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Efficiency of the latex from Euphorbia splendens var. hislopii (N.E. Br.) Ursch & Leandri, Euphorbiaceae, in the control of Rhipicephalus (Boophilus) sanguineus (Latreille, 1806) (Acari: Ixodidae)

Abstract

The aim of this study was to evaluate the effect of the latex from Euphorbia splendens var. hislopii (N.E. Br.) Ursch & Leandri, Euphorbiaceae, on the eggs and engorged larvae of Rhipicephalus (B.) sanguineus (Latreille, 1806) (Acari: Ixodidae). Six aqueous concentrations: 25, 50, 100, 125, 250 and 500 μL/L of the latex of this plant were tested. The control group was tested only with distilled water. The latex of E. splendens var. hislopii presented an LD50 of 18.031 μL/L and LD90 of 84.610 μL/L against the eggs of R. (B.) sanguineus. The larvae of all the groups treated with the latex presented a low survival rate of 0% at 25 μL/L, 1% at 50 μL/L, 2% at 100 μL/L, 3% at 125 μL/L, 9% at 250 μL/L, 5% at 500 μL/L when compared with the control group (91%). On day 7 and 14 after the application the latex killed more efficiently the treated groups (25, 50, 100, 125, 250 and 500 μL/L). As from day 21 the latex became less effective for all treatments. Our results clearly show that the aqueous concentration of the latex have a strong effect on tick eggs and larvae suggesting that it could become an important acaricide.

Phytotherapic; Euphorbia splendens var; hislopii; Rhipicephalus (Boophilus) sanguineus; Acaricide


Efficiency of the latex from Euphorbia splendens var. hislopii (N.E. Br.) Ursch & Leandri, Euphorbiaceae, in the control of Rhipicephalus (Boophilus) sanguineus (Latreille, 1806) (Acari: Ixodidae)

Zeneida T. PintoI, * * E-mail: zeneida@ioc.fiocruz.br, Tel.:+ 55 21 2562 1846. ; Margareth M. C. QueirozII; Júlio V. BarbosaI

ILaboratório de Educação em Ambiente e Saúde, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz, Av. Brasil, 4365, 21045-900 Rio de Janeiro-RJ, Brazil

IILaboratório de Transmissores de Leishmanioses, Setor de Entomologia Médica e Forense, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz, Av. Brasil, 4365, 21045-900 Rio de Janeiro-RJ, Brazil

ABSTRACT

The aim of this study was to evaluate the effect of the latex from Euphorbia splendens var. hislopii (N.E. Br.) Ursch & Leandri, Euphorbiaceae, on the eggs and engorged larvae of Rhipicephalus (B.) sanguineus (Latreille, 1806) (Acari: Ixodidae). Six aqueous concentrations: 25, 50, 100, 125, 250 and 500 μL/L of the latex of this plant were tested. The control group was tested only with distilled water. The latex of E. splendens var. hislopii presented an LD50 of 18.031 μL/L and LD90 of 84.610 μL/L against the eggs of R. (B.) sanguineus. The larvae of all the groups treated with the latex presented a low survival rate of 0% at 25 μL/L, 1% at 50 μL/L, 2% at 100 μL/L, 3% at 125 μL/L, 9% at 250 μL/L, 5% at 500 μL/L when compared with the control group (91%). On day 7 and 14 after the application the latex killed more efficiently the treated groups (25, 50, 100, 125, 250 and 500 μL/L). As from day 21 the latex became less effective for all treatments. Our results clearly show that the aqueous concentration of the latex have a strong effect on tick eggs and larvae suggesting that it could become an important acaricide.

Keywords: Phytotherapic, Euphorbia splendens var. hislopii, Rhipicephalus (Boophilus) sanguineus, Acaricide.

Introduction

Several synthetic acaricides have been used for killing ticks, but resistance of Rhipicephalus (Boophilus) sanguineus (Latreille, 1806) to these products has been noted in some countries (Gladney & Dawkins, 1976; Belot & Mishra, 1979). The indiscriminate use on infested dogs and the environment could cause the inefficiency of the acaricide (Furlong, 1993), in addition to economic injury and poisoning other animals and humans (Fernandes, 1997; 2000).

Plants or crude extracts could become an alternative. Kaaya et al. (1995) and Abdel-Shafy & Zayed (2002) demonstrated that extracts of several plants had a strong acaricide effect, being able to reduce food ingestion and alter the fertility and viability of eggs of Hyalomma anatolicum excavatum, Amblyomma variegatum, Rhipicephalus appendiculatus.

Euphorbia splendens var. hisloppi (N.E. Br.) Ursch & Leandri, Euphorbiaceae, originating from Madagascar, is popularly known in Brazil as "coroa-de-cristo" ("crown-of-christ"), where it is nowadays widespread and cultivated as an ornamental plant and as a hedge (Schall et al., 1992). It has been used as molluscicide since 1930, with the prospect of becoming the most appropriate method to control the snail that is the intermediate host of Schistosoma mansoni. However, in literature there is no mention of the effects of this product on R. (B.) sanguineus. Gomes et al. (2003) tested latex from E. splendens var hislopii, to control Peckya (Peckia) chrysostoma (Wiedemann, 1830) (Diptera: Sarcophagidae) and observed a significant reduction in the body mass of specimens and viability of their whole cycle. Leles & Fernandes (2005) tested the substances extracted from Copaifera langsdorffii (Meliaceae) and Carapa guianensis (Caesalpiniaceae) on larvae of R. (B.) sanguineus, showing a promising activity against these ticks.

The study of the tick R. (B.) sanguineus is important for veterinary medicine, because this arthropod is a transmitter of pathogens to dogs (Simpson et al., 1991), such as Babesia canis, Ehrlichia canis and Hepatozoon canis (Christophers, 1907; Smith et al., 1976).

Some authors highlight the implications of this tick in public health, since parasitizing other domestic animals, R. (B.) sanguineus can also parasitize man (Feldman-Muhsan, 1956; Dipeolu et al., 1982), transmitting pathogens, such as Rickettsia rickettsii, Rickettsia conorii and Coxiella burnetti (Mantovani & Benazzi 1953; Racioppi et al., 1981). Harrison et al. (1997) recently confirmed that the immature forms of R. (B.) sanguineus fed more frequently on humans than reported in the literature, thereby increasing transmission of some anthropozoonoses (Hoogstraal, 1967), as these develop with high tick density and are prevalent in synanthropic environments in various cities of Brazil.

Therefore, this study aims to evaluate the effectiveness of the latex from E. splendens var. hislopii to control the eggs and larvae infestations of R. (B.) sanguineus.

Material and Methods

Latex

For the assays performed in the present study, latex samples were always collected at the same site, to avoid possible variations due to factors such as soil, climate etc, of the plant metabolism and active substance concentration as demonstrated by Lugt (1987). The latex from Euphorbia splendens var. hisloppi (N.E. Br.) Ursch & Leandri, Euphorbiaceae, was extracted by cutting through the stem of a plant in the winter of 2005 on the Fundação Oswaldo Cruz campus, Rio de Janeiro, Brazil. The latex was drained into test tubes. The tubes were hermetically sealed and carried to the laboratory for the preparation of mother solutions. The latex (1 mL) was collected in 9 mL of distilled water, the solution from which the required concentrations were obtained. The concentrations tested were 25, 50, 100, 125, 250 and 500 μL/L. The control group was exposed to distilled water only.

Ticks

A colony of R. (B.) sanguineus was maintained in the Laboratório de Educação em Ambiente e Saúde, Instituto Oswaldo Cruz, Fiocruz, RJ. Gravid females were colected from naturally infested dogs, in Rio de Janeiro-RJ, and free of acaricidal residues for at least thirty days prior to the bioassays. The ticks were reared on the ears of rabbits (Oryctolagus cuniculus) in the laboratory. The females were placed in BOD incubators acclimatized to 27±1 °C, 80% RH and a 12:12 h light/dark photoperiod. In order to obtain eggs of the same age cohort, separated plastic syringes, which were sealed with cotton wool plugs.

The experiments were conducted with 12 day old eggs and engorged larvae (14-21 day-old larvae). After exposure to latex, the samples were kept in BOD incubators acclimatized to 27±1 °C, 80% RH and a 12:12 h light/dark photoperiod until the end of the experiment.

Eggs exposure

For evaluation of latex efficacy on eggs, seven lots of 110 eggs of R. (B.) sanguineus were used for each concentration of latex. Eggs were exposed to 1 mL of each concentration inside the syringe (experimental groups) and the control group received only distilled water, since no other solvent was required to solubilize extracts of E. splendens. The concentration distributed uniformly on the internal surface of the syringes. After 5 min of exposure, the excess humidity was absorbed by the cotton, it was replaced by a dry one, and was returned to the incubator. After the treatment, eggs were observed daily, to check eclosion inhibition and possible changes resulting from the exposure to latex.

Engorged (fed) larvae

Larvae of R. (B.) sanguineus were placed on rabbit ears until engorgement. In order to evaluate the larvicidal efficacy of the latex, seven lots of fifty larvae of R. (B.) sanguineus were placed in plastic syringes and were tested as described above for the eggs. The tests were made in triplicate.

Evaluation of biological parameters

With the aid of an optical microscope the parameters evaluated were the eclosion of the eggs and the number of live and dead larvae (engorged) of R. (B.) sanguineus. The results were confirmed with analysis of variance (ANOVA). The difference between the percentage of hatching eggs and engorged larvae (live and dead) was evaluated through the Chi-Square and Tukey test (significance level: p<0.05) (Zar, 1999). The lethal dose (LD90 and LD50) against egg hatching was computed by Probit analysis (Finney, 1971).

Results and Discussion

The biocontrol activity of the latex from E. splendens var. hislopii, on the eggs of the tick R. (B.) sanguineus is shown in Figure 1. The egg hatching was observed in all groups and there was a significative difference in the eclosion percentage among treatments (Chi-Squared value=389.312, df=6, p<0.001) (Table 2). The egg hatching rate was inversely proportional to the concentration tested, i.e. the lower number of eclosions was observed for the higher concentrations of 125, 250 and 500 μL/L (1% for these concentrations). For the other concentrations tested the egg hatching rates were: 45% with 25 μL/L, 30% with 50 μL/L and 10% with 100 μL/L (Figure 1).


For the control group, the egg hatching rate was approximately 90%. Kaaya et al. (1995) using a different methodology, showed the efficiency of water-soluble extracts of Margaritaria discoidea an Euphorbiacea. The extracts of this plant induced a high mortality in nymphs and adults of R. appendiculatus and A. variegatum but the same was not observed for adults of A. variegatum.

Although eclosion occurred in all groups, for control and eggs treated with 25 μL/L of latex it began 24 h after treatment, while for the groups treated with the other concentrations the eclosions began only 72 h after exposure, thus demonstrating a possible embryogenic action.

The extract of E. splendens var. hislopii presented activity against eggs of R. (B.) sanguineus. The LD50 was 18.031 μL/L and LD90 was 84.610 μL/L, showing significant differences among the concentrations tested (X2=14.15; df=5 p<0.05). Gomes et al. (2003), tested latex from E. splendens var. hislopii as a candidate for as a biological control agent of P. chrysostoma (Wiedemann, 1830) (Sarcophagidae) with concentrations of 0.1, 0.2 and 0.3%, that equaled are equivalent to 100, 200 and 300 mg, respectively, of latex in 100 g of meat and observed interference on the post-embryonic development, promoting a reduction in the number of adults. Due to morphologically alterations these adults were unable to procreate. Mello et al. (2010) also evaluated the effect of crude lyophilized latex of E. splendens var. hislopii on the post-embryonic Megaselia scalaris (Loew, 1866) (Diptera: Phoridae) with concentrations of 5, 10 and 20 μg/mL, inoculated placed directly onto the bodies of the newlyhatched larvae with an automatic pipette (1 μL/larva), i.e., not applied the latex concentrations on the larvae differently as performed from the methodology used in the present study. These authors observed that the larval, pupal and newlyhatched larvae to adult development times were faster in the presence of this substance when compared with control group. This result was the inverse opposite of the obtained in the present study, in other words, in the present study there was a direct relationship in this study, between the increasing the latex concentration (50, 100, 125, 250 and 500 μL/L) there was an increase and the time of development (72 h). It is important detach to point out that the animal insect and the methodology above employed was were different of from the present study, and also that the latex was used in its crude lyophilized form, dissolved in distilled water and the solution was placed topically on the larvae, and whereas in the present study the eggs were exposed to 1mL of each concentration (crude latex dissolved in distilled water) inside the syringe. So this may have caused the observed differences between these studies.

Several studies with plant extracts of Ocimum suave, Gynandropsis gynandra, Azadirachta indica have reported the effectiveness of such plants as repellents, feeding inhibitors and other actions on the biology of these ticks (Malonza et al., 1992; Mwangi et al., 1995).

Based on the conditions related in the present study, the latex of E. splendens var. hislopii demonstrated an anti-embryogenic activity, since the unhatched eggs were pale and showed rough surfaces and the embryos were morphologically altered. Also the extracts influenced the hatching period of the eggs.

The efficacy of the treatments is demonstrated by the results in Table 1. On the first 1 day after treatment the effect of product proved to be was very small or negligible in the treated groups treated with 25 μL/L (4), 125 μL/L (3.33) and 250 μL/L (1.66). Pereira & Famadas (2004), observed mortality of engorged females of Boophhilus microplus (Canestrini, 1887) subjected to treatment with root extract from Dahlstedtia pentaphylla (Leguminosa, Papilionoidae, Millettiedae), which only becomes evident as from second day of exposure to the product. In the present study the best result obtained was seen 1 and 3 days after the application of the extract at a concentration of 100 μL/L (9.66 and 8.66) and 500 μL/L (5.66 and 9.33) respectively when compare to the control group.

On day 7 and 14 after application, the latex show is more efficient in killing at in the treated group (25, 50, 100, 125, 250 and 500 μL/L). As from day 21 the latex became less effective for all treatments, and by day 28 the product already had no effect whatsoever. These results suggest a better effect of the latex against engorged larvae, this because according to Pereira & Famadas (2004), scientific studies have proved that the larval stage of Boophilus microplus (Canestrini, 1887) is about eight times as sensitive to the product as the adult stage. In another study, Pereira & Famadas (2006) observed that the efficiencacy of Dahlstedtia pentaphylla (Leguminosae, Papilionoidae, Millettiedae) at in the concentrations of (1:10 and 1:20 mL) persisted up to day 7, and as from day 14, the product became less effective.

The engorged larvae were observed, displaying a low survival rate with all treatments showing a significant difference (Chi-Squared value=693.78, df=6, p<0.001): 0% at 25 μL/L, 1% at 50 μL/L, 2% at 100 μL/L, 4% at 125 μL/L, 9% at 250 μL/L and 5% at 500 μL/L, respectively (Figure 2 and Table 2).


The larvae that emerged had difficulties to move and were paralyzed. The survival rate of the control group was 91%. Although the results do not provide linearity, the latex presented an activity on eggs and larvae originated from engorged adults of R. (B.) sanguineus, acting directly on the biology of the ticks.

According to Chagas (2004), tests with plant extracts usually give a non-linear relationship between concentrations and action. Still according to the author, this may occur depending on the process of extraction and production of the active compound of the extract.

The results from the present study suggest that latex from E. splendens var. hislopii interfere with the development (eggs and engorged larvae) of R. (B.) sanguineus, thus indicating a potential candidate for biological control.

References

Abdel-Shafy S, Zayed AA 2002. In vitro acaricidal effect of neem seed oil (Azadirachta indica) on egg, immature adult stages of Hyalomma anatolicum excavatum (Ixodoidea:Ixodidae). Vet Parasitol 106: 89-96.

Belot J, Mishra G 1979. Toxité de huit produits acaricides différents sur le tiques de l´espèce Vétérinaire Rhipicephalus sanguineus. Recueil de Médicine 155: 869-871.

Chagas ACS 2004. Controle de parasitas utilizando extratos vegetais. Rev Bras Parasitol Vet 13: 156-160.

Cristophers SR 1907. Piroplasma canis and its life-cycle in the tick. Sci. Mem. Med. & Sanit. Dep. India. 29: 40-43, In: Nuttall, GHF. Biology of ixodides Parasitology, p.7.

Dipeolu OO, Akinboade AO, Ogunji FO 1982. Observations on the epidemiology of house infesting Rhipicephalus sanguineus in a household in Lagos, Nigéria. Bull Anim Hlth Prod Afr 30: 29-30.

Feldman-Muhsam B 1956. Host specificity of Rhipicephalus sanguineus (Latreille) and R. secundus Feldman-Muhsan in Israel. Bull Ent Res 47: 43-45.

Fernandes FF 1997. Dispositivo experimental para manutenção de colônias de ixodídeos visando ao estudo dos parâmetros biológicos da fase de vida livre do ciclo evolutivo. Rev Goiana Med 42: 43-48.

Fernandes FF 2000. In vitro activitty of permethrin, cipermethrin and deltamethrin on larvae of Rhipicephalus sanguineus (Latreille, 1806) (Acari, Ixodidae). Arq Bras Med Vet Zoot 52: 621-626.

Finney DJ 1971. Probit Analysis. Cambridge University Press, New Delhi, 333p.

Furlong J 1993. Controle do carrapato dos bovinos na Região Sudeste do Brasil. Cadastro Técnico da Escola de Veterinária da Universidade Federal de Minas Gerais. 8: 49-61.

Gladney WJ, Dawkins CC 1976. The brown dog tick: laboratory tests of acaricides. Southwestern Entomol 1: 184-189.

Gomes CM, d'Almeida JM, Santos JAA 2003. Avaliação do efeito do látex de Euphorbia splendens var. hislopii (N.E.B.) (Euphorbiacea), no desenvolvimento pós embrionário de Peckia chrysostoma (Wiedemann, 1830) (Diptera: Sarcophagidae), em condições de laboratório. Entomol Vect 10: 109-120.

Harrison BA, Engber BR, Apperson CS 1997. Ticks (Acari:Ixodidae) uncommonly North Carolina found biting humans. J Vector Ecol 22: 6-12.

Hoogstraal H 1967. Ticks in relation to human diseases caused by Rickettsia species, Ann Rev Ent 12: 377-420.

Kaaya GP, Mwangi EN, Malonza MM 1995. Acaricidal activity of Margaritaria discoidea (Euphorbiacea) plant exracts aginst the ticks Rhipicephalus sanguineus and variegatum (Ixodidae). Int J Acarol 21: 123-129.

Leles NR, Fernandes FF 2005. Estudo da bioatividade larvicida das plantas Copaifera langsdorffii e Carapa guianensis para o controle de Rhipicephalus sanguineus (Latreille, 1806). In: Congresso de Pesquisa, Ensino e Extensão da UFG- CONPEEX.

Lugt CB 1987. Feseability of growth and productions of molluscidal plants. In: Mott KE (Eds), Plant Molluscicides. New York, UNDP/World Bank/WHO, p. 231-244.

Malonza MM, Dipeolu OO, Amoo AO, Hassan SM 1992. Laboratory and field observations on anti tick properties of the plant Gynandropsis gynandra (L.) Brig Vet Parasitol 42: 123-136.

Mantovani A, Benazzi P 1953. The isolation of Coxiella burnetti from Rhipicephalus sanguineus on naturally infectes dog. J Am Vet Med Ass 122: 117-118.

Mello, RS, Ferreira, ARS, Queiroz, MMC 2010. Bioactivity of latex from Euphorbia splendens var. hislopii (Euphorbiaceae) on post-embryonic development of Megaselia scalaris (Phoridae). Vet Parasitol 172: 100-104.

Mwangi EN, Essuman S, Kaaya GP, Nyandat E, Munyinyi D, Kimondo G 1995. Repellence of the tick Rhipicephalus appendiculatus by the grass Melinis minutiflora Top Anim Hlth Prod 27: 211-216.

Pereira JR, Famadas KM 2004. Avaliação in vitro da eficiencia do extrato da raíz do timbó (Dahlstedtia pentaphylla) (Leguminosae, Papilionoidae, Millettidae) sobre Boophilus micropluss (Canestrini, 1887) na região do Vale da Paraíba, São Paulo, Brasil. Arq Insect Biol 71: 443-450.

Pereira JR, Famadas KM 2006. The efficieny of the extracts of Dahlstedtia pentaphylla (Leguminosae, Papilionoidae, Millettidae) on Boophilus micropluss (Canestrini, 1887) in artificially infested bovines. Vet Parasitol 142: 191-195.

Racioppi O, Lombardero O, Moriena RA 1981. Presencia de Rhipicephalus sanguineus (Koch, 1844) en perros de la ciudade de Corrientes. Gac Vet B Aires 43: 447-452.

Schall VT, Vasconcellos MC, Vilaca-Coelho AL, Ferreira-Lopes FE, Silva IP 1992. Evaluation of temporal, seasonal and geographic stability of the molluscicidal property of Euphorbia splendens latex. Rev Inst Med Trop 34: 183-191.

Simpson RM, Gaunt SD, Hair JA, Kocan KM, Henk WG, Casey HM 1991. Evaluation of Rhipicephalus sanguineus as a potential biologic vector of Ehrlichia platys. Am J Vet Res 52: 1537-1541.

Smith RD, Sells DM, Stephenson EH, Ristic M, Huxoll DL 1976. Development of Ehrlichia canis, causative agent of canine ehrlichiosis, in the tick R. sanguineus and its differentiation from a symbiotic rickettsia. Am J Vet Res 37: 119-126.

Zar JH 1999. Biostatistical Analysis. Prentice Hall, New Jersey, 831p.

Received 7 Apr 2010

Accepted 6 Oct 2010

  • Abdel-Shafy S, Zayed AA 2002. In vitro acaricidal effect of neem seed oil (Azadirachta indica) on egg, immature adult stages of Hyalomma anatolicum excavatum (Ixodoidea:Ixodidae). Vet Parasitol 106: 89-96.
  • Belot J, Mishra G 1979. Toxité de huit produits acaricides différents sur le tiques de l´espèce Vétérinaire Rhipicephalus sanguineus. Recueil de Médicine 155: 869-871.
  • Chagas ACS 2004. Controle de parasitas utilizando extratos vegetais. Rev Bras Parasitol Vet 13: 156-160.
  • Cristophers SR 1907. Piroplasma canis and its life-cycle in the tick. Sci. Mem. Med. & Sanit. Dep. India. 29: 40-43, In: Nuttall, GHF. Biology of ixodides Parasitology, p.7.
  • Dipeolu OO, Akinboade AO, Ogunji FO 1982. Observations on the epidemiology of house infesting Rhipicephalus sanguineus in a household in Lagos, Nigéria. Bull Anim Hlth Prod Afr 30: 29-30.
  • Feldman-Muhsam B 1956. Host specificity of Rhipicephalus sanguineus (Latreille) and R. secundus Feldman-Muhsan in Israel. Bull Ent Res 47: 43-45.
  • Fernandes FF 1997. Dispositivo experimental para manutenção de colônias de ixodídeos visando ao estudo dos parâmetros biológicos da fase de vida livre do ciclo evolutivo. Rev Goiana Med 42: 43-48.
  • Fernandes FF 2000. In vitro activitty of permethrin, cipermethrin and deltamethrin on larvae of Rhipicephalus sanguineus (Latreille, 1806) (Acari, Ixodidae). Arq Bras Med Vet Zoot 52: 621-626.
  • Finney DJ 1971. Probit Analysis. Cambridge University Press, New Delhi, 333p.
  • Furlong J 1993. Controle do carrapato dos bovinos na Região Sudeste do Brasil. Cadastro Técnico da Escola de Veterinária da Universidade Federal de Minas Gerais. 8: 49-61.
  • Gladney WJ, Dawkins CC 1976. The brown dog tick: laboratory tests of acaricides. Southwestern Entomol 1: 184-189.
  • Gomes CM, d'Almeida JM, Santos JAA 2003. Avaliação do efeito do látex de Euphorbia splendens var. hislopii (N.E.B.) (Euphorbiacea), no desenvolvimento pós embrionário de Peckia chrysostoma (Wiedemann, 1830) (Diptera: Sarcophagidae), em condições de laboratório. Entomol Vect 10: 109-120.
  • Harrison BA, Engber BR, Apperson CS 1997. Ticks (Acari:Ixodidae) uncommonly North Carolina found biting humans. J Vector Ecol 22: 6-12.
  • Hoogstraal H 1967. Ticks in relation to human diseases caused by Rickettsia species, Ann Rev Ent 12: 377-420.
  • Kaaya GP, Mwangi EN, Malonza MM 1995. Acaricidal activity of Margaritaria discoidea (Euphorbiacea) plant exracts aginst the ticks Rhipicephalus sanguineus and variegatum (Ixodidae). Int J Acarol 21: 123-129.
  • Leles NR, Fernandes FF 2005. Estudo da bioatividade larvicida das plantas Copaifera langsdorffii e Carapa guianensis para o controle de Rhipicephalus sanguineus (Latreille, 1806). In: Congresso de Pesquisa, Ensino e Extensão da UFG- CONPEEX.
  • Lugt CB 1987. Feseability of growth and productions of molluscidal plants. In: Mott KE (Eds), Plant Molluscicides. New York, UNDP/World Bank/WHO, p. 231-244.
  • Malonza MM, Dipeolu OO, Amoo AO, Hassan SM 1992. Laboratory and field observations on anti tick properties of the plant Gynandropsis gynandra (L.) Brig Vet Parasitol 42: 123-136.
  • Mantovani A, Benazzi P 1953. The isolation of Coxiella burnetti from Rhipicephalus sanguineus on naturally infectes dog. J Am Vet Med Ass 122: 117-118.
  • Mello, RS, Ferreira, ARS, Queiroz, MMC 2010. Bioactivity of latex from Euphorbia splendens var. hislopii (Euphorbiaceae) on post-embryonic development of Megaselia scalaris (Phoridae). Vet Parasitol 172: 100-104.
  • Mwangi EN, Essuman S, Kaaya GP, Nyandat E, Munyinyi D, Kimondo G 1995. Repellence of the tick Rhipicephalus appendiculatus by the grass Melinis minutiflora Top Anim Hlth Prod 27: 211-216.
  • Pereira JR, Famadas KM 2004. Avaliação in vitro da eficiencia do extrato da raíz do timbó (Dahlstedtia pentaphylla) (Leguminosae, Papilionoidae, Millettidae) sobre Boophilus micropluss (Canestrini, 1887) na região do Vale da Paraíba, São Paulo, Brasil. Arq Insect Biol 71: 443-450.
  • Pereira JR, Famadas KM 2006. The efficieny of the extracts of Dahlstedtia pentaphylla (Leguminosae, Papilionoidae, Millettidae) on Boophilus micropluss (Canestrini, 1887) in artificially infested bovines. Vet Parasitol 142: 191-195.
  • Racioppi O, Lombardero O, Moriena RA 1981. Presencia de Rhipicephalus sanguineus (Koch, 1844) en perros de la ciudade de Corrientes. Gac Vet B Aires 43: 447-452.
  • Schall VT, Vasconcellos MC, Vilaca-Coelho AL, Ferreira-Lopes FE, Silva IP 1992. Evaluation of temporal, seasonal and geographic stability of the molluscicidal property of Euphorbia splendens latex. Rev Inst Med Trop 34: 183-191.
  • Simpson RM, Gaunt SD, Hair JA, Kocan KM, Henk WG, Casey HM 1991. Evaluation of Rhipicephalus sanguineus as a potential biologic vector of Ehrlichia platys. Am J Vet Res 52: 1537-1541.
  • Smith RD, Sells DM, Stephenson EH, Ristic M, Huxoll DL 1976. Development of Ehrlichia canis, causative agent of canine ehrlichiosis, in the tick R. sanguineus and its differentiation from a symbiotic rickettsia. Am J Vet Res 37: 119-126.
  • Zar JH 1999. Biostatistical Analysis. Prentice Hall, New Jersey, 831p.
  • *
    E-mail:
    zeneida@ioc.fiocruz.br, Tel.:+ 55 21 2562 1846.
  • Publication Dates

    • Publication in this collection
      18 Mar 2010
    • Date of issue
      June 2011

    History

    • Received
      07 Apr 2010
    • Accepted
      06 Oct 2010
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