Skip to main content

Thank you for visiting You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

Solanum linnaeanum and Solanum sisymbriifolium as a sustainable strategy for the management of Meloidogyne chitwoodi


Root-knot nematodes (RKN), Meloidogyne spp., are important crop pests that cause severe losses in crop production worldwide, reducing both productivity and crop quality. Meloidogyne chitwoodi Golden, O'Bannon, Santo & Finley, 1980 is considered a quarantine organism by the European and Mediterranean Plant Protection Organization (EPPO) causing damage in tomato and potato crops. The development of nonchemical and sustainable management strategies to reduce nematode damage is crucial. The resistance of Solanum linnaeanum Hepper & P.-M.L. Jaeger and S. sisymbriifolium Lamarck cv. Sis 6001 to M. chitwoodi was evaluated based on gall index (GI), the Bridge & Page (1980) rating chart and reproduction factor (RF). Both plant species were resistant to M. chitwoodi. Solanum linnaeanum had an average of 519 small root swellings/plant, with 45% adult nematodes inside the roots, all males. Solanum sisymbriifolium had GI ≤ 2 and RF ≤ 1 with a high percentage (69%) of nematodes inside the roots that did not develop beyond the sexually undifferentiated second-stage. The use of S. linnaeanum as a new source of resistance is a good alternative for the control of RKN in the quest to develop nonchemical and sustainable management strategies to protect crops.


Plant-parasitic nematodes (PPN) are a focus of intense scientific research because they represent an important constraint for global food production, reducing yields and crop quality worldwide1,2,3,4. Most agricultural fields are infested with at least one PPN species and annual crop losses caused by them are estimated to be between 8.8 and 14.6% of total World crop production5,6. The nematodes with the greatest economic impact are the root-knot nematodes (RKN), Meloidogyne spp. Many species of this genus are quite aggressive, and they are widely distributed across a range of climatic conditions3,7,8. Some species are considered quarantine pests by the European and Mediterranean Plant Protection Organization (EPPO) and interfere with international trade9.

In Europe, RKN are increasingly important and they are responsible for significant yield losses, reaching up to 100% in tomato, S. lycopersicum (L.) H. Karst, one of the major vegetable crops cultivated and consumed internationally10,11.

Potato, S. tuberosum L., is an important staple crop in Portugal and, according to “Instituto Nacional de Estatística” (INE), an average of 431,686 ha of potatoes are produced every year12. Meloidogyne chitwoodi Golden, O'Bannon, Santo & Finley, 1980 is considered a quarantine organism by EPPO (EPPO A2 list: No. 227) causing damage and making tubers unsuitable for consumption or processing. Even though M. chitwoodi is present in most major potato producing areas, its detection in tubers can lead to the rejection of entire shipments. Since the 1990s it has become prevalent in vegetable and potato production areas13,14.

The global distribution and wide range of hosts of RKN explains the high economic impact of these nematodes and the difficulties found in their management11. Although RKN are impossible to eradicate, it is crucial to reduce the amount of damage they cause if productivity is to be sustainable5. Their control is mainly achieved by the cultural practices of crop rotation and the use of resistant cultivars, combined with nematicide application15,16. Despite the fact that the use of chemical pesticides is an effective control strategy, this is an expensive method and European legislation (Directive 69/465/CEE; Directive 2009/128/EC) is very strict regarding the use of nematicides in the field, focusing mainly on environmental safety issues and health risks. The increase of environmental concerns and regulatory restrictions on the application of chemical products in conventional systems have meant that the use of plant resistance to control PPN has increased. The most effective, environmentally friendly, and economical means of controlling Meloidogyne spp. is the use of resistant cultivars10. However, up to now, there are no potato cultivars resistant to RKN9.

Therefore, other control measures are being developed, including the use of plants as trap crops as an alternative to chemical pesticides17,18,19,20. A trap crop is a plant species attractive to pests from another crop but in which the pest fails to survive or reproduce. Many wild Solanum species display resistance to Meloidogyne spp., although the resistance is often not complete, and the nematodes may form a few galls or eggs. A potentially useful source of resistance occurs in S. sisymbriifolium Lamarck21,22.

Solanum sisymbriifolium, originates from warm, temperate South America, is an annual or perennial erect, rhizomatous, shrubby weed with an extensive root system and spiny leaves, currently distributed throughout the world and invasive in some countries. Interest in the study of this plant has increased since it was proved to be a good trap crop against potato cyst nematodes (PCN), Globodera spp. It was introduced in The Netherlands following research that identified the species as the most suitable candidate among a diversity of species tested as potential trap crops17,20,22,23,24,25. Several studies have been done with this plant and it has proved to have effects on hatching, mortality, infectivity and/or reproduction in several nematode species, including PCN, RKN and root-lesion nematodes (RLN)18,20,23,24,26,27,28. The effects of S. sisymbriifolium on nematodes depend on the cultivars used, the genus and species of nematode present and on biotic and abiotic conditions10.

In Portugal, S. sisymbriifolium is not part of the native flora29, but other plants of the same genus, for instance S. linnaeanum Hepper & P.-M.L. Jaeger, which is similar to S. sisymbriifolium (Supplementary Fig. S1), are present in the South of Portugal30,31. It is an invasive species of plant, spiny, with an extensive root system, and is probably native from Southern Africa although it is a common weed in North Africa and Southern Europe30,32.

Solanum sisymbriifolium is also known to be a source of resistance, or partial resistance, to some diseases and plant pests, including fungi, bacteria, nematodes and insects. Solanum linnaeanum has been much less studied but has potential as a source of resistance to some fungi and viruses33,34,35.

The main goals of the present study were: to evaluate the potential value of two wild Solanum plants, S. linnaeanum and S. sisymbriifolium, in controlling agricultural pests such as RKN; to assist in the development of sustainable and ecofriendly management methods of key enemies in agriculture, in order to reduce dependence on chemical pesticides; and to improve crop productivity. The resistance shown by S. linnaeanum and S. sisymbriifolium cv. Sis 6001 was evaluated against M. chitwoodi. Although some studies have been made with S. sisymbriifolium and PPN and it is already used as a trap crop in some places, not much is known about S. linnaeanum and its effects on nematodes. New sources of resistance may result in the development of sustainable and nonchemical management strategies to protect crops against PPN. This is the first report of S. linnaeanum being used in Portugal for the management of PPN.


The environmental conditions used, and the period of the experiments, proved to be appropriate and sufficient for the development and reproduction of the nematodes. The results showed that there was no reproduction of M. chitwoodi in S. linnaeanum and that there was only a little reproduction in S. sisymbriifolium cv. Sis 6001, when compared with the reproduction in the susceptible plants used as controls, tomato cv. Coração de boi and potato cv. Désirée (Fig. 1 and Supplementary Fig. S1).

Figure 1
figure 1

Solanum linnaeanum (A), S. sisymbriifolium cv. Sis 6001 (B), S. lycopersicum cv. Coração de boi (C) and S. tuberosum ssp. tuberosum cv. Désirée (D) roots. Galls with egg masses marked in controls (C, D) with red circles.

Soil sterility was confirmed by the absence of galls and egg masses in uninoculated plants. The values of GI = 5 and RF > 1 (Table 1) obtained in the controls, tomato and potato, confirmed the viability of the inocula and that environmental conditions were favorable for penetration, development and reproduction of M. chitwoodi.

Table 1 Resistance degree (RD) of Solanum linnaeanum, S. sisymbriifolium cv. Sis 6001 and respective controls (tomato and potato), 70 days after inoculation with 5000 eggs of Meloidogyne chitwoodi per plant (averages of ten replicates).

The same was verified by the index in the Bridge & Page (1980) rating chart36, which varied between 4 in tomato plants, 40% roots infested with larger knots but main roots clean, and 5 in potato plants, 50% roots infested with knotting on parts of main roots. All inoculated plants presented symptoms of yellowing, wilting and leaf drop, related to the presence of nematodes.

Solanum linnaeanum was considered resistant to M. chitwoodi (Table 1 and Supplementary Table S1). The index in the Bridge & Page (1980) rating chart36 was 0, because no egg masses developed on the roots. Observation of the stained root systems showed the presence of many small root swellings (average of the 10 replicates was 519 small root swellings/plant) and nematodes inside the roots (total numbers values between 329 and 883 per plant) (Supplementary Table S2). Almost all the nematodes inside the roots were second-stage juveniles (J2) (44%) or adults (45%) and all the adults were males (100%) (Fig. 2).

Figure 2
figure 2

Number of nematodes in different development stages, J2, J4 and adults (all males), on Solanum linnaeanum root systems. The percentages are averages of the two assays (5 replicates/assay).

The values of GI = 0 and RF = 0 (Table 1 and Supplementary Table S1), and the index 0 in the Bridge & Page (1980) rating chart, obtained for S. sisymbriifolium cv. Sis 6001 confirmed its resistance to M. chitwoodi, and are consistent with the results obtained by Dias et al. (2012) for other S. sisymbriifolium cultivars17,36. However, when plants were analyzed separately some variability could be observed between them. Only two replicates (in a total of 10 replicates, 5 per assay) showed the presence of galls, one with one gall and without egg masses and another with 11 galls with 9 egg masses containing 187 eggs in total (Supplementary Table S1). Despite this, there are no statistically significant differences between numbers of galls, egg masses, eggs and RF between S. linnaeanum and S. sisymbriifolium cv. Sis 6001. Observation of stained roots of S. sisymbriifolium cv. Sis 6001 showed some nematodes (total numbers values between 4 and 117 per plant) (Supplementary Table S2). The majority of nematodes inside the roots were J2 (69%); of the remainder, 17% were adults, of which 63% were males (Fig. 3).

Figure 3
figure 3

Number of nematodes in different development stages, J2, J4 and adults (males and females), on Solanum sisymbriifolium cv. Sis 6001 root systems. The percentages are averages of the two assays (5 replicates/assay).


The choice of the classification system of Sasser et al. (1984) and the rating chart of Bridge & Page (1980) for the resistance studies of S. linnaeanum and S. sisymbriifolium cv. Sis 6001 to M. chitwoodi was because they can be applied to any crop and they also allow results from different studies to be compared without the need to include the susceptible controls36,37.

The time that any Meloidogyne species needs to complete a generation depends on external factors, such as temperature, humidity, light and the quality and condition of the host plant in relation to its age and nutritional status. All of these factors are crucial as they determine how and when the effects of nematodes on the plant will be most visible38. In our laboratory, it was observed that M. chitwoodi had a slower rate of development than other Meloidogyne isolates. Thus, the plants were uprooted 70 days after inoculation (DAI) instead of the usual 60 DAI. Any differences found between species or replicates can only be attributed to characteristics inherent to the plants as the assay conditions were always the same.

The control of the population density of PPN in the soil is best achieved by resistance in the plant, characterized as the ability of a plant species to inhibit nematode development or reproduction39. So far, the capacity of J2 penetration into the roots has not been considered as a mechanism for characterization of the resistance. Generally, resistance to nematodes in plants becomes obvious after J2 penetration into the roots (i.e. post-infection)40. The J2 that penetrate the roots of resistant plants may die or leave the roots, but they can also develop to the adult stage, as females without egg production (or the eggs produced are not viable) or as males41. Various procedures for determining the resistance of plants to nematodes are used. The most common procedures are the percentage or number of galls or egg masses formed as well as the RF (Pf/Pi) values37. The low numbers of nematodes that penetrated the roots of S. linnaeanum and S. sisymbriifolium cv. Sis 6001 are probably due to substances produced by the roots of these plants, which prevented their penetration. Conceição and collaborators (2012) analyzed the effects of S. sisymbriifolium (cvs. Domino, Pion, Sharp and Sis 4004) exudates in five Meloidogyne isolates (M. arenaria, M. chitwoodi, M. hapla, M. hispanica and M. javanica) and showed the complexity and variability of the interactions between RKN and S. sisymbriifolium42. In this study, the cultivars studied demonstrated low or no inhibitory effect on M. chitwoodi hatching. The presence of resistance in some S. sisymbriifolium cultivars to PPN, has already been demonstrated for G. pallida, G. rostochiensis, M. chitwoodi and M. javanica17,24. This was confirmed by Hajihassani et al. (2020) for other major species of RKN (M. arenaria, M. haplanaria and M. incognita), although the effectiveness of resistance to M. arenaria varied a lot between S. sisymbriifolium cultivars10.

In S. linnaeanum, in the present work, there was greater nematode penetration of the roots than in S. sisymbriifolium cv. Sis 6001, but there was no reproduction in any of the plants, and all nematodes that developed into adults were males. This reaction is a form of active resistance (i.e. post-infection) in which, although the J2 can penetrate the roots, they do not find favorable conditions for their normal development and reproduction. Adverse nutrition conditions in younger stages can, by themselves, change the physiology of certain nematodes, eliminating formation of females, egg production or population increase14. The larger number of males in the roots may indicate that the plant has a type of resistance that prevents the nematode from feeding normally.

In S. sisymbriifolium cv. Sis 6001, although some nematodes penetrated and established in the roots, there was actual reproduction in only one replicate of the first bioassay. The reduced number of nematodes found in the roots may be related to the existence of exudates or compounds produced by the roots of this cultivar that prevent J2 penetration19. This type of resistance occurs before the nematode penetrates the root (i.e. pre-infection) and is called passive43. From analysis of the results of other authors, S. sisymbriifolium presents great variability, both between and within cultivars. In some cases, resistant and susceptible plants may co-exist within the same cultivar17. In Ali et al. (1992), for M. incognita, although S. sisymbriifolium was invaded by nematodes which formed some (4–5) swellings (not real galls), the nematodes did not develop beyond J2 and there was no egg mass production21. Similar results were also reported by Fassuliotis & Bhatt (1982), possibly due to a tracheid discontinuity, due in turn to the formation of a small, thin-walled giant cell. However, for M. javanica, using regenerated plants rather than seeds, S. sisymbriifolium demonstrated low resistance44. Some reports do not mention the S. sisymbriifolium cultivar and Meloidogyne species used and S. sisymbriifolium may react differently to different species of Meloidogyne. As reported by Daunay & Dalmasso (1985), S. sisymbriifolium was a poor host for M. arenaria and M. incognita but it was a better host for M. javanica45. Therefore, caution should be taken when choosing the S. sisymbriifolium cultivar to control RKN because the results can change with the cultivar and/or the nematode species considered. The effects of some S. sisymbriifolium cultivars, or their plant extracts, on hatching, infectivity and/or reproduction of PCN, RLN and RKN has also been demonstrated by other authors with positive results17,18,26,27.

Although S. sisymbriifolium is tolerant of cold and heat21,46 and is already used as a trap crop in some countries, this plant has already become invasive in some places. However, it is not native to Portugal and is also attacked by pests common to some of our crops47. Taking also in consideration, as already mentioned, that S. sisymbriifolium cultivars have great intra- and inter-cultivar variability42,44 and given the results obtained in this work, S. linnaeanum may be a better plant to use against nematodes. It already exists in Portugal and is also a source of resistance to other pests and plant diseases such as Verticillium wilt33,34. Despite this, care must also be taken with the Meloidogyne species considered and with the plants of S. linnaeanum used. Tzortzakakis and collaborators (2006) tested S. linnaeanum against M. incognita and M. javanica and, in both cases, the nematodes reproduced, although in M. incognita the numbers of galls and egg masses were significantly lower than in the controls48.

The plant species we have considered are resistant, or partially resistant, to some diseases and plant pests. Solanum linnaeanum exhibits resistance to Verticillium wilt and Liu and collaborators (2015) succeeded in the transference of this resistance to eggplants through the introgression of the disease resistance gene34. In the same way, if the S. linnaeanum and S. sisymbriifolium resistance genes are isolated, they can be used to confer resistance to plants susceptible to M. chitwoodi, such as tomato and potato plants. They have a potential to be used as sources for resistance to M. chitwoodi in breeding programs.

In this study, it was demonstrated that S. linnaeanum can reduce RKN densities in the soil. Its roots attract M. chitwoodi juveniles, removing them from the soil but at the same time reducing the reproduction of the nematodes. The fact that the nematodes developed into males, without females, avoids the risk of reproduction or leaving a dangerous, viable population of nematodes in the soil. Since the number of J2 that hatch and penetrate the roots is high, the population density of nematodes in the soil decreases and even those that hatch but do not enter the roots will die. In that way, the use of S. linnaeanum as a trap crop, in a crop rotation system, or even as rootstocks, may be an appropriate component of Integrated Pest Management, keeping RKN populations at levels low enough not to cause economic losses, thereby increasing production and crop quality and avoiding or limiting the use of synthetic nematicides. Using a trap crop does not disturb the ecological balance in the soil and the extensive and deep root systems of S. linnaeanum grow deeper into the soil than nematicides can penetrate. Solanum linnaeanum could be a good alternative to other PPN control measures but more studies are required, including field studies. The crop should be completely removed before flowering or incorporated into the soil as green manure before seeds are produced, preventing it from becoming invasive in areas where it does not yet exist. Also, different conditions should be tested to investigate whether the resistance of the plants is stable at different temperatures. There are no known uses for this plant in Portugal. In this way, it may be possible to find a use for a plant that, despite having existed in Portugal for many years, was only ever considered a weed. In this study, resistance to M. chitwoodi in another cultivar of S. sisymbriifolium (cv. Sis 6001) was also confirmed.


Nematode isolates

Meloidogyne chitwoodi was chosen because it is a problem for potato crops that has already been detected in Portugal and is considered an A2 quarantine pest by EPPO. An isolate of M. chitwoodi from the NEMATO-lab of the University of Coimbra, obtained from a potato field in Porto, Portugal49, was maintained and multiplied on susceptible tomato plants, S. lycopersicum cv. Coração de boi, inoculated with 15 egg masses/plant. The plants were grown in pots filled with 500 g of steam-sterilized soil mix (sand:soil:peat 1:1:1 v/v) and kept in a glasshouse (20–25 °C, 70–75% relative humidity and 12 h photoperiod). Ninety DAI, the plants were uprooted and nematode eggs were extracted with 0.52% sodium hypochlorite (NaOCl) solution, according to Hussey & Barker (1973)50. This culture of M. chitwoodi is a pure isolate started initially from a single egg mass; its identification was confirmed by esterase phenotype analysis at the beginning and at the end of each assay51.

Plant materials

Solanum lycopersicum cv. Coração de boi (tomato), S. linnaeanum and S. sisymbriifolium cv. Sis 6001 were grown from seeds. Our stock of S. linnaeanum is a wild isolate whose seeds were harvested from a plant growing on the roadside in the Algarve. The seeds were germinated at 25–27 °C on moist filter paper in Petri dishes and transplanted singly into 5 cm diameter plastic pots containing 60 cm3 of a steam-sterilized mixture of loam soil and sand (1:2 v/v). Solanum sisymbriifolium seeds were germinated in a glasshouse in polystyrene plates containing sterile peat. Fifteen days after germination the seedlings of this species were transplanted singly into pots filled with 500 g of steam-sterilized soil mix (sand:soil:peat 1:1:1 v/v). The potato plants, S. tuberosum ssp. tuberosum L. (cv. Désirée), were obtained from pieces of potato tubers with sprouts in pots with the same mixture of soil (sand:soil:peat 1:1:1 v/v). All plants were kept in a glasshouse under the same conditions as described above.

Pathogenicity tests

Five four-weeks-old plants from each species were inoculated with 5000 M. chitwoodi eggs (initial population density, Pi). To confirm the soil sterility one plant of each species was potted in the sterilized soil mix and not inoculated. Five susceptible tomato plants cv. Coração de boi and five susceptible potato plants cv. Désirée were also inoculated to confirm the viability of the inocula. Pots were kept in the conditions already mentioned and the plants were watered daily. Seventy DAI the plants were uprooted and the root systems washed. The root systems were stained with phloxine B (0.0015% solution) for 15 min52, and galls and eggs masses were counted. Eggs were extracted as described above and counted to determine the final population (Pf). Resistance rating of the species were based on Gall Index (GI) and Reproduction Factor (RF = Pf / Pi), according to the modified quantitative scheme of Canto-Sáenz (1985)41,53. The evaluation of the degree of resistance of the plants was based on GI and RF37.

Roots that had less than 100 egg masses were stained with acid fuchsin54, and the numbers of the different developmental stages of M. chitwoodi were recorded. Resistance ratings of these plants were based on the RKN rating chart of Bridge & Page (1980)36. This scale is based on the percentage and types of roots galled from 0 (0%, no galls) to 10 (100% galled). The roots were observed using a routine stereo microscope Leica M80, at a magnification of 60 x, and the nematodes found were transferred onto a glass slide and observed with an optical microscope Leica DM2500, at a magnification of 400 ×. The identification of the different developmental stages was done by comparing their morphological characteristics with those described for M. incognita (Supplementary Fig. S2)41,55.

The assay was done twice, using the same conditions each time.

Statistical analysis

The data (values obtained for galls, egg masses and eggs counts and RF), were confirmed to meet the statistical assumptions of normality and homogeneity of variances (one way ANOVA), and were submitted to analysis of variance and the means compared by LSD (P < 0.05) using Statistic 10 software (Statsoft Inc.).


  1. Bernard, G. C., Egnin, M. & Bonsi, C. The impact of plant-parasitic nematodes on agriculturee and methods of control. In Nematology—concepts, diagnosis and control (eds Shah, M. M. & Mahamood, M.) 121–151 (InTech, Croatia, 2017).

    Chapter  Google Scholar 

  2. Chelinho, S. et al. Toxicity of the bionematicide 1,4-naphthoquinone on non-target soil organisms. Chemosphere 181, 579–588. (2017).

    ADS  CAS  Article  PubMed  Google Scholar 

  3. Jones, J. T. et al. Top 10 plant-parasitic nematodes in molecular plant pathology. Mol. Plant. Pathol. 14(9), 946–961. (2013).

    Article  PubMed  PubMed Central  Google Scholar 

  4. Khan, M. R. Taxonomy of plant parasitic nematodes in global context vis-à-vis India. Res. Rev. J. Agric. Allied Sci. 4(3), 1–2 (2015).

    CAS  Google Scholar 

  5. Baidya, S., Timila, R. D., Kc, R. B., Manandhar, H. K. & Manandhar, C. Management of root-knot nematode on tomato through grafting root stock of Solanum sisymbriifolium. J. Nepal Agric. Res. Counc. 3, 27–31. (2017).

    Article  Google Scholar 

  6. Singh, S. K., Hodda, M. & Ash, G. J. Plant-parasitic nematodes of potential phytosanitary importance, their main hosts and reported yield losses. EPPO Bull. 43(2), 334–374. (2013).

    Article  Google Scholar 

  7. Giné, A., Carrasquilla, M., Martínez-Alonso, M., Gaju, N. & Sorribas, F. J. Characterization of soil suppressiveness to root-knot nematodes in organic horticulture in plastic greenhouse. Front. Plant Sci. 7, 1–15. (2016).

    Article  Google Scholar 

  8. Hussey, R. S. & Janssen, G. J. W. Root-knot nematodes: Meloidogynespecies. In Plant resistance to parasitic nematodes (eds Starr, J. L. et al.) 43–70 (CABI Publishing, Wallingford, 2002).

    Chapter  Google Scholar 

  9. Dinh, P. T. Y., Zhang, L., Mojtahedi, H., Brown, C. R. & Elling, A. A. Broad Meloidogyne resistance in potato based on RNA interference of effector gene 16D10. J. Nematol. 47(1), 71–78 (2015).

    CAS  PubMed  PubMed Central  Google Scholar 

  10. Hajihassani, A. et al. Characterization of resistance to major root-knot nematodes (Meloidogyne spp.) in Solanumsisymbriifolium. Phytopathology 110(3), 666–673. (2020).

    Article  PubMed  Google Scholar 

  11. Wesemael, W. M. L., Viaene, N. & Moens, M. Root-knot nematodes (Meloidogyne spp.) in Europe. Nematology 13(1), 3–16. (2011).

    Article  Google Scholar 

  12. Instituto Nacional de Estatística (2020). Accessed 21 April 2020.

  13. Elling, A. Major emerging problems with minor Meloidogyne species. Phytopathology 103(11), 1092–1102. (2013).

    Article  PubMed  Google Scholar 

  14. Ingham, R. E., Hamm, P. B., Williams, R. E. & Swanson, W. H. Control of Meloidogyne chitwoodi in potato with fumigant and non-fumigant nematicides. J. Nematol. 32(4S), 556–565 (2000).

    CAS  PubMed  PubMed Central  Google Scholar 

  15. Schomaker, C. H. & Been, T. H. A model for infestation foci of potato cyst nematodes Globodera rostochiensis and Globodera pallida. Phytophatology 89(7), 583–590. (1999).

    CAS  Article  Google Scholar 

  16. Whitehead, A. G. & Turner, S. J. Management and regulatory control strategies for potato cyst nematodes (Globodera rostochiensis and Globodera pallida). In Potato cyst nematodes, biology, distribution and control (eds Marks, R. J. & Brodie, B. B.) 135–152 (Wallingford, CAB International, 1998).

    Google Scholar 

  17. Dias, M. C., Conceição, I. L., Abrantes, I. & Cunha, M. J. Solanum sisymbriifolium—a new approach for the management of plant-parasitic nematodes. Eur. J. Plant Pathol. 133(1), 171–179. (2012).

    Article  Google Scholar 

  18. Dias, M. C. et al. Effects of Solanum sisymbriifolium on potato cyst nematode populations in Portugal. Plant Soil 421(1), 439–452. (2017).

    CAS  Article  Google Scholar 

  19. Sasaki-Crawley, A. et al. Signalling and behavior of potato cyst nematode in the rhizosphere of the trap crop, Solanum sisymbriifolium. Appl. Biol. 103, 45–52 (2010).

    Google Scholar 

  20. Timmermans, B. G. H., Vos, J., Stomph, T. J., Nieuwburg, J. V. & Putten, P. E. L. Growth duration and root length density of Solanumsisymbriifolium (Lam.) as determinants of hatching of Globoderapallida (Stone). Ann. Appl. Biol. 148(3), 213–222. (2006).

    Article  Google Scholar 

  21. Ali, M., Matsuzoe, N., Okubo, H. & Fujieda, K. Resistance of non-tuberous Solanum to root-knot nematode. J. Jpn. Soc. Hortic. Sci. 60(4), 921–926 (1992).

    Article  Google Scholar 

  22. Fassuliotis, G. & Dukes, P. D. Disease reactions of Solanum melongena and S. sisymbriifolium to Meloidogyne incognita and Verticillium alboatrum. J. Nematol. 4, 222 (1972).

    Google Scholar 

  23. Scholte, K. Screening of non-tuber bearing Solanaceae for resistance to and induction of juvenile hatch of potato cyst nematodes and their potential for trap cropping. Ann. Appl. Biol. 136(3), 239–246. (2000).

    Article  Google Scholar 

  24. Scholte, K. & Vos, J. Effects of potential trap crops and planting date on soil infestation with potato cyst nematodes and root knot nematodes. Ann. Appl. Biol. 137(2), 153–164. (2000).

    Article  Google Scholar 

  25. Turner, S., Martin, T., McAleavey, P. & Fleming, C. The management of potato cyst nematodes using resistant Solanaceae potato clones as trap crops. Ann. Appl. Biol. 149(3), 271–280. (2006).

    Article  Google Scholar 

  26. Dandurand, L.-M. & Knudsen, G. R. Effect of the trap crop Solanumsisymbriifolium and two biocontrol fungi on reproduction of the potato cyst nematode, Globoderapallida. Ann. Appl. Biol. 169(2), 180–189. (2016).

    Article  Google Scholar 

  27. Pestana, M., Gouveia, M. & Abrantes, I. Efeitos de Solanum sisymbriifolium e S. nigrum sobre o nemátode-das-lesões-radiculares, Pratylenchusgoodeyi, parasita da bananeira. Rev. Ciênc. Agrar. 32(2), 173–181 (2008).

    Google Scholar 

  28. Roberts, P. A. & Stone, A. R. Comparisons of invasion and development of Globodera spp. and European potato cyst-nematode pathotypes in roots of resistant Solanum sg. Leptostemonum spp. Nematologica 29, 95–108. (1983).

    Article  Google Scholar 

  29. Global Invasive Species Database (2020). Accessed 21 April 2020.

  30. Marchante, H., Morais, M., Freitas, H. & Marchante, E. Guia prático para a identificação de plantas invasoras em Portugal, ISBN:978-989-26-0785-6 ISBN:978-989-26-0785-6 (Coimbra University Press, Coimbra, 2014).

    Google Scholar 

  31. Naturdata Biodiversidade Online (2020). Accessed 21 April 2020.

  32. Vorontsova, M. S. & Knapp, S. A new species of Solanum (Solanaceae) from South Africa related to the cultivated eggplant. PhytoKeys 8(8), 1–11. (2012).

    Article  Google Scholar 

  33. Collonnier, C. et al. Applications of biotechnology in eggplant. Plant Cell Tissue Organ Cult. 65(2), 91–107. (2001).

    CAS  Article  Google Scholar 

  34. Liu, J., Zheng, Z., Zhou, X., Feng, C. & Zhuang, Y. Improving the resistance of eggplant (Solanum melongena) to Verticillium wilt using wild species Solanum linnaeanum. Euphytica 201(3), 463–469. (2015).

    CAS  Article  Google Scholar 

  35. Nefzi, A. et al. Management of Fusarium crown and root rot of tomato by Solanumlinnaeanum L. extracts. Sci. Hortic. 238, 204–214. (2018).

    CAS  Article  Google Scholar 

  36. Bridge, J. & Page, S. L. J. Estimation of root-knot nematode infestation levels on roots using a rating chart. Trop. Pest Manag. 26(3), 296–298. (1980).

    Article  Google Scholar 

  37. Sasser, J. N., Carter, C. C. & Hartman, K. M. Standardization of host suitability studies and reporting of resistance to root-knot nematodes, ISBN:0-931901-03-0 (Raleigh, North Carolina, 1984).

    Google Scholar 

  38. De Guiran, G. & Ritter, M. Life cycle of Meloidogyne species and factors influencing their development. In Root-knot nematodes (Meloidogyne species) systematic, biology and control (eds Lamberti, F. & Taylor, C. E.) 173–191 (Academic Press Inc, London, 1979).

    Google Scholar 

  39. Minnis, S. et al. Potato cyst nematodes in England and Wales - occurrence and distribution. Ann. Appl. Biol. 140(2), 187–195. (2002).

    Article  Google Scholar 

  40. Campos, H. D., Campos, V. P. & Coimbra, J. L. Efeito do exsudato radicular de Brachiaria decumbens e do sorgoleone de Sorghum bicolor no desenvolvimento de Meloidogyne javanica. Nematol. Bras. 30(1), 59–65 (2006).

    Google Scholar 

  41. Taylor, A. L. & Sasser, J. N. Biology, identification and control of root-knot nematodes (Meloidogyne spp.) 111 (1978); (2020). Accessed 21 April 2020.

  42. Conceição, I. L., Dias, A. M. C., Abrantes, I. & Cunha, M. J. M. Efeitos dos exsudatos radiculares de Solanum sisymbriifolium na eclosão de Meloidogyne spp. Rev. Ciênc. Agrar. 35(26), 274–281 (2012).

    Google Scholar 

  43. Fassuliotis, G. Plant breeding for root-knot nematode resistance. In Root-knot nematodes (Meloidogyne species) systematic, biology and control species) systematic, biology and control (eds Lamberti, F. & Taylor, C. E.) 425–453 (Academic Press Inc, London, 1979).

    Google Scholar 

  44. Fassuliotis, G. & Bhatt, D. P. Potential of tissue culture for breeding root-knot nematode resistance into vegetables. J. Nematol. 14(1), 10–14 (1982).

    CAS  PubMed  PubMed Central  Google Scholar 

  45. Daunay, M. C. & Dalmasso, A. Multiplication de Meloidogyne javanica, M. incognita et M. arenaria sur divers Solanum. Revue Nématol. 8(1), 31–34 (1985).

    Google Scholar 

  46. Timmermans, B. G. H., Vos, J., Nieuwburg, J., Stomph, T. J. & Putten, P. E. L. Germination rates of Solanum sisymbriifolium: temperature response models, effects of temperature fluctuations and soil water potential. Seed Sci. Res. 17(3), 221–231. (2007).

    Article  Google Scholar 

  47. Netherlands Food and Consumer Product Safety Authority. (2020). Accessed 21 April 2020.

  48. Tzortzakakis, E. A., Blotsos, F. A. & Avgelis, A. D. Evaluation of Solanum rootstock accessions for control of root-knot nematodes and tobamoviruses. J. Plant Dis. Prot. 113(4), 188–189. (2006).

    Article  Google Scholar 

  49. Conceição, I. L. P. M. et al. Root-knot nematodes, Meloidogyne spp., on potato in Portugal. Nematology 11(2), 311–313. (2009).

    Article  Google Scholar 

  50. Hussey, R. S. & Barker, K. R. A comparison of methods of collecting inocula of Meloidogyne spp. including a new technique. Plant Dis. Rep. 57, 1027–1028 (1973).

    Google Scholar 

  51. Maleita, C. M., Simões, M. J., Egas, C., Curtis, R. H. C. & Abrantes, I. M. O. Biometrical, biochemical, and molecular diagnosis of Portuguese Meloidogyne hispanica isolates. Plant Dis. 96(6), 865–874. (2012).

    CAS  Article  PubMed  Google Scholar 

  52. Eisenback, J. D. & Hirschmann, H. Identification of Meloidogyne species on the basis of differential host test and perineal-pattern morphology. J. Nematol. 13(4), 513–521 (1981).

    CAS  PubMed  PubMed Central  Google Scholar 

  53. Canto-Sáenz, M. The nature of resistance to Meloidogyne incognita (Kofoid & White, 1919) Chitwood, 1949. In An advanced treatise on Meloidogyne; biology and control (eds Sasser, J. N. & Carter, C. C.) 225–231 (North Carolina State University Graphics, Raleigh, 1985).

    Google Scholar 

  54. Byrd, D. W., Kirkpatrick, T. & Bakker, K. R. An improved technique for clearing and staining tissues for detection of nematodes. J. Nematol. 15(1), 142–143 (1983).

    Google Scholar 

  55. Tryantaphyllou, A. C. & Hirschmann, H. Post infection development of Meloidogyne incognita Chitwood, 1979 (Nematoda: Heteroderidae). Ann. Inst. Phytopathol. Benaki 3(1), 1–11 (1960).

    Google Scholar 

Download references


This work was supported by Centre for Functional Ecology—Science for People and the Planet (CFE), “Instituto do Ambiente, Tecnologia e Vida” (IATV), the European Regional Development Fund (FEDER) through the COMPETE 2020—“Programa Operacional Competitividade e Internacionalização” (POCI) and by National funds through “Fundação para a Ciência e Tecnologia” (FCT), under contracts UID/BIA/04004/2020, POCI-01-0145-FEDER-029283 (PTDC/ASP-PLA/29283/2017) (Ref. HANDLER) and Project ReNATURE—Valorization of the Natural Endogenous Resources of the Centro Region (Centro2020, Centro-01-0145-FEDER-000007). Soraia Perpétuo was funded by FCT/ “Ministério da Ciência, Tecnologia e Ensino Superior” (MCTES) and the European Social Fund through the “Programa Operacional do Capital Humano” (POCH) of the National Strategic Reference Framework (SFRH/BD/129184/2017). Thanks, are also due to the Botanical Garden of the University of Trás-os-Montes and Alto Douro, Bragança, Portugal and to Vandinter Semo, Scheemda, The Netherlands, for supplying Solanum linnaeanum and S. sisymbriifolium seeds, respectively, and to Prof. Óscar Machado and Dr. Filipe Melo, from High School of Agriculture of Coimbra, for multiplying S. linnaeanum seeds and helping with plants maintenance. The authors would like to thank Dr. Kenneth Evans, retired researcher from Rothamsted Research, UK, for valuable comments and suggestions and his review of the final manuscript.

Author information

Authors and Affiliations



Conceived and designed the experiments: L.S.P., M.J.M.C., M.T.B. and I.L.C. Analyzed the data: L.S.P. and I.L.C. Wrote the paper: L.S.P. All authors reviewed and approved the final manuscript.

Corresponding author

Correspondence to Laura Soraia Perpétuo.

Ethics declarations

Competing interests

The authors declare no competing interests.

Additional information

Publisher's note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary information

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Perpétuo, L.S., da Cunha, M.J.M., Batista, M.T. et al. Solanum linnaeanum and Solanum sisymbriifolium as a sustainable strategy for the management of Meloidogyne chitwoodi. Sci Rep 11, 3484 (2021).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI:


By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.


Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing