• Je něco špatně v tomto záznamu ?

Ability of phages to infect Acinetobacter calcoaceticus-Acinetobacter baumannii complex species through acquisition of different pectate lyase depolymerase domains

H. Oliveira, AR. Costa, N. Konstantinides, A. Ferreira, E. Akturk, S. Sillankorva, A. Nemec, M. Shneider, A. Dötsch, J. Azeredo,

. 2017 ; 19 (12) : 5060-5077. [pub] 20171204

Jazyk angličtina Země Anglie, Velká Británie

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/bmc18024527

Bacteriophages are ubiquitous in nature and represent a vast repository of genetic diversity, which is driven by the endless coevolution cycle with a diversified group of bacterial hosts. Studying phage-host interactions is important to gain novel insights into their dynamic adaptation. In this study, we isolated 12 phages infecting species of the Acinetobacter baumannii-Acinetobacter calcoaceticus complex which exhibited a narrow host range and similar morphological features (podoviruses with short tails of 9-12 nm and isometric heads of 50-60 nm). Notably, the alignment of the newly sequenced phage genomes (40-41 kb of DNA length) and all Acinetobacter podoviruses deposited in Genbank has shown high synteny, regardless of the date and source of isolation that spans from America to Europe and Asia. Interestingly, the C-terminal pectate lyase domain of these phage tail fibres is often the only difference found among these viral genomes, demonstrating a very specific genomic variation during the course of their evolution. We proved that the pectate lyase domain is responsible for phage depolymerase activity and binding to specific Acinetobacter bacterial capsules. We discuss how this mechanism of phage-host co-evolution impacts the tail specificity apparatus of Acinetobacter podoviruses.

Citace poskytuje Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc18024527
003      
CZ-PrNML
005      
20180712114913.0
007      
ta
008      
180709s2017 enk f 000 0|eng||
009      
AR
024    7_
$a 10.1111/1462-2920.13970 $2 doi
035    __
$a (PubMed)29076652
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a enk
100    1_
$a Oliveira, Hugo $u CEB - Centre of Biological Engineering, LIBRO - Laboratório de Investigação em Biofilmes Rosário Oliveira, University of Minho, 4710-057 Braga, Portugal.
245    10
$a Ability of phages to infect Acinetobacter calcoaceticus-Acinetobacter baumannii complex species through acquisition of different pectate lyase depolymerase domains / $c H. Oliveira, AR. Costa, N. Konstantinides, A. Ferreira, E. Akturk, S. Sillankorva, A. Nemec, M. Shneider, A. Dötsch, J. Azeredo,
520    9_
$a Bacteriophages are ubiquitous in nature and represent a vast repository of genetic diversity, which is driven by the endless coevolution cycle with a diversified group of bacterial hosts. Studying phage-host interactions is important to gain novel insights into their dynamic adaptation. In this study, we isolated 12 phages infecting species of the Acinetobacter baumannii-Acinetobacter calcoaceticus complex which exhibited a narrow host range and similar morphological features (podoviruses with short tails of 9-12 nm and isometric heads of 50-60 nm). Notably, the alignment of the newly sequenced phage genomes (40-41 kb of DNA length) and all Acinetobacter podoviruses deposited in Genbank has shown high synteny, regardless of the date and source of isolation that spans from America to Europe and Asia. Interestingly, the C-terminal pectate lyase domain of these phage tail fibres is often the only difference found among these viral genomes, demonstrating a very specific genomic variation during the course of their evolution. We proved that the pectate lyase domain is responsible for phage depolymerase activity and binding to specific Acinetobacter bacterial capsules. We discuss how this mechanism of phage-host co-evolution impacts the tail specificity apparatus of Acinetobacter podoviruses.
650    _2
$a Acinetobacter baumannii $x virologie $7 D040981
650    _2
$a Acinetobacter calcoaceticus $x virologie $7 D016954
650    _2
$a Asie $7 D001208
650    _2
$a sekvence nukleotidů $7 D001483
650    _2
$a Evropa $7 D005060
650    _2
$a genom virový $x genetika $7 D016679
650    _2
$a hostitelská specificita $x fyziologie $7 D058507
650    _2
$a Podoviridae $x klasifikace $x genetika $x metabolismus $7 D017902
650    _2
$a polygalakturonasa $x metabolismus $7 D011096
650    _2
$a polysacharid-lyasy $x metabolismus $7 D011133
650    _2
$a proteinové domény $x fyziologie $7 D000072417
650    _2
$a virion $x genetika $7 D014771
655    _2
$a časopisecké články $7 D016428
700    1_
$a Costa, Ana R $u CEB - Centre of Biological Engineering, LIBRO - Laboratório de Investigação em Biofilmes Rosário Oliveira, University of Minho, 4710-057 Braga, Portugal.
700    1_
$a Konstantinides, Nico $u CEB - Centre of Biological Engineering, LIBRO - Laboratório de Investigação em Biofilmes Rosário Oliveira, University of Minho, 4710-057 Braga, Portugal. Laboratory of Microbiology, Wageningen University, Stippeneng, 6708 WE Wageningen, The Netherlands.
700    1_
$a Ferreira, Alice $u CEB - Centre of Biological Engineering, LIBRO - Laboratório de Investigação em Biofilmes Rosário Oliveira, University of Minho, 4710-057 Braga, Portugal.
700    1_
$a Akturk, Ergun $u CEB - Centre of Biological Engineering, LIBRO - Laboratório de Investigação em Biofilmes Rosário Oliveira, University of Minho, 4710-057 Braga, Portugal.
700    1_
$a Sillankorva, Sanna $u CEB - Centre of Biological Engineering, LIBRO - Laboratório de Investigação em Biofilmes Rosário Oliveira, University of Minho, 4710-057 Braga, Portugal.
700    1_
$a Nemec, Alexandr $u Laboratory of Bacterial Genetics, National Institute of Public Health, Šrobárova 48, 100 42 Prague, Czech Republic.
700    1_
$a Shneider, Mikhail $u Laboratory of Molecular Bioengineering, 16/10 Miklukho-Maklaya St, Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry, 117997 Moscow, Russia.
700    1_
$a Dötsch, Andreas $u Institute of Functional Interfaces, Karlsruhe Institute of Technology (KIT), Eggenstein-Leopoldshafen, Germany. Max Rubner-Institute, Institute for Physiologie and Biochemistry of Nutrition, Haid-und-Neu-Str. 9, 76131 Karlsruhe, Germany.
700    1_
$a Azeredo, Joana $u CEB - Centre of Biological Engineering, LIBRO - Laboratório de Investigação em Biofilmes Rosário Oliveira, University of Minho, 4710-057 Braga, Portugal.
773    0_
$w MED00007220 $t Environmental microbiology $x 1462-2920 $g Roč. 19, č. 12 (2017), s. 5060-5077
856    41
$u https://pubmed.ncbi.nlm.nih.gov/29076652 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y a $z 0
990    __
$a 20180709 $b ABA008
991    __
$a 20180712115206 $b ABA008
999    __
$a ok $b bmc $g 1316658 $s 1021448
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2017 $b 19 $c 12 $d 5060-5077 $e 20171204 $i 1462-2920 $m Environmental microbiology $n Environ Microbiol $x MED00007220
LZP    __
$a Pubmed-20180709

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...