Protection of Salmonella by ampicillin-resistant Escherichia coli in the presence of otherwise lethal drug concentrations
Microbial systems have become the preferred testing grounds for experimental work on the evolution of traits that benefit other group members. This work, based on conceptual and theoretical models of frequency-dependent selection within populations, has proven fruitful in terms of understanding the...
Saved in:
Published in | Proceedings of the Royal Society. B, Biological sciences Vol. 276; no. 1674; pp. 3759 - 3768 |
---|---|
Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
The Royal Society
07.11.2009
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | Microbial systems have become the preferred testing grounds for experimental work on the evolution of traits that benefit other group members. This work, based on conceptual and theoretical models of frequency-dependent selection within populations, has proven fruitful in terms of understanding the dynamics of group beneficial or 'public goods' traits within species. Here, we expand the scope of microbial work on the evolution of group-beneficial traits to the case of multi-species communities, particularly those that affect human health. We examined whether β-lactamase-producing Escherichia coli could protect ampicillin-sensitive cohorts of other species, particularly species that could cause human disease. Both β-lactamase-secreting E. coli and, surprisingly, those engineered to retain it, allowed for survival of a large number of ampicillin-sensitive cohorts of Salmonella enterica serovar Typhimurium, including both laboratory and clinical isolates. The Salmonella survivors, however, remained sensitive to ampicillin when re-plated onto solid medium and there was no evidence of gene transfer. Salmonella survival did not even require direct physical contact with the resistant E. coli. The observed phenomenon appears to involve increased release of β-lactamase from the E. coli when present with S. enterica. Significantly, these findings imply that resistant E. coli, that are not themselves pathogenic, may be exploited, even when they are normally selfish with respect to other E. coli. Thus, Salmonella can gain protection against antibiotics from E. coli without gene transfer, a phenomenon not previously known. As a consequence, antibiotic-resistant E. coli can play a decisive role in the survival of a species that causes disease and may thereby interfere with successful treatment. |
---|---|
AbstractList | Microbial systems have become the preferred testing grounds for experimental work on the evolution of traits that benefit other group members. This work, based on conceptual and theoretical models of frequency- dependent selection within populations, has proven fruitful in terms of understanding the dynamics of group beneficial or -public goods- traits within species. Here, we expand the scope of microbial work on the evolution of group-beneficial traits to the case of multi-species communities, particularly those that affect human health. We examined whether beta -lactamase-producing Escherichia coli could protect ampicillin-sensitive cohorts of other species, particularly species that could cause human disease. Both beta - lactamase-secreting E. coli and, surprisingly, those engineered to retain it, allowed for survival of a large number of ampicillin-sensitive cohorts of Salmonella enterica serovar Typhimurium, including both laboratory and clinical isolates. The Salmonella survivors, however, remained sensitive to ampicillin when re-plated onto solid medium and there was no evidence of gene transfer. Salmonella survival did not even require direct physical contact with the resistant E. coli. The observed phenomenon appears to involve increased release of beta -lactamase from the E. coli when present with S. enterica. Significantly, these findings imply that resistant E. coli, that are not themselves pathogenic, may be exploited, even when they are normally selfish with respect to other E. coli. Thus, Salmonella can gain protection against antibiotics from E. coli without gene transfer, a phenomenon not previously known. As a consequence, antibiotic-resistant E. coli can play a decisive role in the survival of a species that causes disease and may thereby interfere with successful treatment. can play a decisive role in the survival of a species that causes disease and may thereby interfere with successful treatment. Microbial systems have become the preferred testing grounds for experimental work on the evolution of traits that benefit other group members. This work, based on conceptual and theoretical models of frequency-dependent selection within populations, has proven fruitful in terms of understanding the dynamics of group beneficial or ‘public goods’ traits within species . Here, we expand the scope of microbial work on the evolution of group-beneficial traits to the case of multi-species communities , particularly those that affect human health. We examined whether β-lactamase-producing Escherichia coli could protect ampicillin-sensitive cohorts of other species, particularly species that could cause human disease. Both β-lactamase-secreting E. coli and, surprisingly, those engineered to retain it, allowed for survival of a large number of ampicillin-sensitive cohorts of Salmonella enterica serovar Typhimurium, including both laboratory and clinical isolates. The Salmonella survivors, however, remained sensitive to ampicillin when re-plated onto solid medium and there was no evidence of gene transfer. Salmonella survival did not even require direct physical contact with the resistant E. coli . The observed phenomenon appears to involve increased release of β-lactamase from the E. coli when present with S. enterica . Significantly, these findings imply that resistant E. coli , that are not themselves pathogenic, may be exploited, even when they are normally selfish with respect to other E. coli . Thus, Salmonella can gain protection against antibiotics from E. coli without gene transfer, a phenomenon not previously known. As a consequence, antibiotic-resistant E. coli can play a decisive role in the survival of a species that causes disease and may thereby interfere with successful treatment. Microbial systems have become the preferred testing grounds for experimental work on the evolution of traits that benefit other group members. This work, based on conceptual and theoretical models of frequency-dependent selection within populations, has proven fruitful in terms of understanding the dynamics of group beneficial or 'public goods' traits within species. Here, we expand the scope of microbial work on the evolution of group-beneficial traits to the case of multi-species communities, particularly those that affect human health. We examined whether β-lactamase-producing Escherichia coli could protect ampicillin-sensitive cohorts of other species, particularly species that could cause human disease. Both β-lactamase-secreting E. coli and, surprisingly, those engineered to retain it, allowed for survival of a large number of ampicillin-sensitive cohorts of Salmonella enterica serovar Typhimurium, including both laboratory and clinical isolates. The Salmonella survivors, however, remained sensitive to ampicillin when re-plated onto solid medium and there was no evidence of gene transfer. Salmonella survival did not even require direct physical contact with the resistant E. coli. The observed phenomenon appears to involve increased release of β-lactamase from the E. coli when present with S. enterica. Significantly, these findings imply that resistant E. coli, that are not themselves pathogenic, may be exploited, even when they are normally selfish with respect to other E. coli. Thus, Salmonella can gain protection against antibiotics from E. coli without gene transfer, a phenomenon not previously known. As a consequence, antibiotic-resistant E. coli can play a decisive role in the survival of a species that causes disease and may thereby interfere with successful treatment. |
Author | Myers, David A. Dugatkin, Lee A. McKenzie, Courtney Patel, Himati Powell, Cayse Perlin, Michael H. Clark, Denise R. Jackson, Nikki Bajorek, Alexander Kormanik, Cecile Atlas, Ronald M. |
AuthorAffiliation | Department of Biology, Program on Disease Evolution , University of Louisville , Louisville, KY 40292 , USA |
AuthorAffiliation_xml | – name: Department of Biology, Program on Disease Evolution , University of Louisville , Louisville, KY 40292 , USA |
Author_xml | – sequence: 1 givenname: Michael H. surname: Perlin fullname: Perlin, Michael H. email: mhperl01@gwise.louisville.edu organization: E-mail: mhperl01@gwise.louisville.edu – sequence: 2 givenname: Denise R. surname: Clark fullname: Clark, Denise R. organization: Department of Biology, Program on Disease Evolution, University of Louisville, Louisville, KY 40292, USA – sequence: 3 givenname: Courtney surname: McKenzie fullname: McKenzie, Courtney organization: Department of Biology, Program on Disease Evolution, University of Louisville, Louisville, KY 40292, USA – sequence: 4 givenname: Himati surname: Patel fullname: Patel, Himati organization: Department of Biology, Program on Disease Evolution, University of Louisville, Louisville, KY 40292, USA – sequence: 5 givenname: Nikki surname: Jackson fullname: Jackson, Nikki organization: Department of Biology, Program on Disease Evolution, University of Louisville, Louisville, KY 40292, USA – sequence: 6 givenname: Cecile surname: Kormanik fullname: Kormanik, Cecile organization: Department of Biology, Program on Disease Evolution, University of Louisville, Louisville, KY 40292, USA – sequence: 7 givenname: Cayse surname: Powell fullname: Powell, Cayse organization: Department of Biology, Program on Disease Evolution, University of Louisville, Louisville, KY 40292, USA – sequence: 8 givenname: Alexander surname: Bajorek fullname: Bajorek, Alexander organization: Department of Biology, Program on Disease Evolution, University of Louisville, Louisville, KY 40292, USA – sequence: 9 givenname: David A. surname: Myers fullname: Myers, David A. organization: Department of Biology, Program on Disease Evolution, University of Louisville, Louisville, KY 40292, USA – sequence: 10 givenname: Lee A. surname: Dugatkin fullname: Dugatkin, Lee A. organization: Department of Biology, Program on Disease Evolution, University of Louisville, Louisville, KY 40292, USA – sequence: 11 givenname: Ronald M. surname: Atlas fullname: Atlas, Ronald M. organization: Department of Biology, Program on Disease Evolution, University of Louisville, Louisville, KY 40292, USA |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/19656787$$D View this record in MEDLINE/PubMed |
BookMark | eNqFks1v1DAQxSNURD_gyg2UE7cstuPE8QVRqrYgVXyDuFmO42y8eONgO5T890zIamEPgBQpit9v3ozn5TQ56l2vk-QhRiuMePXUh6FeEYT4CnHO7iQnmDKcEV7Qo-QE8ZJkFS3IcXIawgYBVlTFveQY87IoWcVOkumtd1GraFyfujb9IO0WGlgr03pK5XYwylhr-szrYEKUfUwvg-q0N6ozMlXOmtT0aex0OgCie6VnGwcH_tYEnVodO2nTxo9roEHuo5dzt3A_udtKG_SD3fss-XR1-fHiZXbz5vrVxflNpkqex6zSuVKlLClHjVQaHo4oazimqFYFwoxoyrlGvC1QgTlvVYNpVTPS1prkTOZnybPFdxjrrW6WCawYvNlKPwknjThUetOJtfsuSAXmrAKDJzsD776NOkSxNUHNO-q1G4MoWckwZ-i_IMGowoSVAK4WUHkXgtftfhqMxByrmGMVc6xijhUKHv95h9_4LkcA8gXwboJlOmV0nMTGjb6Hz7_bPlqqNiE6v3fNEaFFns96tugQvf6x16X_CpfOWSE-V1S8vyb51ZcXr8U74J8vfGfW3a3xWhyM86s7_AQRFi1gDwKXjArw4aIdLUTStGBB_mnhpsGH-rA6_wlf8ffm |
CitedBy_id | crossref_primary_10_1099_mgen_0_000713 crossref_primary_10_1038_s41467_021_27630_9 crossref_primary_10_1038_s41396_023_01393_1 crossref_primary_10_1007_s11306_020_01702_1 crossref_primary_10_1099_mic_0_001442 crossref_primary_10_1038_s41467_019_11571_5 crossref_primary_10_1186_1472_6882_10_64 crossref_primary_10_1371_journal_ppat_1008700 crossref_primary_10_1093_jac_dku466 crossref_primary_10_1021_acssynbio_1c00393 crossref_primary_10_1038_msb_2013_39 crossref_primary_10_1038_s41396_018_0212_z crossref_primary_10_1038_s42003_023_04716_2 crossref_primary_10_1146_annurev_micro_041320_031627 crossref_primary_10_1128_aem_02311_23 crossref_primary_10_3390_ijms222413606 crossref_primary_10_1371_journal_pone_0205202 crossref_primary_10_1016_j_anbehav_2016_06_001 crossref_primary_10_1073_pnas_1523317113 crossref_primary_10_1111_eva_12254 crossref_primary_10_3390_microorganisms10122383 crossref_primary_10_1038_hdy_2017_33 crossref_primary_10_1080_08927014_2015_1124096 crossref_primary_10_1128_mBio_01836_21 crossref_primary_10_1073_pnas_2020956119 crossref_primary_10_1371_journal_pone_0115223 crossref_primary_10_1080_21505594_2018_1426520 crossref_primary_10_1093_femsre_fuw024 crossref_primary_10_1093_femsre_fuac019 crossref_primary_10_1016_j_physrep_2020_05_004 crossref_primary_10_1016_j_tig_2015_05_004 crossref_primary_10_1016_j_mib_2014_09_004 crossref_primary_10_1038_ismej_2015_154 crossref_primary_10_1371_journal_pbio_3002100 crossref_primary_10_1111_mec_17040 crossref_primary_10_2139_ssrn_3188477 crossref_primary_10_7554_eLife_69744 crossref_primary_10_1038_s41396_021_00982_2 crossref_primary_10_1371_journal_pcbi_1006179 crossref_primary_10_1038_s41396_021_01130_6 crossref_primary_10_1038_s41522_019_0109_2 crossref_primary_10_1016_j_mib_2023_102306 crossref_primary_10_1016_j_tim_2014_11_005 crossref_primary_10_1016_j_envint_2018_04_029 crossref_primary_10_1038_s41396_022_01285_w crossref_primary_10_1128_jcm_01558_22 |
Cites_doi | 10.1074/jbc.M508063200 10.1098/rspb.2000.1330 10.1016/0003-2697(76)90527-3 10.1128/MR.47.3.361-409.1983 10.1128/JCM.02147-07 10.1007/s101230100016 10.1038/nature02744 10.1016/S0924-8579(01)00343-0 10.1098/rspb.2004.2916 10.1128/AAC.36.9.1951 10.1128/JB.92.4.1206-1217.1966 10.1128/CMR.15.2.167-193.2002 10.2307/1925895 10.1371/journal.pone.0002763 10.1146/annurev.med.59.110106.132000 10.1128/CMR.18.4.657-686.2005 10.1126/science.1103077 10.1093/genetics/137.4.903 10.3201/eid0702.010205 10.1128/jb.176.11.3140-3147.1994 10.1128/JB.180.20.5478-5483.1998 10.1128/IAI.73.8.5198-5203.2005 10.1038/nrmicro1796 10.1093/clinids/24.Supplement_1.S102 10.1023/B:JANC.0000014736.59554.5c 10.1139/w02-077 10.1128/JB.181.16.4725-4733.1999 10.1006/jtbi.2003.3149 10.2741/3570 10.1093/clinids/24.Supplement_1.S9 10.1586/14787210.5.5.833 10.1128/AAC.39.7.1458 10.1016/j.jtbi.2005.03.021 10.1186/1741-7007-6-20 10.1093/jac/40.5.615 10.1016/S0022-5193(86)80226-0 10.1038/nature05685 10.1371/journal.pbio.0060280 10.1093/jac/45.1.9 10.1128/JB.151.3.1523-1531.1982 10.1016/j.tim.2004.07.003 10.1073/pnas.0811741106 10.1093/jac/dkf021 10.1093/oxfordjournals.molbev.a025984 10.1128/AEM.58.3.900-904.1992 10.1016/0378-1119(77)90000-2 |
ContentType | Journal Article |
Copyright | Copyright 2009 The Royal Society 2009 The Royal Society 2009 The Royal Society 2009 |
Copyright_xml | – notice: Copyright 2009 The Royal Society – notice: 2009 The Royal Society – notice: 2009 The Royal Society 2009 |
DBID | BSCLL CGR CUY CVF ECM EIF NPM AAYXX CITATION 7QL C1K 7X8 5PM |
DOI | 10.1098/rspb.2009.0997 |
DatabaseName | Istex Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed CrossRef Bacteriology Abstracts (Microbiology B) Environmental Sciences and Pollution Management MEDLINE - Academic PubMed Central (Full Participant titles) |
DatabaseTitle | MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) CrossRef Bacteriology Abstracts (Microbiology B) Environmental Sciences and Pollution Management MEDLINE - Academic |
DatabaseTitleList | Bacteriology Abstracts (Microbiology B) MEDLINE CrossRef |
Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 2 dbid: EIF name: MEDLINE url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search sourceTypes: Index Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Sciences (General) Biology |
EISSN | 1471-2954 1471-2945 |
EndPage | 3768 |
ExternalDocumentID | 10_1098_rspb_2009_0997 19656787 30245337 ark_67375_V84_RG23FXBN_Q royprsb_276_1674_3759 |
Genre | Research Support, Non-U.S. Gov't Journal Article Research Support, N.I.H., Extramural |
GrantInformation_xml | – fundername: NIAID NIH HHS grantid: R15 AI060667 – fundername: NIAID NIH HHS grantid: 1 R15 AI060667-01 |
GroupedDBID | - 02 08R 0R 0VX 29P 2WC 36Y 4.4 5RE 85S ABBHK ABFLS ABPTK ACIWK ACNCT ACPRK ADACO ADBBV ADULT ADZLD AEUPB AFRAH ALMA_UNASSIGNED_HOLDINGS AS BAWUL BGBPD CS3 DCCCD DIK DNJUQ DOOOF DWIUU E3Z EBS EJD F5P FRP GX1 H13 HQ3 HTVGU HYE HZ JLS JPM JSG JSODD JST K-O KQ8 MVM O0- O9- OK1 OP1 RHF RPM RRY SA0 V1E X --- -~X 0R~ AACGO AANCE ABPLY ABTLG ABXSQ ACQIA ADACV ADIYS AEXZC AJZGM ALMYZ AOIJS AQVQM AS~ BSCLL BTFSW HZ~ IPSME JAAYA JBMMH JENOY JHFFW JKQEH JLXEF MRS TR2 W8F ~02 CGR CUY CVF ECM EIF NPM AAYXX CITATION 7QL C1K 7X8 5PM |
ID | FETCH-LOGICAL-c693t-8e3cc6a6490daceace9047d9140bc50172e499e09f505199fcd148b72fbe237a3 |
IEDL.DBID | RPM |
ISSN | 0962-8452 |
IngestDate | Tue Sep 17 21:28:02 EDT 2024 Fri Oct 25 09:45:53 EDT 2024 Fri Oct 25 21:05:07 EDT 2024 Tue Sep 24 00:52:50 EDT 2024 Sat Sep 28 07:56:21 EDT 2024 Wed Jan 17 02:37:25 EST 2024 Sun Sep 22 05:19:19 EDT 2024 Wed Oct 30 09:50:21 EDT 2024 Tue Jan 05 21:30:13 EST 2021 Mon May 06 12:21:02 EDT 2019 |
IsDoiOpenAccess | false |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 1674 |
Language | English |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c693t-8e3cc6a6490daceace9047d9140bc50172e499e09f505199fcd148b72fbe237a3 |
Notes | ArticleID:rspb20090997 ark:/67375/V84-RG23FXBN-Q href:rspb20090997.pdf istex:091997C894EF5406403BF65061CAB1C770366551 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
OpenAccessLink | https://europepmc.org/articles/pmc2817278?pdf=render |
PMID | 19656787 |
PQID | 21081276 |
PQPubID | 23462 |
PageCount | 10 |
ParticipantIDs | proquest_miscellaneous_67671970 crossref_primary_10_1098_rspb_2009_0997 pubmed_primary_19656787 istex_primary_ark_67375_V84_RG23FXBN_Q royalsociety_journals_10_1098_rspb_2009_0997 proquest_miscellaneous_21081276 jstor_primary_30245337 highwire_royalsociety_royprsb_276_1674_3759 pubmedcentral_primary_oai_pubmedcentral_nih_gov_2817278 |
ProviderPackageCode | RHF |
PublicationCentury | 2000 |
PublicationDate | 2009-11-07 |
PublicationDateYYYYMMDD | 2009-11-07 |
PublicationDate_xml | – month: 11 year: 2009 text: 2009-11-07 day: 07 |
PublicationDecade | 2000 |
PublicationPlace | England |
PublicationPlace_xml | – name: England |
PublicationTitle | Proceedings of the Royal Society. B, Biological sciences |
PublicationTitleAbbrev | Proc. R. Soc. B |
PublicationTitleAlternate | Proc. R. Soc. B |
PublicationYear | 2009 |
Publisher | The Royal Society |
Publisher_xml | – name: The Royal Society |
References | 7492085 - Antimicrob Agents Chemother. 1995 Jul;39(7):1458-61 10629007 - J Antimicrob Chemother. 2000 Jan;45(1):9-13 9765585 - J Bacteriol. 1998 Oct;180(20):5478-83 18524964 - J Clin Microbiol. 2008 Aug;46(8):2581-9 12123299 - Proc Biol Sci. 2001 Jan 7;268(1462):61-9 12455613 - Can J Microbiol. 2002 Sep;48(9):810-20 8994776 - Clin Infect Dis. 1997 Jan;24 Suppl 1:S9-16 19273370 - Front Biosci (Landmark Ed). 2009;14:4557-64 16223952 - Clin Microbiol Rev. 2005 Oct;18(4):657-86 15899500 - J Theor Biol. 2005 Oct 21;236(4):392-6 15329720 - Nature. 2004 Aug 26;430(7003):1024-7 19018661 - PLoS Biol. 2008 Nov 18;6(11):e280 17937586 - Annu Rev Med. 2008;59:415-28 9656481 - Mol Biol Evol. 1998 Jul;15(7):789-97 17914917 - Expert Rev Anti Infect Ther. 2007 Oct;5(5):833-43 3796009 - J Theor Biol. 1986 Sep 7;122(1):83-93 7982572 - Genetics. 1994 Aug;137(4):903-17 8994788 - Clin Infect Dis. 1997 Jan;24 Suppl 1:S102-5 19332772 - Proc Natl Acad Sci U S A. 2009 Apr 14;106(15):6339-44 942051 - Anal Biochem. 1976 May 7;72:248-54 16041039 - Infect Immun. 2005 Aug;73(8):5198-203 16103114 - J Biol Chem. 2005 Nov 18;280(46):38383-94 1575491 - Appl Environ Microbiol. 1992 Mar;58(3):900-4 11932229 - Clin Microbiol Rev. 2002 Apr;15(2):167-93 1416886 - Antimicrob Agents Chemother. 1992 Sep;36(9):1951-7 11869238 - Clin Microbiol Infect. 1997 Feb;3 Suppl 4:S10-S19 18648645 - PLoS One. 2008;3(7):e2763 8195066 - J Bacteriol. 1994 Jun;176(11):3140-7 4959044 - J Bacteriol. 1966 Oct;92(4):1206-17 344137 - Gene. 1977;2(2):95-113 15875573 - Proc Biol Sci. 2005 Jan 7;272(1558):79-83 7050091 - J Bacteriol. 1982 Sep;151(3):1523-31 18007678 - Nat Rev Microbiol. 2007 Dec;5(12):958-65 11294702 - Emerg Infect Dis. 2001 Mar-Apr;7(2):183-7 17410176 - Nature. 2007 Apr 5;446(7136):668-71 15361616 - Science. 2004 Sep 10;305(5690):1578-9 6355806 - Microbiol Rev. 1983 Sep;47(3):361-409 11463525 - Int J Antimicrob Agents. 2001 Jul;18(1):43-8 19482588 - Front Biosci (Landmark Ed). 2009;14:4815-24 18479522 - BMC Biol. 2008;6:20 10438737 - J Bacteriol. 1999 Aug;181(16):4725-33 11770827 - Int Microbiol. 2001 Jun;4(2):73-80 12453451 - J Theor Biol. 2003 Jan 7;220(1):67-74 12003973 - J Antimicrob Chemother. 2002 May;49(5):793-801 15337159 - Trends Microbiol. 2004 Sep;12(9):401-4 9421308 - J Antimicrob Chemother. 1997 Nov;40(5):615-21 e_1_3_2_28_1 e_1_3_2_49_1 e_1_3_2_20_1 e_1_3_2_22_1 e_1_3_2_24_1 e_1_3_2_16_1 e_1_3_2_39_1 e_1_3_2_9_1 e_1_3_2_18_1 e_1_3_2_7_1 e_1_3_2_31_1 e_1_3_2_10_1 e_1_3_2_12_1 e_1_3_2_35_1 e_1_3_2_14_1 e_1_3_2_37_1 e_1_3_2_3_1 Livermore D. M. (e_1_3_2_34_1) 1997; 4 Travisano M. (e_1_3_2_50_1) 2001; 67 e_1_3_2_29_1 Beveridge T. J. (e_1_3_2_5_1) 1999; 181 Sheratt T. N. (e_1_3_2_47_1) 2009; 14 e_1_3_2_42_1 e_1_3_2_21_1 e_1_3_2_44_1 e_1_3_2_23_1 e_1_3_2_46_1 e_1_3_2_48_1 Katsui N. (e_1_3_2_26_1) 1982; 151 e_1_3_2_40_1 Rapp M. L. (e_1_3_2_41_1) 1992; 58 Rosensweig R. F. (e_1_3_2_43_1) 1994; 137 e_1_3_2_17_1 e_1_3_2_38_1 e_1_3_2_8_1 Foster T. J. (e_1_3_2_19_1) 1983; 47 e_1_3_2_2_1 e_1_3_2_30_1 e_1_3_2_11_1 e_1_3_2_32_1 e_1_3_2_6_1 e_1_3_2_13_1 Li Z. (e_1_3_2_33_1) 1998; 180 e_1_3_2_4_1 e_1_3_2_15_1 e_1_3_2_36_1 e_1_3_2_51_1 Sambrook J. (e_1_3_2_45_1) 2001 Karthikeyan S. (e_1_3_2_25_1) 2001; 4 Knox K. W. (e_1_3_2_27_1) 1966; 92 |
References_xml | – ident: e_1_3_2_40_1 doi: 10.1074/jbc.M508063200 – ident: e_1_3_2_48_1 doi: 10.1098/rspb.2000.1330 – ident: e_1_3_2_7_1 doi: 10.1016/0003-2697(76)90527-3 – volume: 47 start-page: 361 year: 1983 ident: e_1_3_2_19_1 article-title: Plasmid-determined resistance to antimicrobial drugs and toxic metal ions in bacteria publication-title: Microbiol. Rev. doi: 10.1128/MR.47.3.361-409.1983 contributor: fullname: Foster T. J. – ident: e_1_3_2_3_1 doi: 10.1128/JCM.02147-07 – volume: 4 start-page: 73 year: 2001 ident: e_1_3_2_25_1 article-title: Adaptation of bacterial communities to environmental transitions from labile to refractory substrates publication-title: Int. Microbiol. doi: 10.1007/s101230100016 contributor: fullname: Karthikeyan S. – ident: e_1_3_2_21_1 doi: 10.1038/nature02744 – ident: e_1_3_2_20_1 doi: 10.1016/S0924-8579(01)00343-0 – ident: e_1_3_2_15_1 doi: 10.1098/rspb.2004.2916 – ident: e_1_3_2_4_1 doi: 10.1128/AAC.36.9.1951 – volume: 92 start-page: 1206 year: 1966 ident: e_1_3_2_27_1 article-title: Relation between excreted lipopolysaccharide complexes and surface structures of a lysine-limited culture of Escherichia coli publication-title: J. Bacteriol. doi: 10.1128/JB.92.4.1206-1217.1966 contributor: fullname: Knox K. W. – volume: 4 start-page: S10 year: 1997 ident: e_1_3_2_34_1 article-title: β-Lactamases: quantity and resistance publication-title: Clin. Microbiol. Infect. contributor: fullname: Livermore D. M. – ident: e_1_3_2_13_1 doi: 10.1128/CMR.15.2.167-193.2002 – volume: 67 start-page: 403 year: 2001 ident: e_1_3_2_50_1 article-title: Experimental evolution studies yield insights into bacterial diversity publication-title: ASM News contributor: fullname: Travisano M. – ident: e_1_3_2_46_1 doi: 10.2307/1925895 – ident: e_1_3_2_17_1 doi: 10.1371/journal.pone.0002763 – ident: e_1_3_2_35_1 doi: 10.1146/annurev.med.59.110106.132000 – ident: e_1_3_2_39_1 doi: 10.1128/CMR.18.4.657-686.2005 – ident: e_1_3_2_31_1 doi: 10.1126/science.1103077 – volume: 137 start-page: 903 year: 1994 ident: e_1_3_2_43_1 article-title: Microbial evolution in a simple unstructured environment: genetic differentiation in Escherichia coli publication-title: Genetics doi: 10.1093/genetics/137.4.903 contributor: fullname: Rosensweig R. F. – ident: e_1_3_2_42_1 doi: 10.3201/eid0702.010205 – start-page: 2344 volume-title: Molecular cloning: a laboratory manual year: 2001 ident: e_1_3_2_45_1 contributor: fullname: Sambrook J. – ident: e_1_3_2_30_1 doi: 10.1128/jb.176.11.3140-3147.1994 – volume: 180 start-page: 5478 year: 1998 ident: e_1_3_2_33_1 article-title: Gram-negative bacteria produce membrane vesicles which are capable of killing other bacteria publication-title: J. Bacteriol. doi: 10.1128/JB.180.20.5478-5483.1998 contributor: fullname: Li Z. – ident: e_1_3_2_18_1 doi: 10.1128/IAI.73.8.5198-5203.2005 – ident: e_1_3_2_37_1 doi: 10.1038/nrmicro1796 – ident: e_1_3_2_44_1 doi: 10.1093/clinids/24.Supplement_1.S102 – ident: e_1_3_2_2_1 doi: 10.1023/B:JANC.0000014736.59554.5c – ident: e_1_3_2_36_1 doi: 10.1139/w02-077 – volume: 181 start-page: 4725 year: 1999 ident: e_1_3_2_5_1 article-title: Structures of gram-negative cell walls and their derived membrane vesicles publication-title: J. Bacteriol. doi: 10.1128/JB.181.16.4725-4733.1999 contributor: fullname: Beveridge T. J. – ident: e_1_3_2_14_1 doi: 10.1006/jtbi.2003.3149 – ident: e_1_3_2_11_1 doi: 10.2741/3570 – ident: e_1_3_2_32_1 doi: 10.1093/clinids/24.Supplement_1.S9 – ident: e_1_3_2_49_1 doi: 10.1586/14787210.5.5.833 – ident: e_1_3_2_23_1 doi: 10.1128/AAC.39.7.1458 – ident: e_1_3_2_16_1 doi: 10.1016/j.jtbi.2005.03.021 – ident: e_1_3_2_8_1 doi: 10.1186/1741-7007-6-20 – ident: e_1_3_2_24_1 doi: 10.1093/jac/40.5.615 – ident: e_1_3_2_29_1 doi: 10.1016/S0022-5193(86)80226-0 – ident: e_1_3_2_9_1 doi: 10.1038/nature05685 – ident: e_1_3_2_12_1 doi: 10.1371/journal.pbio.0060280 – ident: e_1_3_2_10_1 doi: 10.1093/jac/45.1.9 – volume: 151 start-page: 1523 year: 1982 ident: e_1_3_2_26_1 article-title: Heat-induced blebbing and vesiculation of the outer membrane of Escherichia coli publication-title: J. Bacteriol. doi: 10.1128/JB.151.3.1523-1531.1982 contributor: fullname: Katsui N. – ident: e_1_3_2_22_1 doi: 10.1016/j.tim.2004.07.003 – ident: e_1_3_2_28_1 doi: 10.1073/pnas.0811741106 – ident: e_1_3_2_38_1 doi: 10.1093/jac/dkf021 – volume: 14 start-page: 340 year: 2009 ident: e_1_3_2_47_1 article-title: Evolutionary stable investment in products that confer both and individual benefit and public good publication-title: Front. BioSci. contributor: fullname: Sheratt T. N. – ident: e_1_3_2_51_1 doi: 10.1093/oxfordjournals.molbev.a025984 – volume: 58 start-page: 900 year: 1992 ident: e_1_3_2_41_1 article-title: Model system using coliphage φx174 for testing virus removal by air filters publication-title: Appl. Environ. Microbiol. doi: 10.1128/AEM.58.3.900-904.1992 contributor: fullname: Rapp M. L. – ident: e_1_3_2_6_1 doi: 10.1016/0378-1119(77)90000-2 |
SSID | ssj0009585 |
Score | 2.254603 |
Snippet | can play a decisive role in the survival of a species that causes disease and may thereby interfere with successful treatment. Microbial systems have become the preferred testing grounds for experimental work on the evolution of traits that benefit other group members. This work, based... |
SourceID | pubmedcentral proquest crossref pubmed royalsociety jstor istex highwire |
SourceType | Open Access Repository Aggregation Database Index Database Publisher Enrichment Source |
StartPage | 3759 |
SubjectTerms | Ampicillin - pharmacology Ampicillin Resistance Anti-Bacterial Agents - pharmacology Antibiotic Susceptibility Antibiotics Bacteria beta-Lactamases - genetics beta-Lactamases - metabolism Enzymes Escherichia coli Escherichia coli - drug effects Escherichia coli - enzymology Escherichia coli - genetics Evolution Flasks Genetic Engineering Materials Plasmids Salmonella Salmonella - drug effects Salmonella enterica Salmonella enterica serovar Typhimurium Serovar Typhimurium Β-Lactamase |
Title | Protection of Salmonella by ampicillin-resistant Escherichia coli in the presence of otherwise lethal drug concentrations |
URI | http://rspb.royalsocietypublishing.org/content/276/1674/3759.abstract?cited-by=yes&legid=royprsb;276/1674/3759 https://api.istex.fr/ark:/67375/V84-RG23FXBN-Q/fulltext.pdf https://www.jstor.org/stable/30245337 https://royalsocietypublishing.org/doi/full/10.1098/rspb.2009.0997 https://www.ncbi.nlm.nih.gov/pubmed/19656787 https://search.proquest.com/docview/21081276 https://search.proquest.com/docview/67671970 https://pubmed.ncbi.nlm.nih.gov/PMC2817278 |
Volume | 276 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3db9MwED-tk5B4QWwwCIzhB8SHIGsbJ3H8CNO6CWnT-BjqmxU7zhaxZlHTavS_585JSiutLzxGvSa273fx7-L7AHjDZR6lSG39gaUWZoM88HUWZ742QuRIH7QMKd_57Dw-vQy_jqPxFkRdLowL2je6OCxvJodlce1iK6uJ6XdxYv2Ls6MgoW036feghwDtXPRlpV3XhxOpOZp6GAXLSo1JHz1F3ZaolNK135NIZwSF061uSl2hYOSrtNR_ulDF-0joPbGUU_L76ybmcmWvGj2GRy3JZJ-byezAli134UHTdnKxCzutQdfsfVt1-sMTWFw0FRtQT-w2Zz_SGwQohUYxvWDppCoMfZkpfXTPiXKWM3Zck8ILCpZmCKeCFSVDOskql9FkLN3G5XfdFbVliI9rHFM2nV-hdNlMxIH-KVyOjn8enfptXwbfxJLP_MRyY-I0DuUgSw2-ua0chCKT6KtpE5FTadGPQt3nERFEmZsMnS4tglzbgIuU78F2iVN4DiyN0IPKRKKHmQ4tJZUM8qFNc85NqsXQePCuU4yqmvIbqjk2TxRpk7poSkXa9OBjpze1qgG6qKY1SopYUcqF4iKSHsgN0nRTyhKgHsdrf1F0HqKqLPfgrYPFckDp9DeFx4lI_UpC9f0k4KPxl3P1zYM9h5ulIKdzbs5xrK87ICm0ZjqiSUt7O68VOuDIuES8WYIK7A1xmTx41gDv37q0YPZArEFyKUCVxNd_QQNzFcVbg_Lg09pitK-zesOSv_jvB72Eh-5Ujj7Pi33Ynk3n9hWSu5k-gN7JeHjgTPovdCBUOg |
link.rule.ids | 230,315,730,783,787,888,27936,27937,53804,53806 |
linkProvider | National Library of Medicine |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1bb9MwFLbGEIIXxAaDcJsfEBdB1jRO4vgRppUCazVgQ32zbMdhEWsWNa2g_55znKS00vbCY9TTxD6X-Ds5N0JeMJHHCqCtH1gcYRbkoa-zJPO14TwH-KBFhPXOo3EyPIs-T-LJFom7WhiXtG90cVBeTA_K4tzlVlZT0-vyxHono8MwxWM37d0gN8Feg6hz0le9dt0kTgDnYOxRHK56NaY98BV126RSCDeATwCg4ZhQt34sda2CAbEis_90yYpXwdArsiln6PnXTdbl2mk1uEfutjCTvm-2s0O2bLlLbjWDJ5e7ZKc16Zq-bvtOv7lPlidNzwaQFL3M6Xd1ASqKyVFUL6maVoXBbzOlDw46gs5yTo9qFHmB6dIUFKqgRUkBUNLK1TQZi7dxFV6_i9pS0JBzWFM2W_wE6rLZiFP7B-RscHR6OPTbyQy-SQSb-6llxiQqiUSQKQPvbiuCiGcCvDVtYnQrLXhSIP08RogocpOB26V5mGsbMq7YHtkuYQuPCFUx-FAZT3U_05HFspIg71uVM2aU5n3jkVedYGTVNOCQTeA8lShNnKMpJErTI287ucl1CeBFNauBkicSiy4k47HwiLiGGm-KdQI45XjjLxIjIrLKco-8dGqxWpCa_cIEOR7LH2kkv30M2WDyYSy_emTP6c2KkGGkmzFY636nSBLsGYM0qrSXi1qCCw6YiyfXU2CLvT6wySMPG8X7x5dWmT3CN1RyRYC9xDd_ARNzPcVbk_LIuw1mtC-0-hqWP_7vB-2T28PT0bE8_jT-8oTccTE6_FjPn5Lt-WxhnwHUm-vnzrD_AmduVp8 |
linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1bb9MwFLZgCMQLYoNBuM0PiIsgaxoncfwIY2VcVpXLUN8s23G2aGsWNa2g_55znKS0UvfCY9TTxPb5Tvyd-FwIec5EHiugtn5gsYVZkIe-zpLM14bzHOiDFhHmOx8Pk6OT6PM4Hq-0-nJB-0YX--XFZL8szlxsZTUxvS5OrDc6PghT3HbTXpXlvevkBthskHSO-rLeruvGCQQdDD6Kw2W9xrQH_qJuC1UK4ZrwCSA1HIPqVremrlwwsFZc8D9dwOImKrohonKK3n_dRF6u7FiDu-ROSzXpu2ZK2-SaLXfIzab55GKHbLdmXdNXbe3p1_fIYtTUbQBt0cuc_lAXAFMMkKJ6QdWkKgx-nyl9cNKReJYzelij2gsMmaYAqoIWJQVSSSuX12Qs3sZlef0uaksBJWcwpmw6PwXpspmIg_59cjI4_Hlw5LfdGXyTCDbzU8uMSVQSiSBTBt7fVgQRzwR4bNrE6Fpa8KYAAXmMNFHkJgPXS_Mw1zZkXLFdslXCFB4SqmLwozKe6n6mI4upJUHetypnzCjN-8YjLzvFyKopwiGbw_NUojaxl6aQqE2PvOn0Jlc1gBfVtAZJnkhMvJCMx8ID3G2WxptirgB2Ol77i8RTEQnA88gLB4vlgNT0HIPkeCx_pZH8_jFkg_H7ofzmkV2Hm6Ugw9NuxmCsex2QJNg0HtSo0l7OawluOPAunlwtgWX2-rBMHnnQAO_furRg9ghfg-RSAOuJr_8CZubqirdm5ZG3a4vRvtTqK5b80X8_aI_cGn0YyK-fhl8ek9vumA6_1_MnZGs2ndunwPZm-pmz678h8Fey |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Protection+of+Salmonella+by+ampicillin-resistant+Escherichia+coli+in+the+presence+of+otherwise+lethal+drug+concentrations&rft.jtitle=Proceedings+of+the+Royal+Society.+B%2C+Biological+sciences&rft.au=Perlin%2C+Michael+H.&rft.au=Clark%2C+Denise+R.&rft.au=McKenzie%2C+Courtney&rft.au=Patel%2C+Himati&rft.date=2009-11-07&rft.pub=The+Royal+Society&rft.issn=0962-8452&rft.eissn=1471-2954&rft.volume=276&rft.issue=1674&rft.spage=3759&rft.epage=3768&rft_id=info:doi/10.1098%2Frspb.2009.0997&rft.externalDocID=10_1098_rspb_2009_0997 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0962-8452&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0962-8452&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0962-8452&client=summon |