2021
DOI: 10.1016/j.aqrep.2021.100907
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Comparative analysis of gut bacterial community composition during a single day cycle in Chinese mitten crab (Eriocheir sinensis)

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Cited by 16 publications
(8 citation statements)
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“…When comparing the relative abundances of the 18:00 h group bacterial species, Vibrio rumoiensis was found to be the most abundant taxon. This result is consistent with our previous study involving a single-day microbiota analysis of Chinese mitten crabs 39 . However, many species in the present study were only observed to be highly abundant in the 12:00 h group, which may be due to changing the feeding time of the crabs.…”
Section: Discussionsupporting
confidence: 93%
“…When comparing the relative abundances of the 18:00 h group bacterial species, Vibrio rumoiensis was found to be the most abundant taxon. This result is consistent with our previous study involving a single-day microbiota analysis of Chinese mitten crabs 39 . However, many species in the present study were only observed to be highly abundant in the 12:00 h group, which may be due to changing the feeding time of the crabs.…”
Section: Discussionsupporting
confidence: 93%
“…Previous studies have shown that miRNA expression may be positively correlated with or contrary to corresponding gene expression trends 51 . Combining these data suggest that crab immune response could vary under daily rhythm, possibly upregulated around 18:00, which is consistent with recent studies in our laboratory where diurnal variation in the gut bacterial community of E. sinensis showed that its immune function was more robust at 18:00 52 . Furthermore, we found endopeptidase and catalytic pathways enriched with a large number of putative target genes under circadian.…”
Section: Discussionsupporting
confidence: 92%
“…Briefly, the V3–V4 region of the bacterial 16S ribosomal RNA gene was amplified using PCR with the primers F 5′-ACTCCTACGGGAGGCAGCA-3′ and R 5′-CGGACTACHVGGGTWTCTAAT-3′. The forward primer ITSF (5′-GGAAGTAAAAGTCGTAACAAGG-3′) and reverse primer ITSR (5′-GCTGCGTTCTTCATCGATGC-3′) were used to amplify the fungal internal transcribed spacer (ITS) V1 regions 20 . Thermal cycling consisted of initial denaturation at 98 °C for 5 min, followed by 28 cycles of denaturation at 98 °C for 30 s, annealing at 55 °C for 30 s, and extension at 72 °C for 45 s, with a final extension of 5 min at 72 °C.…”
Section: Methodsmentioning
confidence: 99%