RÉSUMÉ
Objective To analyze the variations and drug resistance of influenza A (H3N2) viruses in Jiangsu Province in 2017, and provide evidence for prevention and control strategies on influenza. Methods Reverse transcription polymerase chain reaction (RT-PCR) was used for the sequencing of H3N2 subtype influenza strains. The influenza reference sequences were obtained from the global shared influenza site GISAID. The sequence alignment and phylogenetic analysis were performed using MAGE7.0 software. Viral resistance was analyzed by a neuraminidase inhibition assay. Results The H3N2 subtype influenza isolates and vaccine strains belonged to the 3C.2a branch of the H3 subtype. Some of the strains showed amino acid mutations on the immune-related sites named N121K, T135K and N171K. The isolates were sensitive to the flu drugs oseltamivir and zanamivir. Conclusion The H3N2 epidemic strains in Jiangsu have genetic recombination within subtypes and are still sensitive to neuraminidase inhibitors. As the H3N2 influenza virus mutations continue, a close monitoring of the viral genetic evolution and the drug resistant genes should be guaranteed.
RÉSUMÉ
Objective To investigate the relation between the rs2070045 locus polymorphism in the SORL1 gene and the onset risk of AD by means of Metβ-analysis. Methods Databases (Medline, Cochrane Library and CBM) were searched using keywords like SORL1, sortilin-related receptor, Alzheimer and so on, and a manual search of citations was also performed from relevant original studies and literatures. All analyses were conducted with Review Manager Version4.2 software. Results 3 literatures with 11 different ethnic groups were studied, totally including the AD group (2927 cases) and the control (3867 cases). The summary OR for studies with frequency of GG+GT genotype at rs2070045 locus in the SORLI gene was 1.19 (95%CI: 1.08-1.31, Z=3.39, P=0.0007), when it compared with the common homozygote ofTT genotype. The summary OR for allele frequency was 1.17 (95%CI: 1.07-1.27, Z=3.67, P=0.0002). Conclusion The metβ-analysis suggests that the polymorphism at rs2070045 locus of SORL1 gene might be a genetic risky factor for AD.