Serological and molecular detection of Tomato chlorosis virus and Tomato infectious chlorosis virus in tomato

Abstract

Tomato chlorosis virus (ToCV) and Tomato infectious chlorosis virus (TICV) are two criniviruses inducing similar yellowing symptoms in tomato. An approximately 4 kb central region of the genomic RNA2 of French ToCV and TICV isolates was sequenced. TICV, for which no other sequences were available, appeared as a distant species in the genus, being close only to LIYV (Lettuce infectious yellows virus) for some, but not all, proteins. ToCV has more than 98% nucleotide identity with isolates from the US and Spain, and sequencing the CP gene of several isolates collected in different regions in southern France during 2 years suggested a unique origin. Polyclonal antisera were produced using capsid proteins of both viruses expressed in Escherichia coli. DAS‐ELISA assays were developed for routine diagnosis and conditions for preparing samples for an optimized detection were determined. No cross‐reactions were observed. However, some false‐negative results, corresponding to samples giving ELISA readings close to the detection limit were regularly detected, particularly for ToCV (approximately 5% of the samples). A triplex RT‐PCR assay was thus developed, which allowed detection of both viruses in a one‐step protocol. An internal PCR control was included, which in addition showed that it could be used as a control for the entire RT‐PCR procedure. Finally, combining DAS‐ELISA in a first round, and triplex RT‐PCR for doubtful samples, appeared the best way to achieve a reliable diagnosis of these viruses.