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Activity of Vetiver Extracts and Essential Oil against Meloidogyne incognita Cover

Figures & Tables

Figure 1

Diagram of a chemotaxis assay. Each plastic plate was divided into three areas: the treatment area (consisting of the treatment point and the surrounding area), the starting area (consisting of the starting point and the surrounding area), and the control area (consisting of the control point and the surrounding area). J2 were placed on the agar at the starting point, treatments were applied to the agar at the treatment point, and sterile distilled water was applied to the agar at the control point. Measurements are given for a plate with an 85-mm-diam. cup (100-mm-diam. lid).

Table 1

Percentage inactive or dead Meloidogyne incognita second-stage juveniles (J2) in Vetiveria zizanioides (vetiver) shoot aqueous (VSA) extracts and vetiver root aqueous (VRA) extracts.

Percentage inactive J2Percentage dead J2
Treatmenta Day 1Day 2Day 3 rinsed
VSA 94%53.4 bAb 70.4 abA68.2 aA
VRA 94%79.6 aAB86.7 aA71.9 aA
VSA 71%46.2 bB63.5 bcA71.1 aA
VRA 71%74.4 aA72.1 abA68.0 aA
VSA 47%39.8 bcB49.3 cdB67.6 aA
VRA 47%50.3 bA49.8 cdA53.4 abA
VSA 24%23.7 cdB38.3 dAB56.3 abA
VRA 24%16.6 deB34.3 deA43.6 bA
0.48 mg/ml streptomycin sulfate14.7 deA18.7 efA22.3 cA
Water6.7 eB9.8 fAB17.5 cA

[i] aAll extracts were from shoots or roots of greenhouse-grown, 2-mon-old vetiver cv. Sierra. Treatments were prepared from 100% extracts (undiluted extracts) containing streptomycin sulfate, diluted to 75%, 50%, and 25% with water, and then added to J2 suspensions in the wells. Final extract dilutions in the wells are presented in the table.

[ii] bValues are means of eight replications in each of the two trials, for a total of N = 16. Differences among treatments were determined by analysis of variance (ANOVA) and means were compared using Tukey-Kramer’s adjustment for multiple comparisons (P ⩽ 0.05). Similar lower case letters indicate that means are not significantly different within a column; similar upper case letters indicate that means are not significantly different within a row.

Table 2

Percentage inactive or dead Meloidogyne incognita second-stage juveniles (J2) in Vetiveria zizanioides (vetiver) root ethanol (VRE) extracts, Tagetes patula (French marigold cv. Durango Mix) root ethanol (FMRE) extract, and in vetiver oil (VO). Extracts were prepared from greenhouse-grown, 2-mon-old and 4-yr-old vetiver cv. Sierra, and from field-grown, 1-yr-old cv. Songkha 3.

Percentage inactive J2Percentage dead J2
Treatmenta Day 1Day 2Day 3 rinsed
FMRE 0.95 mg/ml34.9 aBb 30.7 aB69.1 aA
2-mon VRE 0.95 mg/ml24.9 abcB28.0 abB38.3 bcA
1-yr VRE 0.95 mg/ml27.6 abB26.5 abB42.4 bA
4-yr VRE 0.95 mg/ml29.7 abB30.0 aB41.9 bA
VO 0.95 mg/ml20.3 bcdA12.6 cdA17.1 deA
0.95% CTD12.9 dA8.0 dA11.3 eA
FMRE 0.095 mg/ml13.7 cdB17.0 bcdB35.0 bcA
2-mon VRE 0.095 mg/ml16.2 cdA20.2 abcA24.0 cdeA
1-yr VRE 0.095 mg/ml16.2 cdB13.9 cdB30.5 bcdA
4-yr VRE 0.095 mg/ml14.2 cdB11.0 cdB27.8 bcdA
VO 0.095 mg/ml9.7 dA8.6 cdA9.8 eA
0.095% CTD12.8 dA8.0 dA11.8 eA
Sterile distilled water11.8 dA12.4 cdA15.2 deA

[i] a2-mon VRE = vetiver root ethanol extracts from greenhouse-grown, 2-mon-old cv. Sierra; 1-yr VRE = vetiver root ethanol extracts from field-grown, 1-year-old cv. Songkha 3; 4-yr VRE = vetiver root ethanol extracts from greenhouse-grown, 4-yr-old cv. Sierra; VO = commercial vetiver oil. Treatments were prepared from 1.0 mg/ml and 0.1 mg/ml extracts that were dissolved in a solvent of equal parts castor oil, Tween 80, and dimethyl sulfoxide (CTD) and then added to J2 suspensions in the wells. Final extract dilutions in the wells are presented in the table.

[ii] bValues are means of eight replications in each of the two trials, for a total of N = 16. Differences among treatments were determined by analysis of variance (ANOVA) and means were compared using Tukey-Kramer’s adjustment for multiple comparisons (P ⩽ 0.05). Similar lower case letters indicate that the means are not significantly different within a column; similar upper case letters indicate that the means are not significantly different within a row.

Table 3

Repellent activity of aqueous Vetiveria zizanioides (vetiver) extracts on Meloidogyne incognita second-stage juveniles. The chemotaxis index (CI) was recorded after 24 hr.

Treatmenta CIb
2-mon VRA 0.1 g/ml−0.5 bc
2-mon VSA 0.1 g/ml−0.6 b
Control sterile distilled water0.0 a

[i] aVRA = vetiver root aqueous extracts from greenhouse-grown, 2-mon-old cv. Sierra; VSA = vetiver shoot aqueous extracts from greenhouse-grown, 2-mon-old cv. Sierra.

[ii] bChemotaxis index (CI): ⩾0.2 indicated an attractant; between 0.2 and 0.1, a weak attractant; 0.1 to −0.1, without effect; between −0.1 and −0.2, a weak repellent; and ⩽−0.2, a repellent.

[iii] cValues are means of five replications in each of the two trials, for a total of N = 10. Differences among treatments were determined by analysis of variance (ANOVA) and means were compared using Tukey-Kramer’s adjustment for multiple comparisons (P ⩽ 0.05). Similar lower case letters indicate that means are not significantly different.

Table 4

Repellent activity of Vetiveria zizanioides (vetiver) oil, vetiver root ethanol extracts, and Tagetes patula (French marigold cv. Durango Mix) root ethanol extracts on Meloidogyne incognita second-stage juveniles. The chemotaxis index (CI) was recorded after 24 hr.

Treatmenta CIb
FMRE 0.1 g/ml−0.4 dec
2-mon VRE 0.1 g/ml−0.6 e
1-yr VRE 0.1 g/ml−0.3 bcd
4-yr VRE 0.1 g/ml−0.3 cde
VO 0.1 g/ml−0.1 abc
Ethanol0.1 a
Sterile distilled water0.0 ab

[i] a2-mon VRE = vetiver root ethanol extracts from greenhouse-grown, 2-mon-old cv. Sierra; 1-yr VRE = vetiver root ethanol extracts from field-grown, 1-yr-old cv. Songkha 3; 4-yr VRE = vetiver root ethanol extracts from greenhouse-grown, 4-yr-old cv. Sierra; VO = commercial vetiver oil.

[ii] bChemotaxis Index (CI): ≥0.2 indicated an attractant; between 0.2 and 0.1, a weak attractant; 0.1 to −0.1, without effect; between −0.1 and −0.2, a weak repellent; and ⩽−0.2, a repellent.

[iii] cValues are means of five replications in each of the two trials, for a total of N = 10. Differences among treatments were determined by analysis of variance (ANOVA) and means were compared using Tukey–Kramer’s adjustment for multiple comparisons (P ⩽ 0.05). Similar lower case letters indicate that the means are not significantly different.

Figure 2

GC-MS spectra of crude Vetiveria zizanioides (vetiver) root ethanol (VRE) extracts and commercial vetiver oil (VO). (A) VRE from greenhouse-grown, 2-mon-old cv. Sierra; (B) VRE from field-grown, 1-yr-old cv. Songkha 3; (C) VRE from greenhouse-grown, 4-yr-old cv. Sierra; (D) commercial VO from Haiti.

Figure 3

Chemical structures of the major constituents in vetiver root crude extracts and commercial vetiver oil from Vetiveria zizanioides, determined by GC/MS analysis: (A) 3,3,8,8-tetramethyltricyclo[5.1.0.0(2,4)]oct-5-ene-5-propanoic acid; (B) 6-isopropenyl-4,8a-dimethyl-1,2,3,5,6,7,8,8a-octahydronaphthalen-2-ol; (C) ethyl hexadecanoate; (D) ethyl 9,12-octadecadienoate; (E) 2-(4a,8-dimethyl-1,2,3,4,4a,5,6,7-octahydro-naphthalen-2-yl)-prop-2-en-1-ol.

Table 5

Chemical composition of major constituents in three Vetiveria zizanioides (vetiver) root crude extracts and a commercial vetiver oil, determined by GC/MS analysis.

Sourcea Compound nameb Retention timeComponent percentage under peakc Molecular formulaMolecular weight
2-mon VRE3,3,8,8-Tetramethyltricyclo[5.1.0.0(2,4)]oct-5-ene-5-propanoic acid (a sesquiterpene acid)20.1142.8C15H22O2 234
6-Isopropenyl-4,8a-dimethyl-1,2,3,5,6,7,8,8a-octahydronaphthalen-2-ol (a sesquiterpene alcohol)19.4611.2C15H24O220
1-yr VRE3,3,8,8-Tetramethyltricyclo[5.1.0.0(2,4)]oct-5-ene-5-propanoic acid20.1226.1C15H22O2 234
6-Isopropenyl-4,8a-dimethyl-1,2,3,5,6,7,8,8a-octahydronaphthalen-2-ol19.473.0C15H24O220
Ethyl hexadecanoate (ethyl palmitate)21.8632.3C18H36O2 284
Ethyl 9,12-Octadecadienoate (ethyl linoleate)23.4218.9C20H36O2 308
4-yr VRE3,3,8,8-Tetramethyltricyclo[5.1.0.0(2,4)]oct-5-ene-5-propanoic acid20.1714.1C15H22O2 234
6-Isopropenyl-4,8a-dimethyl-1,2,3,5,6,7,8,8a-octahydronaphthalen-2-ol19.469.9C15H24O220
VO3,3,8,8-Tetramethyltricyclo[5.1.0.0(2,4)]oct-5-ene-5-propanoic acid20.150.7C15H22O2 234
6-Isopropenyl-4,8a-dimethyl-1,2,3,5,6,7,8,8a-octahydronaphthalen-2-ol19.4717.1C15H24O220
2-(4a,8-Dimethyl-1,2,3,4,4a,5,6,7-octahydro-naphthalen-2-yl)-prop-2-en-1-ol(the sesquiterpene alcohol γ-costol)19.9510.5C15H24O220

[i] a2-mon VRE = vetiver root ethanol extracts from greenhouse-grown, 2-mon-old cv. Sierra; 1-yr VRE = vetiver root ethanol extracts from field-grown, 1-yr-old cv. Songkha 3; 4-yr VRE = vetiver root ethanol extracts from greenhouse-grown, 4-yr-old cv. Sierra; VO = commercial vetiver oil.

[ii] bThe components were identified based on the NIST mass spectra library.cRepresents highest area peak of a given compound, and does not include any further isomers.

DOI: https://doi.org/10.21307/jofnem-2018-008 | Journal eISSN: 2640-396X | Journal ISSN: 0022-300X
Language: English
Page range: 147 - 162
Published online: Jun 3, 2018
Published in print: Jan 1, 2018
Published by: Society of Nematologists, Inc.
In partnership with: Paradigm Publishing Services
Publication frequency: 1 issue per year

© 2018 Kansiree Jindapunnapat, Nathan D. Reetz, Margaret H. MacDonald, Ganga Bhagavathy, Buncha Chinnasri, Noppamas Soonthornchareonnon, Anongnuch Sasnarukkit, Kamlesh R. Chauhan, David J. Chitwood, Susan L.F. Meyer, published by Society of Nematologists, Inc.
This work is licensed under the Creative Commons Attribution 4.0 License.