Academic Journal
Genomic characterization of a mobile-element-associated resistance island in trimethoprim-sulfamethoxazole-resistant Stenotrophomonas maltophilia isolates sharing the same PFGE genotype.
| Title: | Genomic characterization of a mobile-element-associated resistance island in trimethoprim-sulfamethoxazole-resistant Stenotrophomonas maltophilia isolates sharing the same PFGE genotype. |
|---|---|
| Authors: | Altan G; Department of Medical Microbiology, Faculty of Medicine, Kocaeli University, Kocaeli, Türkiye., Rakıcı E; Department of Medical Microbiology, Faculty of Medicine, Recep Tayyip Erdoğan University, Rize, Türkiye., Dündar D; Department of Medical Microbiology, Faculty of Medicine, Kocaeli University, Kocaeli, Türkiye., Özgümüş OB; Department of Medical Microbiology, Faculty of Medicine, Recep Tayyip Erdoğan University, Rize, Türkiye. |
| Source: | Frontiers in cellular and infection microbiology [Front Cell Infect Microbiol] 2026 Sep 11; Vol. 16, pp. 1926102. Date of Electronic Publication: 2026 Sep 11 (Print Publication: 2026). |
| Publication Type: | Journal Article |
| Language: | English |
| Journal Info: | Publisher: Frontiers Media SA Country of Publication: Switzerland NLM ID: 101585359 Publication Model: eCollection Cited Medium: Internet ISSN: 2235-2988 (Electronic) Linking ISSN: 22352988 NLM ISO Abbreviation: Front Cell Infect Microbiol Subsets: MEDLINE |
| Imprint Name(s): | Original Publication: Lausanne : Frontiers Media SA |
| MeSH Terms: | Stenotrophomonas maltophilia*/genetics , Stenotrophomonas maltophilia*/drug effects , Stenotrophomonas maltophilia*/isolation & purification , Stenotrophomonas maltophilia*/classification , Trimethoprim, Sulfamethoxazole Drug Combination*/pharmacology , Anti-Bacterial Agents*/pharmacology , Drug Resistance, Multiple, Bacterial*/genetics , Interspersed Repetitive Sequences* , Genomic Islands*, Gram-Negative Bacterial Infections/microbiology ; Levofloxacin/pharmacology ; Minocycline/pharmacology ; Humans ; Microbial Sensitivity Tests ; Electrophoresis, Gel, Pulsed-Field ; Genotype ; Whole Genome Sequencing ; Genome, Bacterial |
| Abstract: | Background: Stenotrophomonas maltophilia is an opportunistic nosocomial pathogen with intrinsic multidrug resistance and limited therapeutic options. This study integrated phenotypic susceptibility testing, targeted molecular screening, PFGE and short-read whole-genome sequencing (WGS) to characterize resistance determinants and their local genomic context in clinical-culture isolates. Methods: Thirty-four non-duplicate clinical-culture isolates were analyzed. Susceptibility to trimethoprim-sulfamethoxazole (TMP-SMX), levofloxacin and minocycline was determined by disk diffusion. Minocycline testing was repeated with acceptable quality control, and the repeat-run zone records were reassessed using current CLSI breakpoints. A predefined, hypothesis-driven PCR panel was used to screen selected resistance-, efflux- and biofilm-associated targets, and gyrA, gyrB, parC and parE were sequenced. Genetic relatedness was assessed by XbaI-PFGE. Three selected isolates (S05, S08 and S25) underwent WGS as a targeted genomic-context analysis rather than a whole-collection population-genomic study. Results: Resistance rates were 5.9% for TMP-SMX, 8.8% for levofloxacin and 11.8% for minocycline after reassessment using current CLSI minocycline breakpoints. Smqnr- and sul1-target PCR positivity was observed in 61.8% and 8.8% of isolates, respectively. A dfrA27-target PCR amplicon was observed in 82.4% of isolates but was not associated with TMP-SMX resistance and was not confirmed in the three sequenced genomes. No QRDR hotspot mutations were identified. The two TMP-SMX-resistant isolates, S05 and S08, shared the same PFGE genotype. Short-read WGS identified an identical 19,361-bp mobile-element-associated resistance region in these isolates, containing a putative Sul-family/folP-like dihydropteroate synthase (DHPS) annotation, two assembly-predicted hits each of bla Conclusions: The identical resistance region in two TMP-SMX-resistant isolates sharing the same PFGE genotype is compatible with shared ancestry, vertical inheritance or persistence of an island-carrying PFGE-defined genotype; horizontal transfer was not demonstrated. The discordance between dfrA27-target PCR positivity, phenotype and WGS highlights the need to interpret molecular screening together with phenotypic susceptibility and orthogonal confirmation. The WGS component provides a local genomic-context characterization rather than evidence of cross-genotype dissemination. (Copyright © 2026 Altan, Rakıcı, Dündar and Özgümüş.) |
| Competing Interests: | The author(s) declared that this work was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. |
| References: | Antimicrob Agents Chemother. 2002 Mar;46(3):665-71. (PMID: 11850246) Int J Antimicrob Agents. 2011 Mar;37(3):230-4. (PMID: 21296557) Antimicrob Agents Chemother. 2006 Nov;50(11):3953-5. (PMID: 16954321) Antimicrob Agents Chemother. 1995 Jan;39(1):185-91. (PMID: 7695304) BMC Microbiol. 2011 Jul 05;11:159. (PMID: 21729271) PLoS One. 2014 Oct 06;9(10):e108409. (PMID: 25285537) Front Med (Lausanne). 2023 May 05;10:1163439. (PMID: 37215718) J Antimicrob Chemother. 2007 Aug;60(2):394-7. (PMID: 17561500) Nucleic Acids Res. 1993 May 11;21(9):2260. (PMID: 8502576) PLoS One. 2016 Jun 16;11(6):e0157693. (PMID: 27310255) Int J Environ Res Public Health. 2015 May 13;12(5):5177-95. (PMID: 25985315) Antimicrob Agents Chemother. 2001 Sep;45(9):2658-61. (PMID: 11502548) Jpn J Infect Dis. 2009 Sep;62(5):372-7. (PMID: 19762987) Int J Med Microbiol. 2011 Jan;301(1):34-43. (PMID: 20952251) J Med Microbiol. 2014 Nov;63(Pt 11):1524-1530. (PMID: 25165124) Expert Rev Anti Infect Ther. 2019 Nov;17(11):877-893. (PMID: 31658838) Biomed Res Int. 2019 Jun 27;2019:3917841. (PMID: 31346516) Antimicrob Agents Chemother. 2010 Jan;54(1):580-1. (PMID: 19841154) Biology (Basel). 2022 Jul 12;11(7):. (PMID: 36101423) Microb Drug Resist. 2002 Winter;8(4):245-51. (PMID: 12523620) Emerg Infect Dis. 2007 Apr;13(4):559-65. (PMID: 17553270) Methods Mol Biol. 2019;1962:227-245. (PMID: 31020564) Antimicrob Agents Chemother. 2006 Aug;50(8):2872-4. (PMID: 16870791) Ann Lab Med. 2015 Mar;35(2):246-9. (PMID: 25729729) J Antimicrob Chemother. 2018 May 1;73(5):1263-1266. (PMID: 29462315) J Comput Biol. 2012 May;19(5):455-77. (PMID: 22506599) Antimicrob Agents Chemother. 2025 Apr 02;69(4):e0012425. (PMID: 40047426) Nucleic Acids Res. 2020 Jan 8;48(D1):D561-D569. (PMID: 31722416) Antimicrob Agents Chemother. 2008 Oct;52(10):3823-5. (PMID: 18644963) Antimicrob Agents Chemother. 2005 May;49(5):1823-9. (PMID: 15855502) Antimicrob Agents Chemother. 2009 Feb;53(2):639-45. (PMID: 19064896) Osong Public Health Res Perspect. 2014 Aug;5(4):193-8. (PMID: 25379369) Curr Res Microb Sci. 2026 May 21;10:100609. (PMID: 42232807) Clin Infect Dis. 2024 Aug 07;:. (PMID: 39108079) J Clin Microbiol. 1995 Sep;33(9):2233-9. (PMID: 7494007) Bioinformatics. 2014 Jul 15;30(14):2068-9. (PMID: 24642063) Mikrobiyol Bul. 2014 Apr;48(2):201-12. (PMID: 24819258) |
| Contributed Indexing: | Keywords: Stenotrophomonas maltophilia; antimicrobial resistance; mobile genetic elements; molecular epidemiology; pulsed-field gel electrophoresis; resistance island; whole-genome sequencing |
| Substance Nomenclature: | 8064-90-2 (Trimethoprim, Sulfamethoxazole Drug Combination) 0 (Anti-Bacterial Agents) 6GNT3Y5LMF (Levofloxacin) FYY3R43WGO (Minocycline) |
| Entry Date(s): | Date Created: 20260926 Date Completed: 20260926 Latest Revision: 20260927 |
| Update Code: | 20260927 |
| PubMed Central ID: | PMC13612193 |
| DOI: | 10.3389/fcimb.2026.1926102 |
| PMID: | 42798368 |
| Database: | MEDLINE |
| FullText | Text: Availability: 0 CustomLinks: – Url: https://resolver.ebsco.com/c/fiv2js/result?sid=EBSCO:cmedm&genre=article&issn=22352988&ISBN=&volume=16&issue=&date=20260911&spage=1926102&pages=1926102&title=Frontiers in cellular and infection microbiology&atitle=Genomic%20characterization%20of%20a%20mobile-element-associated%20resistance%20island%20in%20trimethoprim-sulfamethoxazole-resistant%20Stenotrophomonas%20maltophilia%20isolates%20sharing%20the%20same%20PFGE%20genotype.&aulast=Altan%20G&id=DOI:10.3389/fcimb.2026.1926102 Name: Full Text Finder (for New FTF UI) (ns324271) Category: fullText Text: Full Text Finder MouseOverText: Full Text Finder |
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| Items | – Name: Title Label: Title Group: Ti Data: Genomic characterization of a mobile-element-associated resistance island in trimethoprim-sulfamethoxazole-resistant Stenotrophomonas maltophilia isolates sharing the same PFGE genotype. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Altan+G%22">Altan G</searchLink>; Department of Medical Microbiology, Faculty of Medicine, Kocaeli University, Kocaeli, Türkiye.<br /><searchLink fieldCode="AU" term="%22Rakıcı+E%22">Rakıcı E</searchLink>; Department of Medical Microbiology, Faculty of Medicine, Recep Tayyip Erdoğan University, Rize, Türkiye.<br /><searchLink fieldCode="AU" term="%22Dündar+D%22">Dündar D</searchLink>; Department of Medical Microbiology, Faculty of Medicine, Kocaeli University, Kocaeli, Türkiye.<br /><searchLink fieldCode="AU" term="%22Özgümüş+OB%22">Özgümüş OB</searchLink>; Department of Medical Microbiology, Faculty of Medicine, Recep Tayyip Erdoğan University, Rize, Türkiye. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22101585359%22">Frontiers in cellular and infection microbiology</searchLink> [Front Cell Infect Microbiol] 2026 Sep 11; Vol. 16, pp. 1926102. <i>Date of Electronic Publication: </i>2026 Sep 11 (<i>Print Publication: </i>2026). – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article – Name: Language Label: Language Group: Lang Data: English – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Frontiers+Media+SA%22">Frontiers Media SA </searchLink><i>Country of Publication: </i>Switzerland <i>NLM ID: </i>101585359 <i>Publication Model: </i>eCollection <i>Cited Medium: </i>Internet <i>ISSN: </i>2235-2988 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2222352988%22">22352988 </searchLink><i>NLM ISO Abbreviation: </i>Front Cell Infect Microbiol <i>Subsets: </i>MEDLINE – Name: PublisherInfo Label: Imprint Name(s) Group: PubInfo Data: <i>Original Publication</i>: Lausanne : Frontiers Media SA – Name: SubjectMESH Label: MeSH Terms Group: Su Data: <searchLink fieldCode="MM" term="%22Stenotrophomonas+maltophilia%22">Stenotrophomonas maltophilia*</searchLink>/<searchLink fieldCode="MM" term="%22Stenotrophomonas+maltophilia+genetics%22">genetics</searchLink> <br /><searchLink fieldCode="MM" term="%22Stenotrophomonas+maltophilia%22">Stenotrophomonas maltophilia*</searchLink>/<searchLink fieldCode="MM" term="%22Stenotrophomonas+maltophilia+drug+effects%22">drug effects</searchLink> <br /><searchLink fieldCode="MM" term="%22Stenotrophomonas+maltophilia%22">Stenotrophomonas maltophilia*</searchLink>/<searchLink fieldCode="MM" term="%22Stenotrophomonas+maltophilia+isolation+%26+purification%22">isolation & purification</searchLink> <br /><searchLink fieldCode="MM" term="%22Stenotrophomonas+maltophilia%22">Stenotrophomonas maltophilia*</searchLink>/<searchLink fieldCode="MM" term="%22Stenotrophomonas+maltophilia+classification%22">classification</searchLink> <br /><searchLink fieldCode="MM" term="%22Trimethoprim%2C+Sulfamethoxazole+Drug+Combination%22">Trimethoprim, Sulfamethoxazole Drug Combination*</searchLink>/<searchLink fieldCode="MM" term="%22Trimethoprim%2C+Sulfamethoxazole+Drug+Combination+pharmacology%22">pharmacology</searchLink> <br /><searchLink fieldCode="MM" term="%22Anti-Bacterial+Agents%22">Anti-Bacterial Agents*</searchLink>/<searchLink fieldCode="MM" term="%22Anti-Bacterial+Agents+pharmacology%22">pharmacology</searchLink> <br /><searchLink fieldCode="MM" term="%22Drug+Resistance%2C+Multiple%2C+Bacterial%22">Drug Resistance, Multiple, Bacterial*</searchLink>/<searchLink fieldCode="MM" term="%22Drug+Resistance%2C+Multiple%2C+Bacterial+genetics%22">genetics</searchLink> <br /><searchLink fieldCode="MM" term="%22Interspersed+Repetitive+Sequences%22">Interspersed Repetitive Sequences*</searchLink> <br /><searchLink fieldCode="MM" term="%22Genomic+Islands%22">Genomic Islands*</searchLink><br /><searchLink fieldCode="MH" term="%22Gram-Negative+Bacterial+Infections%22">Gram-Negative Bacterial Infections</searchLink>/<searchLink fieldCode="MH" term="%22Gram-Negative+Bacterial+Infections+microbiology%22">microbiology</searchLink> ; <searchLink fieldCode="MH" term="%22Levofloxacin%22">Levofloxacin</searchLink>/<searchLink fieldCode="MH" term="%22Levofloxacin+pharmacology%22">pharmacology</searchLink> ; <searchLink fieldCode="MH" term="%22Minocycline%22">Minocycline</searchLink>/<searchLink fieldCode="MH" term="%22Minocycline+pharmacology%22">pharmacology</searchLink> ; <searchLink fieldCode="MH" term="%22Humans%22">Humans</searchLink> ; <searchLink fieldCode="MH" term="%22Microbial+Sensitivity+Tests%22">Microbial Sensitivity Tests</searchLink> ; <searchLink fieldCode="MH" term="%22Electrophoresis%2C+Gel%2C+Pulsed-Field%22">Electrophoresis, Gel, Pulsed-Field</searchLink> ; <searchLink fieldCode="MH" term="%22Genotype%22">Genotype</searchLink> ; <searchLink fieldCode="MH" term="%22Whole+Genome+Sequencing%22">Whole Genome Sequencing</searchLink> ; <searchLink fieldCode="MH" term="%22Genome%2C+Bacterial%22">Genome, Bacterial</searchLink> – Name: Abstract Label: Abstract Group: Ab Data: Background: Stenotrophomonas maltophilia is an opportunistic nosocomial pathogen with intrinsic multidrug resistance and limited therapeutic options. This study integrated phenotypic susceptibility testing, targeted molecular screening, PFGE and short-read whole-genome sequencing (WGS) to characterize resistance determinants and their local genomic context in clinical-culture isolates.<br />Methods: Thirty-four non-duplicate clinical-culture isolates were analyzed. Susceptibility to trimethoprim-sulfamethoxazole (TMP-SMX), levofloxacin and minocycline was determined by disk diffusion. Minocycline testing was repeated with acceptable quality control, and the repeat-run zone records were reassessed using current CLSI breakpoints. A predefined, hypothesis-driven PCR panel was used to screen selected resistance-, efflux- and biofilm-associated targets, and gyrA, gyrB, parC and parE were sequenced. Genetic relatedness was assessed by XbaI-PFGE. Three selected isolates (S05, S08 and S25) underwent WGS as a targeted genomic-context analysis rather than a whole-collection population-genomic study.<br />Results: Resistance rates were 5.9% for TMP-SMX, 8.8% for levofloxacin and 11.8% for minocycline after reassessment using current CLSI minocycline breakpoints. Smqnr- and sul1-target PCR positivity was observed in 61.8% and 8.8% of isolates, respectively. A dfrA27-target PCR amplicon was observed in 82.4% of isolates but was not associated with TMP-SMX resistance and was not confirmed in the three sequenced genomes. No QRDR hotspot mutations were identified. The two TMP-SMX-resistant isolates, S05 and S08, shared the same PFGE genotype. Short-read WGS identified an identical 19,361-bp mobile-element-associated resistance region in these isolates, containing a putative Sul-family/folP-like dihydropteroate synthase (DHPS) annotation, two assembly-predicted hits each of bla<subscript>OXA-2</subscript> and ant(3''), multiple insertion sequences and a mercury-resistance module; the region was absent from S25.<br />Conclusions: The identical resistance region in two TMP-SMX-resistant isolates sharing the same PFGE genotype is compatible with shared ancestry, vertical inheritance or persistence of an island-carrying PFGE-defined genotype; horizontal transfer was not demonstrated. The discordance between dfrA27-target PCR positivity, phenotype and WGS highlights the need to interpret molecular screening together with phenotypic susceptibility and orthogonal confirmation. The WGS component provides a local genomic-context characterization rather than evidence of cross-genotype dissemination.<br /> (Copyright © 2026 Altan, Rakıcı, Dündar and Özgümüş.) – Name: Abstract Label: Competing Interests Group: Ab Data: The author(s) declared that this work was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. – Name: Ref Label: References Group: RefInfo Data: Antimicrob Agents Chemother. 2002 Mar;46(3):665-71. (PMID: <searchLink fieldCode="PM" term="%2211850246%22">11850246)</searchLink><br />Int J Antimicrob Agents. 2011 Mar;37(3):230-4. (PMID: <searchLink fieldCode="PM" term="%2221296557%22">21296557)</searchLink><br />Antimicrob Agents Chemother. 2006 Nov;50(11):3953-5. (PMID: <searchLink fieldCode="PM" term="%2216954321%22">16954321)</searchLink><br />Antimicrob Agents Chemother. 1995 Jan;39(1):185-91. (PMID: <searchLink fieldCode="PM" term="%227695304%22">7695304)</searchLink><br />BMC Microbiol. 2011 Jul 05;11:159. (PMID: <searchLink fieldCode="PM" term="%2221729271%22">21729271)</searchLink><br />PLoS One. 2014 Oct 06;9(10):e108409. (PMID: <searchLink fieldCode="PM" term="%2225285537%22">25285537)</searchLink><br />Front Med (Lausanne). 2023 May 05;10:1163439. (PMID: <searchLink fieldCode="PM" term="%2237215718%22">37215718)</searchLink><br />J Antimicrob Chemother. 2007 Aug;60(2):394-7. (PMID: <searchLink fieldCode="PM" term="%2217561500%22">17561500)</searchLink><br />Nucleic Acids Res. 1993 May 11;21(9):2260. (PMID: <searchLink fieldCode="PM" term="%228502576%22">8502576)</searchLink><br />PLoS One. 2016 Jun 16;11(6):e0157693. (PMID: <searchLink fieldCode="PM" term="%2227310255%22">27310255)</searchLink><br />Int J Environ Res Public Health. 2015 May 13;12(5):5177-95. 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(PMID: <searchLink fieldCode="PM" term="%2229462315%22">29462315)</searchLink><br />J Comput Biol. 2012 May;19(5):455-77. (PMID: <searchLink fieldCode="PM" term="%2222506599%22">22506599)</searchLink><br />Antimicrob Agents Chemother. 2025 Apr 02;69(4):e0012425. (PMID: <searchLink fieldCode="PM" term="%2240047426%22">40047426)</searchLink><br />Nucleic Acids Res. 2020 Jan 8;48(D1):D561-D569. (PMID: <searchLink fieldCode="PM" term="%2231722416%22">31722416)</searchLink><br />Antimicrob Agents Chemother. 2008 Oct;52(10):3823-5. (PMID: <searchLink fieldCode="PM" term="%2218644963%22">18644963)</searchLink><br />Antimicrob Agents Chemother. 2005 May;49(5):1823-9. (PMID: <searchLink fieldCode="PM" term="%2215855502%22">15855502)</searchLink><br />Antimicrob Agents Chemother. 2009 Feb;53(2):639-45. (PMID: <searchLink fieldCode="PM" term="%2219064896%22">19064896)</searchLink><br />Osong Public Health Res Perspect. 2014 Aug;5(4):193-8. (PMID: <searchLink fieldCode="PM" term="%2225379369%22">25379369)</searchLink><br />Curr Res Microb Sci. 2026 May 21;10:100609. (PMID: <searchLink fieldCode="PM" term="%2242232807%22">42232807)</searchLink><br />Clin Infect Dis. 2024 Aug 07;:. (PMID: <searchLink fieldCode="PM" term="%2239108079%22">39108079)</searchLink><br />J Clin Microbiol. 1995 Sep;33(9):2233-9. (PMID: <searchLink fieldCode="PM" term="%227494007%22">7494007)</searchLink><br />Bioinformatics. 2014 Jul 15;30(14):2068-9. (PMID: <searchLink fieldCode="PM" term="%2224642063%22">24642063)</searchLink><br />Mikrobiyol Bul. 2014 Apr;48(2):201-12. (PMID: <searchLink fieldCode="PM" term="%2224819258%22">24819258)</searchLink> – Name: SubjectMinor Label: Contributed Indexing Group: Data: <i>Keywords: </i>Stenotrophomonas maltophilia; antimicrobial resistance; mobile genetic elements; molecular epidemiology; pulsed-field gel electrophoresis; resistance island; whole-genome sequencing – Name: NumberCAS Label: Substance Nomenclature Group: ID Data: 8064-90-2 (Trimethoprim, Sulfamethoxazole Drug Combination)<br />0 (Anti-Bacterial Agents)<br />6GNT3Y5LMF (Levofloxacin)<br />FYY3R43WGO (Minocycline) – Name: DateEntry Label: Entry Date(s) Group: Date Data: <i>Date Created: </i>20260926 <i>Date Completed: </i>20260926 <i>Latest Revision: </i>20260927 – Name: DateUpdate Label: Update Code Group: Date Data: 20260927 – Name: PubmedCentralID Label: PubMed Central ID Group: ID Data: PMC13612193 – Name: DOI Label: DOI Group: ID Data: 10.3389/fcimb.2026.1926102 – Name: AN Label: PMID Group: ID Data: 42798368 |
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| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.3389/fcimb.2026.1926102 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 1926102 Subjects: – SubjectFull: Gram-Negative Bacterial Infections microbiology Type: general – SubjectFull: Levofloxacin pharmacology Type: general – SubjectFull: Minocycline pharmacology Type: general – SubjectFull: Humans Type: general – SubjectFull: Microbial Sensitivity Tests Type: general – SubjectFull: Electrophoresis, Gel, Pulsed-Field Type: general – SubjectFull: Genotype Type: general – SubjectFull: Whole Genome Sequencing Type: general – SubjectFull: Genome, Bacterial Type: general – SubjectFull: Stenotrophomonas maltophilia genetics Type: general – SubjectFull: Stenotrophomonas maltophilia drug effects Type: general – SubjectFull: Stenotrophomonas maltophilia isolation & purification Type: general – SubjectFull: Stenotrophomonas maltophilia classification Type: general – SubjectFull: Trimethoprim, Sulfamethoxazole Drug Combination pharmacology Type: general – SubjectFull: Anti-Bacterial Agents pharmacology Type: general – SubjectFull: Drug Resistance, Multiple, Bacterial genetics Type: general – SubjectFull: Interspersed Repetitive Sequences Type: general – SubjectFull: Genomic Islands Type: general Titles: – TitleFull: Genomic characterization of a mobile-element-associated resistance island in trimethoprim-sulfamethoxazole-resistant Stenotrophomonas maltophilia isolates sharing the same PFGE genotype. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Altan G – PersonEntity: Name: NameFull: Rakıcı E – PersonEntity: Name: NameFull: Dündar D – PersonEntity: Name: NameFull: Özgümüş OB IsPartOfRelationships: – BibEntity: Dates: – D: 11 M: 09 Text: 2026 Sep 11 Type: published Y: 2026 Identifiers: – Type: issn-electronic Value: 2235-2988 Numbering: – Type: volume Value: 16 Titles: – TitleFull: Frontiers in cellular and infection microbiology Type: main |
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