Study of the role of type IV secretion system of Xanthomonas citri and Stenotrophomonas maltophilia in the interaction with Dictyostelium discoideum.

• Grant number: 15/25381-2
• Support Opportunities: Scholarships in Brazil - Post-Doctoral
• Start date: March 01, 2016
• End date: February 28, 2018
• Field of knowledge: Biological Sciences - Microbiology - Biology and Physiology of Microorganisms
• Principal Investigator: Shaker Chuck Farah
• Grantee: Ethel Bayer Santos
• Host Institution: Instituto de Química (IQ). Universidade de São Paulo (USP). São Paulo , SP, Brazil
• Associated research grant: 11/07777-5 - Cyclic di-GMP signaling and the Type IV macromolecule secretion system in Xanthomonas citri, AP.TEM

Abstract

Bacterial secretion systems are versatile structures that can secrete proteins and DNA into the extracellular medium or into target cells. Type IV secretion systems (T4SS) are protein complexes formed by 12 proteins (VirB1-VirB11 and VirD4) that play a fundamental role in the virulence of several bacterial species. In the last ten years, our laboratory has been studying interactions involving subunits of the T4SS of Xanthomonas citri, the causative agent of canker citrus, and identified 12 protein substrates secreted by this system. Recently, we demonstrated that T4SS of X. citri is capable of killing other bacterial species, thus working in an analogous manner to the type VI secretion system (T6SS). Once the T4SS of X. citri operates analogously to the T6SS of a variety of bacterial species, such as Vibrio cholerae and Pseudomonas aeruginosa, which are able to inject toxins in both prokaryotic and eukaryotic cells; this project aims to study the role of X. citri T4SS in interactions with a phagocytic eukaryotic cell, such as the social amoeba Dictyostelium discoideum. In addition, this project aims to study the T4SS of the opportunistic pathogen Stenotrophomonas maltophilia to determine whether this secretion system could play a similar role in other species phylogenetically related to Xanthomonas spp. The characterization of the S. maltophilia T4SS and its secreted toxins will be of great value to increase our knowledge about the biology and virulence mechanisms of this emerging pathogen. The knowledge generated at the end of this project will increase our understanding of the ecology of free-living bacteria and the mechanisms by which they survive their environmental predators.

Scientific publications

(4)

(References retrieved automatically from Web of Science and SciELO through information on FAPESP grants and their corresponding numbers as mentioned in the publications by the authors)

BAYER-SANTOS, ETHEL; MARINI, MARJORIE M.; DA SILVEIRA, JOSE F.. Non-coding RNAs in Host-Pathogen Interactions: Subversion of Mammalian Cell Functions by Protozoan Parasites. FRONTIERS IN MICROBIOLOGY, v. 8, MAR 21 2017. (11/51475-3, 15/25381-2)

BAYER-SANTOS, ETHEL; CENENS, WILLIAM; MATSUYAMA, BRUNO YASUI; OKA, GABRIEL UMAJI; DI SESSA, GIANCARLO; MININEL, IZABEL DEL VALLE; ALVES, TIAGO LUBIANA; FARAH, CHUCK SHAKER. The opportunistic pathogen Stenotrophomonas maltophilia utilizes a type IV secretion system for interbacterial killing. PLOS PATHOGENS, v. 15, n. 9, SEP 2019. (15/25381-2, 17/17303-7, 18/04553-8, 15/18237-2, 17/02178-2, 16/00458-5, 11/07777-5)

BAYER-SANTOS, ETHEL; LIMA, LIDIA DOS PASSOS; CESETI, LUCAS DE MORAES; RATAGAMI, CAMILA YURI; DE SANTANA, ELIANE SILVA; DA SILVA, ALINE MARIA; FARAH, CHUCK SHAKER; ALVAREZ-MARTINEZ, CRISTINA ELISA. Xanthomonas citri T6SS mediates resistance to Dictyostelium predation and is regulated by an ECF sigma factor and cognate Ser/Thr kinase. ENVIRONMENTAL MICROBIOLOGY, v. 20, n. 4, SI, p. 1562-1575, APR 2018. (16/08400-6, 14/19720-6, 14/25261-4, 11/07777-5, 15/25381-2)

BAYER-SANTOS, ETHEL; LIMA, LIDIA DOS PASSOS; CESETI, LUCAS DE MORAES; RATAGAMI, CAMILA YURI; DE SANTANA, ELIANE SILVA; DA SILVA, ALINE MARIA; FARAH, CHUCK SHAKER; ALVAREZ-MARTINEZ, CRISTINA ELISA. Xanthomonas citri T6SS mediates resistance to Dictyostelium predation and is regulated by an ECF sigma factor and cognate Ser/Thr kinase. ENVIRONMENTAL MICROBIOLOGY, v. 20, n. 4, p. 14-pg., 2018-04-01. (15/25381-2, 16/08400-6, 11/07777-5, 14/19720-6, 14/25261-4)