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        <datestamp>2026-10-01T05:43:24Z</datestamp>
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          <dc:title>Table 1_Viral metagenomic characterization of HAdV-B-related signals in bronchoalveolar lavage fluid from pediatric and adult clinical cohorts.xlsx</dc:title>
          <dc:creator>Chunyan Zhao (141856)</dc:creator>
          <dc:creator>Jiaheng Chen (23097283)</dc:creator>
          <dc:creator>Ping Wu (46628)</dc:creator>
          <dc:creator>Wen Zhang (7555)</dc:creator>
          <dc:creator>Songyi Ning (11685460)</dc:creator>
          <dc:subject>Public Health and Health Services not elsewhere classified</dc:subject>
          <dc:subject>bronchoalveolar lavage fluid</dc:subject>
          <dc:subject>HAdV-B</dc:subject>
          <dc:subject>human adenovirus</dc:subject>
          <dc:subject>metagenomic next-generation sequencing</dc:subject>
          <dc:subject>pediatric pneumonia</dc:subject>
          <dc:description>&lt;p&gt;Human adenovirus (HAdV) is an important respiratory virus in children, but sequence-level evidence for HAdV-related signals in lower respiratory tract samples remains limited. In this study, we analyzed metagenomic next-generation sequencing data from 189 bronchoalveolar lavage fluid (BALF) libraries from pediatric and adult clinical cohorts, including 30 pediatric and 159 adult patients, together with laboratory environmental controls. MEGAN read-level classification was used to screen for Adenoviridae-related signals. HAdV-related contigs were further reviewed, and a BALF-derived HAdV-B-related representative contig was selected for read recruitment and coverage analysis. Phylogenetic trees were reconstructed using penton base, hexon, and fiber protein sequences. Adenoviridae-classified signals were more apparent in pediatric BALF libraries than in adult BALF libraries or environmental controls. Several pediatric BALF libraries showed broad read coverage across the HAdV-B-related representative contig, whereas adult libraries and environmental controls mainly showed low-coverage-breadth signals. Phylogenetic analysis placed BALF-derived penton base, hexon, and fiber sequences within HAdV-B-related lineages. Twenty-seven capsid protein sequences from 12 pediatric samples had best BLASTp matches to references annotated as HAdV-B3 (n = 23) or HAdV-B7 (n = 4). These findings provide sequence evidence for HAdV-B-related sequence signals in clinically selected pediatric BALF samples and support further investigation using targeted assays and genome sequencing.&lt;/p&gt;</dc:description>
          <dc:date>2026-10-01T05:43:24Z</dc:date>
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          <dc:identifier>10.3389/fpubh.2026.1961482.s003</dc:identifier>
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          <dc:rights>CC BY 4.0</dc:rights>
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