Preferred name: Ipomovirus lycopersici
Taxonomic position: Viruses and viroids: Riboviria: Orthornavirae: Pisuviricota: Stelpaviricetes: Patatavirales: Potyviridae: Ipomovirus
Other scientific names: Eggplant mild leaf mottle virus, TMMoV, Tomato mild mottle virus
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Notes on taxonomy and nomenclature EU Categorization: A1 Quarantine pest (Annex II A)
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EPPO Code: TOMMOV

TMMoV was first reported from Yemen, where it infected Solanum lycopersicum (tomato) and weeds Datura stramonium (jimson weed) and Solanum nigrum (black night-shade) which were growing adjacent to the infected tomato plants (Walkey et al., 1994). Natural infection with TMMoV has also been reported for Nicandra physalodes, another weed species growing near infected tomato plants (Hiskias et al., 1999), and Solanum betaceum (tamarillo) (Monger and Nixon, 2010; Kinoga et al., 2023). Solanum melongena (eggplant) has been found to be infected with the EMLMV strain of TMMoV (Dombrovsky et al., 2012).

Under experimental conditions, TMMoV, including the isolate from eggplant (EMLMV), was also transmitted by mechanical sap inoculation to the following test plants: Nicotiana benthamiana, N. clevelandii, N. glutinosa, N. occidentalis, N. rustica, N. sylvestris and N. tabacum (Walkey et al., 1994; Hiskias et al., 1999; Dombrovsky et al., 2013. In addition, the isolate from tomato was mechanically transferred to Datura metel (Walkey et al., 1994; Hiskias et al., 1999), and the isolate from eggplant was transferred to Physalis floridana, and Petunia sp. (Dombrovsky et al., 2013).

Host list: Datura stramonium, Nicandra physalodes, Solanum betaceum, Solanum lycopersicum, Solanum melongena, Solanum nigrum

The tomato disease caused by TMMoV was first observed in Yemen in 1990 (Walkey et al., 1994), and later, based on a survey of tomato fields in 1994, TMMoV was found to be the predominant and most widespread virus on tomato in Ethiopia (Hiskias et al., 1999). In 2009, TMMoV was also found on tamarillo in Kenya (Monger and Nixon, 2010; Kinoga et al., 2023).

EMLMV has been shown to be the causal agent of a viral disease of eggplant that has been spreading in Israel since 2003 (Dombrovsky et al., 2012). Analysis of samples from the 2020-2021 survey confirmed that EMLMV also infects eggplants in Iraq (Khaffajah et al., 2022) and India (Mishra et al., 2023). Khaffajah et al. (2022) suggested that EMLMV was probably present on eggplant in Iraq before 2020, as a similar virus called eggplant blister mottled virus had been detected in earlier studies (Al-Ani et al., 2011). However, this assumption would need to be verified.

EPPO Region: Israel
Africa: Ethiopia, Kenya
Asia: India (Uttar Pradesh), Iraq, Israel, Yemen

All ipomoviruses are transmissible experimentally by mechanical inoculation and by grafting (Inoue-Nagata et al., 2022). These viruses are also transmitted by the whitefly (Bemisia tabaci) in a non-circulative, semi-persistent manner, the virions being retained on the external surface of the vectors’ mouth parts for a few days or weeks (Dombrovsky et al., 2014).

The first detected TMMoV isolates were reported as a nonpersistent aphid-borne potyvirus (Walkey et al., 1994; Hiskias et al., 2001). However, the sequence of TMMoV shows no relationship with any of the aphid-transmitted genera (Monger et al., 2001), furthermore, repeated vector transmission studies failed to demonstrate transmission of TMMoV by aphids (Abraham et al., 2012). A possible explanation for the discrepancy between these reports is that in the Walkey et al. (1994) and Hiskias et al. (2001) studies, TMMoV unknowingly occurred in a mixed infection with an aphid-transmitted potyvirus, e.g., potato virus Y (PVY), which may have lead to opportunistic transmission of TMMoV by aphids (Abraham et al., 2012; Dombrovsky et al., 2014). When whitefly transmission was attempted with TMMoV using approximately 100 whiteflies per plant, one of five transmission trials with B. tabaci resulted in successful transmission of TMMoV to one plant of N. tabacum cv. Samsun (transmission of TMMoV to other plants included in the same trial failed) (Abraham et al., 2012).

Similar results were reported for the TMMoV isolate from eggplant, EMMLV, which also lacks the motifs in the viral polyprotein that are essential for aphid-vectored transmission of potyviruses but not for transmission by whiteflies (Dombrovsky et al., 2012). Therefore, transmission experiments with aphids failed as expected, whereas EMMLMV was successfully transmitted from infected to healthy eggplant plants or from infected to healthy tobacco plants (N. tabacum cv. Samsun plants) in transmission experiments with whiteflies (B. tabaci) (Dombrovsky et al., 2013). However, the transmission efficiency of B. tabaci was poor and a large number of B. tabaci individuals (a few hundred per plant) were required for successful transmission (Dombrovsky et al., 2013). The transmission of EMLMV by whiteflies occurred in five out of seven independent transmission experiments, yielding the following transmission rates (infected/inoculated test plants): 6/6, 6/8, 0/7, 5/7, 0/6, 8/8 and 6/8. Independent serial transmission experiments on eggplant revealed that the virus was able to persist in the whitefly vector for at least 5 days but was no longer infective after 9 days (Dombrovsky et al., 2013).

Symptoms

The naturally infected tomato plants from which the TMMoV isolate from Yemen was obtained were slightly stunted with mild but distinct mottle symptoms on the leaves (Walkey et al., 1994). In Ethiopia, TMMoV was detected in tomato plants with mottling symptoms on the leaves, whereas severe mosaic, leaf deformation, and plant stunting were observed only when tomato plants were also infected with PVY (Hiskias et al., 1999). No symptoms occur on tomato plants, cvs Marmande and Linda, artificially infected with the TMMoV isolate from eggplant, EMLMV (Dombrovsky et al., 2013).

Mixed infection with TMMoV and PVY in tamarillo from Kenya resulted in leaf mosaic, mottling, and malformation (Kinoga et al., 2023). No sample of tamarillo had a single infection with either virus, making it difficult to associate the observed symptoms with TMMoV or PVY individually.

Solanum nigrum plants infected with TMMoV were just under half the normal size, and the leaves showed distinct mottle symptoms (Walkey et al., 1994). Datura stramonium from Yemen infected with TMMoV was also stunted, and leaves were reduced in size and showed interveinal chlorosis symptoms (Walkey et al., 1994). Virus-like symptoms have also been observed in naturally infected Nicandra physalodes (Hiskias et al., 1999).

In eggplant (Solanum melongena), EMLMV causes mild mottling of leaves and varying degrees of fruit distortion, sometimes accompanied by the formation of blisters on the fruit surface (Dombrovsky et al., 2013). Leaves of eggplant plants infected with EMLMV may also show mosaic, blistered areas, and downward curving leaves (Khaffajah et al., 2022; Mishra et al., 2023).

Morphology

TMMoV particles have a flexible, filamentous morphology and are approximately 720 nm long (Walkey et al., 1994; Dombrovsky et al., 2013). The ssRNA genome of virions comprises approximately 9280 nucleotides (excluding the 3’ poly(A) tail) and encodes a polyprotein of 3011 amino acids (Abraham et al., 2012; Dombrovsky et al., 2012).

Transmission electron microscopy analysis of ultrathin sections from infected leaf tissue revealed the presence of cytoplasmic inclusion bodies with pinwheel and crystalline structures typical of those induced by potyviral infection (Walkey et al., 1994; Dombrovsky et al., 2013).

Detection and inspection methods

The plants, especially the leaves, should be examined for symptoms. Particular attention should be paid if the whitefly B. tabaci is present. If necessary, samples should be taken for laboratory testing for definitive identification of the pest.

Electron microscopy can be used for the detection of Ipomoviruses, as they share a typical morphology, but cannot distinguish TMMoV from the other viruses in the genus. Mechanical inoculation of test plants can be used for detection and subsequent identification by other methods. On mechanically inoculated test plants such as D. stramonium, N. benthamiana, N. clevelandii, N. glutinosa, N. sylvestris and N. tabacum ‘White Burley’, TMMoV can cause vein clearing followed by leaf mottle and deformation or stunting (Hiskias et al., 1999; Dombrovsky et al., 2013).

Antisera prepared against the coat protein of TMMoV have been used in Western blot or ELISA in some studies (Walkey et al., 1994; Hiskias et al., 1999 and 2001; Monger et al., 2001; Abraham et al., 2012; Dombrovsky et al., 2013) but are not currently commercially available. Reverse transcription PCR tests with TMMoV specific primers have also been used for research purposes (Dombrovsky et al., 2013; Kinoga et al., 2023; Mishra et al., 2023), but it should be noted that validation data (performance characteristics according to EPPO Standard PM 7/98) are currently not available for any of these PCR-based tests.

High-throughput sequencing (HTS) analysis can also be used as a screening test for TMMoV. HTS is a technology that can be used to obtain (nearly) complete genome sequences, and analysis of these sequences can be used to identify a virus isolate. Several HTS platforms and sample preparation protocols are available. The performance characteristics of sequencing on the MinION sequencer (Oxford Nanopore Technologies) using the cDNA-PCR protocol for sequencing ribosomal RNA- depleted total RNA to detect TMMoV in tomato leaves are available in the EPPO database on diagnostic expertise (section validation data https://dc.eppo.int/validation_data/validationlist).

In international trade, TMMoV is most likely to be carried by infected vegetative host material, such as seedlings. B. tabaci will spread TMMoV locally.

TMMoV is semipersistent in its whitefly host, and it has been shown that the virus was able to persist in the whitefly vector for at least 5 days but was no longer infective after 9 days(Dombrovsky et al., 2013). This means that B. tabaci can probably spread TMMoV over long distances when carried on infected host material, but when carried on non-host plants, it may not remain virulent long enough to transmit the virus.

In addition, in the case of a mixed infection with an aphid-transmitted potyvirus, local spread of TMMoV by aphids cannot be excluded (see Biology). Mechanical transmission by wounding, although possible under experimental conditions, is highly unlikely to occur (EFSA, 2013). TMMoV is not known to be transmitted by seed.

Economic impact

The disease caused by TMMoV was first observed on tomato in June 1990 at a site in Yemen, but there was no evidence of economic impact, except that the virus slightly stunted many plants of cv. Roma and that these plants showed mild mottle symptoms on the leaves (Walkey et al., 1994). Later, the results of the survey of tomato fields conducted in 1994 in the main growing areas in the Rift Valley and the west of Ethiopia showed that TMMoV is the predominant and most widespread virus in tomato in Ethiopia (Hiskias et al., 1999). Hiskias et al., 1999 reported that in Ethiopia, a single infection with TMMoV resulted in mottle symptoms, while in cases where a mixed infection with PVY was detected, severe mosaic, leaf deformation and plant stunting were observed.

The effects of TMMoV on tamarillo are not assessable as it has only been detected in mixed infections with PVY. However, this mixed infection has been reported to cause mosaic, mottling and malformations on tamarillo leaves (Kinoga et al., 2023).

The TMMoV strain, EMLMV, could have a serious impact on eggplant production, as the fruits of EMLMV-infected plants were deformed to varying degrees, accompanied by hardening of the flesh, making them unmarketable (Dombrovsky et al., 2013). In some cases, complete yield loss was observed in Israel (Dombrovsky et al., 2013). Based on the survey conducted in Iraq in 2020, the infection rate with EMLMV in the eggplant fields surveyed was estimated at 1 to 80 % (Khaffajah et al., 2022).

Control

Control should be based on preventive and cultural practices. The use of healthy seedlings and measures against B. tabaci can help contain the spread. Care should be taken to protect host plant seedlings from infection before transplanting in the field or greenhouse. In regions where B. tabaci occurs in open fields, control should both exclude the insect from entering the area that the host crops are grown (physical barriers, protected cultivation) and reduce whitefly populations using integrated pest management practices, combining biological and chemical control strategies (EPPO, 2023) to suppress the spread of the virus. Crop rotation and planting outside periods of high vector population can also help to reduce the impact of viral diseases. The removal of virus-infected plants, and the removal of the weeds, which are a potential virus reservoir, is also important and would help to prevent further spread of the virus.

Phytosanitary risk

TMMoV has been present in Yemen and Ethiopia since 1990 and 1994 respectively; later it was found in Israel, Iraq, Kenya and India (see Geographical distribution). It can become established in areas where B. tabaci, its whitefly vector, is present. B. tabaci occurs outdoors in coastal areas with a Mediterranean climate and is a greenhouse pest in many EPPO countries (EFSA, 2013; EPPO, 2023). Tomato and eggplant are grown throughout the EPPO region, while tamarillo prefers a subtropical climate but can be grown in Mediterranean climates.

Host plants for planting should only be imported from pest-free areas for the virus. They may also come from areas where the virus occurs if they are produced in pest-free sites of production e.g. under isolation or where measures are implemented to avoid the presence of B. tabaci (e.g. greenhouses, trapping) and no symptoms of the virus are observed during the cycle of vegetation. Surveillance (visual inspection followed by laboratory testing) contributes to early detection of TMMoV infected plants and assessment of vectors for targeted insecticide application. Eradication measures for TMMoV would need to involve both destruction of the affected hosts and target the vector B. tabaci.

Abraham A, Menzel W, Vetten HJ & Winter S (2012) Analysis of the tomato mild mottle virus genome indicates that it is the most divergent member of the genus Ipomovirus (family Potyviridae). Archives of Virology 157, 353-357.

Al-Ani RA, Adhab MA & Ismail KA (2011) Eggplant blister mottled virus (EBMV): A possible new potyvirus characterized from Iraq. Journal of General Molecular Virology 3(3), 49–54.

Dombrovsky A, Reingold V & Antignus Y (2014) Ipomovirus-an atypical genus in the family Potyviridae transmitted by whiteflies. Pest Management Science 70, 1553-1567.

Dombrovsky A, Sapkota R, Lachman O & Antignus Y (2012) Eggplant mild leaf mottle virus (EMLMV), a new putative member of the genus Ipomovirus that harbors an HC-Pro gene. Virus Genes 44, 329-337.

Dombrovsky A, Sapkota R, Lachman O, Pearlsman M & Antignus Y (2013) A new aubergine disease caused by a whitefly-borne strain of Tomato mild mottle virus (TomMMoV). Plant Pathology 62, 750-759.

EFSA Panel on Plant Health (PLH) (2013) Scientific Opinion on the risks to plant health posed by Bemisia tabaci species complex and viruses it transmits for the EU territory. EFSA Journal 11(4), 3162.

EPPO (2021) PM 7/98 (5) Specific requirements for laboratories preparing accreditation for a plant pest diagnostic activity. EPPO Bulletin, 51: 468-498. https://doi.org/10.1111/epp.12780

EPPO (2023) Bemisia tabaci. EPPO datasheets on pests recommended for regulation. https://gd.eppo.int (accessed 2023-11-03)

Hiskias Y, Lesemann D-E & Vetten HJ (1999) Occurrence, distribution and relative importance of viruses infecting hot pepper and tomato in the major growing areas of Ethiopia. Journal of Phytopathology 147, 5–11.

Hiskias Y, Lesemann DE & Vetten HJ (2001) Biological characteristics of tomato mild mottle potyvirus isolated from tomato and thorn apple in Ethiopia. African Crop Science Journal 9(3), 517–525.

Inoue-Nagata AK, Jordan R, Kreuze J, Li F, López-Moya JJ, Mäkinen K, Ohshima K, Wylie S & ICTV Report Consortium (2022) ICTV Virus Taxonomy Profile: Potyviridae 2022. Journal of General Virology 103, 001738.

Khaffajah B, Alisawi O & Fadhl FA (2022) Genome sequencing of eggplant reveals Eggplant mild leaf mottle virus existence with associated two endogenous viruses in diseased eggplant in Iraq. Archives of Phytopathology and Plant Protection 55, 1930-1943. https://doi.org/10.1080/03235408.2022.2123601

Kinoga MN, Kuria PK, Miano DW, Kiambi RG, Mollow DS, Grindstead S & Wasilowa LA (2023) Genome characterisation of two complete coding sequences of tomato mild mottle virus from tree tomato and their distribution in Kenya. Journal of Plant Pathology 105, 15–19.

Mishra R, Verma RK, Mall S & Gaur RK (2023) Complete genome sequence of eggplant mild leaf mottle virus (EMLMV) infecting eggplant in India. Indian Phytopathology 76, 1141-1144. https://doi.org/10.1007/s42360-023-00672-3

Monger WA & Nixon T (2010) Tomato mild mottle virus in Tamarillo in Kenya. NCBI. https://www.ncbi.nlm.nih.gov/nuccore/HQ711860

Monger WA, Spence NJ & Foster GD (2001) Molecular evidence that the aphid transmitted tomato mild mottle virus belongs to the Potyviridae family but not Potyvirus genus. Archives of Virology 146, 2435–2441.

Walkey D, Spence N, Clay CM & Miller A (1994) A potyvirus isolated from solanaceous hosts. Plant Pathology 43, 931–937.

This datasheet was prepared in 2024 by Nataša Mehle. Her valuable contribution is gratefully acknowledged.

EPPO (2024) Ipomovirus lycopersici. EPPO datasheets on pests recommended for regulation. https://gd.eppo.int (accessed 2024-11-21)

This datasheet was first published online in 2024. It is maintained in an electronic format in the EPPO Global Database. The sections on 'Identity', ‘Hosts’, and 'Geographical distribution' are automatically updated from the database. For other sections, the date of last revision is indicated on the right.