High level expression of recombinant mumps nucleoprotein in Saccharomyces cerevisiae and its evaluation in mumps IgM serology.

To develop improved reagents for mumps serology a high-level yeast expression system was employed to produce recombinant mumps nucleoprotein (rNP). The rNP was purified by CsCl gradient centrifugation and yielded approximately 15 mg/l of yeast culture. Electron microscopy of the rNP revealed characteristic herring-bone structures. The electrophoretic mobility of rNP in yeast cells was similar to native NP in SDS-PAGE. Monoclonal antibodies to rNP reacted with native mumps virus nucleoprotein by immunofluorescence assay. A monoclonal antibody to native mumps virus NP reacted with rNP by Western blot assay. The rNP was investigated as antigen in an IgM capture enzyme immunoassay (EIA) using a horseradish peroxidase conjugate of monoclonal antibody to the rNP. Eighteen sera previously found to be positive by IgM capture radioimmunoassay (MACRIA) and 30 sera that were mumps IgM negative by MACRIA were tested by mumps IgM capture EIA. The results for the two test were concordant. In addition, 26 rheumatoid factor positive sera and 35 sera that were IgM positive for measles, rubella or parvovirus B19 were tested. Fifty-nine sera were negative by mumps IgM capture EIA but two sera collected from two infants 3 and 6 weeks after mumps, measles and rubella vaccination were positive. Mumps MACRIA confirmed these results. Compared to MACRIA the overall sensitivity was 100% (20/20) and specificity was 96.8% (30/31). The yeast expressed rNP was highly immunogenic and suitable for use in IgM capture EIA for the diagnosis of mumps.     

Changes in agent variability and time course of disease incidence during a year (as exemplified by dysentery)

The vulnerability of epidemic process during the period of minimum annual incidence of the disease is validated. Biological properties of Shigella sonnei are studied and their variability examined using the index for evaluation of the mean number of variations for a sign. Minimum agent heterogeneity coincides with minimum incidence of disease and maximum heterogeneity with its seasonal rises.     

Nucleotide sequence of the gene encoding the matrix protein of mumps virus (Miyahara strain)

The nucleotide sequence of the gene encoding the matrix (M) protein of mumps virus (MuV), Miyahara strain, has been determined from several overlapping cDNA clones. The M protein mRNA is 1248 nucleotides in length, exclusive of the poly(A) tail, and codes for a protein of 375 amino acids (Mr41,556). Comparison of the deduced amino acid sequence of the M protein of the Miyahara strain with that of the SBL-1 strain revealed that the M proteins of both strains are highly conserved. A significantly lower rate of nucleotide differences conducive to amino acid differences in the M gene compared with other genes appeared to indicate the importance of the conserved primary structure of the M protein for its function.Requests for reprints should be addressed to Kiyoshi Tanabayashi, Department of Measles Virus, National Institute of Health, 4-7-1 Gakuen, Musashimurayama, Tokyo 190-12, Japan.     

Identification of the membrane protein of porcine epidemic diarrhea virus

Sequence information on the genome of porcine epidemic diarrhea virus (PEDV) has only recently been determined. In contrast, very little is known about the viral proteins. In the present report we have identified the membrane glycoprotein (M) of PEDV by use of rabbit anti-peptide sera and transient expression of the cloned M gene in Vero cells and by expression in the baculovirus system. The native M protein of PEDV is incorporated into virions, is N-glycosylated, and migrates with a relative mobility (Mr) of 27 k in polyacrylamide gels. In contrast, the M protein synthesized by recombinant baculoviruses migrates with a Mr of 23 k, that is, with identical mobility as the deglycosylated product of PEDV. Thus, it appears that M protein specified by the recombinant baculovirus is poorly, if at all, glycosylated. Using monoclonal antibodies and rabbit antipeptide sera specific for the N and C termini of the M protein, we were able to show that a 19 k band detected in PEDV-infected cells but not in virions represented a fragment of M from which the C terminus had been cleaved off. Finally, by electron microscopy and immunogold labelling, the relative orientation of M within the virion envelope was determined as NexoCcyt. In conclusion, all of these data strongly support the hypothesis that PEDV should be classified with the group I coronaviruses.     

Mumps vaccine failure investigation in Novosibirsk, Russia, 2002–2004

The aims of this study were to estimate the importance of vaccine failure (VF) in cases of mumps during 2002-2004 in the city of Novosibirsk, Western Siberia, Russia, and to genotype the responsible virus strain. Mumps virus-specific RT-PCR testing of saliva was performed for 18 cases of mumps. Sera were tested for IgM and IgG, IgG avidity, and the ability to neutralise a panel of mumps viruses, including the Leningrad-3 mumps vaccine virus. Of the 12 patients for whom vaccination status was positively determined, 11 showed serological evidence of primary VF. Sequence analysis of virus RNA amplified from saliva revealed a genotype C2 virus in 2002, a genotype H2 virus in 2003, and both genotypes in 2004. Although several vaccinated patients were positive for mumps virus IgG at the time of first sampling, only nominal levels of neutralising antibody were detected, and these were effective in neutralising the vaccine strain, but not genotype C and H mumps virus strains. These results suggest that the majority of cases of mumps in vaccinees are caused by primary VF, defined as either a lack of seroconversion or a lack of IgG maturity, as based on avidity testing. The results also support the hypothesis that sera of low neutralising antibody titre have a limited ability to neutralise heterologous mumps virus strains, suggesting that antigenic differences between circulating and mumps vaccine virus strains may play a role in cases of breakthrough infection. Consistent with previous reports, mumps virus genotypes C and H continue to circulate in Novosibirsk.     

HIV-1 CRF55_01B毒株流行特征的研究进展

CRF55_01B是我国报道的HIV-1主要流行毒株之一,具有较为独特的流行病学和基因进化特征。近几年HIV-1分子流行病学监测发现CRF55_01B已经成为我国第五个主要流行HIV-1毒株。本研究从他的发现起源、流行情况、致病性和耐药性及参与的重组等方面进行综述,并讨论了与其流行密切相关的社会和生物学因素。     

流行性脑脊髓膜炎的流行趋势变化与其疫苗接种

在过去几十年,随着疫苗的广泛使用,不同国家和区域引起流行性脑脊髓膜炎(简称流脑)病原体的血清群也发生了变迁。本文将脑膜炎球菌疫苗免疫接种、感染人群、不同区域和国家流脑的流行趋势及其内在机制研究进展进行综述,为进一步了解流脑流行趋势变化与其疫苗接种和后续制定免疫策略提供参考。     

2005-2019年理塘县法定传染病疫情分析

目的了解理塘县近15年法定传染病疫情形势及流行特征,为政府制定防控措施提供科学依据。方法对2005—2019年理塘县法定传染病疫情进行描述性流行病学分析。采用ArcGIS 10.3软件绘制各乡镇发病情况分布图,SPSS 21.0软件进行χ²检验、趋势性χ²检验。结果2005—2019年理塘县共计报告甲乙丙类传染病21种6154例,年均发病率为644.33/10万,发病呈上升趋势。死亡37例,年均死亡率3.87/10万,病死率0.60%。呼吸道传染病发病最高(341.12/10万);发病前3位的病种为肺结核(271.91/10万)、乙肝(103.24/10万)及包虫病(67.22/10万);肺结核、其他感染性腹泻病、艾滋病/HIV、梅毒发病呈上升趋势。3月、9月分别出现1次发病高峰;20~29岁、30~39岁和10~19岁组发病居前3位;男女性别比为1.24∶1;发病以农民、牧民及学生为主。结论2005-2019年理塘县法定传染病发病率较高且呈上升趋势,应针对高发传染病、上升趋势明显的传染病、重点人群进行分析研究,采取针对性措施控制疫情。     

2018—2020年珠海市学校流感样病例暴发疫情流行特征及影响因素分析

目的 分析珠海市2018—2020年学校流感样病例暴发疫情的流行特征和影响疫情规模的相关因素,为制定防控策略提供依据。方法 采用描述流行病学方法分析学校流感样病例暴发疫情流行特征,采用χ2检验和Logistic回归分析疫情规模的影响因素。结果 2018—2020年珠海市学校累计报告67起流感样病例暴发疫情,累计发病人数1 746例。发病高峰为每年3月—6月和12月—次年1月,主要发生在小学,流感样病例的发病年龄高峰为6～8岁。病原体主要为B型、A(H3N2)亚型和A(H1N1)亚型流感病毒。暴发疫情涉及病例咽痛发生率>50%的学校发生大规模流感样病例暴发疫情的风险是咽痛发生率≤50%学校的4.308倍(95%CI:1.100～16.864)。结论 2018—2020年珠海市学校流感样病例暴发疫情主要集中在冬春季节的小学,高咽痛发生率是学校发生大规模疫情流感样病例暴发疫情的危险因素。     

588名本科护生职业认同及影响因素研究

目的 了解新冠疫情下本科护生职业认同现状及其影响因素。方法 采用一般情况调查表、职业认同量表、护生专业承诺量表对安徽某院校的588名本科护生进行调查。结果 职业认同总分为(58.17±11.27);护生专业承诺总分为(86.55±20.01);职业认同与专业承诺呈显著正相关(r=0.790,P<0.05);专业承诺总分、“有无您崇拜的护理前辈或老师”、“如果有机会,您是否会调换专业”两条目得分对职业认同有影响。结论 新冠疫情下本科护生职业认同处于中等水平且受多种因素影响。