2022
DOI: 10.1101/2022.12.27.522048
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Cataloguing and profiling of the gut virome in Chinese populations uncover extensive viral signatures across common diseases

Abstract: The gut viral community has been linked to human physiology and health, but our knowledge of its genetic and functional contents and disease dependence is far from complete. Here, we collected 11,327 bulk or viral metagenomes from fecal samples from large-scale Chinese populations to establish a Chinese gut virus catalogue (cnGVC) comprising 67,096 nonredundant viral genomes. This catalogue included ~70% of novel viruses that are not represented in existing gut viral databases, and allowed us to characterize t… Show more

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Cited by 6 publications
(15 citation statements)
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“…To establish the composition of the gut viral community, we mapped clean reads of each sample to the cnGVC database, including 67,096 dereplicated vOTUs with high completeness ( 18 ). The rates of reads mapping to cnGVC ranged from 12.68% to 30.24% ( Figure 1A ), suggesting efficient capture of gut viral reads.…”
Section: Resultsmentioning
confidence: 99%
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“…To establish the composition of the gut viral community, we mapped clean reads of each sample to the cnGVC database, including 67,096 dereplicated vOTUs with high completeness ( 18 ). The rates of reads mapping to cnGVC ranged from 12.68% to 30.24% ( Figure 1A ), suggesting efficient capture of gut viral reads.…”
Section: Resultsmentioning
confidence: 99%
“…To analyze the composition of the gut viral community in metagenomic samples, we used a gut virus catalog comprising over 67,000 nonredundant viral operational taxonomic units (vOTUs) as the reference. This Chinese gut virus catalog (cnGVC) was constructed from over 10,000 publicly available fecal metagenomes from the Chinese population (including all samples used in the current study) ( 18 ). Briefly, the clean reads of each metagenomic sample were assembled into contigs using Megahit v1.2.9 ( 26 ).…”
Section: Methodsmentioning
confidence: 99%
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“…Only contigs of ≄5 kb in length were used to identify viral sequences in each sample. The identification, decontamination, and dereplication of viral sequences were performed according to the prior studies ( 20 , 47 – 49 ). Briefly, the assembled contigs underwent a stringent quality assessment as follows: (i) contigs were classified as viral if their viral gene content surpassed that of microbial genes, as determined by CheckV v0.7.0 ( 25 ); (ii) contigs exhibiting a P value of less than 0.01 and a score exceeding 0.90 in DeepVirFinder v1.0 ( 50 ); and (iii) identification as viral sequences by VIBRANT v1.2.1 ( 51 ) using default settings.…”
Section: Methodsmentioning
confidence: 99%