薛成玉, 遇晓杰, 张剑峰, 朱丹丹, 李鑫, 白晶, 朱玉良. 液相悬浮芯片技术在黑龙江省沙门菌血清分型中的应用[J]. 疾病监测, 2019, 34(4): 303-306. DOI: 10.3784/j.issn.1003-9961.2019.04.006
引用本文: 薛成玉, 遇晓杰, 张剑峰, 朱丹丹, 李鑫, 白晶, 朱玉良. 液相悬浮芯片技术在黑龙江省沙门菌血清分型中的应用[J]. 疾病监测, 2019, 34(4): 303-306. DOI: 10.3784/j.issn.1003-9961.2019.04.006
Chengyu Xue, Xiaojie Yu, Jianfeng Zhang, Dandan Zhu, Xin Li, Jing Bai, Yuliang Zhu. Application of liquid suspension chip technique in Salmonella serotyping[J]. Disease Surveillance, 2019, 34(4): 303-306. DOI: 10.3784/j.issn.1003-9961.2019.04.006
Citation: Chengyu Xue, Xiaojie Yu, Jianfeng Zhang, Dandan Zhu, Xin Li, Jing Bai, Yuliang Zhu. Application of liquid suspension chip technique in Salmonella serotyping[J]. Disease Surveillance, 2019, 34(4): 303-306. DOI: 10.3784/j.issn.1003-9961.2019.04.006

液相悬浮芯片技术在黑龙江省沙门菌血清分型中的应用

Application of liquid suspension chip technique in Salmonella serotyping

  • 摘要:
    目的探索液相悬浮芯片技术对黑龙江省食品风险监测的沙门菌分离株的血清分型效果及适用性。
    方法采用玻片凝集试验对分离的451株沙门菌进行分型,采用液相悬浮芯片技术——沙门菌血清型快速分型试剂盒(SSA)对其中256株沙门菌O抗原、H抗原、AT抗原基因进行分型鉴定。
    结果249株分离株可以用SSA完整分型;液相悬浮芯片技术与传统方法血清分型的符合率超过96%。分离鉴定的44种血清型中有7种涉及到的O抗原或H抗原不在SSA检测范围内,其余37种能用SSA成功分型;利用SSA检测15株血清玻片凝集法不能分型的沙门菌,10株可成功分型。
    结论液相芯片技术能对大部分黑龙江省食品源沙门菌进行血清分型,与传统血清分型方法的一致性较高,且比传统方法具有高通量、高速度、准确性高的特点,可考虑常规用于沙门菌血清分型,特别是在应对食源性沙门菌感染暴发及食品风险监测时优先选用该方法进行血清型别的快速判定。

     

    Abstract:
    ObjectiveTo understand the effect and applicability of liquid suspension array Salmonella serotyping assay (SSA) in serotyping of Salmonella isolates from food risk surveillance in Heilongjiang province.
    MethodsThe traditional slide agglutination method was used for the serotyping of 451 Salmonella isolates, SSA kit was used to detect Salmonella O antigen, H antigen and AT antigen genes of 256 strains of these Salmonella isolates.
    ResultsA total of 249 Salmonella isolates could be completely serotyped by SSA kit. The consistent rate between SSA and slide agglutination method was above 96% . Seven of 44 serotypes with O or H antigens were not detected by SSA kit and other 37 serotypes could be successfully serotyped by SSA kit. Fifteen Salmonella isolates could not be serotyped by slide agglutination method, but 10 of them could be successfully serotyped by SSA kit.
    ConclusionSalmonella serotyping assay kit can be used for serotyping of most food-borne Salmonella in Heilongjiang. It has high consistency with traditional serotyping method and has the characteristics of high throughput, high speed and high accuracy. SSA kit could be considered as routine serotyping of Salmonella especially in the response to outbreaks of food-borne Salmonella infection and food risk surveillance, it is preferred for rapid serotyping.

     

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