SUMMARY The fight against adults of Aedes albopictus is temporary, unsatisfied, and polluting for the environment, while larval treatment is more localized in time and space, resulting less dangerous. The most common antilarval product used is a crystal protoxin of Bacillus thuringiensis var. israelensis serum-type 14 produced during the sporulation process and considered harmless for humans, fishes, and other not dipteran insects. Unfortunately the antilarval activity of B. thuringiensis is lost after 24 hours, when larvae can develop undisturbed and its activity is completely absent against eggs and pupae. Acqueous extract of roots of Codonopsis javanica Hook. f. & Thoms (Campanulaceae) was tested to develop new natural formulations against larval and pupal stages of A. albopictus showing poor or no activity against larvae; on the contrary, statistically significant activity was observed against pupae after 48 hrs with 75% of mortality both at 12.79% and 6.39% concentration of the decoction. RIASSUNTO Il trattamento delle forme larvali rappresenta il metodo di lotta più efficace contro Aedes albopictus perché consente di ottenere risultati migliori nel tempo e conseguenze minori sull’ambiente rispetto alla lotta contro la forma adulta. Una tossina batterica prodotta da Bacillus thuringiensis var. israelensis sierotipo H-14 è divenuta il prodotto maggiormente utilizzato nel mondo come larvicida perché ritenuto innocuo nei confronti dell’uomo, dei pesci e di altri insetti che non siano ditteri. L’attività antilarvale di questo prodotto, però, si annulla dopo 24 ore, permettendo alle larve appena nate di svilupparsi indisturbate; inoltre, è del tutto inattivo contro uova e pupe. Con questa indagine sono stati studiati gli effetti dell’estratto acquoso delle radici di Codonopsis javanica (Campanulaceae) contro larve e pupe della zanzara. L’estratto possiede attività scarsa o nulla contro le larve, mentre è significativamente attivo nei confronti delle pupe dopo 48 ore di trattamento con mortalità del 75 % alle diluizioni del 12,79 % e del 6,39%

Braca, Alessandra

Carugini, Silvia

Cecchi, Francesca

Cioni, Pierluigi

Macchioni, Fabio

Morelli, Ivano

Siciliano, Tiziana

English

Università di Pisa

215
(1) Dipartimento di Patologia Animale, Proﬁlassi e Igiene degli alimenti, Direttore Prof. Giovanni Braca.
(2) Dipartimento di Patologia Animale, Direttore Prof. Paolo Verità.
(3) Dipartimento di Chimica Bioorganica e Biofarmacia, Direttore Prof. Ivano Morelli.
AQUEOUS EXTRACT OF CODONOPSIS JAVANICA 
AGAINST LARVAL AND PUPAL STAGES 
OF AEDES ALBOPICTUS
ESTRATTO ACQUOSO DI CODONOPSIS JAVANICA
CONTRO LARVE E PUPE DI AEDES ALBOPICTUS
FABIO MACCHIONI (1), SILVIA CARUGINI (1), FRANCESCA CECCHI (2), 
TIZIANA SICILIANO (3), ALESSANDRA BRACA (3), 
PIERLUIGI CIONI (3), IVANO MORELLI (3)
SUMMARY
The ﬁght against adults of Aedes albopictus is temporary, unsatisﬁed, and polluting for the 
environment, while larval treatment is more localized in time and space, resulting less dange-
rous. The most common antilarval product used is a crystal protoxin of Bacillus thuringiensis 
var. israelensis serum-type 14  produced during the sporulation process and considered harm-
less for humans, ﬁshes, and other not dipteran insects. Unfortunately the antilarval activity of 
B. thuringiensis is lost after 24 hours, when larvae can develop undisturbed and its activity is 
completely absent against eggs and pupae.
Acqueous extract of roots of Codonopsis javanica Hook. f. & Thoms (Campanulaceae) 
was tested to develop new natural formulations against larval and pupal stages of A. albopictus 
showing poor or no activity against larvae; on the contrary, statistically signiﬁcant activity was 
observed against pupae after 48 hrs with 75% of mortality both at 12.79% and 6.39% concen-
tration of the decoction.
Key words: Aedes albopictus, Codonopsis javanica, aqueous extract.
RIASSUNTO
Il trattamento delle forme larvali rappresenta il metodo di lotta più efﬁcace contro Aedes 
albopictus  perché consente di ottenere risultati migliori nel tempo e conseguenze minori sul-
l’ambiente rispetto alla lotta contro la forma adulta. Una tossina batterica prodotta da Bacillus 
thuringiensis var. israelensis sierotipo H-14 è divenuta il prodotto maggiormente utilizzato 
nel mondo come larvicida perché ritenuto innocuo nei confronti dell’uomo, dei pesci e di altri 
insetti che non siano ditteri. L’attività antilarvale di questo prodotto, però, si annulla dopo 24 
ore, permettendo alle larve appena nate di svilupparsi indisturbate; inoltre, è del tutto inattivo 
contro uova e pupe.
216
Con questa indagine sono stati studiati gli effetti dell’estratto acquoso delle radici di Codo-
nopsis javanica (Campanulaceae) contro larve e pupe della zanzara. L’estratto possiede attività 
scarsa o nulla contro le larve, mentre è signiﬁcativamente attivo nei confronti delle pupe dopo 
48 ore di trattamento con mortalità del 75 % alle diluizioni del 12,79 % e del 6,39%. 
Parole chiave: Aedes albopictus, Codonopsis javanica, estratto acquoso.
INTRODUCTION
Aedes albopictus, known as “tiger mosquito”, is an asiatic insect, widespread in 
all continents and recorded in Italy for the ﬁrst time in 1990 imported from China 
(Sabatini et al., 1990).
The “tiger mosquito” is a daytime outdoor ectoparasite, that bites with an unusual 
aggressiveness and it can be vector of dengue virus, encephalitis virus of men and 
animals, and of several arbovirus (Boromisa et al., 1987; Mitchell, 1995; Shroyer, 
1986). Moreover, it is an intermediate host of ﬁlarial species such as Diroﬁlaria 
immitis, D. repens, and Setaria labiatopapillosa (Cancrini et al., 1995;  Cancrini et 
al., 2003).
Aedes albopictus can survive during the cold and dried  winter in temperate 
climates in the egg stage through embryonal diapause (Lyon & Berry, 1991), but it is 
active throughout the year in tropical and subtropical habitats. The females can lay 
40-80 eggs after each blood taking and several hundreds of eggs during their life-time. 
Eggs are laid singly on the sides of water-holding containers such as tires, animal 
watering dishes, birdbaths, ﬂowerpots, hollows of trees and leaves, impermeable 
holes of the soil, and can withstand desiccation up to one year; larval emergence 
occurs when rainfall raises the water level in the containers and several submersions 
are required before hatching; additionally, low O
2
 tension is a more important factor 
than ﬂooding or temperature on inducing egg hatch. Development is temperature 
dependent, but the larvae usually pupate after ﬁve to ten days and the pupal stage 
lasts two days (Hawley, 1988). Larvae are active feeders; they feed on ﬁne particulate 
organic matter in water. Larvae use a breathing siphon to acquire oxygen and, for that 
reason, must periodically come to water surface. Larvae develop through four instars 
prior to pupation and, unlike many other insects, pupae are active and short-lived.
Nowadays the mosquito ﬁght is directed against larvae and, only if it necessary, 
against adults. This is because the ﬁght against adults is temporary, unsatisﬁed, and 
polluting for the environment, while larval treatment is more localized in time and 
space, resulting less dangerous.
Common antilarval products on market are synthetic molecules (temephos, 
clorpyriphos, diﬂubenzuron) or natural compounds such as a crystal protoxin of 
Bacillus thuringiensis var. israelensis produced during the sporulation process. It 
results the most used in the world, because it is considered to be harmless for humans, 
ﬁshes, and other not dipteran insects. Unfortunately the antilarval activity of B. 
thuringensis is lost after 24 hours, when larvae can develop undisturbed and it is 
217
completely ineffective against eggs and pupae. 
The aim of our work is to develop new natural antimosquitos formulations that 
result not toxic for men, animals, and environment and also active for all the stages of 
mosquitos. It’s very important to develop always new antimosquitos drugs to supply 
the farmacoresistance of the nowadays used products. 
Among various tested substances the decoction of the root of  Codonospis javanica  
(Campanulaceae) has shown good activity. This species, known with the popular 
vietnamise name “Dang sam”, has a widespread distribution in South East Asia and 
particularly in the region of Vietnam, where the decoction of the roots is used in 
traditional medicine as tonic and against leukaemia, inﬂammation and hepatitis (Ueda 
et al., 2002). 
Neither phytochemical studies nor biological activity has been carried out on this 
plant till now.
MATERIALS AND METHODS
The dried roots of C. javanica of commercial use were purchased in Sapa 
(Vietnam) on May 2004. The voucher specimen (N° 8658) is deposited at Herbarium 
Horti Botanici Pisani Nuove Acquisizioni, Pisa, Italy.
The powdered dried roots (130.0 g) were heated at 100°C in 1.0 L of water to 
afford a decoction that was lyophilised to obtain 6.5 g of residue. Tests were performed 
against larvae and pupae of A. albopictus. 
Aedes albopictus eggs were captured through ovitraps placed in selected areas 
where the presence of mosquitos was observed  during previous inspections. Masonite 
strips (3x15 cm) were suspended vertically in black pots ﬁlled with 350 ml of water 
to provide a suitable surface for eggs deposition. Every week, pots were rinsed and 
ﬁlled and strips changed and checked for eggs presence. To obtain larvae and pupae 
successively  the strips were left to dry at room temperature for 3 days, then placed 
individually into plastic trays containing dechlorinated tap water after which 1st 
stage larvae were obtained, strips were left to dry again. This alternating wet and dry 
procedure was repeated twice (Toma et al., 2003). 
In each well were placed either 6 larvae at  third and early fourth instar or 6 
pupae;  larvae and pupae showing abnormalities were discarded. In the evaluation of 
the dilutions it was considered the introduction of one drop of water  with each larva 
or pupa changing the initial dilution. For each well was added an amount of food for 
the larval survive. Lyophilised decoction of C. javanica was tested at various dilutions 
from 12,79 % to 0,21 %. For each well were added 20 μl of Amphotericin B (Tab. I). 
Three controls were performed with deionised water, deionised water plus 
amphotericin B, and deionised water plus Bacillus thuringiensis var israelensis 0.25 
mg ﬁnely grinded for each well respectively. The test was repeated three times for 
larvae and pupae. 
The mobility control of larvae and pupae was performed after 24 and 48 hours 
of contact with the substances. To verify mortality, immobile larvae and pupae were 
218
collected one by one after 48 hours and placed in another well with deionised water 
without tested substances; persistence of immobility after their stimulation with a 
needle indicated their death. 
Statistical analysis
Data were subjected to ANOVA in which extract number, observation time (24 and 
48 hours), and stage (pupae or larvae) with all their interactions were considered as 
ﬁxed effects and percentage dead as the independent variable.
RESULTS AND DISCUSSION
Codonopsis javanica extract showed poor or no activity against larvae at each 
concentration tested after 24 and 48 hrs (See Tab.I, Fig1). Results against pupae 
showed 75% of mortality statistically signiﬁcative after 48 hrs at 12.79% and 6.39% 
concentration, while the mortality after 24 hrs resulted not statistically signiﬁcative 
(Tab. II). 
In controls with deionized water only and with amphotericin B were observed no 
death of larvae and pupae  both at 24 and 48 hours. B. thuringiensis var israelensis 
activity appeared high against larvae, determining a mortality of  100% but resulted 
ineffective against pupae (100% mortality of larvae vs. 0% mortality of pupae; P<0.01).
The results obtained may be considered interesting, because the pupicidal 
C. javanica rootsdecoction could be used in combination with the larvicidal  B. 
thuringensis in the ﬁght against Aedes  albopictus.
Tab. I. Initial and ﬁnal diluitions.
Initial
Dilution (%)
Final Dilution (%)
15.00 12.79
7.5 6.39
3.75 3.25
1.87 1.63
0.94 0.81
0.47 0.41
0.23 0.21
Tab. II. Percentage mortality differences of larvae and pupae of Aedes albopictus 
exposed to aqueous extract of Codonopsis javanica at different concentrations for 
24 and 48 hrs. Different letters on the same column indicate signiﬁcant differences; 
A, B: P<0.01.
Larvae Pupae
24 hrs 48 hrs 24 hrs 48 hrs
Controls 0 B 0 B 0 0 B
Amphotericin B 0 B 0 B 0 0 B
B. thuringiensis 100 A 100 A 0 0 B
12.79 % 0 B 16,67 B 50 75 A
6.39 % 0 B 16,67 B 50 75 A
3,25 % 0 B 0 B 50 50 B
1,63 % 0 B 0 B 50 50 B
0,81 % 0 B 0 B 41,66 41,66 B
0,41 % 0 B 0 B 41,66 41,66 B
0,21 % 0 B 0 B 16,66 16,66 B
 
219
Tab. II. Percentage mortality differences of larvae and pupae of Aedes albopictus 
exposed to aqueous extract of Codonopsis javanica at different concentrations for 
24 and 48 hrs. Different letters on the same column indicate signiﬁ cant differences; 
A, B: P<0.01.
Larvae Pupae
24 hrs 48 hrs 24 hrs 48 hrs
Controls 0 B 0 B 0 0 B
Amphotericin B 0 B 0 B 0 0 B
B. thuringiensis 100 A 100 A 0 0 B
12.79 % 0 B 16,67 B 50 75 A
6.39 % 0 B 16,67 B 50 75 A
3,25 % 0 B 0 B 50 50 B
1,63 % 0 B 0 B 50 50 B
0,81 % 0 B 0 B 41,66 41,66 B
0,41 % 0 B 0 B 41,66 41,66 B
0,21 % 0 B 0 B 16,66 16,66 B
Fig. 1. Codonopsis javanica: percentage mortality of larvae and pupae of Aedes 
albopictus exposed to aqueous of Codonopsis javanica at 24 and 48 hrs.
220
REFERENCES
BOROMISA R. D., RAI K.S., GRIMSTAD P.R. (1987). Variation in the vector competence of 
geographic strains of Aedes albopictus for dengue virus. J. Am. Control. Assoc., 3: 378-
386.
CANCRINI G., PIETROBELLI M., FRANGIPANE DI REGALBONO A.F., TAMPIERI M.P., 
DELLA TORRE A. (1995). Development of Diroﬁlaria and Setaria nematodes in Aedes 
albopictus. Parassitol., 37: 141-145. 
CANCRINI G., FRANGIPANE DI REGALBONO A., RICCI I., TESSARIN C., GABRIELLI 
S., PIETROBELLI M. (2003). Aedes albopictus is a natural vector of Diroﬁlaria immitis in 
Italy. Vet. Parasitol. 118 (3-4):195-202. 
 HAWLEY W.A. (1988). The biology of Aedes albopictus. J. Am. Mosq. Contr. Assoc., 
Supplement #1: 1-40. 
LYON W.F., BERRY R.L. (1991). Asian tiger mosquito. Ohio State University Extension Fact 
Sheet HYG-2148-2198. 
MITCHELL CJ. (1995). Geographic spread of Aedes albopictus and potential for involvement 
in arbovirus cycles in the mediterranean. Basin. J. Vect. Ecol., 20: 44-58.
SABATINI A., RANIERI V., TROVATO G., COLUZZI M. (1990). Aedes albopictus in Italia e 
possibile diffusione della specie nell’area mediterranea. Parassitol., 32: 301-304.
SHROYER D.A. (1986).  Aedes albopictus and arboviruses: a coincise review of the litterature. 
J. Am. Mosq. Control. Assoc., 2: 424-428.
TOMA L., SEVERINI F., DI LUCA M., BELLA A., ROMI R. (2003). Seasonal patterns of 
oviposition and egg hatchingrate of Aedes albopictus in Rome. J. Am. Mosq. Contr. Assoc., 
19 (1): 19-22.
UEDA J.Y., TEZUKA Y., BANSKOTA A.H., LE TRAN Q., TRAN Q.K., HARIMAYA Y., 
SAIKI I., KADOTA S. (2002). Antiproliferative activity of Vietnamese medicinal plants. 
Biol. Pharm. Bull., 25 (6): 753-60. 
 


Aqueous extract of codonopsis javanica against larval and pupal stages of aedes albopictus

UnipiEprints

215(1) Dipartimento di Patologia Animale, Proﬁlassi e Igiene degli alimenti, Direttore Prof. Giovanni Braca.(2) Dipartimento di Patologia Animale, Direttore Prof. Paolo Verità.(3) Dipartimento di Chimica Bioorganica e Biofarmacia, Direttore Prof. Ivano Morelli.AQUEOUS EXTRACT OF CODONOPSIS JAVANICA AGAINST LARVAL AND PUPAL STAGES OF AEDES ALBOPICTUSESTRATTO ACQUOSO DI CODONOPSIS JAVANICACONTRO LARVE E PUPE DI AEDES ALBOPICTUSFABIO MACCHIONI (1), SILVIA CARUGINI (1), FRANCESCA CECCHI (2), TIZIANA SICILIANO (3), ALESSANDRA BRACA (3), PIERLUIGI CIONI (3), IVANO MORELLI (3)SUMMARYThe ﬁght against adults of Aedes albopictus is temporary, unsatisﬁed, and polluting for the environment, while larval treatment is more localized in time and space, resulting less dange-rous. The most common antilarval product used is a crystal protoxin of Bacillus thuringiensis var. israelensis serum-type 14  produced during the sporulation process and considered harm-less for humans, ﬁshes, and other not dipteran insects. Unfortunately the antilarval activity of B. thuringiensis is lost after 24 hours, when larvae can develop undisturbed and its activity is completely absent against eggs and pupae.Acqueous extract of roots of Codonopsis javanica Hook. f. & Thoms (Campanulaceae) was tested to develop new natural formulations against larval and pupal stages of A. albopictus showing poor or no activity against larvae; on the contrary, statistically signiﬁcant activity was observed against pupae after 48 hrs with 75% of mortality both at 12.79% and 6.39% concen-tration of the decoction.Key words: Aedes albopictus, Codonopsis javanica, aqueous extract.RIASSUNTOIl trattamento delle forme larvali rappresenta il metodo di lotta più efﬁcace contro Aedes albopictus  perché consente di ottenere risultati migliori nel tempo e conseguenze minori sul-l’ambiente rispetto alla lotta contro la forma adulta. Una tossina batterica prodotta da Bacillus thuringiensis var. israelensis sierotipo H-14 è divenuta il prodotto maggiormente utilizzato nel mondo come larvicida perché ritenuto innocuo nei confronti dell’uomo, dei pesci e di altri insetti che non siano ditteri. L’attività antilarvale di questo prodotto, però, si annulla dopo 24 ore, permettendo alle larve appena nate di svilupparsi indisturbate; inoltre, è del tutto inattivo contro uova e pupe.216Con questa indagine sono stati studiati gli effetti dell’estratto acquoso delle radici di Codo-nopsis javanica (Campanulaceae) contro larve e pupe della zanzara. L’estratto possiede attività scarsa o nulla contro le larve, mentre è signiﬁcativamente attivo nei confronti delle pupe dopo 48 ore di trattamento con mortalità del 75 % alle diluizioni del 12,79 % e del 6,39%. Parole chiave: Aedes albopictus, Codonopsis javanica, estratto acquoso.INTRODUCTIONAedes albopictus, known as “tiger mosquito”, is an asiatic insect, widespread in all continents and recorded in Italy for the ﬁrst time in 1990 imported from China (Sabatini et al., 1990).The “tiger mosquito” is a daytime outdoor ectoparasite, that bites with an unusual aggressiveness and it can be vector of dengue virus, encephalitis virus of men and animals, and of several arbovirus (Boromisa et al., 1987; Mitchell, 1995; Shroyer, 1986). Moreover, it is an intermediate host of ﬁlarial species such as Diroﬁlaria immitis, D. repens, and Setaria labiatopapillosa (Cancrini et al., 1995;  Cancrini et al., 2003).Aedes albopictus can survive during the cold and dried  winter in temperate climates in the egg stage through embryonal diapause (Lyon & Berry, 1991), but it is active throughout the year in tropical and subtropical habitats. The females can lay 40-80 eggs after each blood taking and several hundreds of eggs during their life-time. Eggs are laid singly on the sides of water-holding containers such as tires, animal watering dishes, birdbaths, ﬂowerpots, hollows of trees and leaves, impermeable holes of the soil, and can withstand desiccation up to one year; larval emergence occurs when rainfall raises the water level in the containers and several submersions are required before hatching; additionally, low O2 tension is a more important factor than ﬂooding or temperature on inducing egg hatch. Development is temperature dependent, but the larvae usually pupate after ﬁve to ten days and the pupal stage lasts two days (Hawley, 1988). Larvae are active feeders; they feed on ﬁne particulate organic matter in water. Larvae use a breathing siphon to acquire oxygen and, for that reason, must periodically come to water surface. Larvae develop through four instars prior to pupation and, unlike many other insects, pupae are active and short-lived.Nowadays the mosquito ﬁght is directed against larvae and, only if it necessary, against adults. This is because the ﬁght against adults is temporary, unsatisﬁed, and polluting for the environment, while larval treatment is more localized in time and space, resulting less dangerous.Common antilarval products on market are synthetic molecules (temephos, clorpyriphos, diﬂubenzuron) or natural compounds such as a crystal protoxin of Bacillus thuringiensis var. israelensis produced during the sporulation process. It results the most used in the world, because it is considered to be harmless for humans, ﬁshes, and other not dipteran insects. Unfortunately the antilarval activity of B. thuringensis is lost after 24 hours, when larvae can develop undisturbed and it is 217completely ineffective against eggs and pupae. The aim of our work is to develop new natural antimosquitos formulations that result not toxic for men, animals, and environment and also active for all the stages of mosquitos. It’s very important to develop always new antimosquitos drugs to supply the farmacoresistance of the nowadays used products. Among various tested substances the decoction of the root of  Codonospis javanica  (Campanulaceae) has shown good activity. This species, known with the popular vietnamise name “Dang sam”, has a widespread distribution in South East Asia and particularly in the region of Vietnam, where the decoction of the roots is used in traditional medicine as tonic and against leukaemia, inﬂammation and hepatitis (Ueda et al., 2002). Neither phytochemical studies nor biological activity has been carried out on this plant till now.MATERIALS AND METHODSThe dried roots of C. javanica of commercial use were purchased in Sapa (Vietnam) on May 2004. The voucher specimen (N° 8658) is deposited at Herbarium Horti Botanici Pisani Nuove Acquisizioni, Pisa, Italy.The powdered dried roots (130.0 g) were heated at 100°C in 1.0 L of water to afford a decoction that was lyophilised to obtain 6.5 g of residue. Tests were performed against larvae and pupae of A. albopictus. Aedes albopictus eggs were captured through ovitraps placed in selected areas where the presence of mosquitos was observed  during previous inspections. Masonite strips (3x15 cm) were suspended vertically in black pots ﬁlled with 350 ml of water to provide a suitable surface for eggs deposition. Every week, pots were rinsed and ﬁlled and strips changed and checked for eggs presence. To obtain larvae and pupae successively  the strips were left to dry at room temperature for 3 days, then placed individually into plastic trays containing dechlorinated tap water after which 1st stage larvae were obtained, strips were left to dry again. This alternating wet and dry procedure was repeated twice (Toma et al., 2003). In each well were placed either 6 larvae at  third and early fourth instar or 6 pupae;  larvae and pupae showing abnormalities were discarded. In the evaluation of the dilutions it was considered the introduction of one drop of water  with each larva or pupa changing the initial dilution. For each well was added an amount of food for the larval survive. Lyophilised decoction of C. javanica was tested at various dilutions from 12,79 % to 0,21 %. For each well were added 20 μl of Amphotericin B (Tab. I). Three controls were performed with deionised water, deionised water plus amphotericin B, and deionised water plus Bacillus thuringiensis var israelensis 0.25 mg ﬁnely grinded for each well respectively. The test was repeated three times for larvae and pupae. The mobility control of larvae and pupae was performed after 24 and 48 hours of contact with the substances. To verify mortality, immobile larvae and pupae were 218collected one by one after 48 hours and placed in another well with deionised water without tested substances; persistence of immobility after their stimulation with a needle indicated their death. Statistical analysisData were subjected to ANOVA in which extract number, observation time (24 and 48 hours), and stage (pupae or larvae) with all their interactions were considered as ﬁxed effects and percentage dead as the independent variable.RESULTS AND DISCUSSIONCodonopsis javanica extract showed poor or no activity against larvae at each concentration tested after 24 and 48 hrs (See Tab.I, Fig1). Results against pupae showed 75% of mortality statistically signiﬁcative after 48 hrs at 12.79% and 6.39% concentration, while the mortality after 24 hrs resulted not statistically signiﬁcative (Tab. II). In controls with deionized water only and with amphotericin B were observed no death of larvae and pupae  both at 24 and 48 hours. B. thuringiensis var israelensis activity appeared high against larvae, determining a mortality of  100% but resulted ineffective against pupae (100% mortality of larvae vs. 0% mortality of pupae; P<0.01).The results obtained may be considered interesting, because the pupicidal C. javanica rootsdecoction could be used in combination with the larvicidal  B. thuringensis in the ﬁght against Aedes  albopictus.Tab. I. Initial and ﬁnal diluitions.InitialDilution (%)Final Dilution (%)15.00 12.797.5 6.393.75 3.251.87 1.630.94 0.810.47 0.410.23 0.21Tab. II. Percentage mortality differences of larvae and pupae of Aedes albopictus exposed to aqueous extract of Codonopsis javanica at different concentrations for 24 and 48 hrs. Different letters on the same column indicate signiﬁcant differences; A, B: P<0.01.Larvae Pupae24 hrs 48 hrs 24 hrs 48 hrsControls 0 B 0 B 0 0 BAmphotericin B 0 B 0 B 0 0 BB. thuringiensis 100 A 100 A 0 0 B12.79 % 0 B 16,67 B 50 75 A6.39 % 0 B 16,67 B 50 75 A3,25 % 0 B 0 B 50 50 B1,63 % 0 B 0 B 50 50 B0,81 % 0 B 0 B 41,66 41,66 B0,41 % 0 B 0 B 41,66 41,66 B0,21 % 0 B 0 B 16,66 16,66 B 219Tab. II. Percentage mortality differences of larvae and pupae of Aedes albopictus exposed to aqueous extract of Codonopsis javanica at different concentrations for 24 and 48 hrs. Different letters on the same column indicate signiﬁ cant differences; A, B: P<0.01.Larvae Pupae24 hrs 48 hrs 24 hrs 48 hrsControls 0 B 0 B 0 0 BAmphotericin B 0 B 0 B 0 0 BB. thuringiensis 100 A 100 A 0 0 B12.79 % 0 B 16,67 B 50 75 A6.39 % 0 B 16,67 B 50 75 A3,25 % 0 B 0 B 50 50 B1,63 % 0 B 0 B 50 50 B0,81 % 0 B 0 B 41,66 41,66 B0,41 % 0 B 0 B 41,66 41,66 B0,21 % 0 B 0 B 16,66 16,66 BFig. 1. Codonopsis javanica: percentage mortality of larvae and pupae of Aedes albopictus exposed to aqueous of Codonopsis javanica at 24 and 48 hrs.220REFERENCESBOROMISA R. D., RAI K.S., GRIMSTAD P.R. (1987). Variation in the vector competence of geographic strains of Aedes albopictus for dengue virus. J. Am. Control. Assoc., 3: 378-386.CANCRINI G., PIETROBELLI M., FRANGIPANE DI REGALBONO A.F., TAMPIERI M.P., DELLA TORRE A. (1995). Development of Diroﬁlaria and Setaria nematodes in Aedes albopictus. Parassitol., 37: 141-145. CANCRINI G., FRANGIPANE DI REGALBONO A., RICCI I., TESSARIN C., GABRIELLI S., PIETROBELLI M. (2003). Aedes albopictus is a natural vector of Diroﬁlaria immitis in Italy. Vet. Parasitol. 118 (3-4):195-202.  HAWLEY W.A. (1988). The biology of Aedes albopictus. J. Am. Mosq. Contr. Assoc., Supplement #1: 1-40. LYON W.F., BERRY R.L. (1991). Asian tiger mosquito. Ohio State University Extension Fact Sheet HYG-2148-2198. MITCHELL CJ. (1995). 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Aqueous extract of codonopsis javanica against larval and pupal stages of aedes albopictus

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