湖北农业科学 ›› 2025, Vol. 64 ›› Issue (10): 158-164.doi: 10.14088/j.cnki.issn0439-8114.2025.10.024

• 畜牧·兽医 • 上一篇    下一篇

基于SG-PI双重染色法的单增李斯特菌对苯扎溴铵耐受性快速检测方法的建立

汪国俊, 曹文杰, 季强, 栗绍文, 刘梅   

  1. 华中农业大学动物医学院,武汉 430070
  • 收稿日期:2025-06-04 出版日期:2025-10-25 发布日期:2025-11-14
  • 通讯作者: 刘 梅,女,副教授,博士,主要从事食源性病原菌致病机理、环境适应、流行和传播规律研究,(电话)027-87282091(电子信箱)liumei@mail.hzau.edu.cn。
  • 作者简介:汪国俊(1992-),女,河南信阳人,博士研究生,研究方向为兽医公共卫生学,(电话)027-87282091(电子信箱)wangguojun@webmail.hzau.edu.cn;共同第一作者,曹文杰(2000-),男,湖南娄底人,硕士研究生,研究方向为兽医学,(电话)027-87282091(电子信箱)1971901030@qq.com。
  • 基金资助:
    国家重点研发计划项目(2022YFD1800100)

The establishment of a rapid detection method for benzalkonium bromide tolerance of Listeria monocytogenes based on SG-PI dual-staining

WANG Guo-jun, CAO Wen-jie, JI Qiang, LI Shao-wen, LIU Mei   

  1. College of Veterinary Medicine, Huazhong Agricultural University, Wuhan 430070, China
  • Received:2025-06-04 Published:2025-10-25 Online:2025-11-14

摘要: 为及时掌握单增李斯特菌(Listeria monocytogenes, Lm)对苯扎溴铵的耐受情况,基于SYBR Green I(SG)与碘化丙啶(PI)双重染色,建立了一种能够快速检测Lm对苯扎溴铵耐受性的新方法——SG-PI双重染色法。结果表明,利用稀释法测定104株Lm分离株苯扎溴铵耐受性,检测出11株耐受菌株、93株敏感菌株。首先,确定出SG-PI双染最佳浓度组合为20×SG+5 μmol/L PI,双染最佳时间为5 min;然后,利用双染最佳条件对不同活菌百分比(P)的Lm混合液进行染色和荧光强度测定,计算两染料荧光强度比值(F),确定FP的关系式为F=0.004 996P+0.303 6(R2=0.997 6),得出相对细胞活性(RCA)定量检测模型公式为RCA=[(F-0.303 6)/0.004 996]×100%;最后,通过暴露试验,确定出苯扎溴铵最佳暴露浓度为16 mg/L。与稀释法相比,SG-PI双重染色法对苯扎溴铵耐受菌株的测定是准确的(灵敏性为100%),对耐受菌株的测定比稀释法严格,具有可靠性,可作为验证新方法的评估标准。

关键词: 单增李斯特菌(Listeria monocytogenes), 苯扎溴铵(BAC), 耐受性评估, SYBR Green I(SG), 碘化丙啶(PI)

Abstract: To enhance analytical throughput and enable rapid assessment of bacterial susceptibility to disinfectants, developing an accelerated evaluation protocol is critically required,a new method for rapid phenotypic assessment of Lm's BAC tolerance was established based on SYBR Green I (SG) and propidium iodide (PI) double staining-the SG-PI dual-staining methodology. Results showed that the BAC tolerance of 104 Lm isolates from swine slaughterhouse samples was assessed using the dilution method. Analysis revealed 11 BAC-tolerant and 93 BAC-sensitive isolates, establishing these findings as the reference standard for validating the newly developed methodology. Firstly, the SG-PI dual-staining methodology was optimized, and the optimal concentration combination of the double staining was finally determined to be 20× SG + 5 μmol/L PI, and the optimal double staining incubation time was 5 min. Subsequently, the optimal conditions of the SG-PI dual-staining methodology were applied to Lm suspensions with different percentages of viable bacteria (P), and the fluorescence intensity ratio (F) between SG and PI was calculated. The functional relationship between the F value and the P value was determined to be F=0.004 996P+0.303 6, R2=0.997 6. The quantitative detection model formula for the relative cell activity of Lm derived from the relationship was RCA=[(F-0.303 6)/0.004 996]×100%. Finally, through exposure experiments, the optimal exposure concentration of BAC was determined to be 16 mg/L. The SG-PI double-staining method developed in this study exhibited 100% sensitivity for detecting BAC-tolerant strains, demonstrating superior accuracy compared to traditional dilution methods. The SG-PI dual-staining technique offered simplicity, rapidity, and precision, having been effectively applied in assessing bacterial antibiotic resistance.

Key words: Listeria monocytogenes, benzalkonium bromide(BAC), tolerance assessment, SYBR Green I (SG), propidium iodide (PI)

中图分类号: