Submit or Track your Manuscript LOG-IN

Application of Fatty Acid Esters on Meloidogyne incognita Infected Jew's Mallow Plants

PJN_40_2_127-137

Application of Fatty Acid Esters on Meloidogyne incognita Infected Jew’s Mallow Plants

Oluwatoyin Adenike Fabiyi1*, Mariam Temitope Baker2 and Gabriel Ademola Olatunji2

1Department of Crop Protection, Faculty of Agriculture, University of Ilorin, Ilorin, Nigeria; 2Department of Chemistry, Faculty of Physical Sciences, University of Ilorin, Ilorin, Nigeria.

Abstract | Jew’s mallow (Corchorus olitorius) is a vegetable of importance in Nigeria which is often times infested with root-knot nematodes (RKNs), thus reducing yield and expected income. Principally, synthetic nematicides are employed in the management of RKNs on agricultural fields. The synthetics are confronted with a web of regulations on account of their unhealty negative effect on humans and the environment. Plant protection is primarily saddled with replacing the synthetics. A promising technique is the application of bio-pesticides. Organic fatty acid esters (FAE) are reassuring materials with nematicidal activities. Medicinal plants are rich source of acid esters, hence Alstonia boonei (Apocynaceae) leaves were extracted cold in ethyl acetate. This yielded crude extract that was subjected to column chromatography (silica gel 100-120 mesh grade), which afforded fractions that were analysed with GCMS and FTIR for constituent identification. The result shows octanoic acid; hexanoic acid methyl ester; ethyl octanoate; 9, 12-octadecadienoic acid methyl ester; dodecanoic acid; octadecanoic acid methyl ester; decanoic acid; octadecanoic acid ethyl ester and tetradecanoic acid as the major components while the infra red spectral diagnostic signals agree with the expected vibrational frequencies corresponding to C-H and carbonyl C=O functional groups of fatty acid and esters. Jew’s mallow plants infected with Meloidogyne incognita on the field were treated with the fatty acid esters (FAE) and compared to deionised water and carbofuran as control in two season trials. There was increase in biomass and vegetative growth with notable reduction in M. incognita reproduction in plants treated with FAE at 0.75 mg/ml in the first and repeat experiments. Juvenile population per gram root and soil were reduced significantly at 0.75 and 0.50 mg/ml of FAE in comparison with control. Late flowering was recorded in the untreated control experiment, while plants treated with FAE flowered notably earlier. Application of FAE is recommended for the sustainable management of M. incognita in Jew’s mallow plants.


Received | November 19, 2022; Accepted | December 16, 2022; Published | December 26, 2022

*Correspondence | Oluwatoyin Adenike Fabiyi, Department of Crop Protection, Faculty of Agriculture, University of Ilorin, Ilorin, Nigeria; Email: fabiyitoyinike@hotmail.com

Citation | Fabiyi, O.A., Baker, M.T., and Olatunji, G.A., 2022. Application of fatty acid esters on meloidogyne incognita infected Jew’s mallow plants. Pakistan Journal of Nematology, 40(2): 127-137.

DOI | https://dx.doi.org/10.17582/journal.pjn/2022/40.2.127.137

Keywords | Alstonia boonei, Carbofuran, Chromatographic fractions, Ethyl acetate

Copyright: 2022 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

Plant parasitic nematodes (PPNs) are common pests in agricultural areas (Fabiyi et al., 2020a; Bello et al., 2022; Abiodun et al., 2022). Root-knot nematodes (RKNs) are of high relevance among PPNs. They are distributed worldwide and are obligate parasites of the roots of many plant species (Caveness, 1967; Fabiyi, 2021a, b, 2022a), yield loss of about 78 billion dollars annually around the globe is accredited to them (Caveness, 1967; Barker, 1998; Caillaud et al., 2008; Sun et al., 2006; Verdejo-Lucas, 1999).

Vegetable production is a key source of revenue for women in Nigerian rural communities (AVRDC, 1991). It provides great income to low income earners and small scale farmers, while compensating for the scarcity of animal proteins in the diet. Jew’s mallow (Corchorus olitorius) is a vegetable of importance in Nigeria which is often times infested with RKNs, thus reducing yield and expected income of the farmers. Principally, chemical methods are employed in the management of RKNs. This is flawed with shortcomings and imperfections. Synthetic nematicides are known to be a major pollutant of the ecosystem (Fabiyi and Olatunji, 2021a).

Efforts have been made to study the nematicidal potential of some plant extracts on the survival and reproduction of plant parasitic nematodes (Fabiyi et al., 2020b; Fabiyi, 2022b). Citrus fruit canning waste, thiarubrinc a root extract from Rudbeckia hirta and common agro wastes such as cocoa-pod husk, cassava, orange, pineapple and potato, peels have been reported to be an effective control against nematodes with subsequent significant improvements in crop yield (Egunjobi and Olaitan, 1986; Babatola, 1989; Viala et al., 1998; Fabiyi, 2022c). Bio-pesticides are considered as a good alternative to the synthetic nematicides (Atolani et al., 2014a, b). Soil amendments, plant products and manures have also been found effective and successful in the management of RKNs (Sivakumar and Gunasekara, 2011; Atolani and Fabiyi, 2020; Fabiyi, 2020; Fabiyi and Olatunji, 2021b; Fabiyi, 2021c).

Alstonia boonei belongs to the family Apocynaceae. The leaves have been indicated in the treatment of malaria, snake bites, painful micturition and rheumatic conditions (Kayode and Omotoyinbo, 2008; Ojewole, 1984, 2000). The bark and leaves contain several indole alkaloids, including echitamine, echitamidine, akuammidine, picraline, quebrachidine, and its esters, vincamajine, alstonine, and akuammiline. The triterpenes, 13-amyrine and lupeol were reported as accruing in the bark, and ursolic acid in the leaves (Faparusi and Bassir, 1982). Fatty acid methyl and ethyl esters isolated from Arthrocnemum indicum, Salicornia brachiata, Suaeda maritima, Suaeda monoica and Sesuvium portulacastrum have been reported to have activity against pathogenic fungal and bacterial strains (Chandrasekaran et al., 2008, 2011). This research aims to examine the effectiveness of fatty acid esters (FAE) isolated from A. boonei leaves in ameliorating root knot diseases of Jew’s mallow (C. olitorius) plants caused by Meloidogyne incognita.

Materials and Methods

Sample preparation

The leaves of A. boonei were collected from Fiditi town in Oyo State, Nigeria and authenticated at the University of Ilorin herbarium. The leaves were air dried at ambient temperature (27°C) for four weeks and were milled into powder with the laboratory mill (Christy and Norris Ltd type 8). From the resulting powder, 2 kg was weighed into a 20 liter aspirator for cold extraction with ethyl acetate. The extraction lasted 5 days, it was then decanted, filtered and concentrated with a rotary evaporator under vacuum.

Eight hundred grams (800 g) of the plant crude extract was subjected to open column chromatography on silica gel (I00-120 mesh grade) using a glass column of 10 cm diameter and 50 cm long (Simon, 2006). Column packing was dry. Briefly, after clamping the glass column in a vertical position with its stop­ cock closed, a small plug of cotton wool was introduced into the bottom of the glass column by means of a long glass rod. This was followed by some industrial sea sand to form a layer of 20 cm on the cotton wool. Then silica gel was added to about 40 cm length of the glass column, while tapping the glass for the silica gel to settle, and any entrapped air was allowed to escape (Consden et al., 1994). The plant extract was mixed with silica gel and introduced into the column gently in order not to disturb the bed, while another 3 cm layer of silica gel was placed on top of it, and finally petroleum ether was added. The outlet valve was opened to allow the solvent to flow under gravity at an appropriate steady rate of 1.5 ml per minute. The first eluting solvent was petroleum ether, this was followed by pet ether dichloromethane ratio 1:1 and finally dichloromethane alone. The eluted fractions were collected at 600 ml per fraction. The various fractions were concentrated using rotary evaporator under vacuum.

Spectroscopic measurements

The FTIR was recorded on Shimadzu 84005 Fourier Transform Infra-Red spectrophotometer, while gas chromatography and mass spectroscopy analysis (GC/MS) of the fractions were run on GC/MSQP2010 Plus Shimadzu GCMS equipped with a quadrupole mass spectra detector and an auto-sampler with the following settings; injector, 200 ; interfaced temperature, 250 , solvent cut time, 2.50min; relative detector mode, ACQ mode; scan, start time and end time; 3 minutes and 56 minutes; event time, 0.50 seconds; scan speed, 1428 units. The characteristic mass fragmentation patterns of the fractions were compared with the patterns recorded in NIST.

Field experiment

Vegetable beds of 1.5m2 with a height of 15 cm was prepared after ploughing an area of land measuring 25 m by 25 m. The experimental design was 2x4x3 factorial experiment organized in a randomised complete block design (RCBD). The experiment was conducted twice between the month of April and August in year 2018 and 2019 at the University of Ilorin Teaching an Research farm. Jew’s mallow (C. olitorius) seeds were sown at 50 cm in the row and 75 cm between the rows (Fabiyi and Olatunji, 2021a). C. olitorius plantlets were thinned five days after emergence. At ten days after emergence, each plant on the bed was inoculated with about 1000 eggs and J2 of M. incognita extracted from the infected roots of egg plant (Solanum melongena L.) using the sodium hypoclorite method (Riekert, 1995). The egg and juvenile suspension was introduced into the trench created at the root base of each Jew’s mallow (C. olitorius) plantlet. This was then covered with soil after inoculation. Chromatographic fractions were dissolved in 200 ml of deionised water at 150, 100 and 50 mg to give 0.75, 0.50 and 0.25 mg/ml concentration. Seven days after inoculation, the plants were treated with chromatographic fractions in banded form in the first and repeat experiments. Carbofuran 3G was applied at 1.0, 1.5, and 2.0 kg a.i/ha. The scale of Bridge and Page (1980) was adopted for root gall rating, where 0: root knots absent, 1: very small invisible knots, 2: small but very visible with main roots clean, 3: knots largely visible with main roots clean, 4: large root knots abound with main roots clean, 5: 50% of roots affected, with knots on main root, 6: main root knotted, 7: a handful of main root knotted, 8: all parts of main root knotted, few clean roots visible, 9: severe root knots on root system, 10: severe root knots all over, plant may be dead.

Data collection and statistical analysis

Data were collected from the field on the following parameters: Plant height, number of leaves, and number of branches on weekly basis. Days to 50% flowering was noted before harvest, while shoot weight, nematode population in 250 g soil sample, nematode population in 10 g root sample and root gall rating were assessed in the laboratory after harvest. All data were subjected to analysis of variance. Treatment means were separated using the Duncan’s new multiple range test at 5% level of probability (Gomez and Gomez, 1984).

Results and Discussion

The results of the GCMS analysis are presented in Table 1 and Figure 1. Fifteen compounds were identified and nine were more than 5%. Hexanoic acid methyl ester (15.48%), has the highest percentage among the constituents identified, other compounds present in the fraction include ethyl octanoate (11.44%), dodecanoic acid (11.25%), octanoic acid (9.22%), decanoic acid (11.23%), octadecanoic acid methyl ester (10.30 %), octadecanoic acid ethyl ester (9.19%) and tetradecanoic acid (7.11%). Compounds identified that are lower than 5% include pentadecanoic acid methyl ester (2.01%), 10-octadecenoic acid (1.08%), 9-octadecenoic acid ethyl ester (1.06%), methyl tetradecanoate (2.05%), methyl tetracosanoate (1.01%) and hexadecanoic acid ethyl ester (2.10%). The infra-red analysis of the fatty acid esters revealed several bands like 2924cm-1, 2852 cm-1, 1734cm-1, 1507cm-1, 1464cm-1, 1457cm-1, 1174cm-1, 1095cm-1, 1025cm-1, and 720cm-1

 

Table 1: Constituents of GCMS analysis.

Peak number

Retention time

%

Name of compound

1

26.78

9.22

Octanoic acid

2

29.55

15.48

Hexanoic acid methyl ester

3

30.65

11.44

Ethyl octanoate

4

31.31

5.47

9, 12-octadecadienoic acid methyl ester

5

31.40

11.25

Dodecanoic acid

6

32.05

10.30

Octadecanoic acid, methyl ester

7

32.32

11.23

Decanoic acid

8

33.50

7.11

Tetradecanoic acid

9

9.19

Octadecanoic acid ethyl ester

10

34.01

2.01

Pentadecanoic acid methyl ester

11

34.34

1.08

10-octadecenoic acid

12

35.16

1.06

9-octadecenoic acid ethyl ester

13

35.39

2.05

Methyl tetradecanoate

14

35.46

1.01

Methyl tetracosanoate

15

35.54

2.10

Hexadecanoic acid ethyl ester

 

which agrees with the expected vibrational frequencies corresponding to C-H and carbonyl (C=O) functional groups of fatty acid and esters (Figure 2).

Tables 2, 3 and 4 show the effect of fatty acid esters and carbofuran on the height, number of leaves and branches of Jew’s mallow (C. olitorius) plants under nematode infection on the field. The fatty acid esters at 0.75 mg/ml caused a significant (p<0.05) increase in height of the plants and higher number of leaves and branches was recorded. The untreated control plants presented low mean number of leaves, branches and height. The variation in dosage of application of the treatments was also notable on all the vegetative parameters measured. The highest concentration (0.75mg/ml) produced significantly taller plants and more leaves and branches. Plants treated with the 0.75 mg/ml concentration also flowered significantly earlier (Table 5), while flowering was delayed in lower treatment concentrations. Shoot weights were also significantly (p<0.05) heavier in plants treated with the highest concentrations of fatty acid esters (Table 5). The 0.75 mg/ml dosage of application was the most effective in reducing nematodes in 250 g soil and 10 g root sample at harvest and consequently galling was reduced in the roots of plants administered with the highest concentration in comparison with the untreated control which recorded the highest root gall index (Table 6).

 

Table 2: Comparative effect of fatty acid esters and carbofuran on plant height (cm) of Jew’s Mallow (Corchorus olitorius) plants under Meloidogyne incognita infection.

Treatments

Level Mg/ml

2nd WAT

2nd WAT

4th WAT

4th WAT

6th WAT

6th WAT

Fatty acid esters

1st Trial

2nd Trial

1st Trial

2nd Trial

1st Trial

2nd Trial

0.0

6.21c

7.33c

9.19d

10.26d

12.22d

11.00d

0.25

9.09b

10.14ab

12.30c

13.00c

17.36c

16.27c

0.50

10.16b

11.00a

15.21b

16.02b

21.15b

20.00b

0.75

12.51a

12.10a

19.34a

20.29a

27.23a

26.19a

Carbofuran (kg a.i/ha)

0.0

6.18d

5.48c

8.01d

9.92d

11.04d

10.29d

1.0

10.06c

11.01b

14.07c

13.53c

19.00c

18.11c

1.5

12.19b

12.22b

17.39b

16.02b

23.41b

22.01b

2.0

16.00a

16.77a

20.09a

19.66a

31.05a

30.45a

S.E.M

1.63

0.73

2.06

2.14

3.28

4.33

 

Means in a segment of a given column followed by the same letter are not significantly different using the new Duncan’s multiple range test.

 

Table 3: Comparative effect of fatty acid esters and carbofuran on number of leaves of Jew’s mallow (Corchorus olitorius) plants under Meloidogyne incognita infection.

Treatments

Level Mg/ml

2nd WAT

2nd WAT

4th WAT

4th WAT

6th WAT

6th WAT

Fatty acid esters

1st Trial

2nd Trial

1st Trial

2nd Trial

1st Trial

2nd Trial

0

10.10d

11.04d

17.08d

19.11d

23.06d

21.11d

25

25.26c

29.19c

57.76c

61.29c

70.00c

67.16c

50

46.35b

51.27b

78.06b

83.10b

92.23b

89.51b

75

58.04a

62.16a

91.25a

97.16a

107.08a

105.19a

Carbofuran (kg a.i/ha)

0.0

11.02d

12.37d

15.11d

18.00d

24.29d

20.33d

1.0

31.45c

33.06c

66.13c

73.29c

85.54c

82.21c

1.5

49.36b

53.25b

81.19b

87.00b

103.32b

98.40b

2.0

64.17a

67.00a

99.45a

106.54a

137.28a

131.00a

S.E.M

1.72

1.59

3.71

3.26

4.23

5.11

 

Means in a segment of a given column followed by the same letter are not significantly different using the new Duncan’s multiple range test.

 

Table 4: Comparative effect of fatty acid esters and carbofuran on number of branches of Jew’s mallow (Corchorus olitorius) plants under Meloidogyne incognita infection.

Treatments

Level Mg/ml

2nd WAT

2nd WAT

4th WAT

4th WAT

6th WAT

6th WAT

Fatty acid esters

1st Trial

2nd Trial

1st Trial

2nd Trial

1st Trial

2nd Trial

0

0.00c

0.00b

0.00c

0.00c

2.42d

2.07d

25

0.00c

0.00b

3.08b

2.79b

5.03c

4.78c

50

2.07b

3.19a

4.42b

3.86b

7.15b

6.96b

75

4.11a

4.54a

7.17a

6.37a

10.32a

11.77a

Carbofuran (kg a.i/ha)

0.0

0.00c

0.00b

0.00d

0.00d

2.25d

2.54d

1.0

0.00c

0.00b

4.14c

3.77c

6.09c

5.18c

1.5

3.31b

4.16a

6.22b

5.87b

9.39b

8.00b

2.0

5.22a

5.09a

8.31a

7.92a

11.18a

10.05a

S.E.M

0.01

0.04

0.62

0.11

0.17

0.08

 

Means in a segment of a given column followed by the same letter are not significantly different using the new Duncan’s multiple range test.

 

Table 5: Comparative effect of fatty acid esters and carbofuran on yield attributes of Jew’s mallow (Corchorus olitorius) plants under Meloidogyne incognita infection.

Treatments

Level Mg/ml

Days to 50% flowering

Days to 50% flowering

Fresh shoot

weight (g)

Fresh shoot weight (g)

Fatty acid esters

1st Trial

2nd Trial

1st Trial

2nd Trial

0.0

54.21d

51.33d

88.04d

81.64d

0.25

36.04c

38.09c

128.02c

119.65c

0.50

28.17b

26.02b

135.00b

131.03b

0.75

20.00a

19.79a

169.18a

165.12a

Carbofuran (kg a.i/ha)

0.0

52.06d

56.36c

77.00d

83.25d

1.0

29.05c

28.21b

130.03c

127.76c

1.5

25.07b

26.16b

158.00b

151.29b

2.0

21.15a

20.09a

175.11a

170.31a

S.E.M

1.11

2.08

3.27

3.09

Means in a segment of a given column followed by the same letter are not significantly different using the new Duncan’s multiple range test.

Table 6: Comparative effect of fatty acid esters and carbofuran on nematode populations of Jew’s mallow (Corchorus olitorius) plants under Meloidogyne incognita infection.

Treatments

Level Mg/ml

Nematode population in 250 g soil

Nematode population in 250 g soil sample

Nematode population in 10 g root sample

Nematode population in

10 g root sample

Root gall rating

Root gall rating

Fatty acid esters

1st trial

2nd trial

1st trial

2nd trial

1st trial

2nd trial

0.0

2512.09d

2218.11d

1743.04d

1532.19d

10.00d

10.00d

0.25

163.65c

152.79c

66.36c

57.04c

4.16c

4.03c

0.50

103.59b

92.18b

31.27b

23.15b

2.04b

2.19b

0.75

34.28a

28.06a

14.11a

11.20a

1.17a

1.03a

Carbofuran (kg a.i/ha)

0.0

2617.43d

2508.29d

1105.03d

1028.72d

10.00c

10.00c

1.0

25.34c

18.78c

19.76c

12.88c

1.48b

1.65b

1.5

4.69b

3.57b

5.17b

3.83b

0.32a

0.41a

2.0

0.00a

0.00a

0.00a

0.00a

0.00a

0.00a

S.E.M

2.29

2.05

1.07

2.02

0.11

0.08

 

Means in a segment of a given column followed by the same letter are not significantly different using the new Duncan’s multiple range test.

 

It is worthy to note that the fatty acid esters from Alstonia boonei exhibited some level of nematicidal activity and are close to that of the synthetic nematicide. The fact that the increase in concentration potentiated the toxicity of the fatty acid esters on M incognita underscores the sensitivity of nematodes to the esters and this is a good index for dosage specification. The observed nemato-toxic effects of the fatty acid esters can be attributed to the presence of the identified organic compounds as revealed by the GC/MS and infra-red spectroscopic results of the fraction. Some of these organic compounds are either polar compounds, compounds of intermediate polarity or non polar compounds judging from their respective retention time from the GC/MS result. This however underlies partly the basis for the comparatively higher toxicity of the fatty acid esters to M. incognita on the field. The C-H stretching is associated with long chain hydrocarbons, alicyclics and aromatics. Hydrocarbons are used as soil fumigants against soil insects and nematodes before planting (Symser, 1990). Hydrocarbon oils have played an important role in crop protection as insecticides and ovicides. Fatty acid esters are employed as surfactants, with activities against insect larvae, and nematodes (Abrogat et al., 2009). A variety of fatty acid esters have been used to manage nematodes in vitro and in vivo. Some fatty acid esters and fatty acid derivatives in the group of short carbon chains including C8 to about C14 which could be in the epoxide, cyclopropane, methylated or hydroxylated forms have also been confirmed to be toxic to some nematodes (Feitelson and Dullum, 2000).

The results from this research is corroborated by the findings of Zang et al. (2012). They affirmed that fatty acids are toxic to M. incognita. Their study established that butyric, caprylic, capric, lauric, myristic, palmitic, and oleic acids inhibited egg hatch rate of M. incognita by 15.8%, while 50% juvenile mortality was recorded for capric and caprylic acids after 24 hours of exposure at 2000 μmol/L concentration. The fatty acids equally reduced M. incognita reproduction significantly on Cucumus sativus with an increased biomass growth (Zang et al., 2012). Analogously, the results in this research was sustantiated by Gonçalves da Silva et al. (2021). They demonstrated that 80% egg hatch inhibition was achived with ethyl octanoate at 1000 μg mL−1 concentration, while octanoic acid, ethyl octanoate, and isovaleric acid provided 80% nematostatic action on M. incognita J2. Significant reduction in M. incognita reproduction was noted in further greenhouse experiments where ethyl octanoate was found to be comparable with the commercial fumigant dazomet. Organic acid like palmitoleic acid is reported to be a promising nematicidal substance (Morgunov et al., 2016). Ricineloidic, ricinoleic and 12, 13-epoxy-trans-9-octadecenoic acids were also certified to be nematicidal by William et al. (2005). In their report, fatty acids were evaluated on root-knot nematodes infecting tomato plants at 100 ppm in pot experiments. A significant reduction in root gall damage on the tomato plants was realized. Munamaka (1983) reiterated that myristic, palmitic, and oleic acids from benzene extract of Iris japonica exhibited nematicidal action. Strong nematicidal activity was equally established with the application of 2-undecylenic acid at 10 µg/ml and 80 % mortality was attained (Chitwood, 2002). Similarly, butyric acid, a short chain fatty acid was discovered to be active on M. incognita and Pratylenchus penetrans at 880 µg/ml (Sayre et al., 1965; Chitwood, 2002). The activity of fatty acids was further corroborated by Vrain (1980) he reported twelve fatty acids of C3 to C18 with their derivatives, which include seven methyl esters and four primary alcohols in in vitro and greenhouse trials. Decanoic acid was toxic to all second stage juveniles of Meloidogyne hapla with a high percentage mortality in 24 hours at a concentration of 50 ppm for methyl esters and primary alcohols. Toxicity was noted to increased with increase in carbon chain from C3 to C11.

Concretely, fatty acid esters could be employed to mananage nematodes at lower concentrations. Kim et al. (1996) reported methyl ester of pelargonic acid to be active on root-knot nematodes at 0.005% concentration with 100% mortality after 30 minutes of application, M. javanica galling on tomato roots was prevented. In green house experiments, 1.6µl/liter of methyl pelagonate significantly reduced Heteodera glycine and M. incognita populations on soyabean (Davis et al., 1997), while Globodera tabacum the tobacco cyst nematode population was brought down with some fatty acid esters at 1000 µg/ml (Tarjan and Cheo, 1956).

Some micro-organisms like fungi have presented fatty acid esters with nematicidal activity. 2-decenedioic acid from Pleurotus ostreatus was confirmed by Kwok et al. (1992) as a nematode paralyzing substance, while remarkably higher nematicidal activity was attributed to monoenoic fatty acids with 8-12 carbons (Chitwood, 2002). Furthermore, linoleic acid isolated from Arthrobotrys conoides and A. oligospora was found toxic to M. incogita at 50 µg/ml (Anke et al., 1995; Anke and Sterner, 1997). Similarly, Stadler et al. (1994) isolated linoleic acid, oleic acid, and palmitic acid from Hericium coralloides cultures and they were discovered to be effective towards C. elegans.

Additionally, Pineda-Alegria et al. (2020) confirmed the effectiveness of fatty acid esters in their research on Haemonchus contortus a gastro intestinal nematode of ruminant animals. They found pentadecanoic acid, palmitic acid, stearic acid and linoleic acid to significantly inhibit egg hatch and larval motility of H. contortus at 1.25-20 mg/ml. The fatty acid esters employed in this research remarkably reduced the reproduction of M. incognita on Jew’s mallow plants, thereby improving the vegetative growth which was significantly hindered by M. incognita reproduction on the untreated control plants.

Conclusion and Recommendation

The application of plant metabolites in plant protection would reduce the use of synthetic nematicides and this would also alleviate concerns about environmental toxicity. FAEs are cheap and non-toxic. The application of fatty acid esters could serve as an alternative nematode control option in Nigeria. It will help reduce the losses incurred by the vegetable farmers. FAEs could be derived from several plant secondary metabolites. Although practical applications may be hindered by the lack of industrial production.

Acknowledgement

The authors are grateful to Chemistry Department University of Ilorin, Nigeria.

Novelty Statement

Fatty acid esters are possible option in Meloidogyne incognita management.

Author’s Contribution

O.A.Fabiyi: Conceptualisation, Bench work, Data Collection, Data analysis, Manuscript Draft.

M.T. Baker: Data interpretation Supply of Materials.

G.A. Olatunji: Manuscript Proof Reading, Review and Editing.

Conflict of interest

The authors have declared no conflict of interest.

References

Abiodun, O.A., Dauda, A.O., Fabiyi, O.A. and Akintayo, F.M., 2022. Bio-fortification: Quality improvement of Faba beans. In Faba beans: Chemistry, properties and functionality (eds. S.P. Bangar and S.B. Dhull). pp. 275-300. https://doi.org/10.1007/978-3-031-14587-2_11

Abrogat, S.C., Nigg, H.N. and Becton, R.A., 2009. Use of surfactants for mitigating damage to plants from pests. National Center for Biotechnology Information (2022). PubChem Patent Summary for US-2009186767-A1. Retrieved September 12, 2022 from https://pubchem.ncbi.nlm.nih.gov/patent/US-2009186767-A1

Anke, H. and Sterner, O., 1997. Nematicidal metabolites from higher fungi. Curr. Org. Chem., 1: 361-374. https://doi.org/10.2174/1385272801666220126160657

Anke, H., Stadler, M., Mayer, A. and Sterner O., 1995. Secondary metabolites with nematicidal and antimicrobial activity from nematophagous fungi and Ascomycetes. Can. J. Bot., 73: S932–S939. https://doi.org/10.1139/b95-341

Atolani, O., Fabiyi, O.A. and Olatunji, G.A., 2014a. Nematicidal isochromane glycoside from Kigelia pinnata leaves. Acta Agric. Slovenica., 104(1): 25-31. https://doi.org/10.14720/aas.2014.104.1.3

Atolani, O., Fabiyi, O. A. and Olatunji, G.A. 2014b. Isovitexin from Kigelia pinnata, A Potential Eco-friendly Nematicidal Agent. Tropical Agriculture. Volume 91 (2): 67-74.

Atolani, O. and Fabiyi, O.A., 2020. Plant parasitic nematodes management through natural products: Current progress and challenges. In: Management of phytonematodes: Recent advances and future challenges. (eds. Ansari, R.A., Rizvi, R. and Mahmood, I.,). pp. 297-315. https://doi.org/10.1007/978-981-15-4087-5_13

Atolani, O., Fabiyi, O.A. and Olatunji, G.A., 2014. Isovitexin from Kigelia pinnata, a potential eco-friendly nematicidal agent. Trop. Agric., 91(2): 67-74.

AVRDC, 1991. Asian vegetable research and development center. Culture and agriculture. N. Publ. AVRDC, 11(41).

Babatola, J.O., 1989. Effect of some organic manure on nematode in tomato cultivation. Pak. J. Nematol., 7: 39-46.

Barker, K.R., 1998. Introduction and synopsis of advancements in nematology. In: Plant and Nematode interactions (Barker, K.R., Pederson, G.A., and Windham, G.L.,). Am. Soc. Agron. Inc., Crop Sci. Am. Inc., Soil Sci. Soc. Am. In., Madison, WI, pp. 1–20. https://doi.org/10.2134/agronmonogr36.c1

Bello, T.T., Fabiyi, O.A., Clavero-Camacho, I., Cantalapiedra-Navarrete, C., Palomares-Rius, J.E., Castillo, P. and Archidona-Yuste, A., 2022. First report of Xiphinema ifacolum Luc, 1961 (Dorylaimida: Longidoridae) from Nigeria. J. Nematol., 54: 1-5. https://doi.org/10.2478/jofnem-2022-0015

Bridge, J. and Page, S.L.J., 1980. Estimation of root-knot nematode infestation levels on roots using a rating chart. Trop. Pest Manage., 26(3): 296-298. https://doi.org/10.1080/09670878009414416

Caillaud, M.C., Dubreuil, G., Quentin, M., Perfus-Barbeoch, L., Lecomte, P., Engler, J.D.A., Abad, P., Rosso, M.N., and Favery, B., 2008. Root-knot nematodes manipulate plant cell functions during a compatible interaction. J. Plant Physiol., 165: 104-113. https://doi.org/10.1016/j.jplph.2007.05.007

Caveness, F.E., 1967. Nematodes affecting Western region agric, End of tour progress report on the nematology project USAID/MANR Lagos, Nigeria, pp. 135.

Chandrasekaran, M., Kannathasan, K., and Venkatesalu, V., 2008. Antimicrobial activity of fatty acid methyl esters of some members of Chenopodiaceae. Z. Naturforsch C. J. Biosci., 63(5-6): 331-336. https://doi.org/10.1515/znc-2008-5-604

Chandrasekaran, M., Senthilkumar, A. and Venkatesalu, V., 2011. Antibacterial and antifungal efficacy of fatty acid methyl esters from the leaves of Sesuvium portulacastrum L. Eur. Rev. Med. Pharmacol. Sci., 15(7): 775-780.

Chitwood, D.J., 2002. Phytochemical based strategies for nematode control. Annu. Rev. Phytopathol., 40: 221–249. https://doi.org/10.1146/annurev.phyto.40.032602.130045

Consden, R.A., Gordon, H. and Martin, A.P.J., 1994. Separation of compounds by column chromatography. Biochem. J., 38: 224-232. https://doi.org/10.1042/bj0380224

Davis, E.L., Meyers, D.M., Dullum, C.J., and Feitelson, J.S., 1997. Nematicidal activity of fatty acid esters on soybean cyst and root-knot nematodes. Suppl. J. Nematol., 29: 677-684.

Denton, L., 1997. A review of Corchorus olitorius L, in Nigeria. In: Proceedings of a workshop on African indigenous vegetables (eds. R.R. Schippers and I. Budd). Limbe, Cameroon 13-18 January 1997. Natural Resources Institute/IPGRI Chatham, United Kingdom, pp. 25-30.

Egunjobi, A.O. and Olaitan, J.O., 1986. Response of Meloidogyne incognita on infected cowpea Vigna umguiculata (Ife brown) to some agro waste soil amendment. Nematologica, 16: 33-43.

Fabiyi, O.A., Olatunji, G.A., Atolani, O., and Olawuyi, R.O., 2020a. Preparation of bio-nematicidal nanoparticles of Eucalyptus officinalis for the control of cyst nematode (Heterodera sacchari). J. Anim. Plant Sci., 30(5): 1172-1177. https://doi.org/10.36899/JAPS.2020.5.0134

Fabiyi, O.A. Atolani, O. and Olatunji, G.A., 2020b. Toxicity effect of Eucalyptus globulus on Pratylenchus spp of Zea mays. Sarhad J. Agric., 36(4): 1244-1253. https://doi.org/10.17582/journal.sja/2020/36.4.1244.1253

Fabiyi, O.A., 2020. Growth and yield response of groundnut Arachis hypogaea (Linn.) under Meloidogyne incognita infection to furfural synthesized from agro-cellulosic materials. J. Trop Agric., 58(2): 241-245.

Fabiyi, O.A. and Olatunji, G.A., 2021a. Environmental sustainability: Bioactivity of Leucaena leucocephala leaves and pesticide residue analysis in tomato fruits. Acta Univ.
Agric. Silvic. Mendel. Brun., 69(4): 473-480.

Fabiyi, O.A. and Olatunji, G.A., 2021b. Toxicity of derivatized citrulline and extracts of water melon rind (Citrullus lanatus) on root-knot nematode (Meloidogyne incognita). Trop. Agric., 98(4): 347-355.

Fabiyi, O.A., 2021a. Application of furfural in sugarcane nematode pest management. Pak. J. Nematol., 39(2): 151-155. https://doi.org/10.17582/journal.pjn/2021.39.2.151.155

Fabiyi, O.A., 2021b. Evaluation of Nematicidal activity of terminalia glaucescens fractions against Meloidogyne incognita on capsicum Chinense. J. Hortic. Res., 29(1): 67-74. https://doi.org/10.2478/johr-2021-0006

Fabiyi, O.A., 2021c. Evaluation of plant materials as root-knot nematode (Meloidogyne incognita) suppressant in okro (Abelmuscous esculentus). Agric. Conspec. Sci., 86(1): 51-56.

Fabiyi, O.A., 2022a. Fractions from Mangifera indica as an Alternative in Meloidogyne incognita Management. Pak. J. Nematol., 40(1): 65-74. https://doi.org/10.17582/journal.pjn/2022/40.1.65.74

Fabiyi, O.A., 2022b. Cytotoxicity and nematicidal potential of leaf extracts of Adansonia digitata and Khaya senegalensis on root-knot nematode (Meloidogyne incognita) associated with cabbage (Brassica oleracea). J. Agric. Sci. Sri Lanka., 17(3): 425-436. https://doi.org/10.4038/jas.v17i3.9922

Fabiyi, O.A., 2022c. Application of municipal refuse dump site soil, orange, potato and pineapple peels in the control of root-knot nematode (Meloidogyne incognita) infecting carrots (Daucus carota L.). J. Solid Waste Technol. Manage., 48(3): 474-485. https://doi.org/10.5276/JSWTM/2022.474

Faparusi, S.I., and Bassir, O., 1982. Triterpenes from Alstonia boonei. Phytochemistry, 21: 3083-3084. https://doi.org/10.1016/0031-9422(72)80114-6

Feitelson, J.S. and Dullum, C.J., 2000. Materials and methods for killing nematode and nematode eggs. US Patent for materials and methods for killing nematodes and nematode eggs (Patent No. 6, 124,359). United States Mycogen Corp oration (San Diego, CA) 6124359 https://www.Freepatentsonline.com/6124359.html Retrieved September 14, 2022.

Gomez, K. A. and Gomez, A.A., 1984. Statistical procedures for agricultural reseach, 2nd Ed. New York, USA: John Wiley and Sons.

Gonçalves da Silva, M.S., Campos, V.P., Terra, W.C., Pacheco, P.V.M., Lopes de Paula, L., Barros, A.F., Pedroso, M.P., 2021. Volatile fatty acids from whey volatilome as potential soil fumigants to control Meloidogyne incognita. Crop Protect., pp. 143. https://doi.org/10.1016/j.cropro.2021.105567

Kayode, J. and Omotoyinbo, M.A., 2008. Conservation of botanicals used for dental and oral healthcare in Ekiti State, Nigeria. Ethnobot. Leafl., 12: 7-18.

Kim, L., Jerald, S., Feitelson, J.H. and Zorner, P.S., 1996. Materials and methods for controllling nematodes-Mycogen Corporation (freepatentsonline.com) Patent No. CA2233627A1 (San Diego, CA) https://www.Free patentsonline.com/6124359.html Retrieved September 15, 2022.

Kwok, O.C.H., Plattner, R., Weisleder, D., and Wicklow, D.T., 1992. A nematicidal toxin from Pleurotus ostreatus NRRL 3526. J. Chem. Ecol., 18: 127-136. https://doi.org/10.1007/BF00993748

Morgunov, I.G., Kamzola, S.V., Dedyukhina, E.G., Christyakova, T.L., Lunina, J.N., Mironov, A.A., Stepanova, N.N., Shemshura, O.N., and Vainstein, M.B., 2017. Application of organic acids for plant protection against phytopathogens. Appl. Microbiol. Biotechnol., 101: 921-932. https://doi.org/10.1007/s00253-016-8067-6

Munakata, K., 1983. Nematocidal natural products. In: Natural products for innovative pest management, (ed. D.L. Whitehead, W.S. Bowers), Oxford: Pergamon. pp. 299-310.

Ojewole, J.A.O., 1984. Studies on the pharmacology of echitamine, an alkaloid from the stem bark of A. boonei. Int. J. Crude Drugs Res., 22: 121-143. https://doi.org/10.3109/13880208409070663

Olajide, O.A., 2000. Anti-inflammatory, antipyretic and analgesic properties of Alstonia boonei stem bark. J. Ethnopharm., 71: 179-186. https://doi.org/10.1016/S0378-8741(99)00200-7

Pineda-Alegria, J.A., Sanche, J.E., Gonzalez-Cortazar, M., von Son-de Fernex, E., Gonzalez-Garduno, R., Mendoza-de Gives, P., Zailpa, A., and L. Aguilar-Marcelino. 2020. In vitro nematocial activity of commercial fatty accids and beta sitosterol against Haemonchus contortus. J. Helminthol. Cambridge Univ. Press, 94: e135. https://doi.org/10.1017/S0022149X20000152

Riekert, H., 1995. A modified sodium hypochlorite technique for the extraction of root-knot nematode eggd and larvae from maize root samples. Afr. Plant Prot., 1(1): 41-43.

Sayre, R.M., Patrick, Z.A. and Thorpe, H.J., 1965. Identification of a selective nematicidal component in extracts of plant residues decomposing in soil. Nematologica, 11: 263-268. https://doi.org/10.1163/187529265X00168

Seo, Y. and Kim, Y.H., 2014. Control of Meloidogyne incognita using mixtures of organic acids. Plant Pathol. J., 30(4): 450-455. https://doi.org/10.5423/PPJ.NT.07.2014.0062

Simon, G., 2006. An introduction to planar chromatography. In: Natural products isolation 2nd ed. New Jersey, USA: Humana Press. pp. 77-116. https://doi.org/10.1385/1-59259-955-9:77

Sivakumar, M. and Gunasekaran, K. 2011. Management of root knot nematodes in tomato chilli and brinjal by neem oil formulations. J. Biopest. 4 (2): 198-200.

Smyser, B.P., 1990. Pesticide bio-chemistry and physiology. Pestic. Sci., 38: 374.

Stadler, M., Mayer, A., Anke, H. and Sterner, O., 1994. Fatty acids and other compounds with nematicidal activity from cultures of Basidiomycetes. Planta Med., 60(2): 128-132. https://doi.org/10.1055/s-2006-959433

Sun, M.H., Gao, L., Shi, Y.X., Li, B.J. and Liu, X.Z., 2006. Fungi and actinomycetes associated with Meloidogyne spp. eggs and females in China and their biocontrol potential. J. Invertebr. Pathol., 93: 22–28. https://doi.org/10.1016/j.jip.2006.03.006

Tarjan, A.C., and Cheo, P.C., 1956. Nematocidal value of some fatty acids. Univ. R. I. Agric. Exp. Stn. Bull., pp. 332-341.

Verdejo-Lucas, S., 1999. Namatodes. In: Integrated pest and disease management in Greenhouse crops (eds. Albajes, R. et al.). Kluwer, Netherlands, pp. 61-68. https://doi.org/10.1007/0-306-47585-5_5

Viala, S.S., Brodie, B.B., Rodriguez, E., and Gibson, D.M., 1998. The potential of thiarubrine as a nematicidal agent against plant parasitic nematodes. J. Hematol., 30: 192-200.

Vrain, C., 1980. Fatty acids and their derivatives for nematode control. J. Nematol., 12(4): 240.

Williams, D.J., Kloek, A.P., Hresko, M.C., Shortt, B.J., Davila-aponte, J.A. John, D., Mccarter, J., and Mclaird, M.B., 2005. Nematicidal fatty acid and fatty acid ester related compounds. Patent Application Publication. Sheet 1-9. Patent number 20040157803, https://www.freepatentsonline.com/y2004/0157803.html.

Zang, Wei-pu., Ruan, Wei-bin., Deng, Yun-ying and Gao, Yu-bao. 2012. Potential antagonistic effects of nine natural fatty acids against Meloidogyne incognita. J. Agric. Food Chem., 60(46): 11631-11637. https://doi.org/10.1021/jf3036885

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

Pakistan Journal of Nematology

December

Pakistan Journal of Nematology, Vol. 41, Iss. 2, Pages 101-194

Featuring

Click here for more

Subscribe Today

Receive free updates on new articles, opportunities and benefits


Subscribe Unsubscribe