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pagP基因缺失对禽致病性大肠埃希菌外膜特性的影响

Effect of pagP gene deletion on outer membrane characteristics of avian pathogenic Escherichia coli
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摘要 【目的】研究pagP基因缺失对禽致病性大肠埃希菌(Avian pathogenic Escherichia coli,APEC)外膜特性的影响。【方法】采用最低抑菌浓度(MIC)试验探索pagP基因缺失对菌株生物被膜通透性的影响;通过菌体自聚合试验、外膜疏水性试验以及生物被膜形成条件,分析pagP基因缺失对生物被膜形成能力的影响,并在扫描电镜下观察细菌生物被膜形态。【结果】pagP基因缺失后,菌株MIC降低,菌株的外膜通透性增强且菌体自聚合能力显著增强(P<0.01),其中红霉素和氨苄西林的MIC分别为7和20μg/mL,菌株自聚合能力为87.89%;pagP基因缺失对菌株外膜疏水性无显著影响,疏水性仅为5.337%;随着细菌在LB培养基中静置培养时间的延长,生物被膜形成量增多;pagP基因缺失株的生物被膜形成能力高于野生株。【结论】pagP基因缺失可使APEC外膜特性发生改变,生物被膜形成能力增强。 【Objective】To study the effect of pagP gene deletion on outer membrane characteristics of avian pathogenic Escherichia coli(APEC).【Method】The minimal inhibitory concentration(MIC)experiment was used to explore the effect of pagP deletion on the permeability of outer membrane of strain.Autoaggregation experiment,outer membrane hydrophobicity test,and analysis of biofilm-forming conditions of strain were performed to understand the influence of pagP deletion on biofilm-forming ability.The biofilm morphology was observed by scanning electron microscopy.【Result】The MIC of strain decreased after the deletion of pagP gene,the outer membrane permeability of strain increased,and the autoaggregation ability of strain increased significantly(P<0.01).The MICs of erythromycin and ampicillin were 7 and 20μg/mL respectively.The autoaggregation ability of strain was 87.89%.The deletion of pagP gene had no significant effect on the hydrophobicity of outer membrane of strain,and the hydrophobicity was only 5.337%.The amount of biofilm increased with the increase of time when the strain was cultured in LB medium.The strain with pagP deletion had higher biofilm-forming ability than wild strain.【Conclusion】The deletion of pagP gene can change the characteristics of outer membrane of APEC and enhance the biofilm-forming ability.
作者 束玲玲 徐柳柳 祁克宗 涂建 宋祥军 邵颖 SHU Lingling;XU Liuliu;QI Kezong;TU Jian;SONG Xiangjun;SHAO Ying(College of Animal Science and Technology,Anhui Agricultural University/Anhui Province Key Laboratory of Veterinary Pathobiology and Disease Control,Hefei 230036,China)
出处 《华南农业大学学报》 CAS CSCD 北大核心 2019年第6期8-14,共7页 Journal of South China Agricultural University
基金 国家自然科学基金(31772707)
关键词 禽致病性大肠埃希菌 pagP基因 生物被膜 疏水性 自聚合能力 avian pathogenic Escherichia coli pagP gene biofilm hydrophobicity autoaggregation ability
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  • 1吴希,张双全.抗菌肽对细菌杀伤作用的分子机制[J].生物化学与生物物理进展,2005,32(12):1109-1113. 被引量:17
  • 2李任峰,何启盖,周锐,陈焕春.细菌鞭毛研究概况及进展[J].微生物学通报,2005,32(6):124-127. 被引量:21
  • 3刘玉庆,张怀强,沈建忠,高培基.大肠杆菌群体的生理异质性对药敏实验的影响[J].中国科学(C辑),2007,37(5):524-529. 被引量:6
  • 4Schotulcr C, Schaeffer B, Bree A, et al. Diagnostic strategy for idcmifying avian pathogenic Escherichia col; based on four patterns of virulence genes[J]. Clin Microbi,2012,50(5) : 1673-1678. 被引量:1
  • 5Hem X G,Bai H,Lei L,et al. The luxS gene functions in lhc pathogenesis of avian pathogenic Esccherichia coli[J]. Microbial Pathogenesis, 2013,6 ( 55 ) : 21-27. 被引量:1
  • 6Carniel E, Guilvout I, Prentice M. Characterization of a large chromosomal ‘ high-pathogenicity island ' in hiotype IB Yersinia enterocolitica[J]. Bacteriology, 1996.178(23) :6743-6751. 被引量:1
  • 7Rakin A, Noclting C,Schubert S,et al. Common and spccific eharactcristics of the high-pathogenicity island of Yersimia emerocolitica[J]. Infect Immun, 1999,67 (10) :5265-5271. 被引量:1
  • 8Christoph A,Gregm S,Rakin A,et al, Expression a naiysis of the Yersbdahactin receptor gene fyuA and tile heine receptor hemR of Yersinia enterocolitica in witra. and in vivo using the reporter genes for green fluorescent prmein and lueiferase[J]. Infect Immun, 200! ,69(12) :7772. 被引量:1
  • 9Karch H, Sclmberl S. Zhang D, et al. A genomic is- land, lermcd high pathogenicity island, is present in cerlain non-O 157 Shiga toxin-producing Escherichia coli clonal lineages[J]. Infect immune, 1999,67(11) : 5994-6001. 被引量:1
  • 10Bach S, Almeida A, Carniel E. The Yersinia high- pathogenicity island is present in different members of the family Enteroba cteriaceae[J]. FEMS Microbiol LeE, 2000,183 (2) : 289-294. 被引量:1

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