Inverse Correlation between Promoter Strength and Excision Activity in Class 1 Integrons
Class 1 integrons are widespread genetic elements that allow bacteria to capture and express gene cassettes that are usually promoterless. These integrons play a major role in the dissemination of antibiotic resistance among Gram-negative bacteria. They typically consist of a gene (intI) encoding an integrase (that catalyzes the gene cassette movement by site-specific recombination), a recombination site (attI1), and a promoter (Pc) responsible for the expression of inserted gene cassettes. The Pc promoter can occasionally be combined with a second promoter designated P2, and several Pc variants with different strengths have been described, although their relative distribution is not known. The Pc promoter in class 1 integrons is located within the intI1 coding sequence. The Pc polymorphism affects the amino acid sequence of IntI1 and the effect of this feature on the integrase recombination activity has not previously been investigated. We therefore conducted an extensive in silico study of class 1 integron sequences in order to assess the distribution of Pc variants. We also measured these promoters' strength by means of transcriptional reporter gene fusion experiments and estimated the excision and integration activities of the different IntI1 variants. We found that there are currently 13 Pc variants, leading to 10 IntI1 variants, that have a highly uneven distribution. There are five main Pc-P2 combinations, corresponding to five promoter strengths, and three main integrases displaying similar integration activity but very different excision efficiency. Promoter strength correlates with integrase excision activity: the weaker the promoter, the stronger the integrase. The tight relationship between the aptitude of class 1 integrons to recombine cassettes and express gene cassettes may be a key to understanding the short-term evolution of integrons. Dissemination of integron-driven drug resistance is therefore more complex than previously thought.
Vyšlo v časopise:
Inverse Correlation between Promoter Strength and Excision Activity in Class 1 Integrons. PLoS Genet 6(1): e32767. doi:10.1371/journal.pgen.1000793
Kategorie:
Research Article
prolekare.web.journal.doi_sk:
https://doi.org/10.1371/journal.pgen.1000793
Souhrn
Class 1 integrons are widespread genetic elements that allow bacteria to capture and express gene cassettes that are usually promoterless. These integrons play a major role in the dissemination of antibiotic resistance among Gram-negative bacteria. They typically consist of a gene (intI) encoding an integrase (that catalyzes the gene cassette movement by site-specific recombination), a recombination site (attI1), and a promoter (Pc) responsible for the expression of inserted gene cassettes. The Pc promoter can occasionally be combined with a second promoter designated P2, and several Pc variants with different strengths have been described, although their relative distribution is not known. The Pc promoter in class 1 integrons is located within the intI1 coding sequence. The Pc polymorphism affects the amino acid sequence of IntI1 and the effect of this feature on the integrase recombination activity has not previously been investigated. We therefore conducted an extensive in silico study of class 1 integron sequences in order to assess the distribution of Pc variants. We also measured these promoters' strength by means of transcriptional reporter gene fusion experiments and estimated the excision and integration activities of the different IntI1 variants. We found that there are currently 13 Pc variants, leading to 10 IntI1 variants, that have a highly uneven distribution. There are five main Pc-P2 combinations, corresponding to five promoter strengths, and three main integrases displaying similar integration activity but very different excision efficiency. Promoter strength correlates with integrase excision activity: the weaker the promoter, the stronger the integrase. The tight relationship between the aptitude of class 1 integrons to recombine cassettes and express gene cassettes may be a key to understanding the short-term evolution of integrons. Dissemination of integron-driven drug resistance is therefore more complex than previously thought.
Zdroje
1. StokesHW
HallRM
1989 A novel family of potentially mobile DNA elements encoding site-specific gene-integration functions: integrons. Mol Microbiol 3 1669 1683
2. CollisCM
HallRM
1992 Gene cassettes from the insert region of integrons are excised as covalently closed circles. Mol Microbiol 6 2875 2885
3. CollisCM
HallRM
1992 Site-specific deletion and rearrangement of integron insert genes catalyzed by the integron DNA integrase. J Bacteriol 174 1574 1585
4. CollisCM
RecchiaGD
KimMJ
StokesHW
HallRM
2001 Efficiency of recombination reactions catalyzed by class 1 integron integrase IntI1. J Bacteriol 183 2535 2542
5. BiskriL
BouvierM
GueroutAM
BoisnardS
MazelD
2005 Comparative study of class 1 integron and Vibrio cholerae superintegron integrase activities. J Bacteriol 187 1740 1750
6. BouvierM
DemarreG
MazelD
2005 Integron cassette insertion: a recombination process involving a folded single strand substrate. Embo J 24 4356 4367
7. PartridgeSR
TsafnatG
CoieraE
IredellJ
2009 Gene cassettes and cassette arrays in mobile resistance integrons. FEMS Microbiol Rev 33 757 784
8. MazelD
2006 Integrons: agents of bacterial evolution. Nat Rev Microbiol 4 608 620
9. CollisCM
HallRM
1995 Expression of antibiotic resistance genes in the integrated cassettes of integrons. Antimicrob Agents Chemother 39 155 162
10. JacquierH
ZaouiC
Sanson-le PorsMJ
MazelD
BercotB
2009 Translation regulation of integrons gene cassette expression by the attC sites. Mol Microbiol 72 1475 1486
11. LevesqueC
BrassardS
LapointeJ
RoyPH
1994 Diversity and relative strength of tandem promoters for the antibiotic-resistance genes of several integrons. Gene 142 49 54
12. BunnyKL
HallRM
StokesHW
1995 New mobile gene cassettes containing an aminoglycoside resistance gene, aacA7, and a chloramphenicol resistance gene, catB3, in an integron in pBWH301. Antimicrob Agents Chemother 39 686 693
13. PapagiannitsisCC
TzouvelekisLS
MiriagouV
2009 Relative strengths of the class 1 integron promoter hybrid 2 and the combinations of strong and hybrid 1 with an active p2 promoter. Antimicrob Agents Chemother 53 277 280
14. BrizioA
ConceicaoT
PimentelM
Da SilvaG
DuarteA
2006 High-level expression of IMP-5 carbapenemase owing to point mutation in the −35 promoter region of class 1 integron among Pseudomonas aeruginosa clinical isolates. Int J Antimicrob Agents 27 27 31
15. HouangET
ChuYW
LoWS
ChuKY
ChengAF
2003 Epidemiology of rifampin ADP-ribosyltransferase (arr-2) and metallo-beta-lactamase (blaIMP-4) gene cassettes in class 1 integrons in Acinetobacter strains isolated from blood cultures in 1997 to 2000. Antimicrob Agents Chemother 47 1382 1390
16. PowerP
GalleniM
Di ConzaJ
AyalaJA
GutkindG
2005 Description of In116, the first blaCTX-M-2-containing complex class 1 integron found in Morganella morganii isolates from Buenos Aires, Argentina. J Antimicrob Chemother 55 461 465
17. RiccioML
FranceschiniN
BoschiL
CaravelliB
CornagliaG
2000 Characterization of the metallo-beta-lactamase determinant of Acinetobacter baumannii AC-54/97 reveals the existence of bla(IMP) allelic variants carried by gene cassettes of different phylogeny. Antimicrob Agents Chemother 44 1229 1235
18. NesveraJ
HochmannovaJ
PatekM
1998 An integron of class 1 is present on the plasmid pCG4 from gram-positive bacterium Corynebacterium glutamicum. FEMS Microbiol Lett 169 391 395
19. BurrT
MitchellJ
KolbA
MinchinS
BusbyS
2000 DNA sequence elements located immediately upstream of the −10 hexamer in Escherichia coli promoters: a systematic study. Nucleic Acids Res 28 1864 1870
20. BarneKA
BownJA
BusbySJ
MinchinSD
1997 Region 2.5 of the Escherichia coli RNA polymerase sigma70 subunit is responsible for the recognition of the ‘extended-10’ motif at promoters. EMBO J 16 4034 4040
21. MoyleH
WaldburgerC
SusskindMM
1991 Hierarchies of base pair preferences in the P22 ant promoter. J Bacteriol 173 1944 1950
22. GuerinE
CambrayG
Sanchez-AlberolaN
CampoyS
ErillI
2009 The SOS response controls integron recombination. Science 324 1034
23. BouvierM
Ducos-GalandM
LootC
BikardD
MazelD
2009 Structural features of single-stranded integron cassette attC sites and their role in strand selection. PLoS Genet 5 e1000632 doi:10.1371/journal.pgen.1000632
24. DemarreG
FrumerieC
GopaulDN
MazelD
2007 Identification of key structural determinants of the IntI1 integron integrase that influence attC×attI1 recombination efficiency. Nucleic Acids Res 35 6475 6489
25. FrumerieC
Ducos-GalandM
GopaulDN
MazelD
2009 The relaxed requirements of the integron cleavage site allow predictable changes in integron target specificity. Nucleic Acids Res doi:10.1093/nar/gkp990
26. MacDonaldD
DemarreG
BouvierM
MazelD
GopaulDN
2006 Structural basis for broad DNA-specificity in integron recombination. Nature 440 1157 1162
27. GillingsM
BoucherY
LabbateM
HolmesA
KrishnanS
2008 The evolution of class 1 integrons and the rise of antibiotic resistance. J Bacteriol 190 5095 5100
28. PloyMC
CourvalinP
LambertT
1998 Characterization of In40 of Enterobacter aerogenes BM2688, a class 1 integron with two new gene cassettes, cmlA2 and qacF. Antimicrob Agents Chemother 42 2557 2563
29. YanoH
KugaA
OkamotoR
KitasatoH
KobayashiT
2001 Plasmid-encoded metallo-beta-lactamase (IMP-6) conferring resistance to carbapenems, especially meropenem. Antimicrob Agents Chemother 45 1343 1348
30. LindstedtBA
HeirE
NygardI
KapperudG
2003 Characterization of class I integrons in clinical strains of Salmonella enterica subsp. enterica serovars Typhimurium and Enteritidis from Norwegian hospitals. J Med Microbiol 52 141 149
31. MillerJH
1992 A short course in bacterial genetics: a laboratory manual and handbook for Escherichia coli and related bacteria Cold Spring Harbor, , N.Y. Cold Spring Harbor Laboratory Press
32. DemarreG
GueroutAM
Matsumoto-MashimoC
Rowe-MagnusDA
MarliereP
2005 A new family of mobilizable suicide plasmids based on broad host range R388 plasmid (IncW) and RP4 plasmid (IncPalpha) conjugative machineries and their cognate Escherichia coli host strains. Res Microbiol 156 245 255
33. EspeliO
MoulinL
BoccardF
2001 Transcription attenuation associated with bacterial repetitive extragenic BIME elements. J Mol Biol 314 375 386
Štítky
Genetika Reprodukčná medicínaČlánok vyšiel v časopise
PLOS Genetics
2010 Číslo 1
- Je „freeze-all“ pro všechny? Odborníci na fertilitu diskutovali na virtuálním summitu
- Gynekologové a odborníci na reprodukční medicínu se sejdou na prvním virtuálním summitu
Najčítanejšie v tomto čísle
- A Major Role of the RecFOR Pathway in DNA Double-Strand-Break Repair through ESDSA in
- Kidney Development in the Absence of and Requires
- The Werner Syndrome Protein Functions Upstream of ATR and ATM in Response to DNA Replication Inhibition and Double-Strand DNA Breaks
- Alternative Epigenetic Chromatin States of Polycomb Target Genes