2013
DOI: 10.5897/ajmr2013.6206
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Evaluation of Stropharia sp. 1.2052 nematicidal effects against Meloidogyne incognita on tomato

Abstract: To use unique nematicidal mechanism of Stropharia, the strain 1.2052 was evaluated for its potential to control the root-knot nematode Meloidogyne incognita on tomato. In vitro, the inhibition rate in 24 h of Stropharia sp. 1.2052 isolate was 100% for second-stage juveniles of M. incognita and Panagrellus redivivus, 41.81% for Caenorhabiditis elegans and 99.25% for Bursaphelenchus xylophilus, respectively. In pot experiments, isolate 1.2052 reduced the root-knots to 68.16 to 84.19% in one month and 45.28 to 88… Show more

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Cited by 10 publications
(7 citation statements)
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“…The root-knot nematode M. incognita juveniles (J2s) were collected from pure culture reared on cotton Gossypium barbadense (Gallini) variety (Delta Pin61) at nematode laboratory of the Entomology and Zoology Department, Faculty of Agriculture , Menoufia University; cotton roots were washed with the egg masses in the water to clean it from the soil sticking to the roots, then the roots cutting to pieces of (1 cm) long and stirred in sodium hypochlorite (0.5%) for 3 minutes and shake well in sterile water (Kerry and Bourne, 2002). Nematode eggs were incubated at 25 ± 1°C for 3 to 4 days to obtain second stage juveniles (J2) with modified Baermann funnel method (Gray, 1984) and used in the experimental infection procedure according to Chuixu et al, 2013.…”
Section: Nematode Culturementioning
confidence: 99%
“…The root-knot nematode M. incognita juveniles (J2s) were collected from pure culture reared on cotton Gossypium barbadense (Gallini) variety (Delta Pin61) at nematode laboratory of the Entomology and Zoology Department, Faculty of Agriculture , Menoufia University; cotton roots were washed with the egg masses in the water to clean it from the soil sticking to the roots, then the roots cutting to pieces of (1 cm) long and stirred in sodium hypochlorite (0.5%) for 3 minutes and shake well in sterile water (Kerry and Bourne, 2002). Nematode eggs were incubated at 25 ± 1°C for 3 to 4 days to obtain second stage juveniles (J2) with modified Baermann funnel method (Gray, 1984) and used in the experimental infection procedure according to Chuixu et al, 2013.…”
Section: Nematode Culturementioning
confidence: 99%
“…The cotton roots with egg masses were washed in the water to clean them from soil sticking to the roots, then the roots were cut to pieces of 1 cm long and stirred in sodium hypochlorite (0.5%) for 3 minutes and shake well in sterile water ( Kerry and Bourne, 2002) to free eggs from egg masses. Eggs were incubated at 25 ± 1°C for 3 to 4 days to obtain second stage juveniles (J2s) with the aid of modified Baermann funnel method (Gray, 1984) and used in the experimental infection procedure (Chuixu et al, 2013).…”
Section: Nematode Culturementioning
confidence: 99%
“…On the other hand, the mycelium of another EM, Stropharia sp., was also evaluated in vitro against the free-living nematode P. redivivus at different times of exposure, recording 100% mortality after 36 h exposure [20]. Similarly, Panagrellus sp.…”
Section: Activity Against Free-livingmentioning
confidence: 99%
“…Likewise, the mycelium of Stropharia sp. was assessed against juveniles of the second stage (J 2 ) of M. incognita [20]. Nematodes were exposed to the mycelia on potato dextrose agar (PDA) plates, and 100% mortality was recorded after 36 h postconfrontation.…”
Section: Activity Of Bioproducts From Edible Mushrooms Againstmentioning
confidence: 99%
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