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. 2003 Apr;69(4):1890–1897. doi: 10.1128/AEM.69.4.1890-1897.2003

TABLE 2.

Induction of DJ nematode release of GFP-labeled P. luminescens

Sample Treatment Release activitya
Mean % SD (%) n
M. sexta larva hemolymph None 25 7 3
Incubated at 68°C for 15 min 25 8 2
Pronase (20 μg/ml, 50°C, 2 h) 25 17 3
EDTA (25 mM) 32 2 2
Chelex (10 mg/ml) 33 0 2
Centricon 10-kDa filtrate 27 3 4
Centricon 10-kDa retentate 10 1
Melanized 33 0 2
Dialyzed (5 kDa) 0 1
Dialyzed (10 kDa) 0 1
Diluted 1/10 0 1
Levamisole (0.5 mM) 12 6 4
Ivermectin (100 μg/ml, 1% DMSO) 16 4 4
DMSO (1%, vol/vol) 33 1
Kanamycin (30 μg/ml) 23 3 2
Other arthropod hemolymph
    G. mellonella larvae 42 2 2
    T. molitor larvae 47 5 2
    D. melanogaster larvae 30 1
    Freshwater crab 37 14 2
    A. domestica (feeder cricket) 36 7 2
    Blaberus sp. (tropical cockroach) 55 2 2
    L. alienus Foerster (Ant) 25 2 2
Insect cell culture supernatants
    A. gambiae 4a-3B 31 17 2
    T. ni TN368 24 4 2
    T. ni TNH15 21 2 2
    S. frugiperda SF21 17 3 2
    D. melonogaster DL-1 20 4 2
Nonarthropod fluids
    Fresh human blood 2 1 2
    Culture of P. luminescens NC1/1 3 0 2
    Peptone broth 3 0 2
    Grace's insect cell culture medium 5 4 4
    Schneider's insect cell culture medium + 10% FBS 9 2 2
    Water 3 0 2
a

Percentage of DJ nematodes containing GFP-labeled P. luminescens cells that released bacteria 60 min after incubation. The mean percentage, SD, and number of independent experiments (n) where at least 30 DJ nematodes containing GFP-labeled bacteria were observed are shown.