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1.
Intervirology ; 61(1): 49-52, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-30021210

RESUMO

OBJECTIVE: Human Salivirus (SalV) has been associated with gastroenteritis on all continents. METHODS: This paper presents the real-time RT-PCR assay for the detection of SalV in clinical fecal samples collected from 192 hospitalized children with acute gastroenteritis in Piedmont, Italy. RESULTS: The most commonly detected virus was Norovirus genogroup II (GII) (33.8%), followed by Rotavirus (21.3%), Sapovirus (10.9%), Parechovirus (8%), Norovirus GI (6.7%), and Adenovirus (1%). PCR detected SalV in 1 (0.5%) subject. CONCLUSIONS: Our data show that the detection rate of SalV in diarrheal children (0.5%) is lower than that observed in other countries, where it is reported in diarrheal children in 8.6-1.2% of patients.


Assuntos
Diarreia/epidemiologia , Gastroenterite/epidemiologia , Infecções por Picornaviridae/epidemiologia , Picornaviridae/isolamento & purificação , Doença Aguda/epidemiologia , Criança , Criança Hospitalizada , Pré-Escolar , Diarreia/virologia , Fezes/virologia , Feminino , Gastroenterite/virologia , Humanos , Lactente , Itália/epidemiologia , Masculino , Picornaviridae/genética , Infecções por Picornaviridae/virologia , Prevalência
2.
Minerva Pediatr (Torino) ; 74(4): 412-415, 2022 08.
Artigo em Inglês | MEDLINE | ID: mdl-29968445

RESUMO

BACKGROUND: Human Parechovirus (HPeVs), along with human enteroviruses is associated with gastrointestinal and respiratory infections. The aim of this study was to assess the performance characteristics of two nucleic acid extraction for HPeV-RNA quantitation, the RNAlev Extraction Kit associated with Maxwell automated nucleic acid extractor (Promega, Milan, Italy) and RNAzol manually protocol. METHODS: A total of 137 fecal specimens previously routinely screened for Rotavirus and Adenovirus were tested for HPeV virus. RESULTS: Methods 1 and 2 detected HPeV-RNA in 11 and 10 samples, respectively, with a 96.2% concordance. In particular, 124/137 (90.5%) were concordantly negative by both methods; 8/137 (5.8%) concordantly positive. For the 8 specimens that were positive by both tests, the population mean (SD) was 320 (601) copies/mg with method 1 and 1216 (2338) copies/mg with method 2. By referring to the 8 specimens that were concordantly positive, the correlation value between the two methods was not statistically significant (r=0.381 and P=0.3599). Bland-Altman analysis showed that differences between the two methods were within ±1000 copies/mg of the averaged results for all of the tested specimens. CONCLUSIONS: Method 2, being a semi-automated method, provides benefits over a manual method, in terms of turnaround time, less errors and reliability.


Assuntos
Enterovirus , Parechovirus , Infecções por Picornaviridae , Criança , Enterovirus/genética , Humanos , Parechovirus/genética , Infecções por Picornaviridae/diagnóstico , Infecções por Picornaviridae/epidemiologia , RNA Viral/genética , Reprodutibilidade dos Testes
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