Elucidation of the role of NOA1 and myosins in host response to infection by SACMV
Date
2017
Authors
Mwaba, Imanu Msifu Immaculee
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Abstract
Different host genes playing a role in replication, transcription and movement of
geminiviruses have been identified, allowing a better understanding of host response during
infection. The cytoskeletal protein myosin has been shown to associate with RNA viruses
movement protein and mediate its movement, however no geminivirus association with
myosin has been established. Arabidopsis thaliana nitric oxide associated protein 1
(AtNOA1), once thought to be an enzyme involved in a nitric oxide (NO) production, has
been reported to be differentially regulated in response to biotic and abiotic stress. In this
study we sought to identify the role that myosins and NOA1 play in the development of
disease by south african cassava mosaic virus (SACMV). Using a bioinformatics approach, 24
myosin transcripts were identified in Nicotiana benthamiana, and phylogeny analysis
revealed that seven were class VIII myosins and 17 class XI. Five myosins silencing constructs
M15.1 (transcript Niben101Scf11288g00015.1), MYOSIN XI-F (M11.F), MYOSIN XI-K (M11.K),
MYOSIN XI-2 (M11.2) and MYOSIN VIII.B were selected for silencing using a virus induced
gene silencing (VIGS) approach with SACMV and TRV-VIGS vectors. At 14 days post
inoculation (dpi), both SACMV and TRV-VIGS vectors successfully silenced myosins with
SACMV-VIGS silencing all five and TRV-VIGS silencing all but M11. F. At 28 dpi, SACMV-VIGS
induced silencing of myosin of only two myosins and TRV-VIGS three. TRV-VIGS was found
to be more efficient at silencing as the suppression of myosin induced by TRV-VIGS was
stronger than that of SACMV-VIGS. To assess the effect of myosin silencing on SACMV
infectivity in a separate experiment, 7 dpi of silencing, N. benthamiana plants were
challenged with SACMV and reduction of myosin expression was assessed as well as viral
accumulation. TRV-VIGS did not induce any silencing of myosin at 14 dpi, and at 28 dpi, the
expression of M11.K and M11.F were silenced. SACMV-VIGS induced silencing of M11.F at
both 14 and 28 dpi. In TRV-VIGS silenced M11.K, viral load at 28 dpi was not lower than the
control, however the fold increase in viral load at 28 dpi compared to 14 dpi was 3-fold (p
value 0.03) for M11.K silenced TRV-VIGS plants and 86-fold for the control 6-fold for the
M11.K suggesting that silencing of M11.K decreases the spread of SACMV. In TRV-VIGS
silenced M11.K, viral load at 28 dpi was lower than the control (9-fold p value 0.03) and the
increase in viral load at 28 dpi compared to 14 dpi was insignificant, suggesting that
spreading of SACMV was also hampered. The reduction in myosin M11.F expression induced
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by SACMV-VIGS resulted in an increase in viral load compared to the control. We
hypothesise that the increase in viral load observed in M11.F silenced plants induced by
SACMV-VIGS is due to the perceived resistance of SACMV-VIGS control (SACMV-challenged
no silencing construct) to SACMV-challenge, and therefore results from the SACMV-VIGS
study were inconclusive. From the TRV-VIGS study however, we have identified two
candidate myosins in N. benthamiana myosin XI-K and myosin XI-F as potential interactor of
SACMV during infectivity. Further research into their role in the development of SACMV
disease is warranted.
Nitric oxide associated 1 (NOA1) in plants is a cyclic GTPase involved in protein translation in
the chloroplast and has been indirectly linked to nitric oxide (NO) accumulation. To
understand the role played by NOA1 in response to (SACMV) infection, a bioinformatics
approach was used to identify NOA1 homologues in cassava T200. Using the cassava
genome data on Phytozome, a putative NOA1 namely cassava 4.1_007735m, was identified.
Based on its protein sequence, cassava4.1_007735m shared a 69.6% similarity to
Arabidopsis NOA1 (AtNOA1). The expression of cassava4.1_007735.m (MeNOA1) and N.
benthamiana NOA1 (NbNOA1) and the accumulation of NO in leaf samples was compared
between SACMV-infected and non-infected at early infection stage (14 dpi for N.
benthamiana and 28 dpi for cassava T200) and full systemic stage (28 dpi for N.
benthamiana and 56 dpi for cassava T200). Real-time PCR was used to measure SACMV viral
load which increased significantly by 2-fold (p value 0.05) from 14 to 28 dpi for N.
benthamiana and 8-fold from 28 to 56 dpi in cassava T200 (p value 0.04) as chlorosis and
symptom severity concomitantly progressed. At 14 and 28 dpi, NbNOA1 expression was
significantly lower than mock inoculated plants (2-fold lower at 14 dpi, p value 0.01 and 4
fold lower at 28, (p value 0.00) and the abundance of NO in infected N. benthamiana leaf
tissue was 10% lower at 14 dpi and 40% lower at 28 dpi when compared to mock
inoculated. In cassava T200, MeNOA1 expression was unchanged at 28 dpi and NO levels
were decreased by 40% and at 56 dpi, MeNOA1 expression was 4-fold lower and NO
accumulation was 37 % higher than that of mock inoculated leaf tissue. At 28 dpi for N.
benthamiana and 56 for cassava T200, the decrease in NOA1 expression was accompanied
by chloroplast dysfunction, evident from the significant reduction in chlorophylls a and b
and carotenoids in SACMV-infected leaf samples. Furthermore, the expression of
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chloroplast translation factors (chloroplast RNA binding, chloroplast elongation factor G,
translation initiation factor 3-2, plastid-specific ribosomal protein 6 and) were found to be
repressed in infected N. benthamiana and infected cassava T200 relative to mock inoculated
plants. GC-MS analysis showed a decrease in fumarate and an increase in glucose in
SACMV-infected N. benthamiana in comparison to mock samples suggesting a decrease in
carbon stores. Collectively, these results provide evidence that in response to SACMV
infection in N. benthamiana, decrease in photopigment and carbon stores, accompanied by
an increase in glucose and decrease in fumarate, lead to a decline in NbNOA1 and NO levels.
This is manifested by suppressed translation factors, and disruption of the chloroplast,
resulting in chlorotic disease symptoms. In cassava T200 however, the link could not be
established as the level of glucose was not significantly decreased and fumaric acid was not
detected and although the concomitant decrease in the expression of MeNOA1 and
chloroplast translation factors indicate dysfunction of the chloroplast, the link between
MeNOA1 expression, carbon store, NO and chloroplast activity could not be established.
Description
A dissertation submitted to the Faculty of Science, University of the Witwatersrand, in
fulfilment of the requirements for the degree of Doctor of Philosophy in Science at the
School of Molecular and Cell Biology, 2017
Keywords
Citation
Mwaba, Imanu Msifu (2017) Elucidation of the role of NOA1 and myosins in host response to infection by SACMV, University of the Witwatersrand, Johannesburg, <http://hdl.handle.net/10539/23531>