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  A cryptic plasmid is among the most numerous genetic elements in the human gut

Fogarty, E. C., Schechter, M. S., Lolans, K., Sheahan, M. L., Veseli, I., Moore, R. M., et al. (2024). A cryptic plasmid is among the most numerous genetic elements in the human gut. CELL, 187(5). doi:10.1016/j.cell.2024.01.039.

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 Creators:
Fogarty, Emily C.1, Author
Schechter, Matthew S.1, Author
Lolans, Karen1, Author
Sheahan, Madeline L.1, Author
Veseli, Iva1, Author
Moore, Ryan M.1, Author
Kiefl, Evan1, Author
Moody, Thomas1, Author
Rice, Phoebe A.1, Author
Mimee, Mark1, Author
Chang, Eugene B.1, Author
Ruscheweyh, Hans-Joachim1, Author
Sunagawa, Shinichi1, Author
Mclellan, Sandra L.1, Author
Willis, Amy D.1, Author
Comstock, Laurie E.1, Author
Eren, A. Murat2, Author           
Yu, Michael K.1, Author
Affiliations:
1external, ou_persistent22              
2Max Planck Institute for Marine Microbiology, Max Planck Society, ou_2481692              

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 Abstract: Plasmids are extrachromosomal genetic elements that often encode fitness -enhancing features. However, many bacteria carry "cryptic"plasmids that do not confer clear beneficial functions. We identified one such cryptic plasmid, pBI143, which is ubiquitous across industrialized gut microbiomes and is 14 times as numerous as crAssphage, currently established as the most abundant extrachromosomal genetic element in the human gut. The majority of mutations in pBI143 accumulate in specific positions across thousands of metagenomes, indicating strong purifying selection. pBI143 is monoclonal in most individuals, likely due to the priority effect of the version first acquired, often from one's mother. pBI143 can transfer between Bacteroidales, and although it does not appear to impact bacterial host fitness in vivo, it can transiently acquire additional genetic content. We identified important practical applications of pBI143, including its use in identifying human fecal contamination and its potential as an alternative approach to track human colonic inflammatory states.

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Language(s): eng - English
 Dates: 2024-02-29
 Publication Status: Issued
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Title: CELL
Source Genre: Journal
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Pages: - Volume / Issue: 187 (5) Sequence Number: - Start / End Page: - Identifier: ISSN: 0092-8674