Submit or Track your Manuscript LOG-IN

In Vitro Nematicidal Activity of an Endemic Plant Pulicaria boissieri Hook. F. Against Root-Knot Nematodes Antinematodal Activity of Pulicaria boissieri

PJN_42_1_60-65

In Vitro Nematicidal Activity of an Endemic Plant Pulicaria boissieri Hook. F. Against Root-Knot Nematodes Antinematodal Activity of Pulicaria boissieri

Rauf Khan1, Shazia Mansuri1,2*, Muhammad Abid1, Muneeba Khan2, Anjum Perveen2, Afshan Rehman3 and Rubina Noureen1

1Department of Botany, Federal Urdu University of Arts, Science and Technology, Karachi, Pakistan; 2Centre for Plant Conservation, University of Karachi, Karachi, Pakistan; 3Department of Botany, University of Karachi, Karachi, Pakistan.

Abstract | In this current study, the in vitro nematicidal activity of Pulicaria boissieri against root-knot nematodes has been investigated. The results revealed that all the solvent extracts contained anti-nematodal properties; however, variations in mortality rates were observed. Specifically, the chloroform extract of the leaves of P. boissieri exhibited 84% inhibitory activity against nematodes after 72 hours of exposure. The results indicated that exposure of nematodes for 72 hours resulted in the maximum nematicidal activity compared to exposures of 24 and 48 hours. It was concluded that leaf and stem extracts in chloroform and methanol solvents exhibited the highest activity against nematodes. The sequence of nematicidal activity from high to low was as follows: chloroform > methanol > acetone > ethanol > water. Hence, Pulicaria boissieri demonstrates potential nematicidal activity with various organic solvents.


Received | April 14, 2024; Accepted | May 28, 2024; Published | June 10, 2024

*Correspondence | Shazia Mansuri, Department of Botany, Federal Urdu University of Arts, Science and Technology, Karachi, Pakistan; Email: shazi343@gmail.com

Citation | Khan, R., Mansuri, S., Abid, M., Khan, M., Perveen, A., Rehman, A. and Noureen, R., 2024. In vitro nematicidal activity of an endemic plant Pulicaria boissieri hook. F. against root-knot nematodes Antinematodal activity of Pulicaria boissieri. Pakistan Journal of Nematology, 42(1): 60-65.

DOI | https://dx.doi.org/10.17582/journal.pjn/2024/42.1.60.65

Keywords | Nematicidal activity, Pulicaria boissieri, Plant parasitic nematode (ppn)

Copyright: 2024 by the authors. Licensee ResearchersLinks Ltd, England, UK.

This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).



Introduction

Nematoda is extremely diverse in relationships of species productivity and one of the most abundant metazoan groups on earth (Hugot et al., 2001). Plant-parasitic nematodes (PPNs) are extremely specified parasites that cause diseases in plants using a variety of approaches (Williamson and Hussey, 1996). In terms of nourishing, they might be known as ectoparasitic or endoparasitic (Jasmer et al., 2003). Ectoparasites do not go in the root nevertheless feed by introducing a stylet interested either in epidermal cells or in the root (Wyss, 1997). Plant parasitic nematodes are the greatest damaging group of plant pathogens all over the world and their control is extremely challenging (Sasser, 1998). Plant-parasitic nematodes are the main pests in several countries, especially in the tropical and subtropical regions, where they are renowned for causing severe damages to the yield on a wider variety of crops (Luc et al., 2005). Up till now more than 4,100 nematode species are discovered which have potential to being toxic for plants (Decraemer and Hunt, 2006). Many parasitic nematode species effect leaves and stems but most of the nematodes damage roots of the Plant (Sasser and Freckman, 1987). Plant-parasitic nematodes are the main pests that are affecting economic important crops and loss of billions of dollars. Numerous species of plant-parasitic nematodes belong from the Longidorus and Trichodorus serve as virus vector and carry several viruses from infected plants to healthy plants (Ehlers, 2001; Gaugler, 2002). Entomopathogenic nematodes have been commercialized as environment-friendly agents for numerous insect pests (Brown et al., 1994). Infected plants have different symptoms such as root galling, inhibiting height and nutrient deficiency, predominantly insufficiency of nitrogen (Siddiqui and Mahmood, 1996). They induce the formation of root galls, root system reduction, chlorosis, dwarfism, and wilting in their host plants (Manzanilla et al., 2002). In galled roots, the uptake and transport of water and nutrients are severely altered and therefore, the crop yields are reduced (Sikora and Fernandez, 2005).

It is problematic to control because nematodes have an extensive host variety and a high rate of reproduction, the female nematodes can able to reproduce above a thousand eggs (Natarajan et al., 2006). Currently, several medicinal plants having insecticidal properties are identified (Banerji et al., 1985). Nematicides of plant origin consist of phenolic compounds, isothiocyanates, thiophenics, fatty acids, alkaloids, and glucosides (Andres and Coupland, 2012; Chitwood, 2002). These compounds possibly contain the same compounds that are produced synthetically as respiratory poisons, insecticides, deterrents and repellents (Sukul, 1992). In several plant species belonging to 57 families, antinematicidal compounds have been identified (Banerji et al., 1985). Many plants including Brassicaceae, Asteraceae, Myrtaceae and Rutaceae family member plants contain nematicidal compounds (Sukul, 1992; Gommers, 1973).

Pulicaria boissieri Hook. F. is an endemic plant of Pakistan. P. boissieri belongs to the tribe Inulae from the family Asteraceae. It is a small shrub having villose leaves. There is no research work regarding the nematicidal activity on this plant that has been done yet. In this research, we are going to evaluate antinematodal activity of this plant in different solvent extracts.

Materials and Methods

Extraction of egg masses from galled roots

Egg masses were separated from root knot galls by needle and added into the Petri dishes which contained some amount of distilled water. For hatching egg, masses of nematodes were suspended in water. The Petri dishes were kept at room temperature for 24 hrs. Egg suspension was diluted, and the number of 260/20ml was maintained at about 15-25 nematodes in each block.

Cavity block studies

1ml of extract of each solvent were poured in blocks and left for evaporation for 24 hrs. After complete hatching of egg masses and evaporation of solvents, 1ml of nematodes suspension containing 15-25 living nematodes were added into the cavity blocks, each treatment replicated 3 times. The effect of different extracts on the motility of nematodes was determined at a three-observation time i.e., 24, 48 and 72 hours. Data were recorded, and comparisons of dead percentage were made on basis of the average of dead nematodes.

Plant collection

The plant was collected from the Kerthar range, Thana Bulla khan and adjoint areas. Healthy Stem and leaves were collected and brought to the lab and cleaned with running tap water to remove dust. The collected leaves and stems shade dried for one week. The dried ground to powder form in uniform size with the help of a grinding mill. In total 5 types of plant, solvents were used to extract compounds from plants: Methanol, Ethanol, Acetone, Chloroform and water making the final volume of 1000ppm.

Extraction process through Soxhlet

The first step in qualitative and quantitative analysis of plant constituent is plant extraction. In this process, plant compounds are extracted from crude plant material (Abubakar and Haque, 2020). By this process, phytochemicals from crude plant material with minimum material and solvent usage were extracted. So, we preferred to use the Soxhlet apparatus for purpose of extraction.

Solvent extraction

The powder form of 10g plant material in 150 mL of different solvents chloroform, methanol, ethanol, water and acetone was used. Extraction was done in the Soxhlet apparatus. The extract was air-dried and stored in the refrigerator.

Nematodes culture

For a finding of egg masses and larvae, pure culture of nematodes maintained on eggplants in sterilized soil. Root-knot infected brinjal plants from the culture plate were up-rooted and washed gently under running tap water (Hooper et al., 2005).

Statistical analysis

Statistical analysis was performed by using the software IBM SPSS Statistics 23. One way analysis of variance (ANOVA) followed by Bonferroni post hoc test and student’s t-test were performed to compare the groups with level of confidence P <0.05; (where * = P < 0.05, ** = P < 0.01, *** = P < 0.001). Data are presented as mean ± SE.

Results and Discussions

This study was designed to evaluate the effect of Pulicaria sp. extracts (in different solvents) on living nematodes (Figure 1). The inhibition of nematode mortality was attributed to the exposure period and the extract concentration. However, the mortality rate significantly differed among tested plant extracts in methanol, ethanol, acetone, chloroform and water. All the extracts of leaf and stem showed variation against nematodes as shown in Tables 1-5 and Figure 2. Nematode survival was significantly affected by all types of plant extracts. The length of exposure affected nematode mortality remarkably. The results indicate that leaf and stem extracts of Pulicaria showed significant activity against plant parasitic nematodes.

At 24 hour the highest mortality rate observed in chloroform and methanol extracts as compared to control and other extracts of leaf and stems in different solvents. They showed a significant (p<0.05) nematicidal activity (Tables 1 and 2).

 

 

However, in the next 48 hours time period, a more significant and pronounced mortality rate observed in all solvent extracts of leaf and stem, but stem extract of chloroform showed the highest rate i.e., 51% and leaf extract i.e., 40% as compared to rest of the solvent extracts (p<0.01) (Tables 1-5).

 

Table 1: Nematicidal activity of methanolic extract of Pulicaria boissieri and its statistical analysis.

Methanolic extract

Mean and Standard Error

% of dead Nema-todes in 24 hrs

% of Dead Nema-todes in 48 hrs

% of Dead Nema-todes in 72hrs

Degree of freedom

Means square

Fre-quency

Signi-ficance

Least significant difference

control

14±2.54

7.14

14.28

19

2

2.1

2.71

0.145

0.778

Leaf

15.66 ± 1.47

19.15

21.26

34.03

2

4.77

5.37

0.046

0.889

Stem

15.66 ± 3.55

19.15

31.92

65.96

2

40.11

3.28

0.109

12.22

 

Table 2: Nematicidal activity of Chloroform extract of Pulicaria boissieri and its statistical analysis.

Chloro-form extract

Mean and Stan-dard Error

% of Dead Nematodes in 24hrs

% of Dead Nematodes in 48 hrs

% of Dead Nematodes in 72 hrs

Degree of freedom

Means square

Fre-quency

Signi-ficance

Least significant difference

Control

13.33 ± 1.77

22.5

24.98

37.5

2

3.4

2.38

0.173

1.44

Leaf

14.66 ± 2.16

27.28

40.92

84.1

2

52.11

21.31

0.002

2.44

Stem

13.66 ± 1.47

29.28

51.24

60.98

2

15.44

9.92

0.012

1.55

 

Table 3: Nematicidal activity of acetone extract of Pulicaria boissieri and its statistical analysis.

Acetone Extracts

Mean and Standard Error

% of Dead Nema-todes in 24 hrs

% 0f Dead Nematodes in 48 hrs

% of Dead Nema-todes in 72 hrs

Degree of freedom

Means square

Fre-quency

Signi-ficance

Least significant difference

Control

20.66 ± 1.77

14.51

16.11

24.2

2

0.778

0.875

0.464

0.889

Leaf

20.33 ± 1.77

21.29

22.99

47.51

2

26.77

26.778

0

0.667

stem

21.33 ± 2.85

12.87

17.15

32.8

2

15.44

27.8

0.001

0.556

 

Table 4: Nematicidal activity of ethanolic extract of Pulicaria boissieri and its statistical analysis.

Ethanolic Extracts

Mean and Standard Error

% of Dead Nematodes in 24 hrs

% of Dead Nema-todes in 48 hrs

% of Dead Nema-todes in 72 hrs

Degree of freedom

Means square

Fre-quency

Signi-ficance

Least significant difference

Control

22.33 ± 3.48

13.43

14.91

16.39

2

0.333

0.6

0.579

0.556

Leaf

22.33 ± 2.67

8.99

16.39

32.82

2

22.33

6.931

0.028

3.22

Stem

23.66 ± 3.61

11.24

16.9

36.6

2

27.44

24.76

0.001

1.11

 

Table 5: Nematicidal activity of water extract of Pulicaria boissieri and its statistical analysis.

Water

Mean and Standard Error

% of Dead Nematodes in 24 hrs

% of Dead Nema-todes in 48 hrs

% of Dead Nema-todes in 72 hrs

Degree of freedom (DF)

Means square

Fre-quency

Signi-ficance

Least significant difference

Control

22.33 ± 3.48

13.43

14.91

16.39

2

0.667

1.33

0.385

0.5

Leaf

17.5 ± 2.12

14.28

17.14

28.57

2

3.5

0.95

0.47

3.66

Stem

16 ± 1.41

18.75

21.87

34.37

2

3.5

2.3

0.245

1.5

 

At 72 hours, all the solvent extracts showed highly significant nematicidal activity (p<0.001). The highest mortality rate observed in leaf extract of chloroform solvent i.e., 84% and stem extract of methanol solvent which is 65% (Tables 1-5).

The above result evaluated that all the solvent extracts contained anti-nematodal properties, however, the variation in mortality rate was observed. It was concluded that leaf and stem extract in chloroform and methanol solvent showed the highest activity against nematodes. The sequence of high nematicidal activity to low is as: Chloroform > methanol > acetone > ethanol > water.

In Plants, phytoconstituents are available that are utilized to fix the illness of humanity. Many plants have nematicidal properties in their foundations, shoot, leaves, blossoms, seeds and their concentrates, natural balm, oilseed cakes and items have been successfully tried against an assortment of nematodes (Tsay et al., 2004). In our review, the outcomes demonstrated that the leaf and stem concentrate of Pulicaria plant showed nematicitadal action against plant parasitic nematodes. It has been seen that nematicidal action could be connected with various kinds of compound present in plant. Plant can be the best hotspot for such bioactive mixtures (Bharadwaj and Sharma, 2007).

The quantity of plants contains intensifies that are poisonous to specific nematodes. Neem (Azardirachta indica) has such an assortment of organically dynamic fixings, which have various methods of activity, that it is workable for neem to oppose in excess of 200 types of bugs, parasites and nematodes (Akhtar and Mahmood, 1996). The concentrate fluctuated in their viability in various solvents. In our review, results showed that the plant extract in chloroform showed more viability against nematodes than other solvent’s extract.

The current review has shown that chloroform concentrate of the plant is valuable for nematode control, which will be a prudent and ecofriendly choice for control of nematodes In our review the water concentrate of leaf and stem showed slight adequacy against plant parasitic nematodes with regards to killing and decreased the mortality of nematodes, Klimpel et al. (2011) likewise depicts various concentrates movement against nematodes.

This study exhibits that the plant extract contains gigantic anti-oxidant agent action. Anti-oxidant agents normally produce in plants kills the receptive oxygen species (ROS) created by any injury or stress (Lee et al., 2003). Flavonoid presence demonstrated by the phytochemical examination of plant concentrate might be responsible for this anti-oxidant agent action (Karimi et al., 2010; Prochazkova et al., 2011). Plants produce a wide variety of auxiliary metabolites, some of them of the drug interest and others with antimicrobial properties (e.g., phenylpropanoids, flavonoids, terpenoids, alkaloids, and others), and a significant number of these accumulates assume an indispensable part in the association of plants with their current circumstance (Khalaf et al., 2008).

Conclusions and Recommendations

The results obtained from the testing of leaves and stem extract of P. boissieri against nematodes showed that methanolic extract of leaves of P. boissieri displayed significant inhibition of harmful microbial agents causing damage to plants and humans. It is also reported that the extract showed 84% activity against plant parasitic nematodes. Chloroform extract of leaf and stem showed maximum nematicidal activity as compared to other plant extracts. Thus, this study proved that Pulicaria sp. can be used for biocontrol of plant parasitic nematodes and this plant extract is environment friendly and can control of parasites easily. Antioxidant activity showed 35.35% activity against control from methanolic extract of stem of P. boissieri.

Acknowledgement

The Authors want to acknowledge HEC for funding this research Project.

Novelty Statement

This study is first of its kind in which an Endemic Plant P. boissieri extracts are used for nematicidal activity.

Author’s Contribution

Rauf is the main student who performed main aspect of the research work under the supervision of Dr. Shazia Mansuri.

Conflict of interest

The authors have declared no conflict of interest.

References

Abubakar, A.R. and Haque, M., 2020. Preparation of medicinal plants: Basic extraction and fractionation procedures for experimental purposes. J. Pharm. Bioallied Sci., 12(1): 1-10. https://doi.org/10.4103/jpbs.JPBS_175_19

Akhtar, M. and Mahmood, I., 1996. Control of plant-parasitic nematodes with organic and inorganic amendments in agricultural soil. Appl. Soil Ecol., 4(3): 243-247. https://doi.org/10.1016/S0929-1393(96)00114-X

Andres, F. and Coupland, G., 2012. The genetic basis of flowering responses to seasonal cues. Nat. Rev. Genet., 13(9): 627-639. https://doi.org/10.1038/nrg3291

Banerji, R., Misra, G. and Nigam, S.K., 1985. Role of indigenous plant material in pest control. Pesticides, 19: 32-38.

Bharadwaj, A. and Sharma, S., 2007. Effect of some plant extracts on the hatch of Meloidogyne incognita eggs. Int. J. Bot., 3(3): 312-316. https://doi.org/10.3923/ijb.2007.312.316

Brown, D.J.F., Jones, A.T., Taylor, C.E., Helbrended, J.M. and Lemberti, F., 1994. An appraisal of some aspects of ecology of nematodes vectors of plant viruses. Nematol. Mediterr., 22: 253-263.

Chitwood, D.J., 2002. Phytochemical Based Strategies for Nematode Control. Annu. Rev. Phytopathol., 40(1): 221-249. https://doi.org/10.1146/annurev.phyto.40.032602.130045

Decraemer, W. and Hunt, D.J., 2006. Structure and classification in plant nematology. Wallingford, Oxfordshire: CAB International, pp. 3-32. https://doi.org/10.1079/9781845930561.0003

Ehlers, R.U., 2001. Mass production of entomopathogenic nematodes for plant protection. Appl. Microbiol. Biotechnol., 56: 623-633. https://doi.org/10.1007/s002530100711

Gaugler, R., 2002. Entomopathogenic nematology. CABI Publishing, Wallingford. https://doi.org/10.1079/9780851995670.0000

Gommers, F.J., 1973. Nematicidal principles in compositae. Mededelingen Landbouwhogeschool, Wageningen, The Netherlands, pp. 71-73.

Hooper, D.J., Hallmann, J. and Subbotin, S.A., 2005. Cab international 2005. Plant parasitic nematodes in subtropical and tropical agriculture, 2nd edition (eds. M. Luc, R.A. Sikora, J. Bridge) pp. 53-56. https://doi.org/10.1079/9780851997278.0053

Hugot, J.P., Baujard, P. and Morand, S., 2001. Biodiversity in helminths and nematodes as a field of study: An overview. Nematology, 3(3): 199-208. https://doi.org/10.1163/156854101750413270

Jasmer, D.P., Goverse, A. and Smant, G., 2003. Parasitic nematode interaction with mammals and plants. Annu. Rev. phytopathol., 41: 245-270. https://doi.org/10.1146/annurev.phyto.41.052102.104023

Karimi, E., Oskoueian, E., Hendra, R. and Jaafar, H.Z., 2010. Evaluation of Crocus sativus L. stigma phenolic and flavonoid compounds and its antioxidant activity. Molecules, 15(9): 6244-6256. https://doi.org/10.3390/molecules15096244

Khalaf, N.A., Shakya, A.K., Al-Othman, A., El-Agbar, Z. and Farah, H., 2008. Antioxidant activity of some common plants. Turk. J. Biol., 32(1): 51-55.

Klimpel, S., Abdel-Ghaffar, F., Al-Rasheid, K.A., Aksu, G., FischerStrassen, K.B. and Mehlhorn, H., 2011. The effects of different plant extracts on nematodes. Parasitol. Res., 108(4): 1047-1054. https://doi.org/10.1007/s00436-010-2168-4

Luc, M., Sikora R.A. and Bridge, J., 2005. Plant parasitic nematodes in subtropical and tropical agriculture. CABI Publishing, Wallingford, UK, pp. 871. https://doi.org/10.1079/9780851997278.0000

Lee, S.E., Hwang, H.J. Ha, J.S., Jeong, H.S. and Kim, J.H., 2003. Screening of medicinal plant extracts for antioxidant activity. Life Sci., 73(2): 167-179. https://doi.org/10.1016/S0024-3205(03)00259-5

Manzanilla-López, R.H., Costilla, M.A., Doucet, M., Franco, J., Inserra, R.N., Lehman, P.S., Cid del Prado-Vera, I., Souza, R.M. and Evans, K., 2002. The genus Nacobbus Thorne and Allen (Nematoda: Pratylenchidae): Systematics, distribution, biology and management. Nematropica, 32: 150-227.

Natarajan, N., Cork, A., Boomathi, N., Pandi, R., Velavan, S. and Dhaskshanamoorthy, G., 2006. Cold aqueous extracts of African marigold, Tagetes erecta for control tomato root-knot nematode, Meloidogyne incognita. Crop. Prot., 25: 1210 -1213. https://doi.org/10.1016/j.cropro.2006.03.008

Procházková, D., Boušová, I. and Wilhelmová, N., 2011. Antioxidant and prooxidant properties of flavonoids. Fitoterapia, 82(4): 513-523. https://doi.org/10.1016/j.fitote.2011.01.018

Sasser, J.N., 1998. A perspective on nematode problems worldwide. In: Nematode parasitic to cereals and legumes in temperate Semi Arid regions. ICARDA, Syria, pp. 8-12.

Sasser, J.N. and Freckman, D.W., 1987. A world perspective on nematology: The role of the society. Vistas on nematology. Society of Nematology, pp. 7-14.

Siddiqui, Z.A. and Mahmood, I., 1996. Biological control of plant parasitic nematodes by fungi: A review. Bioresour. Technol., 58(3): 229-239. https://doi.org/10.1016/S0960-8524(96)00122-8

Sikora, R.A. and Fernández, E., 2005. Nematode parasites of vegetables. Plant parasitic nematodes in subtropical and tropical agriculture. 2nd Edition. Wallingford, UK: CAB International. Pp. 319-392. https://doi.org/10.1079/9780851997278.0319

Sukul, N.C., 1992. Plant antagonist to plant-parasitic nematodes. Ind. Rev. Life Sci., 2: 23-52.

Tsay, T.T., Wu, T.S. and Lin, Y.Y., 2004. Evaluation of asteraceae plant for control of Meloidogyne incognita. J. Nematol., 36: 36 -41.

Williamson, V.M. and Hussey, R.S., 1996. Nematode pathogenesis and resistance in plants. Plant Cell, 8(10): 1735. https://doi.org/10.2307/3870226

Wyss, U., 1997. Root parasitic nematodes: An overview. (eds. C. Fenoll, F.M.W. Grundler, S.A. Ohl). Cellular and molecular aspects of plant nematode interactions. Dordrecht, Netherlands: Kluwer Acad. Publ., 10: 5-24. https://doi.org/10.1007/978-94-011-5596-0_2

To share on other social networks, click on any share button. What are these?

Pakistan Journal of Zoology

June

Pakistan J. Zool., Vol. 56, Iss. 3, pp. 1001-1500

Featuring

Click here for more

Subscribe Today

Receive free updates on new articles, opportunities and benefits


Subscribe Unsubscribe