产志贺毒素大肠杆菌基因分型技术的研究进展
Research Progress in Genotyping of Shiga Toxin-Producing Escherichia coli
DOI: 10.12677/AMB.2020.93018, PDF,    科研立项经费支持
作者: 张世钦, 王梓晨, 白芷烨, 李红梅*, 王 翔, 董庆利:上海理工大学医疗器械与食品学院,上海;汪 雯, 吉小凤:农产品质量安全危害因子与风险防控国家重点实验室(筹),浙江省农业科学院农产品质量标准研究所,农业农村部农产品质量安全风险评估实验室(杭州),浙江 杭州
关键词: 产志贺毒素的大肠杆菌分型技术全基因组测序Shiga Toxin-Producing Escherichia coli Genotyping Methods Whole Genome Sequencing
摘要: 产志贺毒素大肠杆菌(Shiga toxin-producing Escherichia coli, STEC)是重要的食源性致病菌,能引起人和动物发生腹泻、出血性肠炎和溶血性尿毒综合症等疾病。为了更好的开展STEC检测、表征、分子进化分析及溯源调查,本文对国内外STEC基因分型技术包括基于酶切扩增分型方法、基于全基因组测序(Whole genome sequencing, WGS)分型方法以及多位点串联重复序列分析(MLVA)、DNA微阵列(DNA microarray)和成簇规律间隔短回文重复序列(CRISPR)分型技术研究进展进行综述,并对基因分型研究方法存在的问题进行探讨,为STEC的溯源追踪和流行病学调查提供参考。
Abstract: Shiga Toxin-producing Escherichia coli (STEC) is an important food-borne pathogen, which can cause diseases, such as diarrhea, hemorrhagic enteritis and hemolytic uremic syndrome in humans and animals. In order to implement the detection, characterization, molecular evolution analysis and traceability investigation of STEC more efficiently, the worldwide STEC genotyping techniques including the genotyping methods based on enzyme-cut amplification and Whole Genome Sequencing (WGS), Multiple Locus Variable number of tandem repeat Analysis (MLVA), DNA microarray and Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) were reviewed, and the issues of genotyping methods were discussed, which could provide the valuable information for the STEC traceability and epidemiological investigation.
文章引用:张世钦, 汪雯, 吉小凤, 王梓晨, 白芷烨, 李红梅, 王翔, 董庆利. 产志贺毒素大肠杆菌基因分型技术的研究进展[J]. 微生物前沿, 2020, 9(3): 125-132. https://doi.org/10.12677/AMB.2020.93018

参考文献

[1] Gonzalez, C.A. (2020) Shiga Toxin-Producing Escherichia coli in the Animal Reservoir and Food in Brazil. Journal of Applied Microbiology, 128, 1268-1282. [Google Scholar] [CrossRef] [PubMed]
[2] Amézquita-López, Bianca, A., Soto-Beltrán, et al. (2018) Isolation, Genotyping and Antimicrobial Resistance of Shiga Toxin-Producing, Escherichia coli. Journal of Microbiology, Immunology and Infection, 51, 425-434. [Google Scholar] [CrossRef] [PubMed]
[3] 顾玲, 祖荣强, 周璐, 等. 徐州地区73株大肠杆菌O157:H7的遗传多样性分析[J]. 江苏预防医学, 2019, 30(1): 36-38.
[4] Karmali, M.A., Mascarenhas, M., Shen, S., et al. (2003) Association of Genomic O Island 122 of Escherichia coli EDL 933 with Verocytotoxin-Producing Escherichia coli Seropathotypes That Are Linked to Epidemic and/or Serious Disease. Clinical Microbiology, 41, 4930-4940. [Google Scholar] [CrossRef
[5] Mathusa, E.C., Chen, Y., Enache, E., et al. (2010) Non-O157 Shiga Toxin-Producing Escherichia coli in Foods. Journal of Food Protection, 73, 1721-1736. [Google Scholar] [CrossRef
[6] Ørskov, I., Ørskov, F., Jann, B., et al. (1977) Serology, Chemistry, and Genetics of O and K Antigens of Escherichia coli. Bacteriological Reviews, 41, 667-710. [Google Scholar] [CrossRef
[7] Brendon, P., Nathan, Z., Byron, B., et al. (2016) Detection, Characterization, and Typing of Shiga Toxin-Producing Escherichia coli. Frontiers in Microbiology, 7, 478-490. [Google Scholar] [CrossRef] [PubMed]
[8] Lacher, D.W., Gangiredla, J., Jackson, S.A., et al. (2014) Novel Microarray Design for Molecular Serotyping of Shiga Toxin-Producing Escherichia coli Strains Isolated from Fresh Produce. Applied & Environmental Microbiology, 80, 4677-4682. [Google Scholar] [CrossRef
[9] Ayala, C.D., Moreno, A.C., Martinez, M.B., et al. (2012) Determination of Flagellar Types by PCR-RFLP Analysis of Enteropathogenic Escherichia coli (EPEC) and Shiga Toxin-Producing E. coli (STEC) Strains Isolated from Animals in São Paulo, Brazil. Research in Veterinary Science, 92, 18-23. [Google Scholar] [CrossRef] [PubMed]
[10] Shima, K., Wu. Y., Sugimoto, N., et al. (2006) Comparison of a PCR-Restriction Fragment Length Polymorphism (PCR-RFLP) Assay to Pulsed-Field Gel Electrophoresis to Determine the Effect of Repeated Subculture and Prolonged Storage on RFLP Patterns of Shiga Toxin-Producing Escherichia coli O157:H7. Journal of Clinical Microbiology, 44, 3963-3968. [Google Scholar] [CrossRef
[11] Pragathi, S., Chris, S., Noll, L.W., et al. (2017) Shiga Toxin Subtypes of Non-O157 Escherichia coli Serogroups Isolated from Cattle Feces. Frontiers in Cellular and Infection Microbiology, 7, 121. [Google Scholar] [CrossRef] [PubMed]
[12] Murgia, M., Rubino, S., Wain, J., et al. (2016) A Novel Broadly Applicable PCR-RFLP Method for Rapid Identification and Subtyping of H58 Salmonella Typhi. Journal of Microbiological Methods, 127, 219-223. [Google Scholar] [CrossRef] [PubMed]
[13] Rousseaux, S., Olier, M., Lemaitre, J., et al. (2004) Use of PCR-Restriction Fragment Length Polymorphism of inlA for Rapid Screening of Listeria monocytogenes Strains Deficient in the Ability to Invade Caco-2 Cells. Applied and Environmental Microbiology, 70, 2180-2185. [Google Scholar] [CrossRef
[14] Sohail, M. and Latif, Z. (2018) Molecular Typing of Methicillin Resistance Staphylococcus aureus (MRSA) Isolated from Device Related Infections by SCCmec and PCR-RFLP of Coagulase Gene. Advancements in Life Sciences, 6, 34-40.
[15] Pieter, V., Rene, H., Marjo, B., et al. (1995) AFLP: A New Technique for DNA Fingerprinting. Nucleic Acids Research, 23, 4407-4414. [Google Scholar] [CrossRef] [PubMed]
[16] Mueller, W. (1999) AFLP Genotyping and Fingerprinting. Trends in Ecology & Evolution, 14, 389-394. [Google Scholar] [CrossRef
[17] Hahm, B.K., Maldonado, Y., Schreiber, E., et al. (2003) Subtyping of Foodborne and Environmental Isolates of Escherichia coli by Multiplex-PCR, rep-PCR, PFGE, Ribotyping and AFLP. Journal of Microbiological Methods, 53, 387-399. [Google Scholar] [CrossRef
[18] Vittorio, L. (2003) AFLP: A Useful Tool for Biodiversity Conservation and Management. Comptes Rendus Biologies, 326, 43-48. [Google Scholar] [CrossRef
[19] Zhi, Y.W., Kwok, H.T. and Ka, H.C. (2004) Applications of AFLP Technology Ingenetic and Phylogenetic Analysis of Penaeid Shrimp. Biochemical Systematics and Ecology, 32, 399-407. [Google Scholar] [CrossRef
[20] Lee, J.H. and Han, T.H. (2006) Identification of Parental Species of the Alstroemeria cv. Jubilee Using AFLP Marker Technique. Scientia Horticulturae, 111, 63-67. [Google Scholar] [CrossRef
[21] 田舜, 李韬. AFLP技术操作流程的变革及其衍生技术[J]. 扬州大学学报(农业与生命科学版), 2006, 27(4): 62-66.
[22] 张平平. 江苏省大肠杆菌O157:H7的RAPD和AFLP分子分型分析[D]: [硕士学位论文]. 南京: 东南大学, 2010.
[23] Neves, E., Lourenc, A., et al. (2008) Pulsed-Field Gelelectrophoresis (PFGE) Analysis of Listeria monocytogenes Isolates from Different Sources and Geographical Originsand Representative of the Twelve Serovars. Systematic and Applied Microbiology, 31, 387-392. [Google Scholar] [CrossRef] [PubMed]
[24] 王丽丽. 我国大肠杆菌O157和猪链球菌脉冲场凝胶电泳分析[D]: [硕士学位论文]. 北京: 中国疾病预防控制中心, 2006.
[25] Codruţa, R.U., Ciontea, A.S., Condei, M., et al. (2017) Molecular Characterisation of Human Shiga Toxin-Producing Escherichia coli O26 Strains: Results of an Outbreak Investigation, Romania, February to August 2016. Eurosurveillance, 22, 17-24. [Google Scholar] [CrossRef
[26] Mariana, C., Carbonari, C., Beatriz, A., et al. (2018) Frequency, Characterization and Genotypic Analysis of Shiga Toxin-Producing Escherichia coli in Beef Slaughterhouses of Argentina. Revista Argentina de Microbiología, 51, 32-38. [Google Scholar] [CrossRef] [PubMed]
[27] Schurch, A.-A., et al. (2018) Whole Genome Sequencing Options for Bacterial Strain Typing and Epidemiologic Analysis Based on Single Nucleotide Polymorphism versus Gene-by-Gene-Based Approaches. Clinical Microbiology and Infection, 24, 350-354. [Google Scholar] [CrossRef] [PubMed]
[28] Abdalhamid, B., et al. (2019) Whole Genome Sequencing to Characterize Shiga Toxin-Producing Escherichia coli O26 in a Public Health Setting. Infect Public Health, 12, 884-889. [Google Scholar] [CrossRef] [PubMed]
[29] Navjot, S., Pascal, L., Tammy, Q., et al. (2019) Whole-Genome Single-Nucleotide Polymorphism (SNP) Analysis Applied Directly to Stool for Genotyping Shiga Toxin-Producing Escherichia coli: An Advanced Molecular Detection Method for Foodborne Disease Surveillance and Outbreak Tracking. Journal of Clinical Microbiology, 57, 307-319. [Google Scholar] [CrossRef
[30] Claire, J., Dallman, T.J. and Grant, K.A. (2019) Impact of Whole Genome Sequencing on the Investigation of Food-Borne Outbreaks of Shiga Toxin-Producing Escherichia coli Serogroup O157:H7, England, 2013 to 2017. Eurosurveillance, 24, 84-90. [Google Scholar] [CrossRef
[31] Maiden, B., et al. (1998) Multilocus Sequence Typing: A Portable Approach to the Identification of Clones within Populations of Pathogenic Microorganisms. Proceedings of the National Academy of Sciences of the United States of America, 95, 3140-3145. [Google Scholar] [CrossRef] [PubMed]
[32] Nüesch-Inderbinen, M., Nicole, C., Wüthrich, D., et al. (2018) Genetic Characterization of Shiga Toxin Producing Escherichia coli Belonging to the Emerging Hybrid Pathotype O80:H2 Isolated from Humans 2010-2017 in Switzerland. International Journal of Medical Microbiology, 308, 534-538. [Google Scholar] [CrossRef] [PubMed]
[33] 邵纯纯. 不同来源产志贺毒素大肠埃希菌的分子流行病学研究[D]: [硕士学位论文]. 济南: 山东大学, 2017.
[34] 唐学明. 数目可变的串联重复顺序(VNTR)的研究方法进展[J]. 国外医学遗传学分册, 1994(3): 120-124.
[35] Bai, L., Guo, Y., Lan, R., et al. (2015) Genotypic Characterization of Shiga Toxin-Producing Escherichia coli O157:H7 Isolates in Food Products from China between 2005 and 2010. Food Control, 50, 209-214. [Google Scholar] [CrossRef
[36] Timmons, C., Trees, E., et al. (2016) Multiple-Locus Variable-Number Tandem Repeat Analysis for Strain Discrimination of Non-O157 Shiga Toxin-Producing Escherichia coli. Journal of Microbiological Methods, 125, 70-80. [Google Scholar] [CrossRef] [PubMed]
[37] Marie-Léone, V., Emeline, C., Muriel, M., et al. (2017) MLVA for Salmonella enterica subsp. enterica Serovar Dublin: Development of a Method Suitable for Inter-Laboratory Surveillance and Application in the Context of a Raw Milk Cheese Outbreak in France in 2012. Frontiers in Microbiology, 8, 295. [Google Scholar] [CrossRef] [PubMed]
[38] Bai, Y., Wang, W., Yan, L., et al. (2018) Molecular Typing Characterization of Food-Borne Methicillin-Resistant Staphylococcus aureus in China. Chinese Journal of Preventive Medicine, 52, 364-371.
[39] Liu, Y.H. and Fratamico, P. (2006) Escherichia coli O Antigen Typing Using DNA Microarrays. Molecular and Cellular Probes, 20, 239-244. [Google Scholar] [CrossRef] [PubMed]
[40] Zhang, F., Hu, S., Huang, J., et al. (2006) Development and Clinical Evaluation of Oligonucleotide Microarray for HLA-AB Genotyping. Pharmacogenomics, 7, 973-985. [Google Scholar] [CrossRef] [PubMed]
[41] Quinones, B., Swimley, M.S., Taylor, A.W., et al. (2011) Identification of Escherichia coli O157 by Using a Novel Colorimetric Detection Method with DNA Microarrays. Foodborne Pathogens and Disease, 8, 705-711. [Google Scholar] [CrossRef] [PubMed]
[42] Quinones, B., Swimley, M.S., Narm, K.E., et al. (2012) O-Antigen and Virulence Profiling of Shiga Toxin-Producing Escherichia coli by a Rapid and Cost-Effective DNA Microarray Colorimetric Method. Frontiers in Cellular Infection Microbiology, 2, Article No. 61. [Google Scholar] [CrossRef] [PubMed]
[43] Kuck, L.R. and Taylor, A.W. (2008) Photopolymerization as an Innovative Detection Technique for Low-Density Microarrays. Bio-Techniques, 45, 179-186. [Google Scholar] [CrossRef] [PubMed]
[44] Shariat, N., Dudley, et al. (2014) CRISPRs: Molecular Signatures Used for Pathogen Subtyping. Applied and Environment Microbiology, 80, 430-439. [Google Scholar] [CrossRef
[45] Groenen, P.M., Bunschoten, A.E., Soolingen, D., et al. (1993) Nature of DNA Polymorphism in the Direct Repeat Cluster of Mycobacterium tuberculosis: Application for Strain Differentiation by a Novel Typing Method. Molecular Microbiology, 10, 1057-1065. [Google Scholar] [CrossRef] [PubMed]
[46] Li, H., Li, P., Xie, J., et al. (2014) A New CRISPR Loci Spacer-Pair Typing (CLSPT) Method Based on The Newly Incorporated Spacer for Salmonella enterica. Journal of Clinical Microbiology, 52, 2955-2962. [Google Scholar] [CrossRef
[47] 狄慧玲. 单核细胞增生李斯特菌分子分型研究及CRISPR/Cas系统解析[D]: [博士学位论文]. 广州: 华南理工大学, 2014.
[48] Schouls, L.M., Reulen, S., Duim, B., et al. (2003) Comparative Genotyping of Campylobacter jejuni by Amplified Fragment Length Polymorphism, Multilocus Sequence Typing, and Short Repeat Sequencing: Strain Diversity, Host Range, and Recombination. Journal of Clinical Microbiology, 41, 15-26. [Google Scholar] [CrossRef
[49] Delannoy, B. and Fach, P. (2012) Use of Clustered Regularly Interspaced Short Palindromic Repeat Sequence Polymorphism for Specific Detection of Enterohemorrhagic Escherichia coli Strains of Serotypes O26:H11, O45:H2, O103:H2, O111:H8, O121:H19, O145:H28, and O157:H7 by Real-Time PCR. Journal of Clinical Microbiology, 50, 4035-4040. [Google Scholar] [CrossRef
[50] 梁文娟. 基于CRISPRs的大肠埃希菌分型方法及其与耐药和毒力关系[D]: [博士学位论文]. 郑州: 郑州大学, 2017.