Acaricidal activities of whole cell suspension, cell-free supernatant, and crude cell extract of Xenorhabdus stokiae against mushroom mite (Luciaphorus sp.)

Acaricidal activities of whole cell suspension, cell-free supernatant, and crude cell extract of Xenorhabdus stokiae against mushroom mite ( Luciaphorus sp.) 1 first-author 1 1 2 corresp ‡Corresponding Author ‡Corresponding Author †E-mail:agramc@ku.ac.th †E-mail:agramc@ku.ac.th agramc@ku.ac.th Biocontrol Research Unit, Department of Biotechnology, Mahasarakham University, Maha Sarakham 44150, Thailand Biocontrol Research Unit, Department of Biotechnology, Mahasarakham University, Maha Sarakham 44150, Thailand Department of Entomology, Kasetsart University, Chatuchak, Bangkok 10900, Thailand Department of Entomology, Kasetsart University, Chatuchak, Bangkok 10900, Thailand Xenorhabdus bacterium has been used as a biological control agent against Luciaphorus sp., a mushroom mite endemic in Thailand. To develop an effective formulation of Xenorhabdus stokiae , treatments using different parts of X. stokiae isolate PB09 culture, including whole cell suspension, cell-free supernatant, and crude cell extract, were performed. The results show that different parts of X. stokiae isolate PB09 culture could induce variable effects on mite mortality and fecundity. Application with cell-free supernatant of X. stokiae culture resulted in both the highest mite mortality rate [(89.00±3.60)%] and the lowest mite fecundity [(41.33±23.69) eggs/gravid female] . Whole cell suspension of X. stokiae isolate PB09 culture was found to be slightly less effective than its cell-free supernatant, suggesting that X. stokiae was more likely to release its metabolites with acaricidal activities to the surrounding culture media. Crude cell extract of X. stokiae was not effective against mites. Cell-free supernatant of X. stokiae isolate PB09 was the most effective biological control agent and it could be conveniently used in future formulations instead of live bacteria. Xenorhabdus Luciaphorus Whole cell suspension Cell-free supernatant Crude cell extract Mushroom mite Introduction 1 Luciaphorus sp. (Acari: Pygmephoridae) is a mushroom mite that has become one of the major threats to the large-scale cultivations of several mushroom species, including Lentinus squarrosulus (Mont.) Singer, Lentinus polychrous Lev., Auricularia auricula-judae (Bull.) Wettst., and Flammulina velutipes Karst. (Bussaman et al., 2004 2004 ). The use of insecticides, such as carbamates and organophosphates, to control this mushroom mite has had little success, and growers can only manage this pest by maintaining the recommended routine horticultural hygiene procedures (Bussaman et al., 2009 2009 ). Biological agents, so-called biocontrol agents, for controlling agricultural pests have been widely used for several years. This is partly due to the strict governmental regulations for the use of hazardous chemicals, as these chemicals can remain protractedly in the food chain (Bro-Rasmussen, 1996 1996 ). The entomopathogenic nematodes of the genera Steinernema and Heterorhabditis have been found to cause the death of several important agricultural insect pests (Chongchitmate et al., 2005 2005 ; Grewal et al., 2005 2005 ). In addition, the bacteria Xenorhabdus sp. and Photorhabdus sp., living symbiotically in the specialized intestinal vesicles of Steinernema and midgut of the intestines of Heterorhabditis nematodes, respectively, are known to contribute to nematodes’ pathogenicity (Gaugler, 2002 2002 ). After the nematodes (in infective juvenile stage) enter the host insects through natural insect openings, the bacteria are released from nematodes’ intestine and enter the host insect haemolymph system. The bacteria then start to replicate rapidly and cause septicemia and cellular apoptosis, leading to death of the host insect (Cho and Kim, 2004 2004 ; Campos-Herrera et al., 2009 2009 ). Both Xenorhabdus and Photorhabdus bacteria have been shown to grow successfully under laboratory conditions, and both cell suspensions and cell-free supernatants of these bacteria have been found to cause adverse effect and cause the death of several insect pests, such as desert locust [ Schistocerca gregaria (Forskål)] (Mahar et al., 2004 2004 ), red flour beetle [ Tribolium castaneum (Herbst)] (Shrestha and Kim, 2010 2010 ), wax moth [ Galleria mellonella (L.)], beet armyworm [ Spodoptera exigua (Hübner)], diamondback moth [ Plutella xylostella (L.)], cotton leafworm moth [ Spodoptera littoralis (Boisduval)] (Campos-Herrera et al., 2009 2009 ), and black vine weevil [ Otiorhynchus sulcatus Germar] (Mahar et al., 2008 2008 ). Hence, these bacteria secrete their metabolic products that are toxic or immunosuppressive to the host insects (Bowen et al., 2000 2000 ; Sharma et al., 2002 2002 ; Mahar et al., 2004 2004 ; 2008 2008 ; Bode, 2009 2009 ; Brivio et al., 2010 2010 ). Moreover, Xenorhabdus sp. and Photorhabdus sp. have been used for controlling Luciaphorus sp., a mushroom mite that has been known to damage several mushroom species (Bussaman et al., 2006 2006 ; 2009 2009 ). Herein, this study was aimed to determine the acaricidal activity of Xenorhabdus stokiae isolate PB09 against a mushroom mite ( Luciaphorus sp.). Materials and methods 1 Bacteria, mushroom culture, and mites 2 X . stokiae isolate PB09 was isolated from surface-sterilized infective juveniles of Steinernema siamkayai nematode obtained from the Department of Agriculture, Ministry of Agriculture and Cooperatives Thailand, using a method previously described (Kaya and Stock, 1997 1997 ). A nutrient bromothymol blue triphenyltetrazolium chloride agar (NBTA) medium, consisting of 37 g nutrient agar (Criterion, USA), 25 mg bromothymol blue powder (Lab-Chem, UK), 4 ml of 0.01 g/ml 2,3,5-triphenyltetrazolium chloride (Sigma-Aldrich, USA), and 1 000 ml distilled water, was used to select the genus Xenorhabdus (Lacey, 1997 1997 ). The bacteria were spread onto NBTA plates, and the plates were sealed and incubated in the dark at 28 °C for 24 h. These bacteria were found to form blue colonies on NBTA agar (indicated Phase I stage) (Stock et al., 1998 1998 ; Grewal et al., 2005 2005 ) and the colonies were selected and sub-cultured to acquire colonies with uniform characteristics. The selected colonies were individually grown in 25 ml of Luria-Bertani (LB) broth (Sigma-Aldrich, USA) and placed in the incubator shaker (200 r/min) at 28 °C for 48 h under complete darkness (Lacey, 1997 1997 ). The concentration of whole bacterial cell suspension was determined by the plate-count technique (Klement et al., 1990 1990 ) and adjusted to 10 8 colony-forming units per ml (CFU/ml) using sterile 1 g/L peptone solution. To obtain cell-free supernatant, cell suspension was centrifuged at 2 500× g and 4 °C for 5 min and filtered using a 0.22-μm filter. The resulting bacterial pellets were collected and used for extraction of crude cell extract. A total of 10 ml of LB broth was added to 0.1 g (approximately 10 9 cells) of bacterial pellets and then placed in a sonicator at 4 °C for 5 min to break the cells before centrifugation at 2 500× g and 4 °C for 5 min, to collect crude cell extract at the top of solution. Lentinus squarrosulus , obtained from the Mushroom Researchers and Growers Society of Thailand, was grown on a mixture of sawdust and sorghum grain to establish a fresh spawn (Bussaman et al., 2009 2009 ). Mushroom mycelia were then inoculated to potato dextrose agar (PDA, Sigma-Aldrich, USA) plates and incubated at 25 °C in the dark for further experiments. Luciaphorus mites were collected from infested L. squarrosulus basidiocarps obtained from the Rapeephan mushroom farm in Khon Kaen Province, northeast Thailand. A fresh L. squarrosulus spawn in a glass bottle was used to maintain a pair of male and female mites at 28 °C for reproduction. These in-house bred mites were used for all of the experiments. Effects of X. stokiae isolate PB09 on mortality of Luciaphorus sp. 2 Acaricidal activities of X. stokiae isolate PB09 were investigated using 50-mm plastic Petri-dish plates containing L. squarrosulus mycelia grown on PDA, as previously described by Bussaman et al. ( 2009 2009 ). One hundred adult Luciaphorus female mites (1 d old) were transferred to each of these 50-mm plastic Petri-dish plates. A total of 500 µl of bacterial whole cell suspension (1×10 8 CFU/ml), cell-free supernatant, or crude cell extract was then sprayed onto the L. squarrosulus mycelia and mushroom mites. The same volumes of LB broth and propargite (a commercial acaricide) at the concentration of 0.04% were used as negative and positive control groups, respectively (four replications/treatment). All plates were covered with lids and placed in a growth chamber at 28 °C and 80% relative humidity in complete darkness. Mite mortality was monitored every 24 h for five consecutive days after treatment. The experiment was repeated twice. Effects of X. stokiae isolate PB09 on progeny production of Luciaphorus sp. 2 The bacterial cell suspension (1×10 8 CFU/ml), cell-free supernatant, and crude cell extract were tested against Luciaphorus mites as described above (four replications/treatment). All plates were covered and placed in a growth chamber at 28 °C and 80% relative humidity in the dark. Five days after the treatment, all living pregnant females were excised using sterile needle and number of eggs/gravid female and the gender of progeny mites were recorded. The experiment was repeated twice. Statistical analysis 2 The data on the percentage of mite mortality were arcsine transformed before analysis. A general linear-model procedure [one-way analysis of variance (ANOVA), SAS Institute, Cary, NC, USA] was used to perform analysis of the treatments. Significant differences between means of the treatment were determined using the least significant difference (LSD) test at P ≤0.05. Results 1 Effects of X. stokiae isolate PB09 on mortality of Luciaphorus sp. 2 Different parts of X. stokiae isolate PB09 culture were found to induce mortality of Luciaphorus mite at different levels (Table 1 1 ). For all the bacterial treatments, the percentages of mite mortality reached a maximum on Day 3 post-treatment and remained unchanged thereafter. Cell-free supernatant of X. stokiae isolate PB09 caused the highest mortality of mites up to (89.00±3.60)%, which was not significantly different from that caused by whole cell suspension [(81.66±2.88)%] . Crude cell extract of X. stokiae isolate PB09 induced mite mortality [(30.00±5.77)%] to a level significantly lower than cell-free supernatant, whole cell suspension, and propargite. No dead mites were observed after application with LB broth. Data are expressed as mean±standard deviation (SD). Means within the same column followed by the same lower case letters are not significantly different ( P (0.05) as compared by LSD test; Means within the same row followed by the same upper case letters are not significantly different ( P (0.05) as compared by LSD test Propargite is a commercial acaricide 2 Treatment 5 Mite mortality (%) Day 1 Day 2 Day 3 Day 4 Day 5 Whole cell suspension 42.66±6.80 cB 58.33±16.07 bA 81.66±2.88 bA 81.66±2.88 bA 81.66±2.88 bA Cell-free supernatant 55.00±5.00 bA 71.66±7.63 bA 89.00±3.60 bA 89.00±3.60 bA 89.00±3.60 bA Crude cell extract 23.00±5.77 dA 28.00±0.00 cA 30.00±5.77 cA 30.00±5.77 cA 30.00±5.77 cA Propargite * * 100.00±0.00 aA 100.00±0.00 aA 100.00±0.00 aA 100.00±0.00 aA 100.00±0.00 aA LB broth 0.00±0.00 eA 0.00±0.00 dA 0.00±0.00 dA 0.00±0.00 dA 0.00±0.00 dA Effects of X. stokiae isolate PB09 on progeny production of Luciaphorus sp. 2 The reproduction of Luciaphorus mite was found to decline after application with X. stokiae isolate PB09 (Table 2 2 ). Both cell-free supernatant and whole cell suspension of X. stokiae isolate PB09 significantly reduced mite fecundity, accounting for (41.33±23.69) and (192.67±11.01) eggs/female, respectively, when compared to the treatment with LB broth [(256.00±19.69) eggs/female]. Furthermore, cell-free supernatant could reduce the number of eggs/female to a level significantly lower than whole cell suspension. In addition, the male:female ratios of mite progeny showed that the number of female offspring was much reduced by applications with cell-free supernatant and whole cell suspension, accounting for 1:4.63 and 1:8.17 male:female, respectively. In contrast, crude cell extract of X. stokiae isolate PB09 showed no effect on mite fecundity [(228.00±23.06) eggs/female] or male:female ratio (1:16.53), similar to LB broth [(256.00±19.69) eggs/female and 1:16.06, respectively] . Also, no mushroom mites were found to survive after propargite application; hence, no fecundity was recorded. Data are expressed as mean±SD. Means within the same column followed by the same letters are not significantly different ( P (0.05) as compared by LSD test Propargite is a commercial acaricide 2 Treatment 2 Fecundity # # (egg/female) 2 Egg hatching # # 2 Male:female ratio Male Female Whole cell suspension 192.67±11.01 b 21.00±6.55 a 171.66±12.58 c 1:8.17 Cell-free supernatant 41.33±23.69 c 7.33±2.31 cd 34.00±7.54 d 1:4.63 Crude cell extract 228.00±23.06 a 13.00±3.46 bc 215.00±13.23 b 1:16.53 Propargite * * 0.00±0.00 d 0.00±0.00 d 0.00±0.00 e 0:0.00 LB broth 256.00±19.69 a 15.00±5.00 ab 241.00±8.54 a 1:16.06 Discussion 1 Different parts of X. stokiae isolate PB09 culture, particularly cell-free supernatant and whole cell suspension, demonstrated harmful effects on Luciaphorus mortality and fecundity. The mite mortality rate caused by whole cell suspension of X. stokiae isolate PB09 in this study was similar to that of Xenorhabdus sp. X1 previously published (Bussaman et al., 2009 2009 ). Also, a decrease of fecundity caused by whole cell suspension of X. stokiae isolate PB09 in this study was equivalent to that in a previous report (Bussaman et al., 2009 2009 ). These results may indicate that whole cell suspension of X. stokiae isolate PB09 in the current study is as effective as the previous one. These high mortality rates caused by X. stokiae isolate PB09 suggest that X. stokiae can transmit horizontally (most likely by direct contact) between infected mites that come in contact with uninfected ones. Moreover, the decrease of fecundity and the changes in sex ratios of mites caused by X. stokiae isolate PB09 infection may indicate vertical transmission of X. stokiae between pregnant females and their offspring, resulting in sexual bias of their offspring. There are some reports of other microorganisms that have produced similar effects on mites, such as Microsporidium phytoseiuli against Phytoseiulus persimilis Athias-Henriot and Wolbachia bacteria against Tetranychus urticae (Koch) (Bjørnson and Keddie, 2001 2001 ; Vala et al., 2004 2004 ). However, more experiments are required to verify the effects of X. stokiae isolate PB09 on Luciaphorus mites. Cell-free supernatant of X. stokiae isolate PB09 in this study was shown to induce both higher mite mortality and lower mite fecundity than the whole cell suspension. This may suggest that metabolites with insecticidal properties that were produced by X. stokiae isolate PB09 are more likely to be secreted to culture supernatant. Mahar et al. ( 2005 2005 ) also found that X. nematophila cell-free metabolites required 4 d to kill 95% G. mellonella larvae whereas cell suspension needed up to 6 d to induce 93% mortality. There are several reports indicated that Xenorhabdus sp. could produce and secrete several secondary metabolites with effective bioactivities such as benzylideneacetone (antibacterial compound), iodinine, phenethylamides, indole derivatives, xenorhabdins, xenorxides, and xenocoumacins (antibiotics), and primary metabolites, such as alkaline protease (Morgan et al., 2001 2001 ; Caldas et al., 2002 2002 ; Ji et al., 2004 2004 ; Mohamed, 2007 2007 ; Bode, 2009 2009 ), whereby all of which are suggested to play roles as insecticidal and immunosuppressive compounds. In contrast, crude cell extract of X. stokiae isolate PB09 had very little effect on mite mortality or fecundity. This is probably due to the loss of important metabolites of bacterial crude cell extract during the extraction process, or they have simply never been present. Conclusions 1 In conclusion, different parts of X. stokiae isolate PB09 culture produced different effects on Luciaphorus mortality and fecundity. 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(Rhabditida: Steinernematidae), an entomopathogenic nematode from Thailand F Vala , M Egas , MW Sabelis . Wolbachia affects oviposition and mating behavior of its spider mite host . J Evol Biol , 2004 . 17 ( 3 ): 692 - 700 . 15149411 DOI: 10.1046/j.1420-9101.2003.00679.x http://doi.org/10.1046/j.1420-9101.2003.00679.x . Wolbachia affects oviposition and mating behavior of its spider mite host Our gratitude goes to Prof. Sunha PANICHAJAYAKUL, the owner of the Rapeephan mushroom farm, for providing the mushroom mites, and Mrs. Vatcharee SOMSOOK of Department of Agriculture, Thailand for providing entomopathogenic nematodes for this study. 10.1631/jzus.B1100155 Project (No. RTA 4880006) supported by the Thailand Research Fund, Kasetsart University and Mahasarakham University 2011-05-15 2012-02-29 2011-09-29 2022-01-05 Copyright © Zhejiang University and Springer-Verlag Berlin Heidelberg 2012 2012 Journal of Zhejiang University-SCIENCE B (Biomedicine and Biotechnology) 04 13