TY - JOUR
T1 - Real-time quantitative PCR assay for the quantification of virus and satellites causing leaf curl disease in cotton in Pakistan
AU - Shafiq, Muhammad
AU - Iqbal, Zafar
AU - Ali, Irfan
AU - Abbas, Qamar
AU - Mansoor, Shahid
AU - Briddon, Rob W.
AU - Amin, Imran
N1 - Funding Information:
MS was supported by the Higher Education Commission (HEC, Pakistan) under the ‘Indigenous 5000 Fellowship Scheme’. RWB was supported by the HEC under the ‘Foreign Faculty Hiring Scheme’. This material is based upon work supported by the “Pak-US cotton productivity enhancement program” of the International Center for Agricultural Research in the Dry Areas (ICARDA) funded by United States Department of Agriculture (USDA), Agricultural Research Service (ARS), under agreement No. 58–6402-0-178F. Any opinions, findings, conclusions or recommendations expressed in this publication are those of the author(s) and do not necessarily reflect the views of the USDA or ICARDA.
Publisher Copyright:
© 2017 Elsevier B.V.
PY - 2017/10
Y1 - 2017/10
N2 - Cotton leaf curl disease (CLCuD) is the major biotic constraint to cotton production in Pakistan and northwestern India. The disease is caused by monopartite begomoviruses in association with a specific DNA satellite, Cotton leaf curl Multan betasatellite. The virus-betasatellite complex is also frequently associated with another DNA satellite-like molecule; an alphasatellite. A quantitative real-time PCR (qPCR) assay to detect all three components of the monopartite begomovirus/betasatellite/alphasatellite complex which causes CLCuD was established. This was used to investigate the relationship between symptoms and virus/satellite titre. Not surprisingly the analysis showed that, overall, there was a reasonable correlation between symptom severity and virus/satellite titre − more severe symptoms usually being associated with more virus/satellite. However, cotton plants were identified with no or very mild symptoms with relatively high virus/satellite titres and plants with severe symptoms but relatively low virus/satellite titres. This may be attributed to the resistance/susceptibility of the cotton variety − tolerant plants being able to sustain a relatively high virus/satellite titre whilst exhibiting mild symptoms. The usefulness of this qPCR procedure in the screening for resistance in cotton against CLCuD is discussed.
AB - Cotton leaf curl disease (CLCuD) is the major biotic constraint to cotton production in Pakistan and northwestern India. The disease is caused by monopartite begomoviruses in association with a specific DNA satellite, Cotton leaf curl Multan betasatellite. The virus-betasatellite complex is also frequently associated with another DNA satellite-like molecule; an alphasatellite. A quantitative real-time PCR (qPCR) assay to detect all three components of the monopartite begomovirus/betasatellite/alphasatellite complex which causes CLCuD was established. This was used to investigate the relationship between symptoms and virus/satellite titre. Not surprisingly the analysis showed that, overall, there was a reasonable correlation between symptom severity and virus/satellite titre − more severe symptoms usually being associated with more virus/satellite. However, cotton plants were identified with no or very mild symptoms with relatively high virus/satellite titres and plants with severe symptoms but relatively low virus/satellite titres. This may be attributed to the resistance/susceptibility of the cotton variety − tolerant plants being able to sustain a relatively high virus/satellite titre whilst exhibiting mild symptoms. The usefulness of this qPCR procedure in the screening for resistance in cotton against CLCuD is discussed.
KW - Cotton leaf curl disease (CLCuD)
KW - Cotton leaf curl Khokhran virus − Burewala (CLCuKoV-Bu)
KW - Cotton leaf curl Multan betasatellite (CLCuMuB)
KW - Polymerase chain reaction (PCR)
KW - Quantitative real-time PCR (qPCR)
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U2 - 10.1016/j.jviromet.2017.05.012
DO - 10.1016/j.jviromet.2017.05.012
M3 - Article
C2 - 28572041
AN - SCOPUS:85021065546
SN - 0166-0934
VL - 248
SP - 54
EP - 60
JO - Journal of Virological Methods
JF - Journal of Virological Methods
ER -