Type VI Secretion System Plays a Role in Type 1 Fimbria Expression and Pathogenesis of an Avian Pathogenic Escherichia coli Strain

• Published in: Infection and Immunity Vol. 78; no. 12; pp. 4990 - 4998
• Main Authors: de Pace, Fernanda, Nakazato, Gerson, Pacheco, Alline, Boldrin de Paiva, Jacqueline, Sperandio, Vanessa, Dias da Silveira, Wanderley
• Format: Journal Article
• Language: English
• Published: Washington, DC American Society for Microbiology 01.12.2010; American Society for Microbiology (ASM)
• Subjects: Animals; Bacterial Adhesion - physiology; Bacterial Secretion Systems - physiology; Bacteriology; Biological and medical sciences; Chickens - microbiology; Escherichia coli; Escherichia coli - genetics; Escherichia coli - metabolism; Escherichia coli - pathogenicity; Escherichia coli Infections - microbiology; Escherichia coli Infections - veterinary; Fimbria; Fimbriae, Bacterial - metabolism; Fundamental and applied biological sciences. Psychology; Gene Expression Regulation, Bacterial - genetics; HeLa Cells - microbiology; Humans; Microbiology; Miscellaneous; Molecular Pathogenesis; Mutation; Oligonucleotide Array Sequence Analysis; Poultry Diseases - microbiology; Reverse Transcriptase Polymerase Chain Reaction; Sepsis - microbiology; Sepsis - veterinary; Vertebrata; Pathogenesis; Escherichia coli; Bacteria; Pilus; Aves; Immunity; Type IV secretion system; Enterobacteriaceae; Strain
• ISSN: 0019-9567; 1098-5522
• DOI: 10.1128/IAI.00531-10

Avian pathogenic Escherichia coli (APEC) strains frequently cause extraintestinal infections and are responsible for significant economic losses in the poultry industry worldwide. APEC isolates are closely related to human extraintestinal pathogenic E. coli (ExPEC) strains and may also act as pathogens for humans. Known APEC virulence factors include adhesins such as type 1 fimbriae and curli, iron acquisition systems, and cytotoxins. Here we show that APEC strain SEPT362, isolated from a septicemic hen, expresses a type VI secretion system (T6SS); causes cytoskeleton rearrangements; and invades epithelial cells, replicates within macrophages, and causes lethal disease in chicks. To assess the contribution of the T6SS to SEPT362 pathogenesis, we generated two mutants, hcp (which encodes a protein suggested to be both secreted and a structural component of the T6SS) and clpV (encoding the T6SS ATPase). Both mutants showed decreased adherence and actin rearrangement on epithelial cells. However, only the hcp mutant presented a mild decrease in its ability to invade epithelial cells, and none of these mutants were defective for intramacrophage replication. Transcriptome studies showed that the level of expression of type 1 fimbriae was decreased in these mutants, which may account for the diminished adhesion and invasion of epithelial cells. The T6SS seems to be important for the disease process, given that both mutants were attenuated for infection in chicks. These results suggest that the T6SS influences the expression of type 1 fimbriae and contributes to APEC pathogenesis.