2023
DOI: 10.1007/s10142-023-01068-2
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Bacterial diversity of middle ear cholesteatoma by 16S rRNA gene sequencing in China

Abstract: In this study, the bacterial diversity of acquired middle ear cholesteatoma (MEC) was evaluated to reveal its pathogenesis and provides a guide for the use of antibiotics. Twenty-nine cases of acquired MEC and eight cases of healthy middle ears undergoing cochlear implantation (CI) were evaluated. Full-length 16S rRNA gene sequencing was performed to profile the bacterial communities in lesions and healthy tissues of the middle ear. ACE (P = 0.043) and Chao1 (P = 0.039) indices showed significant differences i… Show more

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Cited by 4 publications
(3 citation statements)
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“…Replicates within samples were more strongly clustered in the PCoA plot than in the unweighted plot ( Figure 4 ). An R-value closer to 1 in PERMANOVA/Anosim means that the difference between groups is significant and is greater than the difference within groups [ 33 ]. The p -value was less than 0.05, which means the reliability of the test was good.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Replicates within samples were more strongly clustered in the PCoA plot than in the unweighted plot ( Figure 4 ). An R-value closer to 1 in PERMANOVA/Anosim means that the difference between groups is significant and is greater than the difference within groups [ 33 ]. The p -value was less than 0.05, which means the reliability of the test was good.…”
Section: Discussionmentioning
confidence: 99%
“…The "vegan" package in R was used for PERMANOVA/Anosim. PERMANOVA/Anosim was used following the Liang's method [33]. Significant differences between different species were determined via a linear discriminant analysis (LDA) effect size (LEfSe) (https: //github.com/biobakery/lefse/, accessed on 22 June 2023) with two as the default filter value for the LDA score.…”
Section: Discussionmentioning
confidence: 99%
“…The specific forward primer 27F (5 -AGRGTTTGATYNTGGCTCAG-3 ) and reverse primer 1492R (5 -TASGGHTACCTTGTTASGACTT-3 ) that targeted the full 16S rRNA gene of the bacteria were synthesized with the barcodes attached, followed by PCR amplification and then product purification, quantification, and normalization to form the single-molecule real-time (SMRT) Bell sequencing libraries. The libraries were then treated with high-throughput sequencing (HTS) using a PacBio Sequel system (PacBio) [12], which resulted in data in bam format. These data were exported as CCS files via the SMRTlink analysis software (SMRTLink V12.0, Pacific Biosciences of California, Inc., San Diego, CA, USA).…”
Section: The 16s Rrna Full-length Sequencingmentioning
confidence: 99%