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Suppressive Effect of Certain Bacterial Isolates of Pseudomonas fluorescens Suspensions on Root-Knot Nematode, Meloidogyne incognita

PJN_41_1_1-7

Suppressive Effect of Certain Bacterial Isolates of Pseudomonas fluorescens Suspensions on Root-Knot Nematode, Meloidogyne incognita

Ahmed E.A. Mahgoob1, Wafaa M.A. El-Nagdi2, Mahmoud M.A. Youssef2*, Entesar H. Taha1, Mona M.S. Zayed3, Hassan Abd- El-Khair4 and Nora R.A. Saleh2

1Plant Protection Department, Faculty of Agriculture Ain Shams University, P.O. Box 68, Hadayek Shoubra 11241, Cairo, Egypt; 2Department of Plant Pathology, Nematology Laboratory, National Research Centre, Dokki, 12622, Cairo, Egypt; 3Microbiology Department, Faculty of Agriculture, Ain Shams University, P.O. Box 68, Hadayek Shoubra 11241, Cairo, Egypt; 4Department of Plant Pathology, National Research Centre, Dokki, 12622, Cairo, , Egypt.

Abstract | This investigation was planned with the aim to evaluate different suspensions of certain isolates of bacterium, Pseudomonas fluorescens for their nematicidal potentials against root-knot nematode, Meloidogyne incognita under in vitro conditions. The present results indicated that the tested bacterial isolates at two concentrations (25 and 50%) significantly (p≤0.05) inhibited M. incognita- egg hatching at each exposure period (24, 48, 72 and 96 hrs) compared to untreated control. As for the percentages of the second stage juveniles mortality increased with increasing the concentrations and exposure periods. Generally, the highest egg hatching inhibition and juvenile mortality occurred after 96 and 72hrs exposure to the suspensions of the tested isolates of P. fluorescens depending upon their concentrations and exposure periods, respectively.


Received | January 21, 2023; Accepted | March 07, 2023; Published | March 31, 2023

*Correspondence | Mahmoud M. A. Youssef, Department of Plant Pathology, Nematology Laboratory, National Research Centre, Dokki, 12622, Cairo, Egypt; Email: myoussef_2003@yahoo.com

Citation | Mahgoob, A.E.A., El-Nagdi, W.M.A., Youssef, M.M.A., Taha, E.H., Zayed, M.M.S., Abd-El-Khair, H. and Saleh, N.R.A., 2023. Suppressive effect of certain bacterial isolates of Pseudomonas fluorescens suspensions on root-knot nematode, Meloidogyne incognita. Pakistan Journal of Nematology, 41(1): 1-7.

DOI | https://dx.doi.org/10.17582/journal.pjn/2023/41.1.1.7

Keywords | Suppressive effect, Bacterial isolates, Pseudomonas fluorescens, Root-knot nematode, Meloidogyne incognita

Copyright: 2023 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

Root-knot nematodes of the genus, Meloidogyne are sedentary endoparasites that induce root-knot symptoms and cause serious agricultural damage (Trudgill and Blok, 2001). Currently, various attempts have been employed to fight these pests include plant breeding, field sanitation, crop rotation, and chemicals. Although some success has been reported, the use of these methods, particularly agrochemicals, has severe limitations. Increasing interest has been directed toward nematode biological control methods by using antagonistic bacterium, Pseudomonas fluorescens isolates (Saleh et al., 2020; El-Nagdi et al., 2022) and other growth promoting rhizobacteria (Youssef et al., 2017; Abd-El-Khair et al., 2019; Abhishek-Gowda et al., 2022). Under in vitro conditions, El-Hamshary et al. (2006), when studied survival of M. incognita second stage juveniles (J2s) as affected by P. fluorescens and P. aeruginosa, they found that percentages of mortality of the J2s occurred depending upon the bacterial concentration and exposure time. Ashoub and Amara (2010) reported that several bacteria from which P. fluorescens in vitro can cause M. incognita juveniles 100% mortality after 72 hrs. Also, the highest concentration (S) of P. fluorescens was shown to cause the highest nematode mortality (100%) with net mortality (71%) after 72hr compared to other concentrations (Osman et al., 2013). Under greenhouse conditions, Saleh et al. (2020) found that P. fluorescens isolates, Pf1, Pf2, Pf9 and Pf10 were the most effective in reducing M. incognita parameters and consequently improved plant growth criteria. El-Nagdi et al. (2022) proved that the ability of these mentioned isolates to reduce M. incognita depended on the time of addition to infected plants. Yet, little work was done on the bio-efficacy of different isolates of P. fluorescens on root –knot nematode under in vitro and in vivo conditions. Therefore, this research was planned with the purpose to evaluate different isolates of P. fluorescens for their nematicidal potentials against root-knot nematode, M. incognita under in vitro conditions.

Materials and Methods

Pure culture of root-knot nematode and its identification

Root-knot nematode, Meloidogyne sp. pure culture was maintained on eggplant cv. Ice using a single egg-mass in screen house at 30±5 oC. The tested species of root-knot nematode was identified to be M. incognita from adult females based on their morphological characteristics of perineal pattern (Taylor and Sasser 1978).

Extraction of nematode eggs

Root-knot nematode, M. incognita eggs were extracted from egg-masses on infected eggplant roots as described by Hussey and Barker (1973). Then, extracted eggs were counted for bioassay.

Nematode egg hatchability bioassay

The effect of the tested 10 bacterial isolates (each contained 10-7-10-9 colony forming unit (CFU)/ml) was determined based on the number of non- hatched eggs at two concentrations (25 and 50 %) of each bacterial isolate suspension by adding distilled water. A total of 200 nematode eggs in 1 ml of distilled water was put in plastic capsule containing 9 ml suspension of each bacterial isolate in five replicates. Treatment with eggs in distilled water only with the same replicates served as untreated control. After 24, 48, 72 and 96 hr at each concentration, the numbers of non-hatched and hatched eggs were observed by light microscope. The percentages of egg hatching inhibition were calculated according to Abbott’s Formula (Finney, 1971).

Egg inhibition (%) = (m – n)/ (100 – n) × 100

As the percentages of non-hatched eggs were represented by m and n for the treatment and control, respectively.

Extraction of Meloidogyne incognita second stage juveniles (J2s)

M. incognita eggs were extracted from galled eggplant roots bearing their egg masses by washing thoroughly with tap water to avoid debris and cut into small pieces. Then, they were placed in plastic capsule containing sufficient water to help hatching and covered to avoid loss of water by evaporation. After eggs hatching, they were collected every 24 hrs and newly hatched second stage juveniles (J2s) were used for bioassay.

Nematode juvenile survival bioassay

To assess the effect of 10 bacterial isolate suspensions [9 bacterial isolates +1 standard isolate (NRC)] on J2s of M. incognita, the same procedures were carried, when a total of 200 J2s in 1 ml distilled water was added to 9 ml suspension of each bacterial isolate in 5 replicates. Check control treatment in the same number of replicates served as comparison. The percentages of mortality of dead and live juveniles per each treatment were calculated after 24, 48 and 72 hrs following to Abbott’s Formula (Finney, 1971) as follows:

Juvenile mortality (%) = (m – n)/ (100 – n) × 100

As the percentages of dead juveniles in the treatment and control were represented by m and n, respectively.

Source of Pseudomonas fluorescens isolates

Soil samples, each of an aliquot of 200g were gathered from the eggplant, pepper and tomato rhizospheres. The collective samples were root-knot nematode-free. Then, they were transported to Plant Pathology Department (PPD), National Research Centre (NRC) to isolate and identify bacterial isolates.

Isolation and identification of Pseudomonas fluorescens

The total plate counts technique and dilution method were used to isolate P. fluorescens, as described by Ghini et al. (2007), Schaad (1980); Lelliot and Stead (1987) and Goszczynska et al. (2000). Bacterial inoculum for each isolate was justified to 107-109 colony forming unit (CFU)/ml by turbidity method (Baid et al., 2000). Nine P. fluorescens isolates were isolated and identified as reported by Saleh et al. (2020). Bacterial inoculum for each isolate was used as bacterial cells and cultural filtrate mixture.

Source of standard Pseudomonas fluorescens isolate

One standard P. fluorescens Pf10 (NRC isolate) was obtained from PPD, NRC. The inoculum of this isolate was prepared as mentioned before and used.

Statistical procedures

Analysis of the current data was done by using Duncan’s Multiple Range Test for separation the means of treatments (Duncan, 1955). ANOVA test was also used at p≤0.05 to prove the significance of the data (Gomez and Gomez, 1984). This was done by Computer Statistical (COSTAT) software.

 

Table 1: Mean numbers of non- hatched eggs of root- knot nematode, Meloidogyne incognita as influenced by certain isolates of Pseudomonas fluorescens at 25% concentrations after 24, 48, 72 and 96 hrs of exposure.

Treatments

Exposure period (hr)

24

48

72

96

No. of

Non-hatched eggs

Non-hatched eggs

Non-hatched eggs

Non-hatched eggs

Control water +eggs

200a

200a

164a

140b

Pf1+Eggs

200a

200a

167a

143ab

Pf2+Eggs

200a

200a

167a

167ab

Pf3+Eggs

200a

200a

173a

147ab

Pf4+Eggs

200a

200a

171a

165ab

Pf5+Eggs

200a

200a

180a

163ab

Pf6+Eggs

200a

200a

156a

147ab

Pf7+Eggs

200a

200a

177a

171ab

Pf8+Eggs

200a

200a

170a

143ab

Pf9+Eggs

200a

200a

184a

177a

 

-Values are means of 5 replicates. Means followed by the same letter(s) are not significantly (p ≤ 0.05) different according to Duncan’s Multiple Range Test.

 

Results and Discussion

Effect of Pseudomonas fluorescens on egg hatchability of root-knot nematode, Meloidogyne incognita.

The tested bacterial isolates of P. fluorescens at two concentrations (25 and 50%) significantly (p≤0.05) inhibited M. incognita egg hatching at each exposure time compared to that of untreated control as shown in Tables 1 and 2. Generally, In Table 3, egg hatching occurred at 72 and 96 hrs. But after 24 and 48 hrs, no egg hatching occurred. By using 25% concentration, it was noticed that Pf9 recorded the highest percentage of egg inhibition (55.6%) after 72 hrs followed by Pf5 (44.4%) and increased to 61.7 and 70.0% at 96 hrs, respectively. At 50%, the highest percentages of egg inhibition (83.3 and 72.2%) were achieved after 72hr by Pf9 and Pf7, but they decreased to 70 and 58.3%, after 96hr, respectively.

 

Table 2: Mean numbers of non-hatched eggs of root-knot nematode, Meloidogyne incognita as influenced by certain isolates of Pseudomonas fluorescens at concentrations of 50% after 24, 48, 72 and 96 hrs of exposure.

Treatments

Exposure period (hr)

24

48

72

96

No. of

Non-hatched

eggs

Non-hatched

eggs

Non-hatched

eggs

Non-hatched

eggs

Control (eggs + water)

200a

200a

164b

140d

Pf1+Eggs

200a

200a

177ab

168a-c

Pf2 +Eggs

200a

200a

177ab

175a-c

Pf3+Eggs

200a

200a

175ab

167a-c

Pf4+Eggs

200a

200a

173ab

167a-c

Pf5+Eggs

200a

200a

182ab

181a

Pf6+Eggs

200a

200a

177ab

152cd

Pf7+Eggs

200a

200a

190a

175a-c

Pf8+Eggs

200a

200a

182ab

156b-d

Pf9+Eggs

200a

200a

194a

182a

 

-Values are means of 5 replicates. Means followed by same letter(s) are not significantly (p ≤ 0.05) different according to Duncan’s Multiple Range Test.

 

Effect of Pf isolates on nematode juvenile’s mortality

Data in Tables 4, 5 and 6 showed the mean numbers of M. incognita, when treated with different 10 bacterial isolate suspensions of P. fluorescens at 25% and 50% concentrations after different durations (24, 48 and 72 hrs). The results indicated that, the number of dead J2s significantly (p≤0.05) increased with increasing the concentrations of the tested isolates and exposure periods. Table 7 illustrated the mortality percent of

 

Table 3: Egg inhibition % of root-knot nematode, Meloidogyne incognita as influenced by certain isolates of Pseudomonas fluorescens at 25 and 50% concentrations after 24, 48, 72 and 96 hrs of exposure.

Treatments

Egg inhibition% at 25% concentration

Exposure period (hr)

24

48

72

96

Control (water+eggs)

0.0

0.0

٠.0

0.0

Pf1+eggs

0.0

0.0

8.3

5.0

Pf2+eggs

0.0

0.0

8.3

45.0

Pf3+eggs

0.0

0.0

25.0

45.0

Pf4+eggs

0.0

0.0

19.4

41.7

Pf5+eggs

0.0

0.0

44.4

70.0

Pf6+eggs

0.0

0.0

0.0

11.7

Pf7+eggs

0.0

0.0

36.1

51.7

Pf8+eggs

0.0

0.0

16.7

5.0

Pf9+eggs

0.0

0.0

55.6

61.7

% Egg inhibition at 50%

Control (water+eggs)

0.0

0.0

0.0

0.0

Pf1+eggs

0.0

0.0

36.1

46.7

Pf2+eggs

0.0

0.0

36.1

58.3

Pf3+eggs

0.0

0.0

30.5

45.0

Pf4+eggs

0.0

0.0

25.0

45.0

Pf5+eggs

0.0

0.0

50.0

68.3

Pf6+eggs

0.0

0.0

36.1

20.0

Pf7+eggs

0.0

0.0

72.2

58.3

Pf8+eggs

0.0

0.0

50.0

26.7

Pf9+eggs

0.0

0.0

83.3

70.0

 

Table 4: Mean numbers of root-knot nematode, Meloidogyne incognita juveniles (J2s) as affected by certain isolates of Pseudomonas fluorescens at 25 and 50% concentrations, after 24hr of exposure.

Treatments

After 24 hrs exposure

25%

50%

No. of

Live J2s

Dead J2s

Live J2s

Dead J2s

Control (water + J2s)

170a

30d

170a

30g

Pf1+ J2s

60bc

140b-d

10efg

190a-c

Pf2+ J2s

87b

113c

37c-e

163c-e

Pf3+ J2s

Pf4+ J2s

40b-d

163a

160a-c

37d

33c-f

140b

167b-e

60f

Pf5+ J2s

17cd

183ab

3g

197a

Pf6+ J2s

20cd

180ab

17d-f

183a-d

Pf7+ J2s

7d

193a

7fg

193ab

Pf8+ J2s

43b-d

157a-c

30d-g

170a-d

Pf9+ J2s

47b-d

153a-c

43cd

157de

Pf10 (standard) + J2s

60bc

140b-d

30d-g

170a-d

 

-Values are means of 5 replicates. Means followed by same letter(s) are not significantly (p ≤ 0.05) different according to Duncan’s Multiple Range Test.

 

Table 5: Mean numbers of root-knot nematode, Meloidogyne incognita juveniles (J2s) as affected by certain isolates of Pseudomonas fluorescens at 25 and 50% concentrations, after 48hr of exposure.

Treatments

After 48hrs exposure

25%

50%

No. of

Live J2s

Dead J2s

Live J2s

Dead J2s

Control (water + J2s)

140a

60c

140a

60b

Pf1+ J2s

0c

200a

0b

200a

Pf2+ J2s

0c

200a

0b

200a

Pf3+ J2s

0c

200a

0b

200a

Pf4+ J2s

77b

123b

0b

200a

Pf5+ J2s

10c

190a

0b

200a

Pf6+ J2s

0c

200a

0b

200a

Pf7+ J2s

0c

200a

0b

200a

Pf8+ J2s

0c

200a

0b

200a

Pf9+ J2s

0c

200a

0b

200a

Pf10(standard) + J2s

0c

200a

0b

200a

 

-Values are means of 5 replicates. Means followed by same letter(s) are not significantly (p ≤ 0.05) different according to Duncan’s Multiple Range Test.

 

Table 6: Mean numbers of root-knot nematode, Meloidogyne incognita juveniles (J2s) as affected by certain isolates of Pseudomonas fluorescens at 50 and 25% concentrations after 72hr exposure.

Treatments

After 72hrs exposure

25%

50%

No. of

Live J2s

Dead J2s

Live J2s

Dead J2s

Control (Water + J2s)

140a

60b

140a

60b

Pf1+ J2s

0b

200a

0b

200a

Pf2+ J2s

0b

200a

0b

200a

Pf3+ J2s

0b

200a

0b

200a

Pf4+ J2s

0b

200a

0b

200a

Pf5+ J2s

0b

200a

0b

200a

Pf6+ J2s

0b

200a

0b

200a

Pf7+ J2s

0b

200a

0b

200a

Pf8+ J2s

0b

200a

0b

200a

Pf9+ J2s

0b

200a

0b

200a

Pf10(standard) + J2s

0b

200a

0b

200a

 

-Values are means of 5 replicates. Means followed by same letter(s) are not significantly (p ≤ 0.05) different according to Duncan’s Multiple Range Test.

 

M. incognita J2s. Generally, their mortality percent was increased by increasing concentration and exposure time. By using the concentration of 25%, Pf7 induced the highest percentage mortality (95.9%) after exposure time of 24 hrs and reached 100% after 48 and 72 hrs, followed by 90.0% occurred by Pf5 which reached 92.2% after 48 hrs, then 100% after 72 hrs. At 50%, the highest percentage nematode mortality (98.2%) was achieved by using Pf5 after 24 hrs followed by 95.9, 94.1 and 90.0% caused by Pf7, Pf1 and Pf9 at the same period, respectively. However, at 48 and 72 hrs all bacterial treatments caused full mortality of J2s.

 

Table 7: Mortality % of root-knot nematode, Meloidogyne incognita juveniles (J2s) as affected by certain isolates of Pseudomonas fluorescens at 25 and 50% concentrations, after 24, 48 and 72hrs of exposure.

Treatments

Exposure period (hr)

Mortality% at 25%

Mortality% at 50%

24

48

72

24

48

72

Control (Water+J2s)

0

0

0

0

0

0

Pf1+ J2s

64.7

100.0

100

94.7

100

100

Pf2+ J2s

48.8

100.0

100

78.2

100

100

Pf3+ J2s

76.5

100.0

100

80.6

100

100

Pf4+ J2s

4.10

45.0

100

17.6

100

100

Pf5+ J2s

90.0

92.9

100

98.2

100

100

Pf6+ J2s

72.4

100.0

100

74.7

100

100

Pf7+ J2s

95.9

100.0

100

95.9

100

100

Pf8+ J2s

74.4

100.0

100

82.4

100

100

Pf9+ J2s

88.2

100.0

100

90.0

100

100

Pf10 (standard)+J2s

64.7

100.0

100

82.4

100

100

 

Certain genera, species and isolates of bacteria were reported to be highly toxic to nematodes showing the most lethal activity (Ashoub and Amara, 2010; Mokbel and Alharbi, 2014; Elkelany et al., 2020; Mohamed et al., 2021). In the present study, there was great inhibition of egg hatching to J2s, when fresh eggs of M. incognita were exposed to the tested isolates of P. fluorescens suspensions at various concentrations and different periods. The most obvious egg inhibition was caused by Pf9 and Pf5 at 25% after 96hr and by Pf9 and Pf7 at 50% after 72hr. The inability of the eggs to hatch is due to absorption or ingress of bacterial toxic suspensions into the eggs. The mobility of juveniles inside eggs is reduced and finally leading up to death or moribund state. As a result, these juveniles cannot penetrate through the egg shell with their stylet, and hatching will be ceased as shown by El-Gayed et al. (2017). This was emphasized by Hirschmann (1985) who stated that, the egg-mass which is found in posterior region of the nematode female in root-knot allows absorbing the active toxic ingredient secreted by bacterial isolates in the extracts.

As for bioassay of different P. fluorescens isolate suspensions on the newly hatched second stage juveniles of M. incognita in vitro; a great differentiation in nematicidal effects of these isolates on J2s of M. incognita was achieved in the recent study. All isolates of P. fluorescens scored 100% mortality at 72 hrs. This result was consistent to those obtained by Ashoub and Amara (2010) and Osman et al. (2013). Also, the best effective isolates in reducing J2s were Pf7, Pf5 and Pf9 at all exposure times at 25% concentration. At 50% concentration, the most effective isolates were Pf5, Pf7, Pf1 and Pf9 in a descending order for their lethal effects. Hence, it was demonstrated the potentiality of all of the tested bacterial isolates to kill and immobilize J2s of M. incognita at different degrees. This variation may be due to different modes of action of the isolates. In this trend, Tian et al. (2007) showed that certain natural bacterial antagonists of nematode pests can reduce nematodes by producing toxins, antibiotics or enzymes; causing direct inhibition of nematodes. Accordingly, Kerry (2000) explained that, rhizospheric bacteria can act by more mechanisms such as direct effect by production of toxins, enzymes and other secondary metabolites.

Conclusions and Recommendations

There was great inhibition in egg hatching of root-knot nematode to juveniles, when laid eggs of M. incognita were exposed to the tested isolates of P. fluorescens suspensions at various concentrations and exposure periods in vitro. Also, P. fluorescens isolates, when added on newly hatched juveniles of M. incognita in vitro, exhibited a great variation in their nematicidal effects on J2s of M. incognita. Some isolates were more efficient in reducing egg hatchability and juvenile’s mortality than others. More studies on the promising bacterial isolates for reducing root-knot nematodes and their role in integrated pest management under greenhouse and field conditions are needed.

Novelty Statement

The current study indicated that certain isolates of the antagonistic bacterium, P. fluorescens have nematicidal potentials, when used at different concentrations and exposure periods on root-knot nematode, M. incognita egg hatching and juveniles’ mortality. These bacterial isolates proved to be acted as a biocontrol agent within sustainable pest management.

Author’s Contribution

AEAM, WMAEN and MMAY supervised this work, design, writing and execution of this manuscript. EHT and MMSZ supervised the work, provided the facilities during this work and reviewed the manuscript. HAEK isolated and identified the tested bacterial isolates and NRAS carried out the experiment and examined it in the laboratory. All authors read and approved the final manuscript,

Conflict of interest

The authors have declared no conflict of interest.

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Pakistan Journal of Nematology

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Pakistan Journal of Nematology, Vol. 42, Iss. 1, Pages 1-87

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