目的了解副伤寒沙门菌的耐药情况及耐药机制。
Objective To study the antibiotic resistance and its mechanism of salmonella paratyphoid.
目的探讨甲型副伤寒沙门菌的临床特点,以提高诊治水平。
Objective To investigate the clinical characteristic of Paratyphoid fever a infection, and enhance the diagnosis and treatment effects.
同时从现场采集的样品中,检出4株丙型副伤寒沙门菌、3株婴儿沙门菌。
Meanwhile from the scene gathering sample, picks out 4 third paratyphoid salmonella bacilli, 3 baby salmonella bacilli.
将甲型副伤寒沙门菌标准菌株按10- 1 ~ 10 -9稀释后扩增比较PCR的检测灵敏度。
The sensitivity of PCR assay was analyzed with 10 -1 ~10 -9 diluted.
本文综述了疫苗靶标蛋白的识别方法以及可能用于鉴别诊断或者疫苗有效靶标的潜在甲型副伤寒沙门菌抗原蛋白。
This paper summarizes the methods for identifying the vaccine targets and the list of potential s. paratyphi a antigens which could be used in differential diagnosis and as effective vaccine targets.
结果贵州省9个市(州、地)26个县(区)的113株伤寒沙门菌和518株甲型副伤寒沙门菌对10种抗生素进行药物敏感性测定。
Results 113 S. typhi strains and 518 S. paratyphi strains in 26 counties and 9 cities were tested for drug sensitivity to 10 kinds of antibiotics.
随着甲型副伤寒沙门菌atcc 9150全基因组序列的公布,利用基因组和蛋白质组学的方法为研究甲型副伤寒沙门菌的疫苗靶标提供了良好的基础。
Along with the release of ATCC9150 whole genome sequence of S. paratyphi a, the methods using genome and proteomics would be useful for the study of vaccine targets aimed at S. paratyphi a.
近年来,我国南方一些地区以及东南亚某些国家均有甲型副伤寒沙门氏菌流行的报道。
Recently, there has some reports about Salmonella paratyphi a prevalence in our country and some other countries in southeast Asia.
预防和治疗副伤寒沙门氏菌、大肠杆菌、霍乱、细菌性下痢及致病细菌混合感染引起的肠炎病有特效。
Prevention and treatment of paratyphoid salmonella, e. coli, cholera, bacterial diarrhea and bacterial pathogens of enteritis caused by mixed infections with special effects.
猪霍乱沙门氏菌是引起仔猪副伤寒的主要病原菌,给养猪业造成重大危害。
Salmonella choleraesuis(S. choleraesuis) is the main pathogen of piglet paratyphoid, causing severe harm to pig industry.
通过以上研究工作,初步确定了甲型副伤寒沙门氏菌的夹心ELISA检测程序并优化了反应条件。
Through the study above, the detection procedure of sandwich indrect ELISA was decided, and the reacting conditions were optimized.
通过以上研究工作,初步确定了甲型副伤寒沙门氏菌的夹心ELISA检测程序并优化了反应条件。
Through the study above, the detection procedure of sandwich indrect ELISA was decided, and the reacting conditions were optimized.
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