
Received: 2006-11- 24, Accepted: 2003-03-01
* Foundation itims: The 863 projects (2006AA10A210) from MOST.
** Corresponding author. Tel: +86-27-871981, E-mail: sunx1@wh.iov.cnSUN et al. Recent Advances in Biological Control of Pest Insects by Using Viruses in China 159
Table 1. Viruses authorized as commercial insecticide in China
Virus name Target insects Crops No. of producers Helicoverpa armigera NPV Cotton bollworm Cotton, pepper, tobacco 12
Spodoptera litura NPV Cotton
leafworm Vegetable 2 Autographa californica NPV Alfalfa looper Vegetable 3
Spodoptera exigua NPV Beet
armyworm Vegetable 2 Gynaephora sp. NPV Meadow caterpillar Grass 1
Buzura suppressaria NPV Tung tree geometrid Tea 1
Ectropis oblique NPV Apple
geometrid Tea 2 Leucania separate NPV Oriental armyworm Wheat, corn 1
Pieris rapae GV Cabbage white butterfly Vegetable 1
Plutella xylostella GV Diamondback moth Vegetable 2
Pseudaletis separate GV Armyworm Wheat, corn 1
Dendrolimus punctatus CPV Masson pine moth Pine 1
(From “Electronic Manual of Insecticides”, Institute for the Control and Management of Agrochemicals, Chinese Ministry of Agriculture, Data till October, 2006).
median lethal time in 3rd instar H. armigera larvae from 4.90 days to 2.24 days (18). Chitinase, expressed by Serratia marcesscens,was also used to enhance the infectivity of HearNPV (15). An enhancing protein and its truncated fragment from a granulovirus have been expressed and used as synergists of HearNPV and AcMNPV in pest control (2, 3, 4, 6, 16). Techniques have also been developed to increase the yield of viruses in host larvae. For example, incorpo- ration of a juvenile hormone analogue, methoprene, with S. litura NPV might increase virus yield by 227% (5). Similarly, the juvenile hormone analogue ZR515 had been used to increase the yield of HearNPV (Chinese paten:ZL98121687.0).
CONTROL EFFICACY AND BIOSAFETY
ASSESSMENT OF GENETICALLY
MODIFIED BACULOVIRUSES
A major limitation to wide use of baculoviruses for insect control is their slow speed of action. To enhance the efficacy of HearNPV, it was genetically modified either by deletion of the ecdysteroid UDP-glucosyl- transferase (egt) gene from the genome (the recom- binant HearNPV-Δegt) or by insertion of an insect- specific scorpion toxin (AaIT) gene at the egt gene locus (the recombinant HearNPV-AaIT) (13). To devel- op the recombinant HearNPVs as a commercial insec- ticide, the efficacy and biosafety of the recombinant viruses have been investigated.
Control efficacy and economic of the recombinant HearNPV
Application of HearNPV-AaIT on cotton plantations protected the fruit from damage by the bollworm better than HearNPV or HearNPV-Δegt over entire cotton seasons in 2000 and 2001. Yield of cotton lint from HearNPV-AaIT-treated plants was about 22% higher than from plantations treated with wild-type virus alone (13). At an optimal regime to produce the recombinant HearNPV in vivo, the yield of Hear NPV-AaIT was about 44% of the wild-type virus (10). When all conditions are the same, the cost to spray of formulated HearNPV-AaIT was about 50% higher than that of wild-type virus. By all accounts, the increased value of cotton lint after sprays of HearNPV-AaIT formulation is much higher than sprays of the wild- type virus (Table 2). Thus the potential for comer-160V IROLOGICA S INICA V ol.22, No 2 Table 2. Comparison of economic effects of application of wild-type and recombinant HearNPVs in cotton
Treatments Yield of cotton lint a
(kg/ha)
Value of cotton
lint(RMB/ha)
Increased value compared
to control(RMB/ha)
Cost of sprays
(RMB/ha)
Increased income
(RMB/ha)
Control
740 5
921 - - - HearNPV 1
043
8 342 2 421 540 1 881 HearNPV-AaIT 1 299 10 396 4 475 710 3 765
λ-Cyhalothrin EC 1 2 10 313 4 392 720 3 672
a Yield of cotton lint takes average value from experiments conducted in 2001 and 2002 (12).
cialization of the recombinant HearNPV is promising. Biosafety assessments of the recombinant Hear- NPV-AaIT
To assess the risk of releasing recombinant Hear- NPV into the environment, the effects on nontarget species, possibility of AaIT gene flow to other organ- isms, and their environment fitness were studied. Effects on non-target species: The median lethal dose of HearNPV-AaIT was above 2000 mg/kg against female and male rats administered by either intra dermal or per os. This recombinant was also found to be non toxic for bobwhite quail, zebra fish, silkworm and bees. It is not an allergen to a guinea pig skin. Furthermore, it there was no pathological response when rats were inoculated with the recom- binant virus.
In experiments of multiple application of Hear- NPV-AaIT on cotton in 2000, 2001 and 2002, bio- diversity and the dynamics of the natural enemies were also monitored under field conditions. No signifi- cant difference in biodiversity and in the number of natural enemies was observed when plots were treated with either the recombinant or the wild-type virus (Sun et al., unpublished data). Furthermore, the survival time and fecundity of ladybeetles did not differ significantly when they were fed H. armigera larvae infected with either HearNPV-AaIT or wild- type virus (Sun et al., unpublished data). The toxin AaIT expressed by yeast was biologically active against Spodoptera exigua and Argyrogramma agnata larvae when injected into the haemocoel. Whereas, it was not toxic to the two insect species when the toxin was administered per os (14). These data indicate that AaIT was active when it was injected into or ex- pressed in the neurosystem of the insects and it was not active when it was given per os.
Possibility of transferring of AaIT gene from recombinant virus to its surrounding organisms: PCR and dot-blot hybridization were used to test the possiblity AaIT gene flow from HearNPV-AaIT to other organisms after field release. AsIT sequences were not detected in the genome of a pathogen of cotton, Verticillium dahliae Lleb., which was co- cultivated with HearNPV-AaIT DNA or virions for up to 90 days. Similarly, AsIT sequences were not de- tected in the genomic DNA of ladybeetles collected from fields where the recombinant virus was applied several times (9). It is concluded that possibility of the AaIT gene of the recombinant HearNPV transferred to surrounding organisms was very low.
Fitness of the recombinant HearNPV in the envi- ronment: Virus yield per larva, inoculated with HearNPV-AaIT in the 1st, 2nd, 3rd, 4th or 5th larval stage, was 23%, 32%, 41%, 44% and 47% of the yieldSUN et al. Recent Advances in Biological Control of Pest Insects by Using Viruses in China 161
of HearNPV-wt, respectively (14). These data indicate that production of recombinant virus in host larvae was lower than that of wild-type virus.
In the field, there was no significant difference among the inactivation rates of the two recombinant HearNPVs and the wild-type virus on cotton plants (11). Furthermore, the persistence of recombinant viruses in soil was not significantly different from that of wild-type virus (12).
In the field, HearNPV-AaIT exhibited a signifi- cantly lower rate of transmission than the wild-type virus. The vertical transmission of HearNPV-AaIT from infected females to offspring was also signifi- cantly lower than that of wild-type HearNPV (19). Based upon the results mentioned above, there is no evidence that the recombinant baculovirus provides an increased hazard to non target organisms including humans or has a deleterious effect on environmental health in comparison to wild-type viruses. In order to commercialize the genetically modified HearNPV containing AaIT gene, a data package on the safety the virus has been submitted to the Ministry of Agri- culture, P.R. China.
A NEW APPROACH IN THE USE OF
INSECTVIRUSES FOR PEST CONTROL
A new method for delivering viruses to target insects by using Trichogramma spp. as vector has been developed in China (7). By taking into account the biology and the ecology of T. dendrolimi, a special box was designed for releasing the wasps and accom- panying viruses. When T.dendrolimi was released with Dendrolimus punctatus cypovirus to control the masson pine moth (D. punctatus), it was observed that 20%-40% of eggs had been parasitized and 40%-47% of D. punctatus larvae had been infected with the virus (7). In the case of release T. dendrolimi combined with HearNPV to control the cotton bollworm, it was observed that 33%-37% of eggs had been parasitized and 61%-70% of H. armigera larvae had been infected (20).
This technique has also been used for control of H. armigera, S. litura, Plutella xylostella, Ectropis obli- que, Pieris rapae,etc. on more than 20 000 hectares since 1991 in China.
PERSPECTIVE OF USE OF INSECT VIRUSES FORPEST CONTROL IN CHINA
The abuse of chemical insecticides has led to pest resistance, resurgence and environmental problems in many developing countries. Society now demands safer pesticides and less-toxic chemical residues in food and in water. Effective management of pests requires diverse and flexible tools. Among classical biocontrol agents, insect viruses are attractive tools that appear supplement or and, in many cases, replace synthetic chemical pesticides in IPM schemes. Despite their high potential and documented cases of success, the market for viral insecticides is still limited in China. The problem is mainly derived from their relative slow speed of action, relatively low virulence for the older instars and a narrow host range. However, many of these perceived disadvantages can be addressed by modern molecular technologies or in combination with other biocontrol strategies. Geneti- cally modified baculoviruses have already been eluded to and appear to be effective in insect pest control. Furthermore, they can be produced in large amounts by village industries, indicating that they have the potential to deliver sustainable pest control, especially162V IROLOGICA S INICA V ol.22, No 2
in developing countries.
References
1. Chen Q, Li G H, Pang Y, et al.. 2000. Research
developments of Spodoptera exigua Nucleopolyhedro-
virus. Virologica Sinica. (Special issue): 234-235. (in
Chinese)
2. Dong LQ, Zhang K Q, Qiu B S. 200
3. Evaluation of the
feasibility of using lactose as the inducer in producing the
viral enhancing factor from Helicoverpa armigera granu-
lovirus in Escherichia coli BL21DE3. Microbiology, 30:
5-9.
3. Hu R, Meng X L, Xu J P. 2001. Expression of 2.6 kb
enhancin gene fragment from Helicoverpa armigera granulovirus. Virologica Sinica, 16: 3-368. (in Chinese) 4. Liu X G, Yang G, Qiu B S. 2000. Expression of two
truncated enhancin gene from Helicoverpa armigera gra-
nulovirus in E. coli and its preliminary bioassay. Acta
Microbiol Sinica, 41: 168-172. (in Chinese)
5. Liu Y P, Wang F H, Su Z J, et al.2005. Effect of
juvenile hormone analogues on multiplication of Spod
optera litura nucleopolyhedrovirus. Acta Entomol Sini-
ca, 48: 866-870. (in Chinese)
6. Ou Y, Meng X L, Xu J P. 2000. Expression of 2.1kb
enhancin gene fragment from Helicoverpa armigera
granulovirus in Escherichia coli. Chinese J Biotechnol,
16: 595-598. (in Chinese)
7. Peng H Y, Chen X W, Jiang Y, et al.1998. Controlling
Dendrolimus punctatus with Trichogramma dendrolimi
carrying cytoplasmic polyhedrosis virus. Chinese J Biol Control, 14: 111-114. (in Chinese)
8. Su Z, Chen Q, Li G H, Pang Y. 2001. Control of
Spodoptera litura with mixture of SlNPV and its syner-
gist. Chinese J Biol Control, 17: 23-25. (in Chinese)
9. Sun X C, Cheng G Y, Zhou M Z, et al.. 2004, Labora-
tory and field analysis on the transferring of AaIT gene of
recombinant Helicoverpa armigera Nucleopolyhedro- virus (HaSNPV-AaIT) to its surrounding organisms, Virologica Sinica, 20: 420-423. (in Chinese)
10. Sun X L, Sun X C, Bai B K, et al.2005. Production of
polyhedral inclusion bodies from Helicoverpa armigera
larvae infected with wild-type and recombinant HaSNPV.
Biocont Sci Technol,15: 353-366.
11. Sun X L, Sun X C, van der Werf W, et al.. 2004. Field
inactivation of wild-type and genetically modified Heli-
coverpa armigera single nucleocapsid nucleopolyhe- drovirus in cotton. Biocont Sci Technol, 14: 185-192. 12. Sun X L, van der Werf W, Felix F J J A, et al.2006.
Modelling biological control with wild-type and gene-
tically modified baculoviruses in the Helicoverpa armi-
gera-cotton system. Ecological Modelling, 198:387-398.
13. Sun X L, Wang H L, Sun X C, et al.2004. Biological
activity and field efficacy of a genetically modified Helicoverpa armigera SNPV expressing an insect-selec-
tive toxin from a chimeric promote. Biol Control, 29:
124-137.
14. Wang E W, Xu J P, Lu W, et al.2005. Expression and
functional analysis of a recombinant scorpion neuroto-
toxin AaIT. J Wuhan Univ(Nat. Sci. Ed.), 51: 727- 732.
(in Chinese)
15. Xu H G, Peng H Y, Liu J X, et al.2002. Enhancement to
Helicoverpa armigera Nucleopolyhedrovirus by chitinase
of WHS3 strain. Virologica Sinica, 17: 239-242. (in
Chinese)
16. Yuan Z M, Meng X L, Liu S S. 2004. Wide-spectrum
synergy of recombinant enhancin from insect baculovirus
expressed in Escherichia coli. Chinese J Biol Control,
20: 31-33. (in Chinese)
17. Zhang G Y, Sun X L, Zhang Z X, et al. 1995.
Production and effectiveness of the new formulation of
Helicoverpa virus pesticide-emulsifiable suspension.
Virologica Sinica, 10: 242-247. (in Chinese)
18. Zhang Z X, Zhang H Y, Niu G D, et al. 2003. Efficiency
and safety evaluation of HaNPV suspension formulation
containing Chlorfluazuron. Virologica Sinica, 18: 571-
575. (in Chinese)
19. Zhou M Z, Sun X L, Sun X C, et al.. 2005. Horizontal
and vertical transmission of wild-type and recombinant
Helicoverpa armigera single-nucleocapsid nucleopo- lyhedrovirus. J Invert Pathol, : 165-175.
20. Zhu J Q, Lei C L, Peng H Y, et al. 2002. Studies on the
effect of Trichogramma dendrolimi carrying NPV to
suppress Helicoverpa armigera. Natural Enemies of
Insects, 24: 20-25. (in Chinese)
