Acetobacter tropicalis Is a Major Symbiont of the Olive Fruit Fly (Bactrocera oleae)

Following cultivation-dependent and -independent techniques, we investigated the microbiota associated with Bactrocera oleae, one of the major agricultural pests in olive-producing countries. Bacterial 16S rRNA gene libraries and ultrastructural analyses revealed the presence of several bacterial taxa associated with this insect, among which Acetobacter tropicalis was predominant. The recent increased detection of acetic acid bacteria as symbionts of other insect model organisms, such as Anopheles stephensi (G. Favia et al., Proc. Natl. Acad. Sci. USA 104:9047-9051, 2007) or Drosophila melanogaster (C. R. Cox and M. S. Gilmore, Infect. Immun. 75:1565-1576, 2007), prompted us to investigate the association established between A. tropicalis and B. oleae. Using an A. tropicalis-specific PCR assay, the symbiont was detected in all insects tested originating from laboratory stocks or field-collected from different locations in Greece. This acetic acid bacterium was successfully established in cell-free medium, and typing analyses, carried out on a collection of isolates, revealed that different A. tropicalis strains are present in fly populations. The capability to colonize and lodge in the digestive system of both larvae and adults and in Malpighian tubules of adults was demonstrated by using a strain labeled with a green fluorescent protein.Associations of insects with bacteria, protozoa, and fungi are complex and intimate, ranging from parasitism to mutualism, and may be extracellular or intracellular and may play a role in the nutrition, the physiology, or the reproduction of the insect host (10). Petri (1909 to 1910) described one of the first bacterial symbiotic associations in an insect species, the olive fly, Bactrocera (Dacus) oleae (31, 32).The olive fruit fly B. oleae is one of the major pests of the olive tree, strongly affecting olive production worldwide, especially in the Mediterranean area, where more than 90% of the world''s olive tree cultivation takes place (24, 27). Although there have been reports on the isolation of potentially effective Bacillus thuringiensis strains against B. oleae, olive fly control strategies remain almost exclusively based on insecticides, despite the awareness of a need for the use of more environmentally friendly control methods (29). Recently, new concepts are emerging, among which the symbiotic control approach is particularly noteworthy (4). This strategy includes the use of symbionts as vectors of antagonistic factors able to block the life cycle of the plant pathogen in the insect host or, alternatively, their use for the suppression of host natural populations (45). In any case, a prerequisite for developing a symbiotic control approach is the knowledge of the microbiota associated with the insect pest.The nature of the olive fruit fly-associated microbiota is controversial. The culturable bacterium Pseudomonas savastanoi has been suspected to be a mutualist of B. oleae for more than 50 years (6, 17, 22, 25, 32, 33). In addition, traditional microbiological approaches have identified other bacteria of the genera Bacillus, Erwinia, Lactobacillus, Micrococcus, Pseudomonas, Streptococcus, Citrobacter, Proteus, Providencia, Enterobacter, Hafnia, Klebsiella, Serratia, and Xanthomonas as associated with the olive fruit fly (3, 14, 19, 37). Recently, it was suggested that the bacterium housed within the esophageal bulb and the midgut of B. oleae is unculturable, and the novel name “Candidatus Erwinia dacicola” was proposed (7). The presence of “Ca. Erwinia dacicola” was confirmed in Italian natural populations (36).The contradictory results obtained in previous studies prompted us to investigate the microbiota associated with both laboratory and natural populations of the olive fruit fly by employing both cultivation-independent and -dependent methods.     

Biochemical Differences Between Products of the ADH Locus in Olive Fruit Fly (Bactrocera oleae)

Purified alcohol dehydrogenases from olive fruitflies of genotypes SS, II, and SI were biochemicallycompared. The enzymes were found to differ in thespecific activity, in the influence of pH andtemperature on activity, and in the affinity with differentsubstrate-alcohols. The probable relationships of thesefindings with the dramatic changes in allele frequenciesobserved when natural populations are introduced in the laboratory are discussed.     

Aggressive Behavior and Territoriality in the Olive Fruit Fly,Bactrocera oleae (Rossi) (Diptera: Tephritidae): Role of Residence and Time of Day

Bactrocera oleae is a worldwide olive fruit pest. In late afternoon males form swarms on the windward side of trees. Within the swarm, each male occupies a leaf and aggressively excludes male conspecifics before starting courtship displays. Females display aggressive interactions each other too, particularly when they are in close proximity of oviposition sites. In this research, the aggressive behavior displayed by both sexes was quantified. Aggressions were composed by wing waving, fast running towards the opponent, pouncing and boxing on the head and thorax of the foe. High-speed videos highlighted that the parameters characterizing the aggressions did not strongly differ between sexes and between residents and intruders. Resident flies won more combats, both in male-male and female-female aggressive interactions. In both sexes, aggressions were more frequent in the late morning than in the afternoon. Among males, aggressions could be functional to maintain single leaf territories in which each fly can perform courtship displays. Through aggressions females could gain and maintain single oviposition sites. Lastly, by favorable fight outcomes B. oleae could also get access to food sources on olive leaves and fruits.     

Characterization of Two Alcohol Dehydrogenase (Adh) Loci from the Olive Fruit Fly, Bactrocera (Dacus) oleae and Implications for Adh Duplication in Dipteran Insects

We report the cloning and structural characterization of two Adh loci of the olive fruit fly, Bactrocera oleae. Each of the two genes, named Adh1 and Adh2, consists of three exons and two introns for a total length of 1981 and 988 nucleotides, respectively. Their deduced amino acid sequences of 257 and 258 residues exhibit a 77% identity and display the characteristics of the insect ADH enzymes, which belong to the short-chain dehydrogenases/reductases family. The Adh genes of B. oleae are compared to the two genes of the Mediterranean fly, Ceratitis capitata, the only other species of the Tephritidae family in which the Adh genes have been studied. On the basis of amino acid divergence the four genes form two clusters each containing one gene from each species, as expected if there was one duplication event before speciation. On the basis of nucleotide sequence the four sequences form two clusters each containing the two sequences from the same species, as expected if there was a separate duplication event in each species. To help decide between the two alternatives, we compared at both the amino acid and DNA level the Adh genes of five Drosophila species that are known to carry two such genes and observed that, with only one exception at the amino acid level, conspecific loci cluster together. We conclude that the information we have at present does not allow a firm choice between the hypothesis of a single duplication event that occurred before the split of Bactrocera and Ceratitis from their common ancestor and the hypothesis of two independent duplication events, one in each of the two genera. Received: 30 May 2000 / Accepted: 17 August 2000     

Cricket Paralysis Virus, a Potential Control Agent for the Olive Fruit Fly, Dacus oleae Gmel

Representatives of several families of insect viruses were tested for growth and pathogenicity in the olive fruit fly, Dacus oleae Gmel. The viruses included nuclear polyhedrosis viruses, an iridovirus, two picornaviruses, and Trichoplusia ni small RNA virus (a member of the Nudaurelia β family), in addition to two naturally occurring viruses of the olive fruit fly. Two viruses, one of the two picornaviruses (cricket paralysis virus [CrPV] and the iridovirus (type 21 from Heliothis armigera), were found to replicate in adult flies. Flies which were fed on a solution containing CrPV for 1 day demonstrated a high mortality with 50% dying within 5 days and nearly 80% dying within 12 days of being fed. The virus was transmissible from infected to noninfected flies by fecal contamination. The CrPV which replicated in the infected flies was demonstrated to be the same as input virus by infection of Drosophila melanogaster cells and examination of the expressed viral proteins, immunoprecipitation of the virus purified from flies, and electrophoretic analysis of the structural proteins.     

Mitochondrial haplotypes reveal olive fly (Bactrocera oleae) population substructure in the Mediterranean

The olive fly (Bactrocera oleae) is the most important olive tree (Olea europaea) pest. In the Mediterranean basin, where 98?% of its main hosts are concentrated, it causes major agricultural losses, due to its negative effect on production and quality of both olive and olive oil. Previous phylogeographic analyses have established that Mediterranean olive fly populations are distinct from other Old World populations, but did not agree on the specific population substructure within this region. In order to achieve a higher resolution of the diversity of olive fly populations, particularly in Central and Western Mediterranean (home to 70?% of the world production), we comparatively analyzed a set of samples from Portugal in the context of published mitochondrial sequences across the species' worldwide range. Strong evidence of population substructure was found in the Central and Western Mediterranean area, with two clearly separate phylogenetic branches. Together with previously published data, our results strongly support the existence of at least three distinct Mediterranean populations of the olive fly, raise the possibility of additional regional substructure and suggest specific avenues for future research. This knowledge can be instrumental in the development of better management and control strategies for a major pest of Mediterranean agriculture.     

福建地区橘小实蝇田间种群动态监测研究

利用Steiner诱捕器内置诱捕剂Me或Cue与0.2%马拉硫磷混合物制成棉球诱芯,在福建省各个地区共设置50个监测点,诱捕监测橘小实蝇（Bactrocera dorsalis Hendel）种群动态。从2002～2005年,连续4年的诱捕结果表明,橘小实蝇在福建省的发生呈单峰特点,7～9月为发生盛期,高峰出现在8月份。瓜菜园生境、石榴芒果园生境和龙眼香蕉园生境中,石榴芒果园生境橘小实蝇种群密度最高。运用地理信息系统（MapInfo）对该虫监测数据进行地图分析表明,橘小实蝇种群密度的地域特征明显,橘小实蝇有不断向外扩散的趋势。     

Olive fruit fly [Bactrocera (Dacus) oleae (Rossi) (Diptera: Tephritidae)] adult rearing diet without antibiotic

The olive fruit fly [Bactrocera (Dacus) oleae (Rossi) (Diptera: Tephritidae)] adult diet since its development in the 1960’s regularly incorporates antibiotic. Considering recent findings on the importance and function of the indigenous microbial flora of insects, the effects of antibiotic removal were measured on the survival and egg laying of wild flies derived from McPhail trappings and from field infested olive fruits. In the first case wild flies fed no antibiotic laid significantly greater numbers of eggs for two generations (in 5 out of 10 and 2 out of 10 counting dates for G1 and G2 respectively), while there were no significant differences in survival in either test (P = 0.221 for P generation, P = 0.988 for G1 generation from McPhail traps, P = 0.056 for flies from infested fruits). Percent egg–pupa recovery and adult emergence were not significantly affected by lack of antibiotic. An antibiotic‐free strain has been maintained for eight generations, showing acceptable performance when compared to the long‐reared standard ‘Laboratory’ strain. Overall results suggest the feasibility of an adult diet free of antibiotic without negative effects on colony survival and performance.     

Influence of Female Age on Variation of Mate Choice Behavior in Mediterranean Fruit Fly (Diptera: Tephritidae)

In spite of the fact that studies concerning the mate choice by females have largely been based on the idea of the unanimity of the preference for certain male characteristics, variations in this behavior have been reported. Considering this aspect, we studied the influence of female age on mate choice and on the acceptance of courting by males of different ages in lab-reared medflies. The effects of the age of both sexes on the total courtship duration and on the behavioral units performed by males were also examined. Our results demonstrated that: (1) 4 to 12 day-old females prefer younger males; (2) 20 day-old females were less selective; (3) the acceptance of courting was not influenced by male age neither by the duration of behavioral units of courtship; (4) only the duration of continuous wing vibration was affected by the age of both sexes.     

Polymorphic microsatellite markers in the Melon Fruit Fly, Bactrocera cucurbitae (Coquillett) (Diptera: Tephritidae)

Bactrocera cucurbitae (Coquillett) is an important insect pest of melon fruit causing extensive losses of production in Asia and Pacific areas. Twelve polymorphic microsatellite loci were isolated from an enriched DNA library of this species and their amplification characteristics are described. Genetic parameters were estimated on 80 individual flies from four natural populations. Allele numbers per locus ranged from three to 20. These microsatellite markers have potential utility in population structure and gene flow studies of B. cucurbitae.     

Population structure and colonization history of the olive fly, Bactrocera oleae (Diptera, Tephritidae)

The olive fly, Bactrocera oleae, is the major pest of olives in most commercial olive-growing regions worldwide. The species is abundant in the Mediterranean basin and has been introduced recently into California and Mexico, creating problems for quarantine protection and international trade. Here, we use nuclear microsatellite markers and mitochondrial sequences to examine the history of olive fly range expansion and colonization. Sampled populations span the current distribution of the olive fly worldwide, including South and Central Africa, Pakistan, Mediterranean Europe and Middle East, California, and Mexico. The Pakistani populations appear to be genetically well differentiated from the remaining populations, though rooting the origins of the species is problematic. Genetic similarity and assignment tests cluster the remaining populations into two genetic groups--Africa and a group including the Mediterranean basin and the American region. That Africa, and not the Mediterranean, is the origin of flies infesting cultivated olive is supported by the significantly greater genetic diversity at microsatellite loci in Africa relative to the Mediterranean area. The results also indicate that the recent invasion of olive flies in the American region most likely originated from the Mediterranean area.     

Polymorphic microsatellite DNA markers from the Oriental Fruit Fly Bactrocera dorsalis (Hendel)

Six polymorphic microsatellite loci are isolated from the Oriental fruit fly Bactrocera dorsalis (Hendel), an agricultural pest in Asia, including Taiwan. To assess their potential utility as high‐resolution genetic markers, polymerase chain reaction (PCR) primers, amplification conditions, and an automated fluorescence detection protocol were developed. In analyses of 71 individual flies from six different areas of Taiwan, allele numbers ranged from five to 25 were detected for each locus. The observed heterozygosity ranged between 0.268 and 0.737 among these loci. No linkage disequilibrium was found. These microsatellite markers have potential utility to population structure and gene flow studies of B. dorsalis (Hendel).     

Evaluation of Entomopathogenic Nematodes for the Control of Mediterranean Fruit Fly (Diptera: Tephritidae)

The virulence of various entomopathogenic nematode (EPN) strains was evaluated against the Mediterranean fruit fly, C. capitata . The selected nematodes were assessed for their infectivity for the final larval stage of the insect host and under varying environmental conditions. Among 12 EPN strains tested, Steinernema riobrave Texas ( Sr TX) and Heterorhabditis sp. IS-5 (H IS-5), showed high activity and induced >80% mortality. Six EPN strains showed limited activity (>30% mortality), and four strains had no effect (<20% mortality). Sr TX was more effective than H IS-5. Mature C. capitata larvae were most susceptible to nematode infection during the first 4h after they began to emerge from their diet to pupate. Activity of the two nematode strains at a constant inoculation rate was dependent on insect larval density. The highest activity was recorded at 1.88 larvae cm -2 and decreased at higher larval densities. EPN activity was also directly related to nematode density. Maximal activity was shown at a density of 150 infective juveniles cm -2 . A similar activity pattern was also recorded with Sr TX in four different soil types. The persistence of this EPN in the soil extended over 5 days but there was no activity after 14 days. Except for a lower activity under cool conditions (17°C), temperatures ranging between 22 and 41°C, or moisture levels in the treated soil ranging between 3 and 20%, had no significant effect on nematode activity. Our results suggest that application of Sr TX against C. capitata may have potential for controlling C. capitata .     

Climate warming effects on the Olea europaea–Bactrocera oleae system in Mediterranean islands: Sardinia as an example

Global warming will affect all species but in largely unknown ways, with certain regions such as the Mediterranean Basin and its major islands including Sardinia being particularly vulnerable to desertification. Olive ( Olea europaea ) is of eco-social importance in the Mediterranean where it was domesticated. This drought-resistant crop and its major pest, the olive fly ( Bactrocera oleae ), have tight biological links that make them a suitable model system for climate change studies in the Mediterranean. Here a physiologically based weather-driven demographic model of olive and olive fly is used to analyze in detail this plant–pest system in Sardinia under observed weather (10 years of daily data from 48 locations), three climate warming scenarios (increases of 1, 2 and 3 °C in average daily temperature), and a 105-year climate model scenario for the Alghero location (e.g. 1951–2055). grass gis is used to map model predictions of olive bloom dates and yield, total season-long olive fly pupae, and percent fruit attacked by the fly. Island wide simulation data are summarized using multivariate regression. Model calibration with field bloom date data were performed to increase simulation accuracy of olive flowering predictions under climate change. As climate warms, the range of olive is predicted to expand to higher altitudes and consolidate elsewhere, especially in coastal areas. The range of olive fly will extend into previously unfavorable cold areas, but will contract in warm inland lowlands where temperatures approach its upper thermal limits. Consequently, many areas of current high risk are predicted to have decreased risk of fly damage with climate warming. Simulation using a 105-year climate model scenario for Alghero, Sardinia predicts changes in the olive–olive fly system expected to occur if climate continued to warm at the low rate observed during in the past half century.     

Cytogenetic analysis of Malpighian tubule and salivary gland polytene chromosomes of Bactrocera oleae (Dacus oleae) (Diptera: Tephritidae).

Photomaps of the Malpighian tubule and the salivary gland polytene chromosomes of Bactrocera oleae (Dacus oleae) are presented and compared with those of the fat body. Five polytene chromosomes (10 polytene arms) corresponding to the five autosomes of the mitotic nuclei, as well as a heterochromatic mass corresponding to the sex chromosomes, are observed in the nuclei of the three somatic tissues. The most prominent features of each polytene chromosome, the reverse tandem duplications, as well as the rather unusual ectopic pairing of the telomeric regions of different chromosome arms, are described. The constancy of the banding pattern based on the analysis of the three larval tissues is discussed.