Abstract
Methanogens commonly inhabit swine intestine. We analyzed the gut archaeal population by extracting DNA from the
feces of nine piglets. We performed PCR to target the V6–V8 region of the 16S rRNA gene. Subsequent denaturing gradient
gel electrophoresis (DGGE) revealed the presence of Methanobrevibacter boviskoreani, which has not previously been identified
in pigs. We confirmed these data with a PCR-DGGE analysis of the mcrA gene, and subsequent sequencing. At 63 days old,
the only band in fecal samples corresponded to M. boviskoreani. The DGGE analysis also showed that Methanobrevibacter
smithii, which was abundant at 28 days, was dramatically reduced at 42 days, and it completely disappeared at 63 days. To
confirm these data, we quantified M. smithii and the total archaeal population by quantitative PCR (qPCR); moreover, we
designed a new set of species-specific primers based on the 16S rRNA gene of M. boviskoreani. The qPCR results confirmed
the reduction in M. smithii over time and a simultaneous increase in M. boviskoreani. At 63 days, the total numbers of
archaea and M. boviskoreani genomes were comparable, which suggested that M. boviskoreani represented the dominant
archaea. This work showed that the archaeal population shifted during weaning, and M. boviskoreani replaced M. smithii
Lingua originale | English |
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pagine (da-a) | N/A-N/A |
Rivista | FEMS Microbiology Letters |
DOI | |
Stato di pubblicazione | Pubblicato - 2015 |
Keywords
- 16S rRNA gene
- PCR-DGGE
- mcrA gene
- methanogenic archaea
- qPCR