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1.
Chinese Journal of Preventive Medicine ; (12): 40-43, 2013.
Article in Chinese | WPRIM | ID: wpr-274765

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the molecular epidemiological characteristics of norovirus in Guangzhou from 2009 to 2011.</p><p><b>METHODS</b>A total of 183 water samples, 1162 seafood samples and 1066 diarrhea stool specimens were collected from January 2010 to May 2011, June 2009 to June 2011 and July 2009 to December 2010 respectively in Guangzhou. Norovirus was detected by real time reverse transcript-PCR (qRT-PCR). The partial polymerase gene was amplified from norovirus positive samples, then sequenced and compared with the sequences of norovirus in GenBank. The phylogenetic tree was created.</p><p><b>RESULTS</b>The positive rate was 19.67% (36/183), 8.26% (96/1162) and 37.05% (395/1066) in water samples, seafood and diarrhea patients respectively. Noroviruses from positive samples could be divided into 10 representative strains, in which 7 representative strains of genotype of 208 samples was type G2-4. The sequences from water, seafood and stool specimens were highly homologous with the similarity of 94% - 100%.</p><p><b>CONCLUSION</b>In Guangzhou, the predominant Norovirus genotype was G2-4 and the positive rate of samples was high.</p>


Subject(s)
Humans , Base Sequence , Caliciviridae Infections , Epidemiology , Virology , China , Epidemiology , Diarrhea , Virology , Genotype , Molecular Epidemiology , Norovirus , Classification , Genetics , Phylogeny , RNA, Viral , Genetics , Seafood , Virology , Water Microbiology
2.
Chinese Journal of Virology ; (6): 373-378, 2010.
Article in Chinese | WPRIM | ID: wpr-286109

ABSTRACT

To investigate the inhibitory effect of RNA interference (RNAi) on dengue virus I (DENV-1) replication. Small interfering RNA (siRNA) against the PreM gene of dengue virus was synthesized and transfected into C6/36 cells with liposome, which was then attacked by DENV-1 virus. The antiviral effect of siRNA was evaluated by cytopathic effect (CPE), the cell survival rate measured by MTT, and virus RNA quantified by real-time RT-PCR. The results showed that after 7 days post infection of dengue virus, the transfected C6/36 cells showed less CPE. The cell survival rate of the transfected C6/36 cells increased by 2.26 fold, and the amount of virus RNA in the transfected cells was reduced by about 97.54% as well. These findings indicated that the siRNA could effectively inhibit dengue virus RNA replication, and protect C6/36 cells from viral attack, indicating its potential role in prevention and treatment of dengue fever.


Subject(s)
Animals , Cell Line , Dengue Virus , Genetics , Physiology , RNA Interference , Physiology , RNA, Small Interfering , Genetics , RNA, Viral , Genetics , Reverse Transcriptase Polymerase Chain Reaction , Virus Replication , Genetics , Physiology
3.
Journal of Southern Medical University ; (12): 2313-2315, 2009.
Article in Chinese | WPRIM | ID: wpr-325121

ABSTRACT

<p><b>OBJECTIVE</b>To study the relation of the detection rates of the novel influenza virus A/H1N1 RNA in clinically confirmed patients in the 2009 pandemic with the age distribution of the patients and the disease course.</p><p><b>METHODS</b>A total of 151 clinical patients with H1N1 infection were enrolled in this study, from whom 833 dynamic throat swab samples were obtained for detecting the H1N1 RNA using real-time PCR. A statistical analysis of the age distribution was performed among the patients with different disease courses. Chi-square for trend test was used to study the correlation between the detection rates of H1N1 RNA and the time of disease onset.</p><p><b>RESULTS</b>The majority of patients were young with their ages ranging from 10 to 20 years (57.26%) and 20 to 30 years (22.18%). Chi-square for trend test revealed that the positivity rates of the throat swabs in the patients decreased with the prolongation of the disease course (chi(2)=9.784, P=0.002).</p><p><b>CONCLUSION</b>Most of the H1N1 patients are young within the age range of 10-30 years, and the longest disease course can exceed 10 days. The positivity rates of throat swabs from the H1N1 patients decreases with the prolongation of the disease course.</p>


Subject(s)
Adolescent , Adult , Child , Female , Humans , Male , Young Adult , Age Factors , China , Epidemiology , Influenza A Virus, H1N1 Subtype , Genetics , Influenza, Human , Epidemiology , Virology , Pharynx , Virology , RNA, Viral , Reverse Transcriptase Polymerase Chain Reaction
4.
Chinese Journal of Preventive Medicine ; (12): 852-855, 2009.
Article in Chinese | WPRIM | ID: wpr-316104

ABSTRACT

<p><b>OBJECTIVE</b>To timely summarize past experience and to provide more pertinent reference for control and prevention in A/H1N1 cases in influenza season.</p><p><b>METHODS</b>During May 25 to 31, 2009, 2 secondary community cases caused by a influenza A/H1N1 imported case. In the close contacts of 3 A/H1N1 cases, 14 had some aspirator symptoms onset, such as fever (> or = 37.5 degrees C), cough, sore throat and etc. Laboratory tests excluded the infection of A/H1N1 influenza. For throat swab test for the 14 cases, 7 were tested for seasonal influenza virus. A face-to-face or telephone interview was conducted by CDC staff to collect information of 62 close contacts.</p><p><b>RESULTS</b>Of 14 fever cases, there was no significant by differences by age[15-age group: 19.2% (5/26), over 25-age group: 25.0% (9/36); chi(2) = 0.287, P = 0.592]; by sex group [24.0% (6/25) for male and 21.6% (8/37) for female; chi(2) = 0.048, P = 0.826], by working units [dressing and design, photograph, saleroom and others, consumer group: 42.1% (8/19), 27.3% (3/11), 12.5% (2/16) and 6.3% (1/16); chi(2) = 7.653, P = 0.054], by dormitory style [dormitory style = 33.3% (4/12), non-dormitory style = 29.4% (10/34); chi(2) = 0.699, P = 0.403]. All the cases had fever (37.5 - 37.9 degrees C), no case had diarrhea. One in 3 A/H1N1 cases had diarrhea. All the 14 cases were negative result for A/H1N1 RNA. Six from 7 cases were positive for seasonal influenza test.</p><p><b>CONCLUSION</b>This was a seasonal influenza outbreak happened in the close contacts of first confirmed A/H1N1 cases in community in mainland China. It showed that we should exclude the seasonal influenza in the investigation of A/H1N1 cases in the seasonal influenza period in some time. It is necessary to take effective measure to strengthen the control and prevention of seasonal influenza.</p>


Subject(s)
Adolescent , Adult , Female , Humans , Male , Middle Aged , Young Adult , China , Epidemiology , Community-Acquired Infections , Epidemiology , Disease Outbreaks , Influenza A Virus, H1N1 Subtype , Influenza, Human , Epidemiology
5.
Chinese Journal of Preventive Medicine ; (12): 41-44, 2009.
Article in Chinese | WPRIM | ID: wpr-242687

ABSTRACT

<p><b>OBJECTIVE</b>To evaluate the risk of human infection after the outbreak of avian influenza H5N1 in animals, and probe the possibility for virus transmission.</p><p><b>METHODS</b>By means of field epidemiological study, molecular epidemiology, serology and emergency surveillance, persons who had ever closely contacted with sick or dead poultry were observed. While, the RT-PCR and gene sequencing method were used to detect H5 nucleic acid from environmental swabs from 4 epidemic spots, and hemagglutination inhibition assay was also used to detect H5 antibody.</p><p><b>RESULTS</b>Of 22 environmental swabs detected from 4 epidemic spots, one was positive for H5 nucleic acid, and the homogeneity was 95.9% as compared with H5N1 virus A/China/GD01/2006 (H5N1) found in Guangzhou in 2006 by gene sequence analysis. 62 environmental swabs from live poultry stalls of food markets near epidemic spot were detected negative. Six of 68 blood samples of contacts were positive for H9 antibody, and all were negative for H5 antibody. 68 throat swabs of contacts were detected negative for H5 nucleic acid. No close contact was found abnormal after 7 days medical observation. 337 influenza-like cases were reported in emergency surveillance, and no suspicious case was found.</p><p><b>CONCLUSION</b>The current outbreak of H5N1 avian influenza in water fowls has not yet caused further transmission, and human avian influenza case has not been observed. It indicates that the ability of H5N1 virus to transmit to human is not strong yet, and the risk of human infection for H5N1 is still low.</p>


Subject(s)
Animals , Humans , Antibodies, Viral , Blood , China , Epidemiology , Disease Outbreaks , Ducks , Influenza A Virus, H5N1 Subtype , Genetics , Virulence , Influenza in Birds , Epidemiology , Influenza, Human , Epidemiology , Risk Assessment
6.
Chinese Journal of Virology ; (6): 356-359, 2007.
Article in Chinese | WPRIM | ID: wpr-334883

ABSTRACT

To understand the genetic characteristics of hemagglutinin (HA) and neuraminidase (NA) of type B influenza viruses in Guangzhou in 2006, three virus strains from etiology surveillance and seven strains from outbreaks were investigated. Genome RNAs of type B influenza viruses were extracted and reverse-transcripted into cDNAs using random primers. The whole-length DNA of HA and NA were amplified by polymerase chain reaction (PCR), cloned into T-A plasmid and sequenced, and analyzed phylogenetically by DNAstar software. The results showed that the HA of type B influenza viruses were similar and the homology were more than 99%. The type B influenza viruses belong to Victoria lineage. The NA of the type B influenza viruses were similar and the homology were more than 98%. Phylogenetic trees of HA and NA showed that the isolates from etiology surveillance formed a cluster, and the isolates from outbreaks were separated from the cluster. The homology of the type B influenza viruses with B/Shanghai/361/2002, which is the WHO recommended influenza vaccine strain in 2005-2006, were 88.9%-89.7%. It suggested the protective effect of influenza vaccine against type B influenza viruses used in 2005-2006 in Guangzhou may not be afforded.


Subject(s)
China , Hemagglutinin Glycoproteins, Influenza Virus , Genetics , Influenza B virus , Genetics , Neuraminidase , Genetics , Phylogeny , Time Factors
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