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Determination of the virus diversity associated with Grapevine leafroll disease

Thesis (MSc)--Stellenbosch University, 2015. / ENGLISH ABSTRACT: Vitis vinifera is the woody crop most susceptible to intracellular pathogens. Currently 70 pathogens
infect grapevine, of which 63 are of viral origin. Grapevine leafroll-associated virus 3 (GLRaV-3)
is the type species of the genus Ampelovirus, family Closteroviridae. It is considered to be the
primary causative agent of Grapevine leafroll disease (GLD) globally; however, the etiology of
GLD is not completely understood. Here we report on the viral populations present in GLD
symptomatic grapevines across the Western Cape province, South Africa. A widespread survey was
performed to screen 315 grapevines for 11 grapevine-infecting viruses using RT-PCR. Additionally,
GLRaV-3 variant groups were distinguished with high-resolution melt (HRM) curve analysis used
in conjunction with real-time RT-PCR. Members of the family Closteroviridae were detected with
the highest frequency, particularly GLRaV-3 that was detected in 87% of tested plants. Nextgeneration
sequencing (NGS) is capable of detecting known and novel viruses without prior
knowledge of viral sequences and when used in a metagenomic approach is able to detected viral
populations within diseased vines. A total of 17 grapevine samples were subjected to NGS using
either an Illumina MiSeq or HiSeq 2500 instrument to determine the virome within GLD vines.
Collectively, more than 190 million reads were generated through NGS. Read datasets were
trimmed and filtered for quality and subjected to both read-mapping and de novo assembly. Contigs
assembled de novo were analyzed with BLAST (Basic Local Alignment Search Tool) against the
NCBI (National Centre for Biotechnology Information) database and it was determined that
GLRaV-3 was the best-represented virus, comprising 97.5% of the assembled contigs. Grapevine
virus F (GVF) was detected for the first time in South African vineyards through de novo
assemblies and the complete genome sequence validated through direct Sanger sequencing. The
complete genome of GVF isolate V5 spans 7 539 nucleotides and shares 89.11% nucleotide identity
to existing GVF genomes. The data generated through this study will assist in further understanding
the etiology of GLD, support the current hypothesis of GLRaV-3 as the primary contributor to GLD,
aid in understanding virus associations in diseased vines and potentially develop systems in which
to control disease spread and symptom severity. / AFRIKAANSE OPSOMMING: Vitis vinifera is die houtagtige oes wat die mees vatbaarste is vir intrasellulêre patogene. Tans word
wingerde deur 70 patogene geïnfekteer, waarvan 63 van virale oorsprong is. Grapevine leafrollassociated
virus 3 (GLRaV-3) is die tipe spesie van die genus Ampelovirus, familie Closteroviridae.
Dit word globaal beskou as die primêre oorsaak van Wingerd krulblaar-siekte (GLD), alhoewel die
etiologie van GLD nie heeltemal begryp word nie. In hierdie verslag word die virale populasies
teenwoordig in GLD simptomatiese wingerde oor die Wes-Kaap provinsie in Suid-Afrika
gerapporteer. ‘n Wydverspreide opname was uitgevoer om 315 wingerde met 11 wingerdinfekterende
virusse te ondersoek, deur gebruik te maak van tru-transkripsie polimerase ketting
reaksie (PKR). Verder is variantgroepe van GLRaV-3 onderskei met hoë-resolusie smeltingskurweanalise,
tesame met die gebruik van in-tyd tru-transkripsie PKR. Die hoogste frekwensie was van
die lede van die familie Closteroviridae, veral GLRaV-3 wat in 87% van die ondersoekte plante
gevind is. Nuwe-generasie volgorderbepaling (NGS) beskik oor die vermoë om bekende en nuwe
virusse te herken in virale populasies in geaffekteerde wingerde sonder vorige kennis van virale
volgorderbepalings en wanneer dit in ‘n metagenomiese benadering gebruik word kan die virale
bevolkings binne siek wingerde ontdek. ‘n Totaal van 17 wingerd-steekproewe was blootgestel aan
NGS deur die gebruik van of ‘n Illumina MiSeq of ‘n HiSeq 2500 instrument om die virome te
bepaal van GLD wingerde. In totaal is meer 190 miljoen lesings gegenereer deur NGS. Hierdie data
lesings was verwerk en gefilter vir kwaliteit om onderwerp te word vir beide kartering en de novo
samestellings. Contigs verkry deur de novo samestellings was geanaliseer met BLAST (Basic
Local Alignment Search Tool) teenoor die NCBI (National Centre for Biotechnology Information)
databasis en dit was vasgestel dat GLRaV-3 was die mees-verteenwoordigende virus, bestaande uit
97.5% van die saamgestelde contigs. Grapevine virus F (GVF) was vir die eerste keer in Suid-
Afrikaanse wingerde waargeneem deur de novo samestellings en die volledige genoom volgordger
is geverifieer deur middel van direkte Sanger volgorderbepaling. Die volledige genoom van GVF
isoleer V5 spanwydte van 7539 nukleotiedes en deel 89.11% nukleotied identiteite van bestaande
GVF genome. Die gegenereerde data van hierdie studie sal bykomende begrip van die etiologie
van GLD bystaan, die huidige hipotese van GLRaV-3 as die primêre bydraer tot GLD ondersteun,
verhoogde begrip van virus-assosiasies in wingerdsiektes verseker en potensiële sisteme ontwikkel
om siektes en simptome te beheer.

Identiferoai:union.ndltd.org:netd.ac.za/oai:union.ndltd.org:sun/oai:scholar.sun.ac.za:10019.1/97012
Date04 1900
CreatorsMolenaar, Nicholas
ContributorsMaree, Hans Jacob, Burger, Johan T., Stellenbosch University. Faculty of Agrisciences. Dept. of Genetics.
PublisherStellenbosch : Stellenbosch University
Source SetsSouth African National ETD Portal
Languageen_ZA
Detected LanguageEnglish
TypeThesis
Formatxvi, 104 pages : illustrations
RightsStellenbosch University

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