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PARATRANSGENIC STRATEGIES FOR CONTROL OF VECTOR-BORNE

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PARATRANSGENIC STRATEGIES FOR CONTROL OF VECTOR-BORNE DISEASES Ravi V. Durvasula, M.D. Chief of Medicine, NM VA Health Care System Director, Center for Global Health, – PowerPoint PPT presentation

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Title: PARATRANSGENIC STRATEGIES FOR CONTROL OF VECTOR-BORNE


1
PARATRANSGENIC STRATEGIES FOR CONTROL OF
VECTOR-BORNE DISEASES
  • Ravi V. Durvasula, M.D.
  • Chief of Medicine, NM VA Health Care System
  • Director, Center for Global Health,
  • Dept of Internal Medicine
  • UNM School of Medicine

2
AIMS
  • Provide overview of global impact of vector-borne
    diseases
  • Provide overview of Chagas disease
  • Discuss paratransgenic approach to Chagas disease
  • Provide overview of visceral leishmaniasis
  • Discuss paratransgenic approach to visceral
    leishmaniasis in India

3
CONTROL OF VECTOR-BORNE DISEASES
  • Vector-borne diseases remain a leading cause of
    human illness
  • Over 60 billion loss annually to agriculture
  • Impact on commercial livestock
  • Lack of effective vaccines
  • Vector eradication programs mainstay of control
  • Pesticides effective over short term
  • Issues of cost, environmental toxicity, adverse
    health effects and resistance

4
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5
Triatomine Vectors
  • Reduviid bug aka Kissing Bug, Assassin Bug or
    La Chincha
  • Multiple genera Rhodnius, Triatoma,
    Panstrongylus
  • Obligate blood-feeders
  • Humans are innocent bystanders in the cycle

6
Reduviid Bug Habitats
  • Sylvatic and peri-domestic reservoirs
  • Thatch roofing and cracks of adobe walls
  • Up to 10,000 bugs per house
  • Highly sequestered colonies

7
Transmission of T. cruzi
  • Nocturnal
  • Kissing bug attracted to warmth and CO2
  • 30 minutes to repletion
  • Release of fecal/urine droplet at end of blood
    meal
  • Droplet laden with metacyclic trypomastigotes
  • Entry of parasites at site of wound or mucous
    membranes

8
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9
Trypanosoma cruzi
  • Flagellate protozoan
  • Ubiquitous zoonotic agent
  • Silent reservoir in animals
  • Undergoes maturation in arthropod vector

10
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11
Acute Chagas Disease
  • Regional edema, Romanas Sign
  • Fever, flu-like illness
  • Acute myocarditis, hepatosplenomegaly, lymph node
    enlargement
  • Self-limited illness in 70-80 of cases
    indeterminate phase
  • Low level of awareness

12
Chagas Heart Disease
  • Chronic Chagasic Cardiopathy (CCC)
  • Most devastating effect of Chagas disease
  • Progressive dilated cardiomyopathy
  • Arrhythmias, heart blocks
  • Leading cause of heart disease south of US border
  • May occur years to decades after initial infection

13
Gastrointestinal Manifestations of Chagas Disease
  • GI tract involvement in 8-10 of infected
    individuals
  • Syndromes of dysmotility megaesophagus and
    megacolon
  • Dysphagia most common presentation
  • Radiographic and manometric studies similar to
    idiopathic achalasia
  • Megacolon often less symptomatic
  • Chronic constipation

14
AIDS and Chagas Disease
  • Reactivation possible when CD4 count lt 200
  • CNS mass lesion or acute diffuse
    meningoencephalitis
  • May be confused with CNS toxoplasmosis
  • Necrotizing hemorrhagic encephalitis,
    obliterative angiitis
  • Amastigote forms detectable on biopsy

15
TREATMENT OPTIONS
  • Nifurtimox and Benznidazole
  • Nifurtimox has 70 cure rates for acute Chagas
    disease less than 50 cure for Chronic Chagas
  • Benznidazole shows similar efficacy
  • Drugs taken for 60-120 days
  • High rate of side-effects severe GI and neuro
    side-effects with Nifurtimox granulocytopenia,
    rash and neuropathies with Benznidazole
  • WHO recommends treatment course for infected
    patients, regardless of stage
  • No effective vaccine yet

16
Control of Chagas Disease
  • Vector eradication
  • Blood-bank screening
  • 3 highly successful programs Southern Cone,
    Central American and Andean Pact Initiatives
  • Dramatic reductions in new cases
  • Vector resistance and sustainability are issues

17
Prospects for Chagas Control
  • Insecticide use remains the mainstay
  • Many success stories such as Chile
  • Countries such as Bolivia and Guatemala still
    with high prevalence
  • Recent resurgence of disease in Argentina

18
Paratransgenesis Using Gut Symbionts of
Triatomines
  • Triatomines harbor bacterial symbionts that have
    nutritional role
  • The symbionts can be genetically transformed to
    express a gene product that interferes with T.
    cruzi transmission
  • Insect symbionts can be replaced with genetically
    modified symbionts

19
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20
Paratransgenesis
A Novel Approach to Preventing Insect-Borne
Disease. New England Journal of Medicine. Conte
JE Jr. Sept 1997 337(11) 785-6.
21
PARATRANSGENIC EXPRESSION IN R. PROLIXUS
  • shuttle plasmid pRrThioCec with cDNA for
    L-cecropin A
  • clearance of T. cruzi in 65 of experimental
    group (n100) and log 2-3 reduction in parasites
    in 35 (Durvasula et al. PNAS 1997)
  • shuttle plasmid pRrMDWK6 with gene encoding rDB3
  • Expression of functional VH-Kappa in R. prolixus
    (Durvasula et al. Med. Vet . Entomology 1998 )
  • Shuttle plasmid pBAP5 with L1 mycobacteriophage
    integrase (Dotson et al. Inf Gen Imm 2003)
  • Rhodococcal expression plasmids with genes
    encoding AMPs
  • (Fieck et al 2009)

22
T.cruzi coated with mAb WIC29.26
  • Glycan epitope of gp72
  • Related glycans of T. cruzi surface
  • Targets for single chain antibodies expressed via
    recombinant R. rhodnii

23
Red Fluorescent Protein- sFv
  • Engineered single chain antibody
  • VH-RFP-VL structure
  • Recognizes sialic acid residues
  • Photoactivation by white light

24
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25
Surface of T.cruzi
  • Arthrobacter-derived lyticase
  • Alpha mannosidase
  • Genes encoding endoglucanases expressed via R.
    rhodnii

26
Activity of recombinant lyticase against
Trypanosoma cruzi
  • cDNA encoding lyticase of Arthrobacter cloned
    into Rhodococcal-E. coli shuttle plasmid
  • Extracts of E. coli transformed to express
    lyticase
  • Marked decline in OD 600nm of T. cruzi culture
    exposed to cell extracts
  • Lyticase-treated T. cruzi failed to propagate in
    fresh LIT
  • Transformation of R. rhodnii underway

27
Table 1 Minimal Inhibitory and Bactericidal
Peptide Concentration Determinations 24
Hour Single AMP Treatment All
samples plated in triplicate
Values averaged from three independent trials
28
SYMBIONT SPREAD
29
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30
Greenhouse Study of Transgenic Insects
31
Greenhouse Study Summary
32
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33
Potential Modes of Environmental Spread of GM
Bacteria
  • Transfer of GM bacteria to non-target arthropods
  • Ants, cockroaches, or flies ingesting GM bacteria
  • Horizontal Gene Transfer (HGT) amongst compatible
    host bacteria

34
A Paratransgenic Approach to Visceral
Leishmaniasis
  • Heidi Hillesland
  • University of New Mexico School of Medicine
  • Howard Hughes Medical Fellow
  • Mentors Ravi Durvasula, M.D. and Ivy Hurwitz,
    Ph.D.

35
Visceral Leishmaniasis (VL) Endemic Regions
Visceral leishmaniasis what are the needs for
diagnosis, treatment and control? François
Chappuis, Shyam Sundar, Asrat Hailu, Hashim
Ghalib, Suman Rijal, Rosanna W. Peeling, Jorge
Alvar Marleen Boelaert. Nature Reviews
Microbiology 5, S7-S16 (November 2007)
36

40 species of Phlebotomus Old world
30 species of Lutzomyia- Americas
Lutzomyia longipalpis Lutzomyia migonei Lutzomyia
ovalesi Lutzomyia verrucarum Lutzomyia peruensis
Phlebotomus argentipes Phlebotomus
papatasi Phlebotomus ariasi Phlebotomus duboscqi
37
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38
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39
VL Clinical Manifestations
  • Incubation period varying from weeks to months to
    years
  • Prolonged fever
  • Cachexia
  • Hepatosplenomegaly with predominance of
    splenomegaly
  • Pancytopenia
  • Hypergammaglobulinemia , mostly IgG
  • Hypoalbuminemia
  • Death most commonly due to secondary infection

www.sfgate.com/.../a/2002/08/19/MN33767.DTLo1
40
VL in Bihar, India
National Vector Borne Disease Control Programme,
22, Shamnath Marg, Delhi - 110054.
www.nvbdcp.gov.in/kal9.html
41
Life cycle of sandfly
Larvae-4 instar
Egg
Pupae
Adult fly
34-70 days, 28ºC
  • Terrestrial lifecycle
  • Breeding sites characterized at periphery of
  • cattle sheds in Bihar for P. argentipes
  • Moist microhabitats-rock crevices, animal
  • burrows, termite mounds, cavities of tree,
  • domestic animal shelters, organic debris

42
Paratransgenesis
  • Transform commensal bacteria to express
    anti-leishmania compound

4. Larvae undergo pupation
  • Introduce transformed commensal bacteria to soil
    breeding sites

5. Sandfly emerges with transformed bacteria
within its gut
  • Larvae feed on soil containing transformed
    bacteria
  • Blocked parasite development in adult sandfly

43
P. argentipes Samples From Four Regions in Bihar
Identification of Aerobic Gut Bacteria from the
Kala Azar Vector Phlebotomus argentipes A
Platform for Potential Paratransgeneic
Manipulation of Sand flies. American Journal of
Tropical Medicine and Hygiene. Hillesland H,
Read A, Subhadra B, Hurwitz I, McKelvey R, Ghosh
K, Durvasula R, Das P. 2008 76 (6) 881-6.
44
P. argentipes Gut Bacteria Isolates
Candidates for paratransgenesis non-pathogenic
soil bacteria that are amenable to transformation
45
Transformation of Candidate Bacteria B.
megaterium, B. subtilis, and B. pumilus
46
Development of Paratransgenic Sand Fly
No bacteria added
Bacillus subtilis
Bacillus subtilis pAD43-25 GFP
47
Development of Paratransgenic Sand Fly
Bright field and fluorescent microscopy of gut
dissection
  • and b. Bacillus subtilis fly at 10x
  • c. and d. Bacillus subtilis pAD43-25 at 10x

a
b
c
d
48
Development of Paratransgenic Sand Fly
Fluorescent microscopy of gut dissection Bacillus
subtilis pAD43-25 fly at 40x
49
NEXT STEPS
  • Evaluation of antimicrobial peptide activity
    against strains of L. donovani
  • Cloning of AMP-encoding genes into Bacillus
    expression plasmids
  • Testing of RFP activity clone VH-RFP-VL encoding
    gene
  • Potential killing of sandflies with light
    exposure

50
THE FUTURE
  • Laying down blankets of insecticides over cities
    does not appear to have a bright future. And only
    50 years after penicillin seemed a cure-all, the
    efficacy of nearly all of the roughly 150
    antibiotics in the doctors satchel is waning. If
    the arsenal for disease prevention continues
    emptying, the decision will become more focused
    how do we weigh the fear of knowingly disrupting
    our own natural habitat with transgenics versus
    the fear of taking no action in face of a new
    epidemic? Jack Hitt, The New York Times
    Magazine May 6, 2001

51
ACKNOWLEDGEMENTS
  • NIH/NIAID
  • HHMI
  • USDA
  • Burroughs Wellcome Foundation
  • The Yale/ UNM Team
  • Dr. Ranjini Sundaram
  • Dr. Sahar Usmani
  • Dr. D. V. Subba Rao
  • Scott Matthews
  • Bobban Subhadra
  • Dr. Ivy Hurwitz
  • Annabeth Fieck
  • Heidi Hillesland
  • Sarah Weiss
  • Dr. V.Sree Hari Rao
  • Dr. Gabriel Lopez
  • Dr. Amber Read
  • Dr. Robin McKelvey
  • MERTU/G , UDV, Guatemala
  • Celia Cordon-Rosales
  • Dr. Pamela Pennington
  • Walter Reed Army Institute of Research, Bethesda
  • Dr. Ed Rowton
  • Dr. Kashinath Ghosh
  • APTIV Inc., Portland, Oregon
  • Philipp Kirch
  • Dr. John McLaughlin
  • Univ. Buenos Aires, Argentina
  • Dr. Ricardo Gurtler
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