Next Article in Journal
Synchronous Langat Virus Infection of Haemaphysalis longicornis Using Anal Pore Microinjection
Previous Article in Journal
Molecular Mechanisms of Human Papillomavirus Induced Skin Carcinogenesis
Open AccessArticle

Novel Fri1-like Viruses Infecting Acinetobacter baumannii—vB_AbaP_AS11 and vB_AbaP_AS12—Characterization, Comparative Genomic Analysis, and Host-Recognition Strategy.

1
Institute of Antimicrobial Chemotherapy, Smolensk State Medical University, Smolensk, Russian Federation
2
Moscow Institute of Physics and Technology (State University), Moscow region, Dolgoprudny, Russian Federation
3
State Researсh Center for Applied Microbiology and Biotechnology, Moscow region, Obolensk, Russian Federation
4
Institute of Molecular Genetics and Gene Biology, Russian Academy of Sciences, Moscow, Russian Federation
5
Skolkovo Institute of Science and Technology, Skolkovo, Russian Federation
6
Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Moscow, Russian Federation
7
North-Western State Medical University named after I.I. Mechnikov, Saint-Petersburg, Russian Federation
8
Institute of Experimental Medicine, Saint-Petersburg, Russian Federation
9
Saint Petersburg State University, Saint-Petersburg, Russian Federation
10
Peter the Great St. Petersburg Polytechnic University, St. Petersburg, Russian Federation
11
Waksman Institute, Rutgers, the State University of New Jersey, Piscataway, NJ, USA
*
Author to whom correspondence should be addressed.
Viruses 2017, 9(7), 188; https://doi.org/10.3390/v9070188
Received: 14 June 2017 / Revised: 6 July 2017 / Accepted: 6 July 2017 / Published: 17 July 2017
(This article belongs to the Section Bacterial Viruses)
Acinetobacter baumannii is a gram-negative, non-fermenting aerobic bacterium which is often associated with hospital-acquired infections and known for its ability to develop resistance to antibiotics, form biofilms, and survive for long periods in hospital environments. In this study, we present two novel viruses, vB_AbaP_AS11 and vB_AbaP_AS12, specifically infecting and lysing distinct multidrug-resistant clinical A. baumannii strains with K19 and K27 capsular polysaccharide structures, respectively. Both phages demonstrate rapid adsorption, short latent periods, and high burst sizes in one-step growth experiments. The AS11 and AS12 linear double-stranded DNA genomes of 41,642 base pairs (bp) and 41,402 bp share 86.3% nucleotide sequence identity with the most variable regions falling in host receptor–recognition genes. These genes encode tail spikes possessing depolymerizing activities towards corresponding capsular polysaccharides which are the primary bacterial receptors. We described AS11 and AS12 genome organization and discuss the possible regulation of transcription. The overall genomic architecture and gene homology analyses showed that the phages are new representatives of the recently designated Fri1virus genus of the Autographivirinae subfamily within the Podoviridae family. View Full-Text
Keywords: bacteriophage; Acinetobacter baumannii; Podoviridae; Fri1virus; RNA polymerase; tail spike; capsule types bacteriophage; Acinetobacter baumannii; Podoviridae; Fri1virus; RNA polymerase; tail spike; capsule types
Show Figures

Figure 1

MDPI and ACS Style

Popova, A.V.; Lavysh, D.G.; Klimuk, E.I.; Edelstein, M.V.; Bogun, A.G.; Shneider, M.M.; Goncharov, A.E.; Leonov, S.V.; Severinov, K.V. Novel Fri1-like Viruses Infecting Acinetobacter baumannii—vB_AbaP_AS11 and vB_AbaP_AS12—Characterization, Comparative Genomic Analysis, and Host-Recognition Strategy.. Viruses 2017, 9, 188.

Show more citation formats Show less citations formats
Note that from the first issue of 2016, MDPI journals use article numbers instead of page numbers. See further details here.

Article Access Map by Country/Region

1
Back to TopTop