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André A. Grassmann, PhDAssistant Professor
Pronouns:
He/Him
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I am a molecular microbiologist studying how bacterial pathogens sense host environments and remodel gene expression and cell surface architecture to promote infection, persistence, and transmission. My work focuses on spirochetes, including Borrelia burgdorferi, Leptospira interrogans, and Treponema pallidum, and integrates genetics, transcriptomics, structural biology, and infection-relevant models. A central goal of my research is to define how regulatory responses to host signals generate biologically meaningful phenotypes at the host–pathogen interface, with direct implications for pathogenesis and vaccine development.
| Degree | Institution | Major |
|---|---|---|
| BS | Universidade Federal de Pelotas (UFPel) | Biological Sciences |
| MSc | Universidade Federal de Pelotas (UFPel) | Biotechnology |
| PhD | Universidade Federal de Pelotas (UFPel) | Biotechnology |
Post-Graduate Training
| Training | Institution | Specialty |
|---|---|---|
| Postdoctoral | Universidade Federal de Pelotas (UFPel) | Postdoctoral Fellow, Supervisor: Dr. Alan McBride |
| Postdoctoral | UConn Health | Postdoctoral Fellow, Spirochete Research Labs, Department of Medicine, PIs: Drs. Justin Radolf and Melissa Caimano |
Awards
| Name of Award/Honor | Awarding Organization |
|---|---|
| Merit Award, 15th North Eastern Structure Symposium (NESS), Farmington, CT, USA | North Eastern Structure Symposium (NESS) |
| Merit Award, Biological Sciences, 23rd UFPel Scientific Congress, Pelotas, Brazil | UFPel Scientific Congress |
Within the Spirochete Research Laboratories, my research focuses on molecular mechanisms that enable spirochetes to adapt to complex life cycles spanning arthropod vectors, environmental reservoirs, and mammalian hosts. One major area of emphasis is transcriptional regulation in Borrelia burgdorferi, where I study how the Fur-family regulator BosR integrates host-derived signals to control RpoS-dependent and RpoS-independent gene expression during tick and mammalian infection. A second research focus centers on the outer membrane biology of Leptospira interrogans, including the regulation, function, and assembly of outer membrane proteins that contribute to virulence, persistence, and immune recognition. These studies combine several state-of-the-art molecular biology assays, structural modeling, and in vivo infection models to link regulatory mechanisms to pathogenic outcomes.
The Spirochete Research Laboratories offer research opportunities for graduate students, MD/PhD students, postdoctoral fellows, and motivated undergraduate trainees. Ongoing projects include defining gene regulatory networks across the Borrelia enzootic cycle, mapping protein–DNA interactions, and characterizing infection-relevant outer membrane proteins in Leptospira. Trainees are encouraged to develop interdisciplinary skill sets spanning molecular microbiology, bioinformatics, and translational research, and to actively participate in manuscript preparation and grant-related activities.
Rotation students joining the Spirochete Research Laboratories are exposed to interdisciplinary approaches for studying bacterial gene regulation, host adaptation, and cell envelope biology. Rotation projects emphasize hypothesis-driven experimental design, quantitative data analysis, and integration of computational and wet-lab methods. Trainees gain hands-on experience with transcriptomics, molecular genetics, protein biochemistry, and infection-relevant models while developing independent research questions within a collaborative, multi-PI environment.
Journal Articles
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DNA Binding by BosR Controls RpoS-Dependent and -Independent Gene Expression in Borrelia burgdorferi.
Molecular microbiology 2025 Nov;
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Sequence variability of BamA and FadL candidate vaccinogens suggests divergent evolutionary paths of Treponema pallidum outer membrane proteins.
Journal of bacteriology 2025 Aug;207(8):e0015925
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Immunodominant extracellular loops of Treponema pallidum FadL outer membrane proteins elicit antibodies with opsonic and growth-inhibitory activities.
PLoS pathogens 2024 Dec;20(12):e1012443
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Leptospira interrogans encodes a canonical BamA and three novel noNterm Omp85 outer membrane protein paralogs.
Scientific reports 2024 Aug;14(1):19958
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BosR and PlzA reciprocally regulate RpoS function to sustain Borrelia burgdorferi in ticks and mammals.
The Journal of clinical investigation 2023 Jan;
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Challenges for the development of a universal vaccine against leptospirosis revealed by the evaluation of 22 vaccine candidates.
Frontiers in cellular and infection microbiology 2022 Jan;12940966
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TonB-dependent receptor epitopes expressed in M. bovis BCG induced significant protection in the hamster model of leptospirosis.
Applied microbiology and biotechnology 2022 Jan;106(1):173-184
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The FUR-like regulators PerRA and PerRB integrate a complex regulatory network that promotes mammalian host-adaptation and virulence of Leptospira interrogans.
PLoS pathogens 2021 Dec;17(12):e1009078
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PlzA is a bifunctional c-di-GMP biosensor that promotes tick and mammalian host-adaptation of Borrelia burgdorferi.
PLoS pathogens 2021 Jul;17(7):e1009725
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Role of glucosyltransferase R in biofilm interactions between Streptococcus oralis and Candida albicans.
The ISME journal 2020 Feb;
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Cultivation of Leptospira interrogans Within Rat Peritoneal Dialysis Membrane Chambers.
Methods in molecular biology (Clifton, N.J.) 2020 Jan;2134229-242
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Discovery of Novel Leptospirosis Vaccine Candidates Using Reverse and Structural Vaccinology.
Frontiers in immunology 2017 Jan;8463
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Pathogenic Leptospires Modulate Protein Expression and Post-translational Modifications in Response to Mammalian Host Signals.
Frontiers in cellular and infection microbiology 2017 Jan;7362
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Lectin I from Bauhinia variegata (BVL-I) expressed by Pichia pastoris inhibits initial adhesion of oral bacteria in vitro.
International journal of biological macromolecules 2016 Dec;93(Pt A):913-918
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Draft genome of the Leptospira interrogans strains, Acegua, RCA, Prea, and Capivara, obtained from wildlife maintenance hosts and infected domestic animals.
Memorias do Instituto Oswaldo Cruz 2016 Apr;111(4):280-3
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Generation of Mammalian Host-adapted Leptospira interrogans by Cultivation in Peritoneal Dialysis Membrane Chamber Implantation in Rats.
Bio-protocol 2015 Jul;5(14):
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Evaluation of the Leptospira interrogans Outer Membrane Protein OmpL37 as a Vaccine Candidate.
PloS one 2015 Jan;10(11):e0142821
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A model system for studying the transcriptomic and physiological changes associated with mammalian host-adaptation by Leptospira interrogans serovar Copenhageni.
PLoS pathogens 2014 Mar;10(3):e1004004
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Protection against lethal leptospirosis after vaccination with LipL32 coupled or coadministered with the B subunit of Escherichia coli heat-labile enterotoxin.
Clinical and vaccine immunology : CVI 2012 May;19(5):740-5
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Highly virulent Leptospira borgpetersenii strain characterized in the hamster model.
The American journal of tropical medicine and hygiene 2011 Aug;85(2):271-4
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Preliminary characterization of Mus musculus-derived pathogenic strains of Leptospira borgpetersenii serogroup Ballum in a hamster model.
The American journal of tropical medicine and hygiene 2010 Aug;83(2):336-7
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B subunit of Escherichia coli heat-labile enterotoxin as adjuvant of humoral immune response in recombinant BCG vaccination.
Canadian journal of microbiology 2008 Aug;54(8):677-86
Reviews
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Reverse Vaccinology: An Approach for Identifying Leptospiral Vaccine Candidates.
International journal of molecular sciences 2017 Jan;18(1):
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A Universal Vaccine against Leptospirosis: Are We Going in the Right Direction?
Frontiers in immunology 2017 Jan;8256
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Recombinant vaccines against leptospirosis.
Human vaccines 2011 Nov;7(11):1215-24