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Updated: Aug 24, 2026

Phage Phenomics: Physiological Approaches to Characterize Novel Viral Proteins
Published on: June 11, 2015
The Mycoplasma fermentans prophage phiMFV1: genome organization, mobility and variable expression of an encoded
K Röske1, M J Calcutt, K S Wise
1Department of Molecular Microbiology and Immunology, University of Missouri-Columbia, Columbia, MO 65212, USA.
Abstract:
The approximately 16 kb genome of the Mycoplasma fermentans phiMFV1 prophage is described, and its mobility, replication and effect on the mycoplasma surface phenotype are demonstrated. In various M. fermentans strains, phiMFV1 was either absent or integrated at diverse (and sometimes multiple) chromosomal sites, each marked by a conserved TTTTTA target sequence that is duplicated upon integration. Precise excision, replication of an extrachromosomal form and loss of phiMFV1 from the mycoplasmal genome were documented in a series of clonal derivatives of M. fermentans propagated in culture. Of 18 open reading frames (ORFs) encoded by phiMFV1, most can be ascribed functions related to phage biology, whereas one encodes a unique coiled-coil membrane surface protein, Mem, that was confirmed to be expressed in propagating populations of M. fermentans. With the exception of Mem and other minor ORFs, the striking similarity between the deduced proteomes of phiMFV1 and the recently described phiMAV1 of arthritogenic strains of Mycoplasma arthritidis, along with the prominent gene synteny between these elements, provides the taxonomic basis for a new family of prophage. Their coding features are consistent with long-term residence in mycoplasma genomes and the divergence of species within a phylogenetic clade of mycoplasmas. The unique Mem protein expressed from phiMFV1 and the unique hypothetical surface lipoproteins encoded by phiMAV1 and phiMFV1 also suggest that prophage-associated genes may provide specific, selectable phenotypic traits during co-evolution of mycoplasma species with their respective mammalian hosts. Retention of these labile prophage elements in organisms with such drastically reduced genome sizes implies a significant role in adaptation and survival.
Insights
The Mycoplasma fermentans phiMFV1 prophage exhibits mobility and encodes a unique surface protein, Mem. Its similarity to phiMAV1 suggests a new prophage family crucial for mycoplasma adaptation.
Area of Science:
- Microbiology
- Virology
- Genomics
Background:
- Mycoplasma fermentans harbors the phiMFV1 prophage, a mobile genetic element.
- Prophages can influence host cell phenotype and genome evolution.
Purpose of the Study:
- To characterize the Mycoplasma fermentans phiMFV1 prophage.
- To investigate its mobility, replication, and impact on the host's surface phenotype.
- To establish its taxonomic relationship with other prophages.
Main Methods:
- Genomic analysis of phiMFV1.
- Tracking prophage integration and excision in M. fermentans strains.
- Identification and characterization of open reading frames (ORFs) and encoded proteins, including the Mem protein.
- Comparative proteomic and syntenic analysis with phiMAV1.
Main Results:
- phiMFV1 is approximately 16 kb and integrates into M. fermentans chromosomes at specific target sites.
- The prophage can excise, replicate as an extrachromosomal form, and be lost from the host genome.
- phiMFV1 encodes 18 ORFs, including the unique surface protein Mem, which is expressed by the host.
- phiMFV1 shares significant genomic and proteomic similarity with phiMAV1, supporting a new prophage family classification.
- Prophage-encoded genes likely confer selectable phenotypic traits, aiding mycoplasma adaptation and survival.
Conclusions:
- phiMFV1 is a mobile genetic element with implications for Mycoplasma evolution and host adaptation.
- The discovery of phiMFV1 and its relationship to phiMAV1 establishes a new prophage family.
- Prophage-derived surface proteins may play a role in the co-evolution of mycoplasmas with their hosts.
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