Molecular characteristics of salmonella genomic island 1 in Proteus mirabilis isolates from poultry farms in China

Antimicrobial Agents and Chemotherapy

Volumn 58, Issue 12, 2014, Pages 7570-7572

  Lei, Chang Wei ^a   Zhang, An Yun ^a   Liu, Bi Hui ^a   Wang, Hong Ning ^a   Guan, Zhong Bin ^a   Xu, Chang Wen ^a   Xia, Qing Qing ^a   Cheng, Han ^a   Zhang, Dong Dong ^a  

^a SICHUAN UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

LINCOSAMIDE; SPECTINOMYCIN; STREPTOMYCIN; ANTIINFECTIVE AGENT;

ANIMAL EXPERIMENT; ANTIBIOTIC RESISTANCE; ARTICLE; BACTERIUM IDENTIFICATION; BACTERIUM ISOLATION; CHINA; CHROMOSOME; CONTROLLED STUDY; FARM ANIMAL; GENE CASSETTE; GENE MAPPING; GENETIC ANALYSIS; GENETIC SCREENING; GENOMIC ISLAND; GROUP STRUCTURE; HOMOLOGOUS RECOMBINATION; INTESTINE; NONHUMAN; NUCLEOTIDE SEQUENCE; PERITONITIS; POLYMERASE CHAIN REACTION; POULTRY; POULTRY FARMING; PROTEUS MIRABILIS; SALMONELLA; SALMONELLA GENOMIC ISLAND 1; ANIMAL; ANIMAL HUSBANDRY; BACTERIAL GENE; CHICKEN; CHROMOSOME MAP; DRUG EFFECTS; GENETICS; ISOLATION AND PURIFICATION; MICROBIAL SENSITIVITY TEST; MICROBIOLOGY; MOLECULAR GENETICS; MULTIDRUG RESISTANCE; POULTRY DISEASES; PROTEUS INFECTIONS;

ANIMAL HUSBANDRY; ANIMALS; ANTI-BACTERIAL AGENTS; BASE SEQUENCE; CHICKENS; CHINA; CHROMOSOME MAPPING; DRUG RESISTANCE, MULTIPLE, BACTERIAL; GENES, BACTERIAL; GENOMIC ISLANDS; MICROBIAL SENSITIVITY TESTS; MOLECULAR SEQUENCE DATA; POULTRY; POULTRY DISEASES; PROTEUS INFECTIONS; PROTEUS MIRABILIS;

EID: 84912112326     PISSN: 00664804     EISSN: 10986596     Source Type: Journal    
DOI: 10.1128/AAC.03992-14     Document Type: Article

References (20)

1. Juhas M, van der Meer JR, Gaillard M, Harding RM, Hood DW, Crook DW. 2009. Genomic islands: tools of bacterial horizontal gene transfer and evolution. FEMS Microbiol. Rev. 33:376-393. http://dx.doi.org/10 .1111/j.1574-6976.2008.00136.x.
2. Boyd D, Peters GA, Cloeckaert A, Boumedine KS, Chaslus-Dancla E, Imberechts H, Mulvey MR. 2001. Complete nucleotide sequence of a 43-kilobase genomic island associated with the multidrug resistance region of Salmonella enterica serovar Typhimurium DT104 and its identification in phage type DT120 and serovar Agona. J. Bacteriol. 183:5725-5732. http://dx.doi.org/10.1128/JB.183.19.5725-5732.2001.
3. Doublet B, Boyd D, Mulvey MR, Cloeckaert A. 2005. The Salmonella genomic island 1 is an integrative mobilizable element. Mol. Microbiol. 55:1911-1924. http://dx.doi.org/10.1111/j.1365-2958.2005.04520.x.
4. Levings RS, Lightfoot D, Partridge SR, Hall RM, Djordjevic SP. 2005. The genomic island SGI1, containing the multiple antibiotic resistance region of Salmonella enterica serovar Typhimurium DT104 or variants of it, is widely distributed in other S. enterica serovars. J. Bacteriol. 187:4401-4409. http://dx.doi.org/10.1128/JB.187.13.4401-4409.2005.
5. Hall RM. 2010. Salmonella genomic islands and antibiotic resistance in Salmonella enterica. Future Microbiol. 5:1525-1538. http://dx.doi.org/10 .2217/fmb.10.122.
6. Hu YY, Cai JC, Zhang R, Zhou HW, Sun Q, Chen GX. 2012. Emergence of Proteus mirabilis harboring blaKPC-2 and qnrD in a Chinese Hospital. Antimicrob. Agents Chemother. 56:2278-2282. http://dx.doi.org/10.1128 /AAC.05519-11.
7. Ahmed AM, Hussein AI, Shimamoto T. 2007. Proteus mirabilis clinical isolate harbouring a new variant of Salmonella genomic island 1 containing the multiple antibiotic resistance region. J. Antimicrob. Chemother. 59:184-190. http://dx.doi.org/10.1093/jac/dkl471.
8. Boyd DA, Shi X, Hu QH, Ng LK, Doublet B, Cloeckaert A, Mulvey MR. 2008. Salmonella genomic island 1 (SGI1), variant SGI1-I, and new variant SGI1-O in Proteus mirabilis clinical and food isolates from China. Antimicrob. Agents Chemother. 52:340-344. http://dx.doi.org/10.1128 /AAC.00902-07.
9. Bi S, Yan H, Chen M, Zhang Z, Shi L, Wang H. 2011. New variant Salmonella genomic island 1-U in Proteus mirabilis clinical and food isolates from South China. J. Antimicrob. Chemother. 66:1178-1179. http: //dx.doi.org/10.1093/jac/dkr030.
10. Siebor E, Neuwirth C. 2011. The new variant of Salmonella genomic island 1 (SGI1-V) from a Proteus mirabilis French clinical isolate harbours blaVEB-6 and qnrA1 in the multiple antibiotic resistance region. J. Antimicrob. Chemother. 66:2513-2520. http://dx.doi.org/10.1093/jac/dkr335.
11. Siebor E, Neuwirth C. 2013. Emergence of Salmonella genomic island 1 (SGI1) among Proteus mirabilis clinical isolates in Dijon, France. J. Antimicrob. Chemother. 68:1750-1756. http://dx.doi.org/10.1093/jac/dkt100.
12. Seiffert SN, Tinguely R, Lupo A, Neuwirth C, Perreten V, Endimiani A. 2013. High prevalence of extended-spectrum-cephalosporin-resistant enterobacteriaceae in poultry meat in Switzerland: emergence of CMY-2-and VEB-6-possessing Proteus mirabilis. Antimicrob. Agents Chemother. 57:6406-6408. http://dx.doi.org/10.1128/AAC.01773-13.
13. th Informational Supplement. CLSI document M100-S22. Clinical and Laboratory Standards Institute, Wayne, PA.
14. Levings RS, Hall RM, Lightfoot D, Djordjevic SP. 2006. linG, a new integron-associated gene cassette encoding a lincosamide nucleotidyltransferase. Antimicrob. Agents Chemother. 50:3514-3515. http://dx.doi .org/10.1128/AAC.00817-06.
15. Wu JJ, Ko WC, Chiou CS, Chen HM, Wang LR, Yan JJ. 2008. Emergence of Qnr determinants in human Salmonella isolates in Taiwan. J. Antimicrob. Chemother. 62:1269-1272. http://dx.doi.org/10.1093/jac/dkn426.
16. Fortini D, Garcia-Fernandez A, Veldman K, Mevius D, Carattoli A. 2009. Novel genetic environment of plasmid-mediated quinolone resistance gene qnrB2 in Salmonella Bredeney from poultry. J. Antimicrob. Chemother. 64:1332-1334. http://dx.doi.org/10.1093/jac/dkp356.
17. Doublet B, Poirel L, Praud K, Nordmann P, Cloeckaert A. 2010. European clinical isolate of Proteus mirabilis harbouring the Salmonella genomic island 1 variant SGI1-O. J. Antimicrob. Chemother. 65:2260-2262. http://dx.doi.org/10.1093/jac/dkq283.
18. Carlson SA, Sharma VK, McCuddin ZP, Rasmussen MA, Franklin SK. 2007. Involvement of a Salmonella genomic island 1 gene in the rumen protozoan-mediated enhancement of invasion for multiple-antibioticresistant Salmonella enterica serovar Typhimurium. Infect. Immun. 75: 792-800. http://dx.doi.org/10.1128/IAI.00679-06.
19. Ogunleye AO, Carlson SA. 2012. Emergence of an SGI1-bearing Salmonella enterica serotype Kentucky isolated from septic poultry in Nigeria. J. Infect. Dev. Ctries. 6:483-488. http://dx.doi.org/10.3855/jidc.1988.
20. Douard G, Praud K, Cloeckaert A, Doublet B. 2010. The Salmonella genomic island 1 is specifically mobilized in trans by the IncA/C multidrug resistance plasmid family. PLoS One 5:e15302. http://dx.doi.org/10.1371 /journal.pone.0015302.