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. 2005 Jul;71(7):4052-6.
doi: 10.1128/AEM.71.7.4052-4056.2005.

Mediterranean fruit fly as a potential vector of bacterial pathogens

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Mediterranean fruit fly as a potential vector of bacterial pathogens

Shlomo Sela et al. Appl Environ Microbiol. 2005 Jul.

Abstract

The Mediterranean fruit fly (Ceratitis capitata) is a cosmopolitan pest of hundreds of species of commercial and wild fruits. It is considered a major economic pest of commercial fruits in the world. Adult Mediterranean fruit flies feed on all sorts of protein sources, including animal excreta, in order to develop eggs. After reaching sexual maturity and copulating, female flies lay eggs in fruit by puncturing the skin with their ovipositors and injecting batches of eggs into the wounds. In view of the increase in food-borne illnesses associated with consumption of fresh produce and unpasteurized fruit juices, we investigated the potential of Mediterranean fruit fly to serve as a vector for transmission of human pathogens to fruits. Addition of green fluorescent protein (GFP)-tagged Escherichia coli to a Mediterranean fruit fly feeding solution resulted in a dose-dependent increase in the fly's bacterial load. Flies exposed to fecal material enriched with GFP-tagged E. coli were similarly contaminated and were capable of transmitting E. coli to intact apples in a cage model system. Washing contaminated apples with tap water did not eliminate the E. coli. Flies inoculated with E. coli harbored the bacteria for up to 7 days following contamination. Fluorescence microscopy demonstrated that the majority of fluorescent bacteria were confined along the pseudotrachea in the labelum edge of the fly proboscis. Wild flies captured at various geographic locations were found to carry coliforms, and in some cases presumptive identification of E. coli was made. These findings support the hypothesis that the common Mediterranean fruit fly is a potential vector of human pathogens to fruits.

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Figures

FIG. 1.
FIG. 1.
Acquisition of GFP-tagged E. coli by Mediterranean fruit flies exposed to contaminated feed. Flies were exposed for 24 h to a 20% sucrose solution supplemented with different numbers of tagged E. coli cells. Male and female flies were collected separately, and the number of Ampr, GFP-expressing bacteria in 20 flies was determined.
FIG. 2.
FIG. 2.
Mediterranean fruit flies acquire E. coli from contaminated fecal material. Flies were exposed to a 20% sucrose solution or fecal material enriched with 2 × 109 CFU/ml GFP-labeled E. coli for 20 h. The numbers of labeled bacteria in males and females were determined. Flies could efficiently acquire E. coli from both the sucrose solution and fecal material in similar numbers. Bacteriological determinations were performed with batches of 10 males and 10 females per replicate (three replicates per treatment).
FIG. 3.
FIG. 3.
Survival of E. coli on contaminated Mediterranean fruit flies. Flies were exposed to a sucrose solution supplemented with 4.6 × 109 CFU/ml of E. coli for 20 h. After this, a sample of 10 to 20 flies was collected each day from the cage and subjected to microbiological analysis. Day 1 refers to the 24 h after the beginning of exposure. No E. coli was detected on preexposure flies.
FIG. 4.
FIG. 4.
Visualization of E. coli in the Mediterranean fruit fly by fluorescence microscopy. Flies were fed a 20% sucrose solution supplemented with 109 CFU/ml GFP-expressing E. coli. (A) Micrograph of the labelum under UV light, with bacteria clearly present in the pseudotrachea of the labelum (arrows). (B) Fine structure of the labelum with associated fluorescent bacteria at a higher magnification. Bars, 100 μm.

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