Memórias do Instituto Oswaldo Cruz
Fundação Oswaldo Cruz, Fiocruz
ISSN: 1678-8060
Vol. 90, Num. 3, 1995, pp. 329-330
Mem Inst Oswaldo Cruz, Rio de Janeiro, Vol. 90(3): 329-330, may/jun. 1995

RESEARCH NOTE

Fate of Bacillus sphaericus after Ingestion by the Predator Belostoma micantulurn ( Hemiptera: Belostomatidae)

CJ Carvalho-Pinto, L Rabinovitch*, RSA Alves*, CMB Silva*, RAGB Consoli**

Code Number: OC95065 Size of Files: Text: 6K Graphics: Line Drawings (gif) 18K

Departamento de Microbiologia e Parasitologia, Universidade Federal de Santa Catam, Caixa Postal 476, 88040- 900 Florianopolis, SC, Brasil *Laboratorio de Fisiologia Bacteriana, Departamento de Bacteriologia, Instituto Oswaldo Cruz, Rio de Janeiro, RJ, Brasil **Centro de Pesquisas Rene Rachou - HOCRUZ, Belo Honzonte, MG, Departamento de Parasitologia, ICB, UFMG, Bdo Honzonte, MG, Brasil

Key words: Bacillus sphaericus - Culex quinquefasciatus - Belostoma micantulum biological control

The persistence of Bacillus sphaericus in the environment can be influenced by the activity of other organisms present in the mosquito larval habitat and its controling efficacy can be related to the density of non- target arthropods (S Karch et al. 1990 J Am Mosq ControIAssoc 6: 47-54).

Belostoma micantulum, commonly known as water-bug, is an aquatic hemiptera prevalent in South America from Guiana to Argentina (GR Spinelli et al. 1983 Neotropica 29: 27- 34) which coexists with mosquito larvae and is an efficient predator of them (AS Mijares, RG Broche 1985 Rev Cub Hyg y Epid 37: 203-209).

With the aim of assessing the fate of the bacteria after their ingestion by the hemiptera as well as their behavior in cadavers of these insects, 90 adults of B. micantulum each placed in a plastic cup containing 200 ml of dechlorinated water was fed each with ten 4th instar larvae of Culex quinquefasciatus previously infected with B. sphaericus 2362 strain (8.1 x 10^4 spores/ml for 30 min). A group of 50 mosquitoes larvae was transferred to a cup containing only distilled water to confirm the bacterial infection showed by observation of 100% of morality after 48 hr. Forty-five hemiptera were killed by crushing their heads immediately after feeding on larvae and were kept isolated in plastic cups in sterile dechlorinated water. The rest of the hemiptera was kept alive in the same conditions. Staing from the first day after feeding the water-bugs, their guts were dissected, ground and homogenized in 1 ml of sterile dechlorinated water. This material was split into two subsamples, one of which was submitted to a heat shock (80 C/15 min) to kill all vegetative cells and non spore forming bacteria. Of each subsample, 0.1 ml or a dilution of it was plated in NYSM medium (PS Myers, AA Yousten 1978 Infect Immun 19: 1047-1053) in Petri dishes containing 100 mg/l of streptomycin. Three hemiptera were dissecated in each day and their guts were individually ground, homogeinized in water and plated in culture medium.

The colony counts were recorded after a 24 hr growth period at 35 C. B. sphaericus presence was confirmed by the observations of morfology colonies as well as microscopic observation of smears stained by the Gram's method. Also, the material of some randomly selected colonies of each dish was diluted in water and transferred to plastic cups each containing dechlorinated water and ten 4th instar larvae of Cx. quinquefasciatus to confirm entomopathogenicity after 48 hr. All larvae died after this period of time.

Figure shows the observed results. The number of colony- forming units (CFU) and spores found in the gut of live water- bugs decreased to very low levels in the first days after ingestion of infected mosquito larvae. After 30 and 60 days no more bacterial presence was detected (Fig. A). The platings of feces of water-bugs collected in the cups which contained them, in the first days of experiment, were also positive for B. sphaericus, showing that this bacteria is released through water-bugs feces during the first days after ingestion of infected mosquitoes larvae. In water-bugs cadavers, after a little initial decrease, we observed a strong increase of CFU number and spores, that showed to be stable from the 10th until the 60th day when the experiment was finished (Fig. B). It seems that these bacteria are able to make use of water-bug cadavers in order to grow and posteriorly esporulate.

B. sphaericus grows in dead larval tissues of Cx. quinquefasciatus larvae (S Silapanuntaknl et al. 1983 J Invertebr Pathol 42: 387-392, B Des Rochers, R Garcia 1984 Mosq News 44 (2-Pan I): 160-165). The present work confirms the hypothesis that, in the absence of dead mosquito larvae, this bacteria can still multiply if sufficient proteinaceous material is available in its environment (VL Kramer 1990 J F. con Entomol 83: 1280-1285). This replication in cadavers may occur in other animals Which, somehow, ingest B. sphaericus.

    Figure 1. Number of colony-forming umts - CFU (.) and spores (1) of Bacillus sphaericus in the guts of alive (A) and dead (B) Belostoma micantulura fed with Culex quinquefasciatus larvae infected by B. sphaericus for different pe- riods of time. Each point represents the mean of three observations.

The ability of B. sphaericus to reproduce in cadaverts of other animals besides mosquito larvae could be an impoaant factor to increase its persistence in mosquito breeding sites and consequently result in its better efficacy as a larval control agent.

Copyright 1995 Fundacao Oswaldo Cruz


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