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1.
Braz J Microbiol ; 55(3): 2767-2782, 2024 Sep.
Article in English | MEDLINE | ID: mdl-39012425

ABSTRACT

Norovirus is an important etiologic agent of acute gastroenteritis and has become even more relevant in Brazil after the implementation of the monovalent rotavirus vaccine in 2006 through the public health system, now representing a significant portion of the etiology of acute diarrheal diseases. Although diagnosing acute gastroenteritis caused by norovirus is a relatively simple process, and the infection tends to be self-limited, the virus can be considerably harmful to vulnerable populations, such as children, the elderly, and immunocompromised individuals. The spread of norovirus is also particularly favorable among such groups due to its mode of transmission, favored by cluttered environments such as in hospitals and densely populated regions. Additionally, norovirus' ability to spread through water and food creates the need for measures to ensure adequate sanitation and the development of effective measures to prevent outbreaks and severe manifestations of the disease. This review aims to address the main reports of human norovirus detected in Brazil over the years, focusing on clinical-hospital, food-related, and urban conglomerate contexts, including the circulating strains.


Subject(s)
Caliciviridae Infections , Gastroenteritis , Norovirus , Norovirus/genetics , Norovirus/isolation & purification , Norovirus/classification , Brazil/epidemiology , Humans , Caliciviridae Infections/epidemiology , Caliciviridae Infections/virology , Gastroenteritis/virology , Gastroenteritis/epidemiology , Disease Outbreaks
2.
Mem. Inst. Oswaldo Cruz ; 114: e180574, 2019. tab, graf
Article in English | LILACS | ID: biblio-1040626

ABSTRACT

Human sapoviruses (HSaV) are considered important causative agents of acute gastroenteritis in humans worldwide. However, knowledge of the genetic characteristics of the whole genome of HSaV in Brazil is limited. Here we report the complete genome sequences of six HSaVs GI.2 and two GI.3 strains obtained from children with acute gastroenteritis in the Northern region of Brazil. Next generation sequencing was used to obtain the full genome and molecular characterization of the genome was performed. Phylogenetic analysis of the genome was also performed. Only one complete HSaV GI.2 genome characterization in the country precedes that of the present study. This is the first complete genome sequence of genotype GI.3 in Brazil. The data obtained in this investigation can contribute to the augmentation of the database on the molecular diversity of HSaVs strains circulating in Brazil, and to the improvement of current typing protocols.


Subject(s)
Humans , Child , Caliciviridae Infections/virology , Sapovirus/genetics , Gastroenteritis/virology , Phylogeny , Brazil , Acute Disease , Sequence Analysis, DNA , High-Throughput Nucleotide Sequencing , Genotype
3.
J Virol Methods ; 258: 49-53, 2018 08.
Article in English | MEDLINE | ID: mdl-29800592

ABSTRACT

Human norovirus (HuNoV) is one of the main causes of acute gastroenteritis worldwide and is responsible for at least 20% of all cases. The detailed molecular mechanism of this norovirus remains unknown due to the lack of a suitable in vitro culturing system. An infectious clone of HuNoV would be a useful tool for elucidating the processes of viral infection and the mechanisms of replication. We developed an infectious cDNA clone of HuNoV using the rapid technique of Gibson Assembly. The complete genome of the HuNoV GII.4 Sydney subtype was cloned into a previously modified pcDNA3.1-based plasmid vector downstream from a cytomegaloviral promoter. We monitored the viral infection in vitro by inserting the reporter gene of the green fluorescent protein (GFP) between the NTPase and p22 genes, also by Gibson Assembly, to construct a HuNoV-GFP replicon. Human Caco-2 cells were transfected with the full-length genomic clone and the replicon containing GFP. The gene encoding the VP1/VP2 capsid protein was expressed, which was indirect evidence of the synthesis of subgenomic RNAs and thus the negative strand of the genome. We successfully constructed the infectious clone and its replicon containing GFP for the HuNoV GII.4 Sydney subtype, a valuable tool that will help the study of noroviral infection and replication.


Subject(s)
Norovirus/growth & development , Norovirus/genetics , Replicon , Caco-2 Cells , Cytomegalovirus/genetics , Gene Expression , Genes, Reporter , Genetic Vectors , Green Fluorescent Proteins/analysis , Green Fluorescent Proteins/genetics , Humans , Plasmids , Promoter Regions, Genetic , Reverse Genetics , Staining and Labeling , Transfection
4.
Epidemiol Infect ; 144(9): 1876-8, 2016 07.
Article in English | MEDLINE | ID: mdl-26796080

ABSTRACT

Nebovirus is a new genus of viruses belonging to the Caliciviridae family recently characterized in cattle, and is associated with gastrointestinal disorders, such as diarrhoea, anorexia and intestinal lesions particularly in calves. The aim of this study was to investigate the prevalence of neboviruses in Brazilian cattle and analyse phylogenetically the virus strains detected. A prevalence of 4·8% of neboviruses in faecal samples from 62 head of cattle from different Brazilian states was detected. All positive animals were aged 96·0% nt (100% aa) sequence identity between the virus sequences in this study and >88·8% nt (>94·4% aa) identity with Newbury1/UK. Our results indicate, for the first time, the occurrence of neboviruses in Brazil as well as in South America, and the first Newbury1-like nebovirus found outside the UK.


Subject(s)
Caliciviridae Infections/veterinary , Caliciviridae/classification , Caliciviridae/isolation & purification , Cattle Diseases/epidemiology , Cattle Diseases/virology , Genotype , Animals , Brazil/epidemiology , Caliciviridae/genetics , Caliciviridae Infections/epidemiology , Caliciviridae Infections/virology , Cattle , Cluster Analysis , Diarrhea/epidemiology , Diarrhea/veterinary , Diarrhea/virology , Feces/virology , Female , Gastroenteritis/epidemiology , Gastroenteritis/veterinary , Gastroenteritis/virology , Humans , Male , Phylogeny , Prevalence , Sequence Homology, Nucleic Acid
5.
Rev. Soc. Bras. Med. Trop ; Rev. Soc. Bras. Med. Trop;43(3): 277-280, May-June 2010. graf
Article in Portuguese | LILACS | ID: lil-548523

ABSTRACT

INTRODUÇÃO: O norovírus foi recentemente identificado como o principal causador de surtos de gastroenterite aguda de origem não bacteriana em todo o mundo e está envolvido em episódios de origem alimentar. Neste estudo, foram avaliados pacientes com sintomas de gastroenterite aguda pelo período de um ano, a fim de se avaliar duas metodologias na identificação do NoV - a reação em cadeia por polimerase convencional e em tempo real -, incidência, sazonalidade e genótipo predominante. MÉTODOS: Após a extração do RNA, 50 amostras foram analisadas pela metodologia de PCR convencional e 365 amostras foram analisadas pela metodologia de PCR em tempo real. Todas as amostras que apresentaram resultado positivo pelas duas metodologias ou discordante foram sequenciadas, ao todo, 13 amostras foram sequenciadas. RESULTADOS: Das 50 amostras testadas pelas duas metodologias, 7 apresentaram resultado positivo pelo método convencional e 15 pelo método da PCR em tempo real. Do total de 365 amostras testadas pela metodologia de PCR, em tempo real, 48 foram positivas. Em relação às amostras sequenciadas, todas mostraram ser NoV do genogrupo II. Em relação à distribuição da incidência de amostras, positivas para NoV, ao longo do ano, pôde ser observada uma frequência de casos positivos maior na primavera, chegando a 29,7 por cento em novembro. CONCLUSÕES: Observamos que o PCR em tempo real é o método mais sensível para a identificação do Nov, que a incidência do NoV é de 13,2 por cento e o genogrupo II prevalece na população avaliada, sendo a primavera o período de maior taxa de infecção.


INTRODUCTION: Norovírus was recently identified as the main cause of outbreaks of acute gastroenteritis of non-bacterial origin worldwide and it is involved in episodes of foodborne origin. In this study, patients with symptoms of acute gastroenteritis were evaluated over a one-year period, in order to evaluate two methods for identifying norovírus (real-time and conventional polymerase chain reaction), along with its incidence, seasonality and predominant genotype. METHODS: After RNA extraction, 50 samples were analyzed using conventional PCR and 365 were analyzed using real-time PCR. All the samples that presented positive results using both methods or discordant results were sequenced. In all, 13 samples were sequenced. RESULTS: Out of the 50 samples tested using both methods, seven presented a positive result from the conventional method and 15 from real-time PCR. Out of the total of 365 samples tested using real-time PCR, 48 were positive. All of the sequenced samples were shown to present norovírus of genogroup II. Regarding the distribution of norovírus-positive sample incidence over the course of the year, higher frequency of positive cases was observed during the southern hemisphere spring, reaching 29.7 percent in November. CONCLUSIONS: We observed that real-time PCR was more sensitive for identifying norovírus. The incidence of norovírus was 13.2 percent and genogroup II predominated among the population evaluated, with the greatest infection rate in the southern hemisphere spring.


Subject(s)
Humans , Feces/virology , Gastroenteritis/virology , Norovirus/genetics , RNA, Viral/analysis , Acute Disease , Brazil/epidemiology , Genotype , Incidence , Norovirus/isolation & purification , Polymerase Chain Reaction/methods , Seasons
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