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Abstract

81 Pseudomonas aeruginosa from Guangdong Provincial Institute of Food Inspection were identified by 16S rRNA sequence analysis. The DNA was isolated and the sequences of 16S rRNA gene were amplified by PCR with the bacterium universal primers, and then the PCR products were sequenced after 2% agarose gel electrophoresis. Moreover, the corrected sequences were aligned with Clustal X and the phylogenetic tree was constructed by MEGA5.1. Consequently, the identified results of the 81 strains confirmed their original identification before. On the phylogenetic tree, No. 24-3-QY strain formed a separate branch with No. 100-5-JM strain and No. 106-3-JM strain. No.2 8-1-DW formed one branch and the other 77 strains formed a separate branch with P. aeruginosa ATCC 27853. This was the first research about waterborne P. aeruginosa in Guangdong Province when China began to implement GB 19298—2014 “National food safety standards of packaged drinking water” since May 24, 2015. The waterborne P. aeruginosa culture collection in Guangdong was preliminarily established basing on these strains. These data will provide a powerful tool for effectively tracing source of P. aeruginosa and controlling the water contamination in future.

Publication Date

11-28-2016

First Page

21

Last Page

24,89

DOI

10.13652/j.issn.1003-5788.2016.11.005

References

[1] 闻玉梅. 现代医学微生物学[M]. 上海: 上海医科大学出版社, 1999: 383-389.
[2] KIM W, TENGRA FARAH K, YOUNG Z, et al. Spaceflight promotes Biofilm Formation by Pseudomonas aeruginosa[J]. PLOS One, 2013, 8(4): 624-627.
[3] WALKER T S, BAIS H P, DEZIEL E, et al, Pseudomonas aeruginosa-plant root interactions. Pathogenicity, biofilm formation, and root exudation [J]. Plant Physiol, 2004, 134(1): 320-331.
[4] RAHME L G, STEVENS E J, WOLFORT S F, et al. Common virulence factors for bacterial pathogenicity in plants and animals[J]. Science, 1995, 268(5 219): 1 899-1 902.
[5] RAHME L G, TAN M W, LE L, et al. Use of model plant hosts to identify Pseudomonas aeruginosa virulence factors[J]. Proc Natl Acad Sci USA, 1997, 94(24): 13 245-13 250.
[6] MAHAJAN-MIKLOS S, TAN M W, RAHME L G, et al. Molecular mechanisms of bacterial virulence elucidated using a Pseudomonas aeruginosa-Caenorhabditis elegant pathogenesis model [J]. Cell, 1999, 96(1): 47-56.
[7] MARTINEZ C, PONS E, PRATS G, et al. Salicylic acid regulates flowering time and links defense responses and reproductive development[J]. Plant J, 2004, 37(2): 209-217.
[8] DARGENIO D A, GALLAGHER L A, BERG C A, et al. Drosophila as a model host forPseudomonas aeruginosa infection [J]. J Bacterial, 2001, 183(4): 1 466-1 471.
[9] MIYATA S, CASEY M, FRANK D W, et al. Use of the Galleria mellondla caterpillar as a model host to study the role of the type III secretion system in Pseudomonas aeruginosa pathogenesis[J]. Infect Immune, 2003, 71(5): 2 404-2 413.
[10] BALTCH A L, SMITH R P. Pseudomonas aeruginosa: infections and treatment[J]. New York: M.Dekler,1994: 83-84.
[11] 李飞. 包装饮用泉水食源性致病菌分布规律和遗传多样性研究[D]. 广州: 华南理工大学, 2013: 35-36.
[12] 徐励琴, 薛计泉, 罗泽燕, 等. 桶装饮用水铜绿假单胞菌检测及耐药性分析[J]. 海峡预防医学杂志, 2015, 21(3): 56-57.
[13] 魏磊, 吴清平, 张菊梅, 等. 矿泉水和山泉水中铜绿假单胞菌污染调查及分离菌株毒力基因与耐药性分析[J]. 微生物通报, 2015, 42(1): 125-132.
[14] 蔡双福, 张琴, 黄耀雄. 食品中铜绿假单胞菌的监测分析[J]. 中国卫生检验杂志, 2015, 26(3): 875-905.
[15] SILVA M E, FILHO I C, ENDO E H, et al. Characterisation of potential virulence markers in pseudomonas aeruginosa isolated from drinking water[J]. Antonie Van Leeuwenhoek, 2008, 93(4): 323-334.
[16] VENIERI D, VANTARAKIS A, KOMNINOU G, et al. Microbiological evaluation of bottled non-carbonated(“still”) water from domestic brands in Greece[J]. Int J Food Microbiol, 2006, 107(1): 68-72.
[17] LAVENIR R, JOCKTANE D, LAURENT F, et al. Improved reliability of Pseudomonas aeruginosa PCR detection by the use of the species-specific ecfX gene target [J]. Journal of Microbiological Methods, 2007, 70: 20-29.
[18] 程池, 刘光全, 李金霞, 等. 55株芽孢杆菌16S rRNA基因序列测定与系统发育学分析[J]. 食品与发酵工业, 2006, 32(10): 20-24.
[19] TENG L J, HSUEH P R, HUANG Y H, et al. Identification of Bactericides thetaiotaomicron on the basis of an unexpected specific applicant of Universal 16S Ribosomal DNA PCR[J]. Journal of Clinical Microbiology, 2004, 42(4): 1 727-1 730.
[20] STACKEBRANDT E B, GOEBEL B M. Taxonomic note:a place for DNA-RNA reassociation and 16S rRNA sequence analysis in the present species definition in bacteriology[J]. Int J Syst Bacteriol, 1994, 44: 842-849.
[21] 张晓娟, 宋萍, 王柱, 等. 23株芽孢杆16S rRNA基因序列扩增与系统发育分析[J]. 食品与发酵科技, 2012, 48(2): 9-12.
[22] 朱飞舟, 陈利玉, 陈汉春. 16S rRNA基因序列分析法鉴定病原细菌[J]. 中南大学学报: 医学版, 2013, 38(10): 1 035-1 041.
[23] 刘大佳, 杨明, 陈利玉, 等. 采用16S rRNA基因分析技术鉴定正畸患者矫治前龈沟液的细菌种类[J]. 中国现代医学杂志, 2016, 26(2): 43-46.
[24] 吴至成, 伍丽娴, 李丽花, 等. 不同地理种群栖稻假单胞菌株的16S rRNA基因序列分析[J]. 中国热带医学, 2012,12(12): 1 453-1 456.
[25] 邹寰, 喻子牛, 孙明. 蜡状芽胞杆菌群16S rDNA分析[J]. 华中农业大学学报, 2008, 27(4): 478-482.
[26] 赵耘, 杜昕波, 李伟杰, 等. 袋鼠源铜绿假单胞菌分离鉴定[J]. 中国预防兽医学报, 2010, 32(2): 139-141.

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