2020
DOI: 10.1007/s10126-020-09987-y
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Elucidation of Gut Microbiota in Mud Crab Scylla paramamosain Challenged to WSSV and Aeromonas hydrophila

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Cited by 11 publications
(7 citation statements)
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“…Firmicutes represented 78% of analyzed sequences in the current study. Previous studies reported that other phyla, such as Proteobacteria , Acidobacteria , and Bacteroidetes , dominated the intestinal assemblage of Chinese mitten crabs (Shi et al 2019 ; Su et al 2020 ), fiddler crabs (Cuellar-Gempeler and Leibold 2018 , 2019 ), mud crabs (Wei et al 2019b ; Lin et al 2020 ), and vent crabs (Zhang et al 2017 ). We also found that Proteobacteria and Bacteroidetes dominated wild and pond-raised Chinese mitten crabs (Li et al 2007 ).…”
Section: Discussionmentioning
confidence: 99%
“…Firmicutes represented 78% of analyzed sequences in the current study. Previous studies reported that other phyla, such as Proteobacteria , Acidobacteria , and Bacteroidetes , dominated the intestinal assemblage of Chinese mitten crabs (Shi et al 2019 ; Su et al 2020 ), fiddler crabs (Cuellar-Gempeler and Leibold 2018 , 2019 ), mud crabs (Wei et al 2019b ; Lin et al 2020 ), and vent crabs (Zhang et al 2017 ). We also found that Proteobacteria and Bacteroidetes dominated wild and pond-raised Chinese mitten crabs (Li et al 2007 ).…”
Section: Discussionmentioning
confidence: 99%
“…Based on our previous studies ( 55 , 56 ), the period 24 h postinfection was chosen for sampling in this study. Total RNA of hemolymph collected from mud crabs was isolated using TRIzol reagent (Ambion, USA) according to the manufacturer’s instructions.…”
Section: Methodsmentioning
confidence: 99%
“…The V4 region of the bacterial 16S rRNA gene was amplified using the primers 515F (5 -GTGCCAGCMGCCGCGGTAA-3 ) and 806R (5 -GGACTACHVGGGTWTCTAAT-3 ) in PCR reactions. Each PCR reaction performed consisted of 10 ng of DNA templates, 2 µM of forward and reverse primers, and 15 µL of Phusion ® High-Fidelity PCR Master Mix (New England Biolabs, Ipswich, MA, USA) [31]. Thermal cycling was carried out with an initial denaturation at 98 • C for 1 min, followed by 30 cycles of denaturation at 98 • C for 10 s, annealing at 50 • C for 30 s, and elongation at 72 • C for 30 s, with a final extension at 72 • C for 5 min.…”
Section: Dna Extraction Pcr Amplification Library Preparation and Seq...mentioning
confidence: 99%
“…Thermal cycling was carried out with an initial denaturation at 98 • C for 1 min, followed by 30 cycles of denaturation at 98 • C for 10 s, annealing at 50 • C for 30 s, and elongation at 72 • C for 30 s, with a final extension at 72 • C for 5 min. The PCR products were detected on a 2% agarose gel and purified using a Qiagen Gel Extraction Kit (Qiagen, Hilden, Germany) [31]. Sequencing libraries were generated using a TruSeq ® DNA PCR-Free Sample Preparation Kit (Illumina, San Diego, CA, USA), and index codes were added.…”
Section: Dna Extraction Pcr Amplification Library Preparation and Seq...mentioning
confidence: 99%
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