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        <datestamp>2026-09-23T05:44:44Z</datestamp>
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          <dc:title>Table 1_Pan-genome analysis identifies a Burkholderia cepacia-specific gene marker for rapid species-level identification.xlsx</dc:title>
          <dc:creator>Kun Cheng (1395379)</dc:creator>
          <dc:creator>Shuaicheng Mu (11136369)</dc:creator>
          <dc:creator>Huifen Feng (151840)</dc:creator>
          <dc:creator>Rui Liu (54031)</dc:creator>
          <dc:creator>Jie Liu (15128)</dc:creator>
          <dc:creator>Ling Li (38566)</dc:creator>
          <dc:creator>Jiaqi Liu (309587)</dc:creator>
          <dc:creator>Weiwei Wu (244139)</dc:creator>
          <dc:creator>Yuanyuan Ge (1567765)</dc:creator>
          <dc:creator>Lei Zhai (1853257)</dc:creator>
          <dc:creator>Su Yao (3627038)</dc:creator>
          <dc:subject>Microbiology</dc:subject>
          <dc:subject>Burkholderia cepacia</dc:subject>
          <dc:subject>gene marker</dc:subject>
          <dc:subject>pan-genome</dc:subject>
          <dc:subject>PCR</dc:subject>
          <dc:subject>species-level identification</dc:subject>
          <dc:description>Inroduction&lt;p&gt;Burkholderia cepacia is a representative member of the Burkholderia cepacia complex (Bcc) and is widely distributed in water and soil environments. It has a propensity to form biofilms in water-based products, making it a significant contaminant in the pharmaceutical, cosmetic, and food industries and posing threats to product quality control and public health. Therefore, rapid and accurate species-level identification of B. cepacia is of great importance.&lt;/p&gt;Methods&lt;p&gt;To achieve rapid and accurate species-level identification of B. cepacia, we performed a pan-genome analysis based on 138 high-quality genome sequences covering B. cepacia and its closely related Bcc species with taxonomic positions validated by average nucleotide identity (ANI) analysis. A conserved core gene encoding a glycosyl hydrolase family 18 (GH18) protein was identified as a species-specific molecular marker. A specific primer pair comprising SEQ ID NO.2 and SEQ ID NO.3 was designed based on this marker and validated with both genome sequences and bacterial pure cultures.&lt;/p&gt;Results&lt;p&gt;The GH18-encoding gene is highly conserved across 115 B. cepacia strains (sequence identities ranging from 90.3 to 100.0%) and is absent in all other Bcc species examined. The primer pair exhibited high inclusivity and exclusivity for B. cepacia. The established PCR method achieved a detection limit of 5 pg/μL for pure genomic DNA and 10&lt;sup&gt;3&lt;/sup&gt; CFU/mL in artificially contaminated water-based personal care and medical device products.&lt;/p&gt;Discussion&lt;p&gt;The identification of this conserved core gene provides a promising basis for the rapid and accurate species-level detection of B. cepacia. Given the widespread occurrence of B. cepacia in water and soil environments and its ability to form biofilms in water-based products, such a species-specific molecular marker may help improve contamination monitoring and quality control in the pharmaceutical, cosmetic, and food industries, thereby contributing to public health protection.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-23T05:44:44Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Dataset</dc:type>
          <dc:identifier>10.3389/fmicb.2026.1915686.s001</dc:identifier>
          <dc:relation>https://figshare.com/articles/dataset/Table_1_Pan-genome_analysis_identifies_a_Burkholderia_cepacia-specific_gene_marker_for_rapid_species-level_identification_xlsx/33971038</dc:relation>
          <dc:rights>CC BY 4.0</dc:rights>
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