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Pathogenomic s Goal: Identify previously unrecognized mechanisms by which bacteria cause disease, using a unique combination of informatics, evolutionary biology, microbiology and genetics.

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Page 1: Pathogenomics Goal: Identify previously unrecognized mechanisms by which bacteria cause disease, using a unique combination of informatics, evolutionary

Pathogenomics

Goal:

Identify previously unrecognized mechanisms by which bacteria cause disease, using a unique combination of informatics, evolutionary biology, microbiology and genetics.

Page 2: Pathogenomics Goal: Identify previously unrecognized mechanisms by which bacteria cause disease, using a unique combination of informatics, evolutionary

Pathogenicity

Processes that pathogenic bacteria use to cause disease are still minimally understood

Bacterial proteins identified that manipulate host cells by interacting with, or mimicking, host proteins.

Idea: Could we identify novel disease factors by identifying bacterial genes more similar to host genes than you would expect based on evolutionary relationships?

Page 3: Pathogenomics Goal: Identify previously unrecognized mechanisms by which bacteria cause disease, using a unique combination of informatics, evolutionary

Informatics screen for candidate bacterial genes. - genes similar to host genes

Rank candidates.- how much like host protein?

Prioritize for further biological study. - previously studied?- UBC microbiologists study bacterium?- gene in model host that UBC geneticists may study?

Evaluate evolutionary significance.

Modify screening method

Initial Approach

Collectgene data

Page 4: Pathogenomics Goal: Identify previously unrecognized mechanisms by which bacteria cause disease, using a unique combination of informatics, evolutionary

New gene data available for many pathogens

Anthrax PlagueCat scratch disease Peptic ulcersChlamydia Pneumonia Cholera Periodontal diseaseDental caries Paratyphoid/enteric feverDiarrhea (E. coli etc.) SalmonellosisDiphtheria Scarlet feverEpidemic typhus Shigellosis (bacillary dysentery)Mediterranean fever Sleeping sicknessGastroenteritis Strep throatGiardia SyphilisGonorrhea Toxic shock syndromeLegionnaires' disease Tuberculosis Leishmaniasis TularemiaLeprosy Typhoid feverLeptospirosis UrethritisListeriosis Urinary Tract InfectionsLyme disease Whooping coughMalaria MeningitisNecrotizing fasciitis Yeast infection

Some hospital-acquired infections, animal/plant infections

Page 5: Pathogenomics Goal: Identify previously unrecognized mechanisms by which bacteria cause disease, using a unique combination of informatics, evolutionary

First finding: Surprising evidence of transfer of a gene from a bacterial pathogen to a protozoan pathogen

ProtozoaBacteria

Why did we find this? Why do we care?

Page 6: Pathogenomics Goal: Identify previously unrecognized mechanisms by which bacteria cause disease, using a unique combination of informatics, evolutionary

Evidence that a gene was transferred between a bacterial pathogen and a

protozoan pathogen

H. influenzae: Causes respiratory tract infections and meningitis

T. vaginalis: Causes the STD Trichomonas

A gene in the bacterium Haemophilus influenzae, and related bacteria, is highly similar to a gene in the protozoan Trichomonas vaginalis.

Page 7: Pathogenomics Goal: Identify previously unrecognized mechanisms by which bacteria cause disease, using a unique combination of informatics, evolutionary

Evidence that a gene was transferred between a bacterial pathogen and a

protozoan pathogen

Unusual occurrence of gene transfer.

Did this gene transfer confer a benefit to Trichomonas?

In bacteria: - Gene participates in system that parasitizes the mucous membranes of animals for nutritional purposes.- Definitive role in disease still unstudied

In this protozoan: - Similar role?

Page 8: Pathogenomics Goal: Identify previously unrecognized mechanisms by which bacteria cause disease, using a unique combination of informatics, evolutionary

Publication in Preparation

Keeling, Patrick F., Fiona S. L. Brinkman, Audrey de Koning and Steven J. Jones.

“Evidence supporting horizontal gene transfer from a pathogenic bacteria to a pathogenic protozoan.”

To be submitted to the journal Molecular Biology and Evolution.

Page 9: Pathogenomics Goal: Identify previously unrecognized mechanisms by which bacteria cause disease, using a unique combination of informatics, evolutionary

Back to the focus: Identifying bacterial genes similar to host genes

Page 10: Pathogenomics Goal: Identify previously unrecognized mechanisms by which bacteria cause disease, using a unique combination of informatics, evolutionary

Pathogenomics Database

Page 11: Pathogenomics Goal: Identify previously unrecognized mechanisms by which bacteria cause disease, using a unique combination of informatics, evolutionary

World Research Community

Prioritized candidates

Study function of similar gene in model host, C. elegans.

Study function of gene.

Investigate role of bacterial gene in disease: Infection study in model host

Further biological study

The worm C. elegans

DATABASE

Contact other groups for possible collaborations.

Page 12: Pathogenomics Goal: Identify previously unrecognized mechanisms by which bacteria cause disease, using a unique combination of informatics, evolutionary

Summary: Strengths

• Interdisciplinary team

• Automated informatics approach - continually updated

• Better understanding: pathogen gene and similar host gene

• Insight into gene transfer events between organisms and evolution of pathogen-host interactions

• Public database: – Exposure for UBC research– Foster collaborations– Benefit world research

community

Page 13: Pathogenomics Goal: Identify previously unrecognized mechanisms by which bacteria cause disease, using a unique combination of informatics, evolutionary

• Pathogenomics group– Ann M. Rose, Yossef Av-Gay, David L.

Baillie, Fiona S. L. Brinkman, Robert Brunham, Stefanie Butland, Rachel C. Fernandez, B. Brett Finlay, Robert E.W. Hancock, Christy Haywood-Farmer, Steven J. Jones, Patrick Keeling, Audrey de Koning, Don G. Moerman, Sarah P. Otto, B. Francis Ouellette, Iain E. P. Taylor.

• Peter Wall Institute for Advanced Studies

Acknowledgements