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Circulating 16S RNA in Biofluids: Extracellular Vesicles as Mirrors of Human Microbiome?
Ricci, Veronica; Carcione, Davide; Messina, Simone; Colombo, Gualtiero I; D'Alessandra, Yuri.
Affiliation
  • Ricci V; Unit of Immunology and Functional Genomics, Centro Cardiologico Monzino-IRCCS, 20138 Milan, Italy.
  • Carcione D; Dipartimento di Medicina Clinica e Chirurgia, Università degli Studi di Napoli Federico II, 80138 Napoli, Italy.
  • Messina S; Unit of Laboratory Medicine, Centro Cardiologico Monzino-IRCCS, 20138 Milan, Italy.
  • Colombo GI; Unit of Immunology and Functional Genomics, Centro Cardiologico Monzino-IRCCS, 20138 Milan, Italy.
  • D'Alessandra Y; Unit of Immunology and Functional Genomics, Centro Cardiologico Monzino-IRCCS, 20138 Milan, Italy.
Int J Mol Sci ; 21(23)2020 Nov 25.
Article in En | MEDLINE | ID: mdl-33255779
The human body is inhabited by around 1013 microbes composing a multicomplex system, termed microbiota, which is strongly involved in the regulation and maintenance of homeostasis. Perturbations in microbiota composition can lead to dysbiosis, which has been associated with several human pathologies. The gold-standard method to explore microbial composition is next-generation sequencing, which involves the analysis of 16S rRNA, an indicator of the presence of specific microorganisms and the principal tool used in bacterial taxonomic classification. Indeed, the development of 16S RNA sequencing allows us to explore microbial composition in several environments and human body districts and fluids, since it has been detected in "germ-free" environments such as blood, plasma, and urine of diseased and healthy subjects. Recently, prokaryotes showed to generate extracellular vesicles, which are known to be responsible for shuttling different intracellular components such as proteins and nucleic acids (including 16S molecules) by protecting their cargo from degradation. These vesicles can be found in several human biofluids and can be exploited as tools for bacterial detection and identification. In this review, we examine the complex link between circulating 16S RNA molecules and bacteria-derived vesicles.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: RNA, Ribosomal, 16S / Dysbiosis / Extracellular Vesicles / Cell-Free Nucleic Acids Limits: Humans Language: En Journal: Int J Mol Sci Year: 2020 Type: Article Affiliation country: Italy

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: RNA, Ribosomal, 16S / Dysbiosis / Extracellular Vesicles / Cell-Free Nucleic Acids Limits: Humans Language: En Journal: Int J Mol Sci Year: 2020 Type: Article Affiliation country: Italy