Our understanding of the interactions between microbial communities
and their niche in the host gut has improved owing
to recent advances in environmental microbial genomics.
Integration of metagenomic and metataxonomic sequencing
data with other omics data to study the gut microbiome
has become increasingly common, but downstream analysis
after data integration and interpretation of complex omics
data remain challenging. Here, we review studies that have
explored the gut microbiome signature using omics approaches,
including metagenomics, metataxonomics, metatranscriptomics,
and metabolomics. We further discuss recent
analytics programs to analyze and integrate multi-omics datasets
and further utilization of omics data with other advanced
techniques, such as adaptive immune receptor repertoire sequencing,
microbial culturomics, and machine learning, to
evaluate important microbiome characteristics in the gut.
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A Gram-stain-negative, mucus-forming, motile by gliding,
non-spore-forming and short rod-shaped bacterial strain
designated R1-15T was isolated from soil and its taxonomic
position was evaluated using a polyphasic approach. Strain
R1-15T grew at 15–37°C (optimum, 30°C), at pH 6–7 (optimum,
pH 6) and in the presence of 0–1% (w/v) NaCl (optimum,
0%) on 0.1X TSA. On the basis of 16S rRNA gene sequence
similarity, the novel strain was assigned to the family
Chitinophagaceae of the phylum Bacteroidetes, and its closest
related taxa were species of the genera Taibaiella (88.76–
90.02% sequence similarity), Lacibacter (89.24–90.00%), Chitinophaga
(88.61–89.76%), and Terrimonas (89.04%). Flexirubin-
type pigments were produced. The only isoprenoid
quinone was MK-7, and the major polar lipid was phosphatidylethanolamine.
Based on whole genome comparisons
between the strain R1-15T and the type strains of relatives,
the orthologous average nucleotide identity values were 66.9–
67.0%. The DNA G+C content of strain R1-15T was 43.8
mol%. The combination of phylogenetic, chemotaxonomic
and phenotypic data clearly supported separation of strain
R1-15T from related taxa, and thus the name Mucibacter
soli gen. nov., sp. nov. is proposed. The type strain is R1-15T
(= KCTC 62274T = JCM 31190T).
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Pseudomonas aeruginosa has been identified as an important
causative agent of airway infection, mainly in cystic fibrosis.
This disease is characterized by defective mucociliary clearance
induced in part by mucus hyper-production. Mucin is
a major component of airway mucus and is heavily O-glycosylated,
with a protein backbone. Airway infection is known
to be established with bacterial adhesion to mucin. However,
the genes involved in mucin degradation or utilization remain
elusive. In this study, we sought to provide a genetic basis of
P. aeruginosa airway growth by identifying those genes. First,
using RNASeq analyses, we compared genome-wide expression
profiles of PAO1, a prototype P. aeruginosa laboratory
strain, grown in M9-mucin (M9M) and M9-glucose (M9G)
media. Additionally, a PAO1 transposon (Tn) insertion mutants
library was screened for mutants defective in growth
in M9M medium. One mutant with a Tn insertion in the
xcpU gene (PA3100) was determined to exhibit faulty growth
in M9M medium. This gene contributes to the type II secretion
system, suggesting that P. aeruginosa uses this secretion
system to produce a number of proteins to break down and
assimilate the mucin molecule. Furthermore, we screened
the PAO1 genome for genes with protease activity. Of 13 mutants,
one with mutation in PA3247 gene exhibited defective
growth in M9M, suggesting that the PA3247-encoded protease
plays a role in mucin utilization. Further mechanistic
dissection of this particular process will reveal new drug targets,
the inhibition of which could control recalcitrant P. aeruginosa
infections.
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Citrobacter rodentium
possesses a functional type II secretion system necessary for successful host infection
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Pseudomonas aeruginosa type IV pili actively induce mucus contraction to form biofilms in tissue-engineered human airways Tamara Rossy, Tania Distler, Lucas A. Meirelles, Joern Pezoldt, Jaemin Kim, Lorenzo Talà, Nikolaos Bouklas, Bart Deplancke, Alexandre Persat, Victor Sourjik PLOS Biology.2023; 21(8): e3002209. CrossRef
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Structural and functional analysis of the carotenoid biosynthesis genes of aPseudomonasstrain isolated from the excrement of Autumn Darter Yuki Fukaya, Miho Takemura, Takashi Koyanagi, Takashi Maoka, Kazutoshi Shindo, Norihiko Misawa Bioscience, Biotechnology, and Biochemistry.2018; 82(6): 1043. CrossRef
Evolutionary conservation of the antimicrobial function of mucus: a first defence against infection Cassie R Bakshani, Ana L Morales-Garcia, Mike Althaus, Matthew D Wilcox, Jeffrey P Pearson, John C Bythell, J Grant Burgess npj Biofilms and Microbiomes.2018;[Epub] CrossRef
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Bacterial lectins are carbohydrate-binding adhesins that recognize
glycoreceptors in the gut mucus and epithelium of
hosts. In this study, the contribution of lectin-like activities
to adhesion of Lactobacillus mucosae LM1 and Lactobacillus
johnsonii PF01, which were isolated from swine intestine,
were compared to those of the commercial probiotic Lactobacillus
rhamnosus GG. Both LM1 and PF01 strains have
been reported to have good adhesion ability to crude intestinal
mucus of pigs. To confirm this, we quantified their adhesion
to porcine gastric mucin and intestinal porcine enterocytes
isolated from the jejunum of piglets (IPEC-J2). In addition,
we examined their carbohydrate-binding specificities by suspending
bacterial cells in carbohydrate solutions prior to adhesion
assays. We found that the selected carbohydrates affected
the adherences of LM1 to IPEC-J2 cells and of LGG to
mucin. In addition, compared to adhesion to IPEC-J2 cells,
adhesion to mucin by both LM1 and LGG was characterized
by enhanced specific recognition of glycoreceptor components
such as galactose, mannose, and N-acetylglucosamine.
Hydrophobic interactions might make a greater contribution
to adhesion of PF01. A similar adhesin profile between a probiotic
and a pathogen, suggest a correlation between shared
pathogen–probiotic glycoreceptor recognition and the ability
to exclude enteropathogens such as Escherichia coli K88 and
Salmonella Typhimurium KCCM 40253. These findings extend
our understanding of the mechanisms of the intestinal
adhesion and pathogen-inhibition abilities of probiotic Lactobacillus
strains.
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