DISTRIBUTION OF MAIZE LETHAL NECROSIS, ITS VECTORS AND HOST PLANTS IN MAJOR MAIZE GROWING AREAS OF UGANDA - PowerPoint PPT Presentation

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DISTRIBUTION OF MAIZE LETHAL NECROSIS, ITS VECTORS AND HOST PLANTS IN MAJOR MAIZE GROWING AREAS OF UGANDA

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DISTRIBUTION OF MAIZE LETHAL NECROSIS, ITS VECTORS AND HOST PLANTS IN MAJOR MAIZE GROWING AREAS OF UGANDA PhD proposed research in Uganda by Mudde Barnabas – PowerPoint PPT presentation

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Title: DISTRIBUTION OF MAIZE LETHAL NECROSIS, ITS VECTORS AND HOST PLANTS IN MAJOR MAIZE GROWING AREAS OF UGANDA


1
DISTRIBUTION OF MAIZE LETHAL NECROSIS, ITS
VECTORS AND HOST PLANTS IN MAJOR MAIZE GROWING
AREAS OF UGANDA
PhD proposed research in Uganda by Mudde
BarnabasPhD student, University of Nairobi
Presented During The Workshop To Develop
Strategic Plan For Maize Lethal Necrosis Disease
For Eastern And Central Africa, Jacaranda Hotel,
Nairobi, Kenya 21st -23rd August,
2013 Supervisors 1. Prof . Olubayo Florence,
Faculty of Agriculture, University of Nairobi 2.
Dr. Miano Douglas, Faculty of Agriculture,
University of Nairobi
3. Dr. Asea
Godfrey, National Agricultural Research
Organisation (NARO)
2
Background
  • Maize Zea mays (L.) is one of the chief starchy
    cereal crops in East Africa
  • It is the vital staple for over 70 million people
  • Uganda ranked 10th in Africa
  • Annual production estimate at 1,373,000 tonnes
  • Annual yield is 1.5 tons per hectare
  • Low yields majorly attributed to biotic
    constraints
  • Major biotic constraints include diseases caused
    by
  • Fungi
  • Bacteria
  • Viruses
  • Most important viruses are
  • Maize streak virus, Maize rough dwarf virus
  • And the new Maize lethal necrosis

3
Maize lethal necrosis disease
  • Maize Lethal Necrosis disease (MLN) first
    identified in USA in 1976 In East Africa from
    Kenya and Tanzania (2011) In Uganda (2012).
  • Symptoms include drying of leaves, premature
    plant death failure to tassel / sterility in
    male plants malformed /no ears premature drying
    or rotting of cobs
  • Potential yield losses 30 -100 . (Wangai et al.,
    2012)
  • MLN caused by double infection with Maize
    chlorotic mottle virus (MCMV) and any of cereal
    viruses in Potyviridae group Sugarcane mosaic
    virus (SCMV), Maize dwarf mosaic virus (MDMV) or
    Wheat streak mosaic virus (WSMV).
  • MLN-causing viruses are transmitted by several
    insect vectors. MCMV (thrips and beetles) MDMV
    and SCMV (aphids).
  • Alternate hosts of MLN causing viruses include
    Maize, sugarcane, grasses of family poaceae,
    sorghum, millet and johnson grass.

4
Symptoms
Fine chlorotic streaks
Dead heart symptoms
Complete necrosis
5
Problem statement
  • Maize Lethal Necrosis disease (MLN) stands out as
    greatest threat to African food security crop
    (maize).
  • In 2012, this MLN disease outbreak was first
    reported in Busia district in eastern Uganda, it
    is not known to what extent this disease is now
    prevalent and distributed in Uganda.
  • It is not known which maize viruses of the
    Potyviridae group in Uganda could be combining
    with MCMV to cause the MLN symptoms observed in
    maize fields so far.
  • Apart from maize, the maize lethal necrosis
    causing viruses are haboured by alternate plant
    hosts. The potential plant hosts for MLN causing
    viruses in Uganda not known.
  • The vectors of the MLN-causing viruses in Uganda
    are not known and their virus transmission
    efficiency.
  • Plant virus epidemics are multi-component systems
    resulting from interactions between the virus
    (es), vectors and host plant (s).
  • A full understanding of the epidemiology of MLN
    disease is critical for development of
    sustainable management strategies

6
Objectives
  • General Objective
  • To provide a better understanding of the
    epidemiology, host plants, vector range of MLN
    disease for improved control
  • Specific objectives of the study
  • 1. To establish the distribution and incidence
    of MLN in Uganda
  • 2. To determine alternate hosts of MLN causing
    viruses in Uganda
  • 3. To identify potential insect vectors of MLN
    causing viruses in Uganda
  • 4. To determine transmission efficiencies of
    vectors of MLN causing viruses in Uganda

7
Methodology
8
Methodology
  • Objective. 1 . Distribution, incidence and
    severity of MLN in major maize growing districts
    of Uganda
  • Data from 13 major maize-growing districts of
    Uganda
  • Disease incidence Estimate of percentage of
    maize plants infested
  • Severity assessed using a 1 to 5 scale by
    Biswanath et al. 2013
  • GPS coordinates recorded

9
Methodology contd
  • Activity 1.1. Serological and molecular detection
    of MLN in maize samples
  • Lab studies at National Crop Resources Research
    Institute, Namulonge in Uganda.
  • ELISA against MLN causing viruses (MCMV, SCMV,
    MDMV, WSMV) as well as antibodies against the
    entire Potyvirus genus (AGDIA, Elkhart,IN).
  • Confirmation with reverse transcription-polymerase
    chain reaction (RT-PCR) using specific primers
    (Wangai et al., 2012)

10
Methodology contd
  • Objective 2 Identification of alternate plant
    hosts of MLN in Uganda
  • Alternate MLN host plants collected from
    confirmed hotspots of MLN in Uganda.
  • Identified to species level in collaboration with
    Botany and Zoology department of Makerere
    University Institute of Environment and Natural
    Resources
  • ELISA against MLN causing viruses (MCMV, SCMV,
    MDMV, WSMV) as well as antibodies against the
    entire Potyvirus genus (AGDIA, Elkhart,IN).

11
Methodology contd
  • Objective 3 Identification of potential insect
    vectors in Uganda
  • Activity 3.1. Vector collection
  • Sampling vectors from confirmed hotspots of MLN
    in Uganda.
  • Potential vectors colonizing maize will be
    identified to species level in collaboration with
    ICIPE.
  • Insect vector viral content MLN causing viruses
    will be determined using Enzyme Linked
    Immunosorbent Assay as previously described by
    Chu and Francki, (1982).
  • Real time PCR will be also be used to quantify
    viral load in potential vectors

12
Methodology contd
  • Objective 4 Determine transmission efficiencies
    of potential vectors in Uganda to transmit MLN
  • Vectors transferred to MLN-infected 3 week old
    maize
  • For each insect vector, 3 species selected for
    transmission studies
  • MCMV symptoms noted in seedlings at 5, 10, 15,
    20, after feeding
  • Viral content will be measured at each of these
    stages using ELISA
  • Percent transmission rates based on number of
    infected plants out of total observed

13
Expected budget and output
  • Budget USD 90,000
  • Outputs
  • 1. Incidence and distribution of MLN in Uganda
    established.
  • 2. Knowledge of alternative hosts and
    vectors of MLN causing viruses prevalent in
    Uganda
  • 3. At least 4 scientific papers and PhD thesis
    published.

14
Acknowledgements
  • NARO
  • Government of Uganda
  • Development Partners
  • University of Nairobi

15
  • THANK YOU FOR LISTENING
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