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The distribution of a phage-related insertion sequence element in the cyanobacterium, Microcystis aeruginosa
Sotaro Kuno1, Takashi Yoshida, Ryoma Kamikawa
1Department of Agriculture, Kyoto University, Kitashirakawa-Oiwake, Sakyo-ku, Kyoto 606–8502, Japan.
Abstract:
The cyanophage Ma-LMM01, specifically-infecting Microcystis aeruginosa, has an insertion sequence (IS) element that we named IS607-cp showing high nucleotide similarity to a counterpart in the genome of the cyanobacterium Cyanothece sp. We tested 21 strains of M. aeruginosa for the presence of IS607-cp using PCR and detected the element in strains NIES90, NIES112, NIES604, and RM6. Thermal asymmetric interlaced PCR (TAIL-PCR) revealed each of these strains has multiple copies of IS607-cp. Some of the ISs were classified into three types based on their inserted positions; IS607-cp-1 is common in strains NIES90, NIES112 and NIES604, whereas IS607-cp-2 and IS607-cp-3 are specific to strains NIES90 and RM6, respectively. This multiplicity may reflect the replicative transposition of IS607-cp. The sequence of IS607-cp in Ma-LMM01 showed robust affinity to those found in M. aeruginosa and Cyanothece spp. in a phylogenetic tree inferred from counterparts of various bacteria. This suggests the transfer of IS607-cp between the cyanobacterium and its cyanophage. We discuss the potential role of Ma-LMM01-related phages as donors of IS elements that may mediate the transfer of IS607-cp; and thereby partially contribute to the genome plasticity of M. aeruginosa.
Insights
A cyanophage insertion sequence element, IS607-cp, was found in multiple Microcystis aeruginosa strains. This element may transfer between cyanobacteria and phages, influencing genome plasticity.
Area of Science:
- Microbiology
- Genetics
- Molecular Biology
Background:
- Cyanophages, viruses that infect cyanobacteria, play roles in marine ecosystems.
- Insertion sequences (IS) are mobile genetic elements that can alter host genomes.
- The cyanophage Ma-LMM01 infects Microcystis aeruginosa, a globally significant bloom-forming cyanobacterium.
Purpose of the Study:
- To identify and characterize an insertion sequence (IS) element in the cyanophage Ma-LMM01.
- To investigate the presence and distribution of this IS element in different strains of Microcystis aeruginosa.
- To explore the potential for horizontal gene transfer of the IS element between cyanobacteria and their phages.
Main Methods:
- Polymerase Chain Reaction (PCR) was used to detect the IS607-cp element.
- Thermal Asymmetric Interlaced PCR (TAIL-PCR) was employed to determine the insertion sites and copy numbers of the IS element.
- Phylogenetic analysis was conducted using nucleotide sequences of IS elements from various bacteria.
Main Results:
- The cyanophage Ma-LMM01 harbors an insertion sequence element, designated IS607-cp, with high similarity to elements in cyanobacteria.
- IS607-cp was detected in four out of 21 tested M. aeruginosa strains, with multiple copies present in each.
- Different insertion patterns of IS607-cp were observed across the strains, suggesting replicative transposition.
- Phylogenetic analysis indicated potential transfer of IS607-cp between M. aeruginosa and Cyanothece spp., mediated by phages.
Conclusions:
- The cyanophage-associated insertion sequence IS607-cp is present in several M. aeruginosa strains.
- Ma-LMM01-related phages may act as vectors for IS607-cp transfer, contributing to genome plasticity in M. aeruginosa.
- Understanding IS element dynamics is crucial for comprehending cyanobacterial evolution and adaptation.
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