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<p>Drinking-water distribution systems (DWDS) impose ecological pressures shaped by oligotrophy, surface attachment, hydraulic fluctuation, and residual disinfectants. These conditions may favor stress-tolerant and biofilm-capable microorganisms, including members of the <i>Stenotrophomonas maltophilia</i> complex. Although this complex is clinically relevant because of intrinsic multidrug resistance and opportunistic pathogenic potential, the strain-level genomic features that may support persistence in disinfectant-managed water systems remain incompletely characterized. We applied an integrated genome-resolved framework to <i>Stenotrophomonas</i> sp. NG-SM01, a drinking-water isolate assigned to the <i>S. maltophilia</i> complex genomospecies Sgn4. Hybrid sequencing was used to generate a closed genome assembly, followed by phylogenomics and MLST for taxonomic placement, pangenome analysis for gene-content context, and genomic-island mapping to identify candidate accessory regions. Functional profiling included BacMet screening for metal/biocide tolerance-associated loci and genome-scale metabolic reconstruction using gapseq.&#xa0;Phenotypic assays assessed crystal-violet biofilm biomass and acute hydrogen peroxide (H₂O₂) survival as a general oxidative-stress proxy. NG-SM01 clustered within the Sgn4 genomospecies of the <i>S. maltophilia</i> complex and formed a strongly supported sister lineage to its closest available reference genome, GCF_025642255.1 (UFboot = 100). MLST confirmed a newly curated <i>guaA</i> allele (<i>guaA</i>-909), and the allelic profile was assigned ST1409. Disk diffusion showed limited inhibition by several antimicrobial agents; however, categorical interpretation using <i>S. maltophilia</i>-specific CLSI criteria was applied only to levofloxacin and trimethoprim–sulfamethoxazole, both of which were susceptible. Genomic-island analysis highlighted two candidate loci potentially relevant to stress adaptation: GI_6, carrying an EPS/envelope-remodeling cassette including <i>algL</i> and a GT26-family glycosyltransferase within a panel-restricted architecture, and GI_4, an IME-associated region located near SOS-response genes including <i>recA</i>, <i>recX</i>, and <i>lexA</i>. NG-SM01 formed reproducible moderate biofilm biomass under static microtiter conditions and showed plateau-like survival dynamics during acute H₂O₂ exposure. BacMet screening prioritized Tier-1 metal/biocide tolerance-associated signals, including CzcR-like and AdeL-like regulators and a YfeB-like transport component, while gapseq reconstruction predicted broad transport capacity, including 1,920 transporter entries, of which 23% were metal-related. This single-isolate study identifies genomic and phenotypic features potentially relevant to persistence in a drinking-water <i>S. maltophilia</i> complex Sgn4 isolate. The combined evidence supports a hypothesis-generating “Switch–Shield” framework, in which stress-response regulation and mobilome-associated plasticity may represent a candidate “switch,” while EPS/envelope remodeling may represent a candidate protective “shield.” However, direct causality between GI_4/GI_6 and the observed phenotypes was not demonstrated. Future validation using transcriptomics, mutant-based assays, and DWDS-mimetic free-chlorine or chloramine exposure models, including flow/pipe reactors with detachment and shedding measurements, will be required to test this model.</p>

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Genomic analysis identifies candidate SOS-associated and EPS/envelope-remodeling islands in a drinking-water Stenotrophomonas maltophilia complex isolate

  • 期刊论文

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  • 发表日期：

    2026年6月28日

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  • Farouk Hassan,
  • Süheyla Türkyılmaz,
  • Taghrid S. El-Mahdy

摘要

Drinking-water distribution systems (DWDS) impose ecological pressures shaped by oligotrophy, surface attachment, hydraulic fluctuation, and residual disinfectants. These conditions may favor stress-tolerant and biofilm-capable microorganisms, including members of the Stenotrophomonas maltophilia complex. Although this complex is clinically relevant because of intrinsic multidrug resistance and opportunistic pathogenic potential, the strain-level genomic features that may support persistence in disinfectant-managed water systems remain incompletely characterized. We applied an integrated genome-resolved framework to Stenotrophomonas sp. NG-SM01, a drinking-water isolate assigned to the S. maltophilia complex genomospecies Sgn4. Hybrid sequencing was used to generate a closed genome assembly, followed by phylogenomics and MLST for taxonomic placement, pangenome analysis for gene-content context, and genomic-island mapping to identify candidate accessory regions. Functional profiling included BacMet screening for metal/biocide tolerance-associated loci and genome-scale metabolic reconstruction using gapseq. Phenotypic assays assessed crystal-violet biofilm biomass and acute hydrogen peroxide (H₂O₂) survival as a general oxidative-stress proxy. NG-SM01 clustered within the Sgn4 genomospecies of the S. maltophilia complex and formed a strongly supported sister lineage to its closest available reference genome, GCF_025642255.1 (UFboot = 100). MLST confirmed a newly curated guaA allele (guaA-909), and the allelic profile was assigned ST1409. Disk diffusion showed limited inhibition by several antimicrobial agents; however, categorical interpretation using S. maltophilia-specific CLSI criteria was applied only to levofloxacin and trimethoprim–sulfamethoxazole, both of which were susceptible. Genomic-island analysis highlighted two candidate loci potentially relevant to stress adaptation: GI_6, carrying an EPS/envelope-remodeling cassette including algL and a GT26-family glycosyltransferase within a panel-restricted architecture, and GI_4, an IME-associated region located near SOS-response genes including recA, recX, and lexA. NG-SM01 formed reproducible moderate biofilm biomass under static microtiter conditions and showed plateau-like survival dynamics during acute H₂O₂ exposure. BacMet screening prioritized Tier-1 metal/biocide tolerance-associated signals, including CzcR-like and AdeL-like regulators and a YfeB-like transport component, while gapseq reconstruction predicted broad transport capacity, including 1,920 transporter entries, of which 23% were metal-related. This single-isolate study identifies genomic and phenotypic features potentially relevant to persistence in a drinking-water S. maltophilia complex Sgn4 isolate. The combined evidence supports a hypothesis-generating “Switch–Shield” framework, in which stress-response regulation and mobilome-associated plasticity may represent a candidate “switch,” while EPS/envelope remodeling may represent a candidate protective “shield.” However, direct causality between GI_4/GI_6 and the observed phenotypes was not demonstrated. Future validation using transcriptomics, mutant-based assays, and DWDS-mimetic free-chlorine or chloramine exposure models, including flow/pipe reactors with detachment and shedding measurements, will be required to test this model.