First report of Meloidogyne javanica (Nematoda: Meloidogynidae) infecting Scoparia dulcis, a medicinal plant in Brazil

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Journal of Nematology

Society of Nematologists

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First report of Meloidogyne javanica (Nematoda: Meloidogynidae) infecting Scoparia dulcis, a medicinal plant in Brazil

Cristiano Bellé * / Rodrigo Ferraz Ramos / Andressa Lima de Brida / Tiago Edu Kaspary

Keywords : Detection, Diagnosis, Identification, Root-knot nematodes, Sweet broom

Citation Information : Journal of Nematology. Volume 51, Pages 1-3, DOI: https://doi.org/10.21307/jofnem-2019-072

License : (CC-BY-4.0)

Received Date : 14-August-2019 / Published Online: 14-October-2019

ARTICLE

ABSTRACT

Medicinal plants Scoparia dulcis showing symptoms caused by root-knot nematodes were detected in the municipality of Cachoeira do Sul, Rio Grande do Sul State, Brazil. Based on the morphological, esterase phenotypes, and molecular analyses of the mitochondrial DNA region between the cytochome oxidase subunit II and 16S rRNA genes (mtDNA) and species-specific sequence characterized amplified region (SCAR), the causal agent of the observed symptoms was identified as Meloidogyne javanica. Pathogenicity was confirmed by fulfilling a modified version of Koch’s postulates. To our knowledge, this is the first report of M. javanica infecting S. dulcis in Brazil.

Graphical ABSTRACT

Scoparia dulcis L. (Scrophulariaceae), commonly known as sweet broom, is a perennial plant, widely distributed in tropical and subtropical regions, especially in flooded environments (Jain and Singh, 1989; Zhang et al., 2014). Scoparia dulcis is an erect, annual herb with serrated leaves, producing white flowers. Its ethnomedicinal uses among various indigenous tribes in the rain-forest is well-documented (Murtl et al., 2012). Pharmacological properties of S. dulcis have been speculated and traditionally used as a treatment for diabetes mellitus, hypertension, stomach troubles, hypertension, inflammation, bronchitis, hemorrhoids, hepatosis, and as an analgesic and antipyretic (Das and Chakraborty, 2011; Murtl et al., 2012).

Medicinal plants can be attacked by pests, diseases, and plant-parasitic nematodes, which can qualitatively and quantitatively impair curative properties and production (Bellé et al., 2017; Pandey, 2017). Among the plant-parasitic nematodes, the most important genus is Meloidogyne Göldi, 1887, which, cause to direct damage such as root galls and reduction in the number of roots, and predisposition to fungal and bacterial diseases, causing losses in crop yields (Karssen, 2002; Rich et al., 2008).

Sweet broom plants showing distinctive root galls (Fig. 1A) were collected on August 2018 in the municipality of Cachoeira do Sul, Rio Grande do Sul State, Brazil. In order to identify the plant-parasitic nematode species, a combination of morphological, biochemical, and molecular analyses were performed.

Figure 1:

Sweet broom (Scoparia dulcis L.) roots showing galls caused by Meloidogyne javanica (Treub, 1885) Chitwood, 1949 infection.

10.21307_jofnem-2019-072-f001.jpg

To identify this Meloidogyne population, the following techniques were used: esterase phenotypes (n = 40 females) (Carneiro and Almeida, 2001); morphology and morphometrics of second-stage juveniles (J2) (n = 40) and females (n = 20), and perineal patterns (n = 20); and molecular characterization of the mitochondrial DNA region between the cytochome oxidase subunit II (COII) and 16S rRNA genes (mtDNA) using the primers C2F3 (5´-GGTCAATGTTCAGAAATTTGTGG-3´) and 1108 (5´-TACCTTTGACCAATCACGCT-3´) (Powers and Harris, 1993) along with PCR species-specific sequence characterized amplified region (SCAR) for confirmation, using a primer set composed of Fjav (5´-GGTGCGCGATTGAACTGAGC-3´) and Rjav (5´-CAGGCCCTTCAGTGGAACTATAC-3´) (Zijlstra et al., 2000).

The nematode population density observed in the sample was 1,976 J2s/g of roots. The morphometric study showed the following results; J2s: length (L) = 414.5 ± 36.1 (345.0–470.5) µm, a = 33.7 ± 2.8 (28.1–32.5), c = 8.4 ± 0.9 (6.3–10.1), stylet length = 11.5 ± 1.2 (10.1–14.2) µm, dorsal esophageal gland orifice (DGO)  = 3.5 ±  0.4 (3.0–4.6) µm, tail length = 51.1 ± 3.3 (45.8–54.4) µm and hyaline tail terminus = 11.5 ± 1.7 (9.1–14.7) µm; and females L = 850.5 ± 90.5 (640.5–995.5) µm, stylet length = 14.5 ± 0.8 (12.5–15.8) µm, and DGO = 3.4 ± 0.7 (2.8–4.2) µm. The perineal patterns showed a low dorsal arch, trapezoid shape, smooth striae interrupted by a pair of incisures on both sides corresponding to lateral fields, clearly demarcated from striae by parallel lines, tail whorl often distinct. The overall morphology and morphometrics of the population of M. javanica (Treub, 1885) Chitwood, 1949 are in agreement with the original description (Rammah and Hirschmann, 1990; Hunt and Handoo, 2009).

The polymorphisms of the esterase bands by electrophoresis revealed the phenotype J3 (Rm = 1.00, 1.25, and 1.40) typical of M. javanica (Carneiro et al., 1996). The mtDNA sequence (1639 bp) was submitted to GenBank with Accession No. MN227142. Searches on BLAST showed that 99% identity with sequences of M. javanica isolates from South Africa (GenBank JX987326), Taiwan (GenBank JX100439), Turkey (GenBank LT602894), and Vietnam (GenBank MK033441). The PCR amplification using SCAR technique produced a specific fragment of expected size (∼670 bp) for M. javanica (Zijlstra et al., 2000).

In greenhouse tests, S. dulcis plantlets were maintained in pots with 2,000 dm3 sterilized soil. In total, 10 replicates were inoculated with 5,000 eggs and J2s from the original population of M. javanica, in addition to a non-inoculated control. Plants were well maintained under greenhouse conditions at 25 to 27°C. After 55 days, the inoculated plants exhibited galled root systems similar to plants observed in the field, with a nematode reproduction factor (final population/initial population) of 24.5. The non-inoculated plants did not exhibit any galls. The morphological and molecular characterization of this re-isolated root-knot nematode were identical those of M. javanica.

This is the first report of M. javanica parasitising S. dulcis in Brazil. Globally, M. javanica is considered an economically important agricultural nematode reported over 770 plant species, including tea [(Camellia sinensis (L.) Kuntze], grape (Vitis sp. L.), many vegetables, fruit trees, weeds, cereals, and ornamentals, causing severe yield losses (CABI, 2019). Hence, further studies are necessary to investigate the damage it can causes to specific crops, such as S. dulcis, grown in tropical, subtropical, and temperate regions.

References


  1. Bellé, C. , Kaspary, T. E. , Kuhn, P. R. , Schmitt, J. and Lima-Medina, I. 2017. Reproduction of Pratylenchus zeae on weeds. Planta Daninha 35: e017158528.
  2. CABI 2019. Meloidogyne javanica (sugarcane eelworm). Invasive Species Compendium, available at: www.cabi.org/isc/datasheet/33246 (accessed April 29, 2019).
  3. Carneiro, R. M. D. G. and Almeida, M. R. A. 2001. Técnica de eletroforese usada no estudo de enzimas dos nematoides de galhas para identificação de espécies. Nematologia Brasileira 25: 555–60.
  4. Carneiro, R. M. D. G. , Almeida, M. R. A. and Carneiro, R. G. 1996. Enzyme phenotypes of Brazilian populations of Meloidogyne spp. Fundamental & Applied Nematology 3: 555–60.
  5. Chitwood, B. G. 1949. Root-knot nematodes – part I. A revision of the genus Meloidogyne Göldi, 1887. Proceedings of the Helminthological Society of Washington 16:90–104.
  6. Das, H. and Chakraborty, U. 2011. Anti-hyperglycemic effect of Scoparia dulcis in streptozotocin induced diabetes. Research Journal of Pharmaceutical, Biological and Chemical Sciences 2: 334–42.
  7. Göldi, E. A. 1887. Relatório sôbre a molestia do cafeiro na provincial da Rio de Janeiro. Archuivos do Museu Nacional do Rio de Janeiro 8:7–123.
  8. Hunt, D. J. and Handoo, Z. A. 2009. Taxonomy, identification and principal species, in Perry, R. N. , Moens, M. and Starr, J. (Eds), Root-knot Nematodes, CABI Publishing, Wallingford, pp. 55–118.
  9. Jain, R. and Singh, M. 1989. Factors affecting goatweed (Scoparia dulcis) seed germination. Weed Science 37: 766–70.
  10. Karssen, G. 2002. The plant-parasitic Nematode Genus Meloidogyne Goldi, 1892 (Tylenchida) in Europe, Brill, Leiden.
  11. Murtl, K. , Panchal, M. , Taya, P. and Raghuveer, S. R. 2012. Pharmacological properties of Scoparia dulcis: a review. Pharmacologia 3: 344–47.
  12. Pandey, R. 2017. Diseases of medicinal and aromatic plants: insights in nematode biomanagement. Indian Phytopathology 70: 12–21.
  13. Powers, T. O. and Harris, T. S. 1993. A polymerase chain reaction method for identification of five major Meloidogyne species. Journal of Nematology 25: 1–6.
  14. Rammah, A. and Hirschmann, H. 1990. Morphological comparison of three host races of Meloidogyne javanica . Journal of Nematology 22: 56–68.
  15. Rich, J. R. , Brito, J. A. , Kaur, R. and Ferrel, J. A. 2008. Weed species as hosts of Meloidogyne: a review. Nematropica 39: 157–85.
  16. Treub, M. 1885. Onderzoekingen over Sereh-Ziek Suikkeriet gedaan in s Lands Plantentium te Buitenzorg. Mededeelingen uit's Lands Plantentium, Batavia 2: 1–39.
  17. Zhang, W. J. , Wang, R. , Zhang, D. , Wei, W. and Chen, H. 2014. Interspecific associations of weed species around rice fields in Pearl River Delta, China: a regional survey. Selforganizology 1: 143–205.
  18. Zijlstra, C. , Fargette, M. and Donkers-Venne, D. T. H. M. 2000. Identification of Meloidogyne incognita, M. javanica and M. arenaria using sequence characterised amplified region (SCAR) based PCR assays. Nematology 2: 847–53.
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FIGURES & TABLES

Figure 1:

Sweet broom (Scoparia dulcis L.) roots showing galls caused by Meloidogyne javanica (Treub, 1885) Chitwood, 1949 infection.

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REFERENCES

  1. Bellé, C. , Kaspary, T. E. , Kuhn, P. R. , Schmitt, J. and Lima-Medina, I. 2017. Reproduction of Pratylenchus zeae on weeds. Planta Daninha 35: e017158528.
  2. CABI 2019. Meloidogyne javanica (sugarcane eelworm). Invasive Species Compendium, available at: www.cabi.org/isc/datasheet/33246 (accessed April 29, 2019).
  3. Carneiro, R. M. D. G. and Almeida, M. R. A. 2001. Técnica de eletroforese usada no estudo de enzimas dos nematoides de galhas para identificação de espécies. Nematologia Brasileira 25: 555–60.
  4. Carneiro, R. M. D. G. , Almeida, M. R. A. and Carneiro, R. G. 1996. Enzyme phenotypes of Brazilian populations of Meloidogyne spp. Fundamental & Applied Nematology 3: 555–60.
  5. Chitwood, B. G. 1949. Root-knot nematodes – part I. A revision of the genus Meloidogyne Göldi, 1887. Proceedings of the Helminthological Society of Washington 16:90–104.
  6. Das, H. and Chakraborty, U. 2011. Anti-hyperglycemic effect of Scoparia dulcis in streptozotocin induced diabetes. Research Journal of Pharmaceutical, Biological and Chemical Sciences 2: 334–42.
  7. Göldi, E. A. 1887. Relatório sôbre a molestia do cafeiro na provincial da Rio de Janeiro. Archuivos do Museu Nacional do Rio de Janeiro 8:7–123.
  8. Hunt, D. J. and Handoo, Z. A. 2009. Taxonomy, identification and principal species, in Perry, R. N. , Moens, M. and Starr, J. (Eds), Root-knot Nematodes, CABI Publishing, Wallingford, pp. 55–118.
  9. Jain, R. and Singh, M. 1989. Factors affecting goatweed (Scoparia dulcis) seed germination. Weed Science 37: 766–70.
  10. Karssen, G. 2002. The plant-parasitic Nematode Genus Meloidogyne Goldi, 1892 (Tylenchida) in Europe, Brill, Leiden.
  11. Murtl, K. , Panchal, M. , Taya, P. and Raghuveer, S. R. 2012. Pharmacological properties of Scoparia dulcis: a review. Pharmacologia 3: 344–47.
  12. Pandey, R. 2017. Diseases of medicinal and aromatic plants: insights in nematode biomanagement. Indian Phytopathology 70: 12–21.
  13. Powers, T. O. and Harris, T. S. 1993. A polymerase chain reaction method for identification of five major Meloidogyne species. Journal of Nematology 25: 1–6.
  14. Rammah, A. and Hirschmann, H. 1990. Morphological comparison of three host races of Meloidogyne javanica . Journal of Nematology 22: 56–68.
  15. Rich, J. R. , Brito, J. A. , Kaur, R. and Ferrel, J. A. 2008. Weed species as hosts of Meloidogyne: a review. Nematropica 39: 157–85.
  16. Treub, M. 1885. Onderzoekingen over Sereh-Ziek Suikkeriet gedaan in s Lands Plantentium te Buitenzorg. Mededeelingen uit's Lands Plantentium, Batavia 2: 1–39.
  17. Zhang, W. J. , Wang, R. , Zhang, D. , Wei, W. and Chen, H. 2014. Interspecific associations of weed species around rice fields in Pearl River Delta, China: a regional survey. Selforganizology 1: 143–205.
  18. Zijlstra, C. , Fargette, M. and Donkers-Venne, D. T. H. M. 2000. Identification of Meloidogyne incognita, M. javanica and M. arenaria using sequence characterised amplified region (SCAR) based PCR assays. Nematology 2: 847–53.

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