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Biography

Dr. Lampe received his PhD in Entomology from the University of Illinois at Urbana-Champaign in 1992. He has a BS in Biology from St. Louis University and an MS in Entomology from Purdue University; he joined the faculty at Duquesne University in 1998.

Dr. Lampe's laboratory investigates novel ways to halt the spread of insect transmitted diseases like malaria by creating bacterial strains that express anti-malarial proteins and peptides. We aim to design bacterial strains suitable for field release in Africa as part of a multipronged approach to controlling this deadly disease. 

Education

  • PhD, Entomoogy, University of Illinois at Urbana-Champaign, 1992
  • MS, Entomology, Purdue University, 1987
  • BS, Biology, St. Louis University, 1985

Research Interests

I.  Symbiotic control of insect-transmitted diseases of plants and animals

Insects are vectors for many of the most deadly plant and animal diseases and are a crucial link in these disease cycles. In the past, cultural methods or insecticide treatments have been used to control insect vectors. These methods are still widely practiced, but in many cases insects have evolved resistance to insecticides. In some areas of the world, notably Africa, public health measures used in developed countries to reduce vector populations are difficult to apply. Clearly, new methods are necessary to aid in the control of insect-vectored diseases.

Symbiotic control is a method that takes advantage of basic microbial ecology. The phenotype of all plants and animals is the product of genetic and environmental effects. One large environmental effect is provided by the microorganisms that form various kinds of sybioses with plants and animals. In symbiotic control, we genetically engineer symbiotic microbes to deliver effector proteins that can interfere with disease causing organisms. In this way, we can alter the disease-causing phenotype of insect vectors by modifying the bacteria that they normally carry.

Blocking mosquito transmission of malaria to humans: We are genetically modifying two species of bacteria to deliver antimalarial effector proteins. Malaria is the most widespread and dangerous insect-transmitted human disease in the world. It infects more than 500 million people (ca. 1 in 14 humans) and causes between 1 and 2 million deaths each year. The incidence of malaria is increasing and new measures to combat it are desperately needed.

Both Pantoea agglomerans and Asaia borogensis are bacterial species that are found in the midguts of Anopheles gambiae, the most important malaria vector mosquito in Africa. We are developing secretion systems for use in both of these species in order to secrete anti-malarial effectors into the midgut of An. gambiae. These effector molecules include single chain antibodies that bind directly to the Plasmodium parasites that cause malaria and to receptors on the mosquito midgut epithelium that the parasite uses to invade mosquito tissues. We are also developing ways to control the gene expression of antimalarial effector genes and methods to develop genetically stable strains of bacteria carrying these effectors.

II. Microbial ecology of mosquitoes

A related focus of my lab is uncovering the microbiota of mosquitoes in Pennsylvania with an eye toward expanding our repertoire of microbes suitable for symbiotic control. We are identifying a large number of culturable bacteria found in mosquitoes and also working to uncover the complete gut and ovary microbiomes of several species of Pennsylvania mosquitoes in collaboration with Gina Lamendella at Juniata College and Mike Hutchinson at the PA Dept. of Environmental Protection. Abundant culturable strains are being tested for their ability to colonize different mosquito tissues and for their ability to block the development of malaria parasites in Anopheles.


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  1. Grogan C, Bennett M, Lampe DJ. An evaluation of fusion partner proteins for paratransgenesis in Asaia bogorensis. PLoS One. 2022;17(9):e0273568. doi: 10.1371/journal.pone.0273568. eCollection 2022. PubMed PMID: 36048823; PubMed Central PMCID: PMC9436115.
  2. Guido ML, Kelly TP, Bongio NJ, Lampe DJ. Paratransgenesis in mosquitoes and other insects: microbial ecology and bacterial genetic considerations. In: Benedict MQ, Scott MJ, editors. Transgenic Insects: techniques and applications, second edition 2nd ed. Wallingford, UK: CAB International 2022. Chapter 16; p.320-339. 594p.
  3. O'Neill CE, Skilton RJ, Forster J, Cleary DW, Pearson SA, Lampe DJ, Thomson NR, Clarke IN. An inducible transposon mutagenesis approach for the intracellular human pathogen Chlamydia trachomatis. Wellcome Open Res. 2021;6:312. doi: 10.12688/wellcomeopenres.16068.1. eCollection 2021. PubMed PMID: 35087955; PubMed Central PMCID: PMC8767425.
  4. Skilton RJ, O'Neill C, Thomson NR, Lampe DJ, Clarke IN. Progress towards an inducible, replication-proficient transposon delivery vector for Chlamydia trachomatis. Wellcome Open Res. 2021;6:82. doi: 10.12688/wellcomeopenres.16665.1. eCollection 2021. PubMed PMID: 33997299; PubMed Central PMCID: PMC8097735.
  5. Grogan C, Bennett M, Moore S, Lampe D. Novel Asaia bogorensis Signal Sequences for Plasmodium Inhibition in Anopheles stephensi. Front Microbiol. 2021;12:633667. doi: 10.3389/fmicb.2021.633667. eCollection 2021. PubMed PMID: 33664722; PubMed Central PMCID: PMC7921796.
  6. Shane JL, Grogan CL, Cwalina C, Lampe DJ. Blood meal-induced inhibition of vector-borne disease by transgenic microbiota. Nat Commun. 2018 Oct 8;9(1):4127. doi: 10.1038/s41467-018-06580-9. PubMed PMID: 30297781; PubMed Central PMCID: PMC6175951.
  7. Bongio NJ, Lampe DJ. Inhibition of Plasmodium berghei Development in Mosquitoes by Effector Proteins Secreted from Asaia sp. Bacteria Using a Novel Native Secretion Signal. PLoS One. 2015;10(12):e0143541. doi: 10.1371/journal.pone.0143541. eCollection 2015. PubMed PMID: 26636338; PubMed Central PMCID: PMC4670117.
  8. Shane JL, Bongio NJ, Favia G, Lampe DJ. Draft Genome Sequence of Asaia sp. Strain SF2.1, an Important Member of the Microbiome of Anopheles Mosquitoes. Genome Announc. 2014 Jan 9;2(1). doi: 10.1128/genomeA.01202-13. PubMed PMID: 24407652; PubMed Central PMCID: PMC3886965.
  9. Wang S, Ghosh AK, Bongio N, Stebbings KA, Lampe DJ, Jacobs-Lorena M. Fighting malaria with engineered symbiotic bacteria from vector mosquitoes. Proc Natl Acad Sci U S A. 2012 Jul 31;109(31):12734-9. doi: 10.1073/pnas.1204158109. Epub 2012 Jul 16. PubMed PMID: 22802646; PubMed Central PMCID: PMC3412027.
  10. Bisi DC, Lampe DJ. Secretion of anti-Plasmodium effector proteins from a natural Pantoea agglomerans isolate by using PelB and HlyA secretion signals. Appl Environ Microbiol. 2011 Jul;77(13):4669-75. doi: 10.1128/AEM.00514-11. Epub 2011 May 20. PubMed PMID: 21602368; PubMed Central PMCID: PMC3127683.
  • BIOL 112 Evolution, Ecology, and Diversity
  • BIOL 340W/540 Evolution
  • BIOL 417/517 Invertebrate Biology and Biotechnology