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不同品系小鼠对炭疽芽胞杆菌弱毒株芽胞的敏感性研究
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作者 袁璐 陈楠 +5 位作者 王东澍 吕宇飞 郭艳 陈杰 刘先凯 王恒樑 《微生物学杂志》 CAS CSCD 2023年第3期30-38,共9页
通过比较四种品系小鼠对炭疽芽胞杆菌(Bacillus anthracis)(简称炭疽杆菌)弱毒株芽胞的敏感性,确定炭疽杆菌弱毒株芽胞攻毒合适的动物模型。采用炭疽杆菌弱毒株A16Q1(pXO1-、pXO2+)和A16PI2(pXO1+、pXO2-)的芽胞对四种品系小鼠(DBA/2、K... 通过比较四种品系小鼠对炭疽芽胞杆菌(Bacillus anthracis)(简称炭疽杆菌)弱毒株芽胞的敏感性,确定炭疽杆菌弱毒株芽胞攻毒合适的动物模型。采用炭疽杆菌弱毒株A16Q1(pXO1-、pXO2+)和A16PI2(pXO1+、pXO2-)的芽胞对四种品系小鼠(DBA/2、KM、ICR和BALB/c)进行腹腔攻毒,记录小鼠死亡时间,计算LD50、绘制存活曲线并统计分析。运用较敏感的KM小鼠研究不同canSNP基因型毒素缺陷株(含pXO2拷贝数不同)芽胞的毒力差异。利用更为敏感的DBA/2小鼠评价S-层蛋白BA3338对荚膜缺陷株芽胞毒力的影响。结果表明,在四种品系小鼠中,毒素缺陷株芽胞的毒力均高于荚膜缺陷株芽胞的毒力。DBA/2小鼠对炭疽杆菌弱毒株芽胞的剂量依赖关系最好,最为敏感,其次是KM小鼠,而ICR小鼠和BALB/c小鼠对炭疽杆菌弱毒株芽胞不敏感。确定了DBA/2小鼠和KM小鼠在炭疽杆菌弱毒株芽胞研究中的适用性。使用KM小鼠评价了不同canSNP基因型炭疽杆菌芽胞的毒力差异,结果表明,不同canSNP基因型炭疽杆菌由于所含pXO2质粒拷贝数的差异导致芽胞的毒力不同。使用DBA/2小鼠评价了S-层蛋白BA3338缺失对炭疽杆菌芽胞毒力的影响,表明BA3338基因的缺失导致炭疽杆菌芽胞毒力降低。 展开更多
关键词 炭疽芽胞杆菌 弱毒株 小鼠品系 cansnp基因型 S-层蛋白
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利用荧光定量PCR快速鉴定炭疽疫情和种群分型
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作者 石一 马琳 +7 位作者 张恩民 刘玮 贺莉 纪建军 魏建春 李伟 马国柱 刘东立 《职业与健康》 CAS 2017年第9期1189-1192,共4页
目的应用实时荧光定量PCR技术对2015年陕西炭疽疫情快速鉴定和种群分析。方法对甘泉县炭疽病例水泡液或病灶涂抹物及血液标本进行细菌分离,同时提取核酸进行荧光定量PCR试验。结果从1例病灶涂抹物中分离到1株炭疽芽胞杆菌。在19例病例... 目的应用实时荧光定量PCR技术对2015年陕西炭疽疫情快速鉴定和种群分析。方法对甘泉县炭疽病例水泡液或病灶涂抹物及血液标本进行细菌分离,同时提取核酸进行荧光定量PCR试验。结果从1例病灶涂抹物中分离到1株炭疽芽胞杆菌。在19例病例中检出16例核酸阳性,疫情相关菌株种群确定为A.Br.001/002群。结论炭疽杆菌实时荧光定量PCR可用于炭疽疫情迅速判定,确定病例菌株种群,可克服传统病原培养分离阳性率低,血清学诊断时间长的缺点。 展开更多
关键词 炭疽 实时荧光定量PCR 单核苷酸多态性 cansnp
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Genetic source tracking of an anthrax outbreak in Shaanxi province,China 被引量:1
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作者 Dong-Li Liu Jian-Chun Wei +21 位作者 Qiu-Lan Chen Xue-Jun Guo En-Min Zhang Li He Xu-Dong Liang Guo-Zhu Ma Ti-Cao Zhou Wen-Wu Yin Wei Liu Kai Liu Yi Shi Jian-Jun Ji Hui-Juan Zhang Lin Ma Fa-Xin Zhang Zhi-Kai Zhang Hang Zhou Hong-Jie Yu Biao Kan Jian-Guo Xu Feng Liu Wei Li 《Infectious Diseases of Poverty》 SCIE 2017年第1期110-117,共8页
Background:Anthrax is an acute zoonotic infectious disease caused by the bacterium known as Bacillus anthracis.From 26 July to 8 August 2015,an outbreak with 20 suspected cutaneous anthrax cases was reported in Ganqua... Background:Anthrax is an acute zoonotic infectious disease caused by the bacterium known as Bacillus anthracis.From 26 July to 8 August 2015,an outbreak with 20 suspected cutaneous anthrax cases was reported in Ganquan County,Shaanxi province in China.The genetic source tracking analysis of the anthrax outbreak was performed by molecular epidemiological methods in this study.Methods:Three molecular typing methods,namely canonical single nucleotide polymorphisms(canSNP),multiple-locus variable-number tandem repeat analysis(MLVA),and single nucleotide repeat(SNR)analysis,were used to investigate the possible source of transmission and identify the genetic relationship among the strains isolated from human cases and diseased animals during the outbreak.Results:Five strains isolated from diseased mules were clustered together with patients’isolates using canSNP typing and MLVA.The causative B.anthracis lineages in this outbreak belonged to the A.Br.001/002 canSNP subgroup and the MLVA15-31 genotype(the 31 genotype in MLVA15 scheme).Because nine isolates from another four provinces in China were clustered together with outbreak-related strains by the canSNP(A.Br.001/002 subgroup)and MLVA15 method(MLVA15-31 genotype),still another SNR analysis(CL10,CL12,CL33,and CL35)was used to source track the outbreak,and the results suggesting that these patients in the anthrax outbreak were probably infected by the same pathogen clone.Conclusions:It was deduced that the anthrax outbreak occurred in Shaanxi province,China in 2015 was a local occurrence. 展开更多
关键词 ANTHRAX OUTBREAK Bacillus anthracis Molecular typing cansnp MLVA SNR Shaanxi province China
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