Female , Humans , Infant , Middle Aged , Young Adult , Diarrhea/virology , Rotavirus Infections/virology , Rotavirus/genetics , Acute Disease , Chromatography , Electrophoresis, Polyacrylamide Gel , Feces/virology , Genotype , Latex Fixation Tests , Microscopy, Electron , Negative Staining , Reverse Transcriptase Polymerase Chain Reaction , Rotavirus Infections/diagnosis , Rotavirus/isolation & purification
7.
J Med Virol ; 82(10): 1797-802, 2010 Oct.
Article in English | MEDLINE | ID: mdl-20827779

ABSTRACT

A total of 162 rotavirus strains detected between 1996 and 2006 among individuals with diarrhea in Rio de Janeiro, Brazil, were analyzed by multiple-gene genotyping. Characterization of strains was done by RT-PCR assay for amplification and typing of the VP7-, VP4-, VP6-, and NSP4-encoding genes. Overall, 139 (85.8%) strains belonged to the common group A rotavirus combinations: 67 (41.4%) belonged to genotype G1-P[8]-I1-E1; 18 (11.1%) were G2-P[4]-I2-E2; 11 (6.8%) were G3-P[8]-I1-E1; 12 (7.4%) were G4-P[8]-I1-E1; and 31 (19.1%) were G9-P[8]-I1-E1. Two samples presented mixed genotypes (G1 + G3-P[8]-I1-E1 and G1 + G9-P[9]-I1-E1) and rare combinations, such as G2-P[6]-I2-E2 and G9-P[6]-I2-E2, were detected in six (3.7%) strains. The results suggest a linkage among all four genes. Genotypes G1/G3/G4/G5/G9-P[8] were correlated strongly to I1-E1 genotypes and G2-P[4]/P[6] were correlated to I2-E2 genotypes. Unusual combinations of genes, such as G3-P[9]-I2-E2, G9-P[9]-I1-E2, and G3-P[9]-I3-E3, were observed in 15 (9.3%) strains. The characterization of multiple genes allows a more complete analysis of the rotavirus isolates and provides evidence of natural reassortment of strains.


Subject(s)
Antigens, Viral/genetics , Capsid Proteins/genetics , Genetic Linkage , Glycoproteins/genetics , Rotavirus/genetics , Toxins, Biological/genetics , Viral Nonstructural Proteins/genetics , Brazil , Child, Preschool , Cluster Analysis , Diarrhea/virology , Genotype , Humans , Infant , Infant, Newborn , RNA, Viral/genetics , Recombination, Genetic , Reverse Transcriptase Polymerase Chain Reaction , Rotavirus Infections/virology , Sequence Analysis, DNA
8.
J Clin Virol ; 48(2): 127-30, 2010 Jun.
Article in English | MEDLINE | ID: mdl-20382557

ABSTRACT

BACKGROUND: The newly described human bocavirus (HBoV) species 2 and 3 have been repeatedly detected in stool strengthening the possibility that these viruses might present a tropism for the gastrointestinal tract and may be etiological agents of diarrhea. OBJECTIVE: In this study we assessed the presence of HBoV2 and HBoV3 in stool specimens from Brazilians with acute gastroenteritis. STUDY DESIGN: Stool samples from Brazilian patients with acute diarrhea were analyzed for HBoV2 and HBoV3 by PCR assay. Full or partial genome sequences were obtained for selected isolates. Electron microscopy analysis was used to investigate virus morphology. RESULTS: Electron microscopy confirmed the presence of virus-like particles in HBoV PCR-positive specimens, with morphology similar to other members of the Parvoviridae family. Five samples out of 807 (0.6%) were positive for HBoV3. Three of the HBoV3-positive patients were HIV/AIDS positive. A selected group of 144 samples was also tested for HBoV2 and 30 samples (20.8%) were positive, 11 of which were HIV/AIDS positive. CONCLUSION: This study reports the detection and genetic characterization of HBoV3 and HBoV2 in the stool of Brazilian patients with acute diarrhea. This is the first description of HBoV3 outside Australia, suggesting a wide global distribution of this virus. Further studies are needed to better understand the role of HBoV in gastrointestinal infections, particularly among patients with HIV/AIDS.


Subject(s)
Feces/virology , Gastroenteritis/epidemiology , Gastroenteritis/virology , Human bocavirus/classification , Human bocavirus/isolation & purification , Parvoviridae Infections/epidemiology , Parvoviridae Infections/virology , Brazil/epidemiology , Child , Cluster Analysis , DNA, Viral/chemistry , DNA, Viral/genetics , DNA, Viral/isolation & purification , Humans , Infant , Male , Microscopy, Electron, Transmission , Molecular Sequence Data , Phylogeny , Polymerase Chain Reaction , Sequence Analysis, DNA , Sequence Homology , Virion/ultrastructure
9.
Braz J Infect Dis ; 14(6): 553-7, 2010.
Article in English | MEDLINE | ID: mdl-21340294

ABSTRACT

UNLABELLED: Acute diarrheal disease is still one of the major public health problems worldwide. Rotaviruses (RV) are the most important viral etiologic agents and children under five years of age are the target population. OBJECTIVE: To investigate the rate of RV infection in hospitalized patients due to acute diarrhea in the cities of Ponta Grossa, Londrina and Assai - Paraná. METHODS: Latex agglutination (LA); immunochromatography (ICG); polyacrylamide gel electrophoresis (PAGE) and negative staining electron microscopy (ME) tests were used to detect the virus. For the genotyping, RT-PCR and RT-PCR-ELISA were used, respectively, for NSP4 and VP4/VP7. RESULT: Out of 124 samples there were 69 positive stool samples for RV, for at least one of the used tests, 67 of them being RV group A (RV-A). Overall, most of the RV positive stool samples came from children under thirteen years of age. However, 12 positive cases occurred in patients aged 13 years or above, including an 81-year old patient. CONCLUSION: The data showed similar electropherotypes and genotypes G, P and NSP4 of the inland wild circulating strains of RV.


Subject(s)
Diarrhea/virology , Rotavirus Infections/virology , Rotavirus/genetics , Acute Disease , Adolescent , Adult , Aged, 80 and over , Child , Child, Preschool , Chromatography , Electrophoresis, Polyacrylamide Gel , Feces/virology , Female , Genotype , Humans , Infant , Latex Fixation Tests , Microscopy, Electron , Middle Aged , Negative Staining , Reverse Transcriptase Polymerase Chain Reaction , Rotavirus/isolation & purification , Rotavirus Infections/diagnosis , Young Adult
10.
Braz J Infect Dis ; 14(6): 549-52, 2010.
Article in English | MEDLINE | ID: mdl-21340293

ABSTRACT

BACKGROUND: Diarrhea is a major cause of morbidity and mortality among HIV-infected patients worldwide. OBJECTIVE: We sought to determine the frequency of viral gastrointestinal infections among Brazilian HIV-infected patients with diarrhea. METHODS: A collection of 90 fecal specimens from HIV-infected individuals with diarrhea, previously tested for the presence of bacteria and parasite was analyzed by polymerase chain reaction and sequence analysis for the presence of enteric viruses such as astrovirus, norovirus, rotavirus groups A, B and C, adenovirus, herpes simplex virus, Epstein-Barr virus, cytomegalovirus, and human bocavirus. RESULTS: Twenty patients (22.2%; n = 90) were infected with parasites (11 single infections and nine coinfected with virus). Enteropathogenic bacteria were not found. Virus infections were detected in 28.9% (26/90) of the specimens. Cytomegalovirus was the most common virus detected (24.4%; 22/90). Coinfections with viruses and/or parasite were observed in 10 (11.1%) samples. CONCLUSION: Gastrointestinal virus infections were more frequent than parasitic or bacterial infections in this patient population.


Subject(s)
AIDS-Related Opportunistic Infections/virology , Diarrhea/virology , Gastroenteritis/virology , AIDS-Related Opportunistic Infections/parasitology , Adolescent , Adult , Diarrhea/parasitology , Feces/parasitology , Feces/virology , Female , Gastroenteritis/parasitology , Humans , Male , Middle Aged , Polymerase Chain Reaction , Young Adult
11.
J Med Virol ; 80(1): 113-7, 2008 Jan.
Article in English | MEDLINE | ID: mdl-18041001

ABSTRACT

We analyzed 379 stool samples collected from January 1998 through December 2004, from hospitalized and non-hospitalized children with diarrhea in Rio de Janeiro, Brazil. These samples had prior negative results for other enteric viruses and bacterial pathogens. The specimens were analyzed for HAstV detection by RT-PCR. HAstV genotypes were determined by sequence analysis of the RT-PCR products. Twenty (5.3%) out of 379 samples were positive for astrovirus. Astrovirus was equally common among inpatients and outpatients and among different age groups. Of 20 HAstV-infected children, 13 (65%) were either hospitalized or received medical care in the emergence department, which suggests that they had a more severe illness. Only 7 (35%) of the 20 HAstV-infected children attended walk-in clinics, which suggests that they had mild disease. Other then diarrhea, fever was the most common symptom among the HAstV-positive patients, followed by vomit and bloody diarrhea. HAstV-1 was the predominant strain although genotypes 2 and 4 were also found. There was no obvious difference among HAstV strains detected from inpatients or outpatients or among different age groups. The study documented that astrovirus is an agent of acute diarrhea in children who are inpatients or outpatients in Rio de Janeiro, Brazil although it seems to be less common as a single cause of childhood diarrhea then rotavirus.


Subject(s)
Astroviridae Infections/epidemiology , Astroviridae Infections/virology , Mamastrovirus/classification , Brazil/epidemiology , Child , Child, Hospitalized , Child, Preschool , Diarrhea/epidemiology , Diarrhea/virology , Diarrhea, Infantile/epidemiology , Diarrhea, Infantile/virology , Feces/virology , Humans , Infant , Mamastrovirus/genetics , Mamastrovirus/isolation & purification , Molecular Epidemiology , Retrospective Studies , Reverse Transcriptase Polymerase Chain Reaction
12.
Microbiol Res ; 163(2): 136-9, 2008.
Article in English | MEDLINE | ID: mdl-16735108

ABSTRACT

We investigated the antiviral activity of an aliphatic nitro compound (NC) isolated from Heteropteris aphrodisiaca O. Mach. (Malpighiaceae), a Brazilian medicinal plant. The NC was tested for its antiviral activity against poliovirus type 1 (PV-1) and bovine herpes virus type 1 (BHV-1) by plaque reduction assay in cell culture. The NC showed a moderate antiviral activity against PV-1 and BHV-1 in HEp-2 cells, and the 50% inhibitory concentration (IC50) were 22.01 microg/ml (selectivity index (SI)=2.83) and 21.10 microg/ml (SI=2.95), respectively. At the highest concentration of the drug (40 microg/ml) a reduction of approximately 80% in plaque assay was observed for both viruses. The treatment of cells or virus prior to infection did not inhibit the replication of virus strains.


Subject(s)
Antiviral Agents/pharmacology , Herpesvirus 1, Bovine/drug effects , Nitro Compounds/pharmacology , Plants, Medicinal/chemistry , Poliovirus/drug effects , Animals , Brazil , Cattle , Cell Line, Tumor , Cytopathogenic Effect, Viral/drug effects , Humans , Inhibitory Concentration 50 , Plant Extracts/pharmacology , Plant Roots/chemistry , Viral Plaque Assay
13.
Braz. arch. biol. technol ; 50(1): 39-44, Jan. 2007. graf
Article in English | LILACS | ID: lil-452546

ABSTRACT

An indirect solid-phase enzyme immunoassay (EIA) was developed for the detection of poliovirus antigen. Virus antigen was obtained in LLC-MK2 cell cultures and used to prepare antibodies in rabbit and guinea pig. Antibodies were evaluated by double immunodiffusion and neutralization test. Optimal concentrations of guinea pig and rabbit immunoglobulins were determined by checkerboard titration. Microtitre plates were coated with 15.0 µg/ml guinea pig anti-polio immunoglobulin and rabbit anti-polio immunoglobulin at the concentration of 7.94 µg/ml was used as detecting antibody. The standard curve with eight different antigen concentrations in eight replicates resulted in a coefficient of variation (CV) between 2.1 percent to 7.8 percent. The dose-response relationship was determined by simple linear regression with a coefficient of correlation (R²) equal to 96.4 percent. The assay detected a minimum of 2.3 µg/ml poliovirus antigen.


O trabalho apresenta o desenvolvimento de um ensaio imunoenzimático indireto para a detecção de antígeno de poliovírus. O antígeno viral foi obtido em cultura de células LLC-MK2 e usado para imunização de coelho e cobaia. Os soros hiperimunes foram avaliados por imunodifusão dupla e teste de neutralização. Após padronização, o soro de captura, produzido em cobaia, foi usado na concentração protéica de 15.0 µg/ml para sensibilizar microplacas de poliestireno e o soro de coelho (detector) foi usado na concentração de 7.94 µg/ml. A curva padrão resultante da utilização de oito diferentes concentrações do antígeno padrão definiu um coeficiente de variação de 2.1 por cento a 7.8 por cento. A relação dose-resposta foi determinada por regressão linear simples com o estabelecimento do coeficiente de correlação (R²) igual a 96.4 por cento. O ensaio possibilitou a detecção mínima de 2.3 µg/ml de antígeno de poliovírus.

14.
Emerg Infect Dis ; 13(11): 1756-8, 2007 Nov.
Article in English | MEDLINE | ID: mdl-18217564

ABSTRACT

Human bocavirus (HBoV) was detected in 14 (2%) of 705 fecal specimens from Brazilian children with gastroenteritis. Coinfection with rotavirus, adenovirus, or norovirus was found in 3 (21.4%) HBoV-positive specimens. None of the HBoV-positive patients had respiratory symptoms.


Subject(s)
Bocavirus/isolation & purification , Gastroenteritis/virology , Parvoviridae Infections/virology , Adolescent , Bocavirus/genetics , Brazil , Child , Child, Preschool , Feces/virology , Female , Humans , Infant , Male , Parvoviridae Infections/complications , Phylogeny , Polymerase Chain Reaction/methods , Retrospective Studies
15.
Braz. j. microbiol ; 37(4): 561-565, Oct.-Dec. 2006. tab
Article in English | LILACS | ID: lil-442212

ABSTRACT

The aqueous extract of Agaricus blazei Murill ss. Heinem, a basidiomycete native from Brazil, frequently used by popular medicine, mainly in the form of tea, was assessed to its antiviral action against herpes simplex type 1 (HSV-1) and bovine herpes type 1 (BoHV-1) in HEp-2 cell culture. Viral replication inhibition was evaluated by plaque assay and immunofluorescence test. The extract demonstrated virucide action for both viruses, being more effective against HSV-1, inhibiting its infectivity in 78.4 and 73.9 percent at the concentrations of 50 and 100 æg/mL, respectively moreover, reduction in 47 percent the number of fluorescent cells was observed for both concentrations. The extract also showed discrete therapeutic activity. These results suggest that A. blazei extract acts mainly in the viral particle, however, the effect during virus replication can not be ruled out.


O extrato aquoso de Agaricus blazei Murill ss. Heinem, um basidiomiceto nativo do Brasil, usado na medicina popular, na forma de chá, foi avaliado quanto suas propriedades antivirais contra herpes simplex tipo 1 (HSV-1) e herpes bovino tipo 1 (BoHV-1) em cultura de células HEp-2. A inibição da replicação viral foi monitorada pelos ensaio de placa e reação de imunofluorescência. O extrato apresentou atividade virucida mais efetiva do que terapêutica para ambos os vírus, sendo mais efetivo portanto para HSV-1, inibindo em mais de 70 por cento o número de plaques e em cerca de 47 por cento o número de células apresentando fluorescência específica, nas concentrações de 50 e 100 æg/mL, nas duas técnicas utilizadas. Os resultados obtidos sugerem que o extrato aquoso de A. blazei deve agir principalmente sobre a partícula viral, embora a inibição durante o ciclo replicativo do vírus não deva ser excluída.


Subject(s)
Humans , Cattle , Agaricus , Herpesvirus 1, Bovine , Herpesvirus 1, Human , In Vitro Techniques , Viral Plaque Assay , Cell Culture Techniques , Fluorescent Antibody Technique , Methods
16.
J Med Virol ; 78(9): 1241-9, 2006 Sep.
Article in English | MEDLINE | ID: mdl-16847962

ABSTRACT

Between May and August in 2003, a total of 251 fecal samples were collected from children and adults with diarrhea (5 inpatients and 246 outpatients) at a private hospital in the city of Ponta Grossa, the state of Paraná, Brazil. Group A rotavirus was detected in 71 of 251 (28.3%) specimens: 55 (77.5%) from children under 5 years of age and 16 (22.5%) from individuals aged 6-72 years. All 71 strains exhibited a "long" RNA pattern when analyzed by PAGE. Sixty-one positive samples that yielded enough RNA were submitted to PCR genotyping. The most frequent G/P genotype combination detected was G1P[8] (86.9%; 53/61) followed by G9P[8] (3.3%; 2/61) and G12P[9] (1.6%; 1/61). Rotaviruses with G2, G3, G4, P[4], or P[6] specificity were not detected. For three strains (4.9%) bearing G1 genotype, the VP4 specificity could no be determined, and two specimens (3.3%) remained G/P non-typeable. One rotavirus strain (HC91) bearing G12P[9] genotype with a "long" electropherotype was isolated from an 11-month-old boy with diarrhea for the first time in Brazil. The cell-culture grown HC91 strain was shown to belong to serotype G12 by neutralization.


Subject(s)
Diarrhea/epidemiology , Rotavirus Infections/epidemiology , Rotavirus/genetics , Adolescent , Adult , Aged , Brazil/epidemiology , Child , Child, Preschool , Data Collection , Feces/virology , Hospitals, Private , Humans , Infant , Infant, Newborn , Middle Aged , Molecular Epidemiology , Neutralization Tests , Phylogeny , RNA, Viral/genetics , Rotavirus/classification , Rotavirus/immunology , Rotavirus/isolation & purification , Species Specificity , Urban Population
17.
Biol Pharm Bull ; 29(6): 1092-5, 2006 Jun.
Article in English | MEDLINE | ID: mdl-16754999

ABSTRACT

Crude extract (CE) and aqueous (AqF) and ethyl acetate (EtOAcF) fractions of Guazuma ulmifolia Lam., Sterculiaceae and the corresponding AqF, EtOAcF of Stryphnodendron adstringens (Mart.) Coville, Leguminosae were tested for their antiviral activity against poliovirus 1 (P-1) and bovine herpesvirus 1 (BHV-1) in HEp-2 cultured cells. The antiviral activity was monitored by plaque assay and immunofluorescence assay (IFA) under virucidal and therapeutic protocols. The therapeutic protocol demonstrated statistically significant positive results with both plants and for both virus strains. The highest percentages of viral inhibition were found for G. ulmifolia EtOAcF which inhibited BHV-1 and P-1 replication by 100% and 99%, respectively (p<0.05, Student's t-test). For S. adstringens, AqF was the most efficient, inhibiting BHV-1 and P-1 by 97% and 93%, respectively (p<0.05). In the virucidal protocol, G. ulmifolia CE inhibited the replication of BHV-1 and P-1 by 60% and 26%, respectively (p<0.05), while, for S. adstringens, inhibition of 62% (p<0.05) was demonstrated only with EtOAcF for P-1. IFA demonstrated that the greatest reduction in fluorescent cell number occurred with G. ulmifolia, under the therapeutic protocol for both virus strains. However, AqF and EtOAcF of S. adstringens were most efficient with the virucidal protocol for P-1. In conclusion, we demonstrated that G. ulmifolia and S. adstringens inhibited BHV-1 and P-1 replication, as well as, blocked the synthesis of viral antigens in infected cell cultures.


Subject(s)
Antiviral Agents/pharmacology , Fabaceae/chemistry , Herpesvirus 1, Bovine/drug effects , Malvaceae/chemistry , Plant Extracts/pharmacology , Poliovirus/drug effects , Antigens, Viral/biosynthesis , Antiviral Agents/isolation & purification , Cell Line, Tumor , Chromatography, High Pressure Liquid , Cytopathogenic Effect, Viral , Dose-Response Relationship, Drug , Ethanol/chemistry , Herpesvirus 1, Bovine/physiology , Humans , Plant Bark/chemistry , Plant Extracts/isolation & purification , Poliovirus/physiology , Virus Replication/drug effects , Water/chemistry
18.
J Virol Methods ; 114(1): 29-35, 2003 Dec.
Article in English | MEDLINE | ID: mdl-14599676

ABSTRACT

Acridine orange is a metachromatic intercalator used extensively in histochemistry to differentiate double- from single-stranded (ds, ss) nucleic acid by the emission of green and red fluorescence, respectively, under ultraviolet light. In the present study we standardised a protocol in order to use acridine orange to detect rotavirus ds RNA in polyacrylamide gels and compared it to silver and ethidium bromide staining. We demonstrated that the simplest and best condition was attained when gels containing rotavirus ds RNA bands, stained in green, were treated with 4.3 microM acridine orange after electrophoresis and destained with distilled water pH 6 at 37 degrees C. Under this protocol, rotavirus RNA concentration was calculated and the mean minimum amounts of nucleic acid detected by acridine orange, ethidium bromide, and silver staining were 26.0 +/- 4.29, 15.6 +/- 1.48 and 1.06 +/- 0.11 ng, respectively. The comparison of acridine orange sensitivity with ethidium bromide and silver staining, for 25 field strains of rotavirus and one cell-adapted strain (SA11), demonstrated concurrent results in 80% of the specimens. Red colour emission resulting from the interaction of acridine orange with ss nucleic acid was also shown by testing denatured 0.5 kb HindIII digest of lambda phage DNA. Furthermore, it was demonstrated that rotavirus ds RNA could be used for reverse transcription activity, followed by PCR amplification, after acridine orange staining. In conclusion, although acridine orange is less sensitive than ethidium bromide and silver staining, its practicality, low cost, metachromatic properties, and its non-interference on RT-PCR should be considered. It is suggested the use of acridine orange as an appropriate stain for various purposes in virology, as well as for the molecular biology of nucleic acid.


Subject(s)
Acridine Orange , Electrophoresis, Polyacrylamide Gel/methods , RNA, Bacterial/analysis , Rotavirus/genetics , Staining and Labeling/methods , Animals , Cattle , Feces/virology , Humans , RNA, Double-Stranded/analysis , Rotavirus/isolation & purification , Rotavirus Infections/virology , Virology/methods
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