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Different subtype strains of Akkermansia muciniphila abundantly colonize in southern China.


ABSTRACT: This study investigates the colonization rate of Akkermansia muciniphila in the gastrointestinal tracts of people living in southern China and applies a modified method for the isolation and subtyping of A. muciniphila strains from faecal samples.Fresh faecal samples were collected and bacterial DNA was extracted from these samples for real-time PCR analysis. Strains were separated using a culture-dependent sPCR-directed method and classified using an enterobacterial repetitive intergenic consensus (ERIC-PCR) DNA fingerprinting method. The colonization rate for the sample population from southern China was 51·74%. We isolated 22 strains from human faeces. The results revealed that all strains were identifiable as A. muciniphila with 99-100% identity to the type-strain ATCC BAA-835. ERIC-PCR resulted in grouping of the DNA fingerprints showed that 12 distinct clusters were distinguished with a delineation level of 100%.Southern China has a high rate of A. muciniphila colonization and over 12 different subtype strains reside in faecal samples.Akkermansia muciniphila has a beneficial role in human gastrointestinal tract. These studies provide a better understanding of A. muciniphila and details of its colonization in the human gastrointestinal tract.

SUBMITTER: Guo X 

PROVIDER: S-EPMC4736461 | biostudies-literature | 2016 Feb

REPOSITORIES: biostudies-literature

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Different subtype strains of Akkermansia muciniphila abundantly colonize in southern China.

Guo X X   Zhang J J   Wu F F   Zhang M M   Yi M M   Peng Y Y  

Journal of applied microbiology 20160201 2


<h4>Aim</h4>This study investigates the colonization rate of Akkermansia muciniphila in the gastrointestinal tracts of people living in southern China and applies a modified method for the isolation and subtyping of A. muciniphila strains from faecal samples.<h4>Methods and results</h4>Fresh faecal samples were collected and bacterial DNA was extracted from these samples for real-time PCR analysis. Strains were separated using a culture-dependent sPCR-directed method and classified using an ente  ...[more]

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