scholarly journals Comparative genomics of the type VI secretion systems of Pantoea and Erwinia species reveals the presence of putative effector islands that may be translocated by the VgrG and Hcp proteins

BMC Genomics ◽  
2011 ◽  
Vol 12 (1) ◽  
Author(s):  
Pieter De Maayer ◽  
Stephanus N Venter ◽  
Tim Kamber ◽  
Brion Duffy ◽  
Teresa A Coutinho ◽  
...  
BMC Genomics ◽  
2014 ◽  
Vol 15 (1) ◽  
pp. 163 ◽  
Author(s):  
Divine Shyntum ◽  
Stephanus Venter ◽  
Lucy Moleleki ◽  
Ian Toth ◽  
Teresa Coutinho

2018 ◽  
Vol 9 ◽  
Author(s):  
Min Wang ◽  
Hengchun Cao ◽  
Qian Wang ◽  
Tingting Xu ◽  
Xi Guo ◽  
...  

2020 ◽  
Vol 2 (7A) ◽  
Author(s):  
Stephanie Sibinelli de Sousa ◽  
Julia Takuno Hespanhol ◽  
Bruno Matsuyama ◽  
Stephane Mesnage ◽  
Gianlucca Nicastro ◽  
...  

Type VI secretion systems (T6SSs) are contractile nanomachines widely used by bacteria to intoxicate competitors. Salmonella Typhimurium encodes a T6SS within the Salmonella pathogenicity island 6 (SPI-6) that is used during competition against species of the gut microbiota. We characterized a new SPI-6 T6SS antibacterial effector named Tlde1 (type VI L,D-transpeptidase effector 1). Tlde1 is toxic in target-cell periplasm and its toxicity is neutralized by co-expression with immunity protein Tldi1 (type VI L,D-transpeptidase immunity 1). Time-lapse microscopy revealed that intoxicated cells display altered cell division and lose cell envelope integrity. Bioinformatics analysis showed that Tlde1 is evolutionarily related to L,D-transpeptidases. Point mutations on conserved histidine121 and cysteine131 residues eliminated toxicity. Co-incubation of purified recombinant Tlde1 and peptidoglycan tetrapeptides showed that Tlde1 displays both L,D-carboxypeptidase activity by cleaving GM-tetrapeptides between meso-diaminopimelic acid3 and D-alanine4, and L,D-transpeptidase exchange activity by replacing D-alanine4 for a non-canonical D-amino acid. Tlde1 constitutes a new family of T6SS effectors widespread in Proteobacteria. This work increases our knowledge about the bacterial effectors used in interbacterial competitions and provides molecular insight into a new mechanism of bacterial antagonism.


2020 ◽  
Vol 11 ◽  
Author(s):  
Jorge Soria-Bustos ◽  
Miguel A. Ares ◽  
Carlos A. Gómez-Aldapa ◽  
Jorge A. González-y-Merchand ◽  
Jorge A. Girón ◽  
...  

2020 ◽  
Vol 21 (8) ◽  
pp. 1055-1069 ◽  
Author(s):  
Namgyu Kim ◽  
Jin Ju Kim ◽  
Inyoung Kim ◽  
Mohamed Mannaa ◽  
Jungwook Park ◽  
...  

Nitrogen ◽  
2020 ◽  
Vol 1 (2) ◽  
pp. 81-98
Author(s):  
Martina Lardi ◽  
Yilei Liu ◽  
Sebastian Hug ◽  
Samanta Bolzan de Campos ◽  
Leo Eberl ◽  
...  

Rhizobia have two major life styles, one as free-living bacteria in the soil, and the other as bacteroids within the root/stem nodules of host legumes where they convert atmospheric nitrogen into ammonia. In the soil, rhizobia have to cope with changing and sometimes stressful environmental conditions, such as nitrogen limitation. In the beta-rhizobial strain Paraburkholderia phymatum STM815, the alternative sigma factor σ54 (or RpoN) has recently been shown to control nitrogenase activity during symbiosis with Phaseolus vulgaris. In this study, we determined P. phymatum’s σ54 regulon under nitrogen-limited free-living conditions. Among the genes significantly downregulated in the absence of σ54, we found a C4-dicarboxylate carrier protein (Bphy_0225), a flagellar biosynthesis cluster (Bphy_2926-64), and one of the two type VI secretion systems (T6SS-b) present in the P. phymatum STM815 genome (Bphy_5978-97). A defined σ54 mutant was unable to grow on C4 dicarboxylates as sole carbon source and was less motile compared to the wild-type strain. Both defects could be complemented by introducing rpoNin trans. Using promoter reporter gene fusions, we also confirmed that the expression of the T6SS-b cluster is regulated by σ54. Accordingly, we show that σ54 affects in vitro competitiveness of P. phymatum STM815 against Paraburkholderia diazotrophica.


PLoS ONE ◽  
2013 ◽  
Vol 8 (10) ◽  
pp. e76030 ◽  
Author(s):  
Thibault G. Sana ◽  
Chantal Soscia ◽  
Céline M. Tonglet ◽  
Steve Garvis ◽  
Sophie Bleves

2017 ◽  
Vol 20 (1) ◽  
pp. 1-15 ◽  
Author(s):  
Patricia Bernal ◽  
María A. Llamas ◽  
Alain Filloux

2016 ◽  
Vol 113 (36) ◽  
pp. 10174-10179 ◽  
Author(s):  
Carina R. Büttner ◽  
Yingzhou Wu ◽  
Karen L. Maxwell ◽  
Alan R. Davidson

Contractile phage tails are powerful cell puncturing nanomachines that have been co-opted by bacteria for self-defense against both bacteria and eukaryotic cells. The tail of phage T4 has long served as the paradigm for understanding contractile tail-like systems despite its greater complexity compared with other contractile-tailed phages. Here, we present a detailed investigation of the assembly of a “simple” contractile-tailed phage baseplate, that of Escherichia coli phage Mu. By coexpressing various combinations of putative Mu baseplate proteins, we defined the required components of this baseplate and delineated its assembly pathway. We show that the Mu baseplate is constructed through the independent assembly of wedges that are organized around a central hub complex. The Mu wedges are comprised of only three protein subunits rather than the seven found in the equivalent structure in T4. Through extensive bioinformatic analyses, we found that homologs of the essential components of the Mu baseplate can be identified in the majority of contractile-tailed phages and prophages. No T4-like prophages were identified. The conserved simple baseplate components were also found in contractile tail-derived bacterial apparatuses, such as type VI secretion systems, Photorhabdus virulence cassettes, and R-type tailocins. Our work highlights the evolutionary connections and similarities in the biochemical behavior of phage Mu wedge components and the TssF and TssG proteins of the type VI secretion system. In addition, we demonstrate the importance of the Mu baseplate as a model system for understanding bacterial phage tail-derived systems.


2019 ◽  
Vol 38 (18) ◽  
Author(s):  
Johannes Paul Schneider ◽  
Sergey Nazarov ◽  
Ricardo Adaixo ◽  
Martina Liuzzo ◽  
Peter David Ringel ◽  
...  

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