2016年4月—2022年3月深圳市和济南市流感病原学监测及流行特征

目的 分析在新型冠状病毒肺炎流行背景下,2016年4月—2022年3月国内深圳市和济南市流感流行特点,了解我国南北方地区流感流行差异。 方法 使用深圳市和济南市国家级哨点医院2016—2022监测年度流感样病例(ILI)和流感病原学监测资料,分析流感流行特征和趋势。 结果 2016—2022监测年度深圳市和济南市国家级哨点医院的门急诊病例中流感样病例百分比(ILI%)分别为2.25%、3.45%。两地区ILI%最高的年份均为2021—2022监测年度。ILl年龄构成均以0~4岁为主(分别占40%、46%)。按月分析两地区流感病毒分离阳性率与ILI%变化的相关性,两者趋势均存在正相关(r=0.238,P<0.05;r=0.425,P<0.001)。两地区不同监测年度流感优势毒株型别均不相同,呈交替变化,但每年流行的型别及高峰期的优势毒株型别基本一致。 结论 2020—2021监测年度即新型冠状病毒肺炎流行初期,深圳市和济南市流感活跃程度明显低于往年平均水平且流行毒株型别单一,其余监测年度基本符合我国南、北方地区流感流行特征。     

Incomplete effector/memory differentiation of antigen-primed CD8+ T cells in gene gun DNA-vaccinated mice

DNA vaccination is an efficient way to induce CD8+ T cell memory, but it is still unclear to what extent such memory responses afford protection in vivo. To study this, we induced CD8+ memory responses directed towards defined viral epitopes, using DNA vaccines encoding immunodominant MHC class I-restricted epitopes of lymphocytic choriomeningitis virus covalently linked to beta2-microglobulin. This vaccine construct primed for a stronger recall response than did a more conventional minigene construct. Despite this, vaccinated mice were only protected against systemic infection whereas protection against the consequences of peripheral challenge was limited. Phenotypic analysis revealed that DNA vaccine-primed CD8+ T cells in uninfected mice differed from virus-primed CD8+ T cells particularly regarding expression of very-late antigen (VLA)-4, an adhesion molecule important for targeting T cells to inflammatory sites. Thus, our DNA vaccine induces a long-lived memory CD8+ T cell population that provides efficient protection against high-dose systemic infection. However, viral replication in solid non-lymphoid organs is not curtailed sufficiently fast to prevent significant virus-induced inflammation. Our results suggest that this is due to qualitative limitations of the primed CD8+ T cells.     

广东省2005-2007年麻疹病原学监测

目的 开展有效的麻疹病原学监测,分离麻疹病毒,了解广东省2005-2007年流行的麻疹野病毒分离株基因特征,为控制、消除麻疹提供科学依据.方法 用Veto/Slam细胞从暴发和散发麻疹疑似病例的咽拭子和尿液标本中分离麻疹病毒,并对所有分离到的麻疹病毒通过逆转录-聚合酶链反应(RT-PCR)方法,扩增出核蛋白(N)基因碳末端450个核苷酸片段,对其产物测定基因序列以定型.结果 2005-2007年共收到380份标本,包括咽拭子或尿液标本.共分离到82株麻疹野病毒.2005年病毒分离率为23.58%,2006年病毒分离率为17.11%,2007年病毒分离率为39.13%.病毒分离成功率与病例出疹天数和标本的采集质量有密切关系.结论 我省已经掌握了麻疹病毒的分离和分子生物学鉴定技术,分离率较高;我省多年来流行的麻疹毒株均为H1基因型,与国内流行的优势基因型一致.     

Keratin immunohistochemistry in renal cell carcinoma subtypes and renal oncocytomas: a systematic analysis of 233 tumors

Keratin immunohistochemistry represents a widely applied differential diagnostic tool in surgical pathology. To investigate the value of keratin subtyping for the diagnosis among histological subtypes of renal cell carcinoma and oncocytomas, we performed a detailed immunohistochemical study, applying 22 different monoclonal keratin antibodies on a large series of 233 renal tumors [125 conventional, 22 chromophobe, and 20 papillary (12 type-1, 8 type-2 tumors) cancers and 66 oncocytomas] using a tissue microarray technique. Immunoreactivity for keratin 7, 8, 18, and 19 was present in all tumor entities, albeit in varying quantities. With antibodies directed against keratins 8 and 18, oncocytomas showed a distinct perinuclear and punctate dot-like pattern, which was not observed in renal cancer specimens. The only tumors showing immunoreactivity for keratin 20 were two type-2 papillary cancers. All other monospecific keratin antibodies yielded consistently negative results. Overall, in contrast to some recent publications, keratin subtyping generally appeared to be of additional value only for the differentiation of renal epithelial tumors. Hence, with respect to differential diagnostic value, Hales colloidal iron stain and vimentin immunostaining are still the most useful tools in renal tumor pathology.     

卵巢切除对大鼠子宫雌激素受体亚型表达的影响

目的 通过对去卵巢大鼠雌激素受体亚型在子宫表达的观察，研究卵巢切除对大鼠子宫影响的机制。方法 选择成年Wistar大鼠30只，10只为正常组，10只为假手术组，10只为模型组(去卵巢组)。6周后处死大鼠，分离摘取子宫，常规石蜡包埋、切片，分别进行ERα、ERβ抗体的免疫组织化学染色。结果 1．ERα在正常组、假手术组及模型组子宫的上皮细胞、间质细胞及肌细胞核均有表达，其中以腺上皮细胞表达最强。图像分析表明，模型组腺上皮ERα表达较其他2组弱。2．ERα在去卵巢子宫中未见明显表达，只在正常组和假手术组子宫腺上皮细胞核中表达，且较ERα表达弱。结论卵巢切除后明显影响大鼠子宫ERα、ERα的表达，尤其对ERα的影响较为显著。     

巢式PCR检测龈下菌斑中HCMV、EBV、HSV-1与慢性牙周炎活动性的关系

目的　建立临床检测龈下菌斑标本中人巨细胞病毒 (HCMV)、Epstein Barr病毒 (EBV)、单纯疱疹病毒 1型 (HSV 1 )巢式PCR方法 ,研究这 3种病毒与慢性牙周炎活动性的关系。方法　收集6 2例慢性牙周炎患者 (男性 2 7例、女性 35例 ,平均年龄 5 3岁 )的牙周炎活动部位、牙周炎静止部位的龈下菌斑 ,提取DNA后使用巢式PCR检测HCMV、EBV、HSV 1 ,比较分析其在同一病人不同部位的检出率。结果　牙周炎活动部位的HCMV检出率为 38.7%,EBV的检出率为 5 8%,HSV 1的检出率为30 .6 %,两种以上病毒合并感染的检出率为 4 0 .3%;牙周炎静止部位的HCMV检出率为 1 4 .5 %,EBV为 2 2 .6 %,HSV 1为 1 1 .3%,两种以上病毒合并感染的检出率为 1 1 .3%。这 3种病毒及其合并感染在牙周炎活动部位的检出率均高于牙周炎静止部位 ,差异有统计学意义 (P <0 .0 5 )。结论　提示HC MV、EBV、HSV 1与慢性牙周炎的活动性相关。     

Sequence of Echinochloa hoja blanca tenuivirus RNA-5

The sequence is presented of RNA-5 of Echinochloa hoja blanca tenuivirus, a second tenuivirus associated with rice cultivation in Latin America (after rice hoja blanca virus). The RNA is 1334 nucleotides long and contains in the complementary sense RNA a single long open reading frame. The deduced amino acid sequence of this open reading frame shows that it encodes a highly basic and hydrophilic 44 kD protein (pc5) with about 50% similarity to the pc5 protein of maize stripe virus (MStV). This and other features of the RNA are discussed.The GenBank accession number of the sequence reported in this paper is L47430.     

Influenza A virus-induced apoptosis is a multifactorial process: exploiting reverse genetics to elucidate the role of influenza A virus proteins in virus-induced apoptosis

Three influenza viruses, A/Puerto Rico/8/34-A/England/939/69 clone 7a (H3N2), A/Fiji/15899/83 (H1N1), and A/Victoria/3/75 (H3N2), induce different levels of apoptosis in vitro at equal moi; Clone 7a > A/Victoria > A/Fiji. Previous studies have shown that several viral proteins from clone 7a and A/Fiji, including PB2, NA, NS1, M1, and M2, induce apoptosis when expressed individually fused to the herpes simplex virus tegument protein, VP22. However, this did not reflect viral protein-protein-RNA interactions known to occur within infected cells. To explore the role of viral proteins in apoptosis under infection conditions, recombinant viruses with single or triple gene exchanges were generated using A/Victoria or clone 7a as the background virus. Inserting the A/Fiji NS or PB2 gene into A/Victoria or clone 7a significantly reduced the level of apoptosis compared to the parent virus while clone 7a PA or NP genes increased apoptosis. Inserting A/Fiji NA or HA or clone 7a NS, M, NA, or HA genes individually into A/Victoria had no significant effect on apoptosis. Surprisingly, inserting the M, NA, and HA genes of A/Fiji together into clone 7a reduced apoptosis, whereas inserting clone 7a M, NA, and HA together into A/Fiji increased apoptosis. These results suggest that no single virus protein induces apoptosis and that the combination of genes required may be strain specific, highlighting the difficulty of predicting the virulence of new strains that arise in nature. No support for the view that apoptosis is essential for high virus yields was obtained as high virus yields were obtained with viruses that induced both high and low levels of apoptosis.