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Journal of General Virology (2000), 81, 1839-1849.
© 2000 Society for General Microbiology


Plant

Multiple infection, recombination and genome relationships among begomovirus isolates found in cotton and other plants in Pakistan

Ana I. Sanzb,1, Aurora Fraile1, Fernando García-Arenal1, Xueping Zhouc,2, David J. Robinson2, Saif Khalid3, Tahir Buttd,2 and Bryan D. Harrison2

Departmento de Biotecnologia, E.T.S. Ingenieros Agronomos, Universidad Politecnica, 28040 Madrid, Spain1
Scottish Crop Research Institute, Invergowrie, Dundee DD2 5DA, UK2
National Agricultural Research Centre, Islamabad 45500, Pakistan3

Author for correspondence: Bryan Harrison. Fax +44 1382 562426. e-mail djrobi{at}scri.sari.ac.uk

Begomoviruses occur in many plant species in Pakistan and are associated with an epidemic of cotton leaf curl disease that has developed since 1985. PCR analysis with primer pairs specific for each of four already sequenced types of DNA-A of cotton leaf curl virus (CLCuV-PK types a, 26, 72b and 804a), or for okra yellow vein mosaic virus (OYVMV), indicated that many individual naturally infected plants of cotton and other malvaceous species contained two or three begomovirus sequences. Similarly, sequence differences among overlapping fragments of begomovirus DNA-A, amplified from individual naturally infected plants, indicated much multiple infection in malvaceous and non-malvaceous species. Some cotton plants contained DNA-A sequences typical of begomoviruses from non-malvaceous species, and some non-malvaceous plants contained sequences typical of CLCuV-PK. Some DNA-A sequences were chimaeric; they each included elements typical of different types of CLCuV-PK, or of different malvaceous and/or non-malvaceous begomoviruses. Often an apparent recombination site occurred at the origin of replication. No complete CLCuV-PK DNA-A sequence was found in malvaceous or non-malvaceous species collected in Pakistan outside the area of the cotton leaf curl epidemic but chimaeric sequences, including a part that was typical of CLCuV-PK DNA-A, did occur there. We suggest that recombination among such pre-existing sequences was crucial for the emergence of CLCuV-PK. Recombination, following multiple infection, could also explain the network of relationships among many of the begomoviruses found in the Indian subcontinent, and their evolutionary divergence, as a group, from begomoviruses causing similar diseases in other geographical regions.




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