Development of insecticide resistance has been a serious concern worldwide, whose mechanisms have been attributed to evolutionary changes in pest insect genomes such as alteration of drug target sites, up-regulation of degrading enzymes, and enhancement of drug excretion. Here, we report a previously unknown mechanism of insecticide resistance: Infection with an insecticide-degrading bacterial symbiont immediately establishes insecticide resistance in pest insects. The bean bug Riptortus pedestris and allied stinkbugs harbor mutualistic gut symbiotic bacteria of the genus Burkholderia , which are acquired by nymphal insects from environmental soil every generation. In agricultural fields, fenitrothion-degrading Burkolderia strains are present at very low densities. We demonstrated that the fenitrothion-degrading Burkholderia strains establish a specific and beneficial symbiosis with the stinkbugs and confer a resistance of the host insects against fenitrothion. Experimental applications of fenitrothion to field soils drastically enriched fenitrothion-degrading bacteria from undetectable levels to >80% of total culturable bacterial counts in the field soils, and >90% of stinkbugs reared with the enriched soil established symbiosis with fenitrothion-degrading Burkholderia . In a Japanese island where fenitrothion has been constantly applied to sugarcane fields, we identified a stinkbug population wherein the insects live on sugarcane and ≈8% of them host fenitrothion-degrading Burkholderia . Our finding suggests the possibility that the symbiont-mediated insecticide resistance may develop even in the absence of pest insects, quickly establish within a single insect generation, and potentially move around horizontally between different pest insects and other organisms.
eThe vertical transmission of symbiotic microorganisms is omnipresent in insects, while the evolutionary process remains totally unclear. The oriental chinch bug, Cavelerius saccharivorus (Heteroptera: Blissidae), is a serious sugarcane pest, in which symbiotic bacteria densely populate the lumen of the numerous tubule-like midgut crypts that the chinch bug develops. Cloning and sequence analyses of the 16S rRNA genes revealed that the crypts were dominated by a specific group of bacteria belonging to the genus Burkholderia of the Betaproteobacteria. The Burkholderia sequences were distributed into three distinct clades: the Burkholderia cepacia complex (BCC), the plant-associated beneficial and environmental (PBE) group, and the stinkbug-associated beneficial and environmental group (SBE). Diagnostic PCR revealed that only one of the three groups of Burkholderia was present in ϳ89% of the chinch bug field populations tested, while infections with multiple Burkholderia groups within one insect were observed in only ϳ10%. Deep sequencing of the 16S rRNA gene confirmed that the Burkholderia bacteria specifically colonized the crypts and were dominated by one of three Burkholderia groups. The lack of phylogenetic congruence between the symbiont and the host population strongly suggested host-symbiont promiscuity, which is probably caused by environmental acquisition of the symbionts by some hosts. Meanwhile, inspections of eggs and hatchlings by diagnostic PCR and egg surface sterilization demonstrated that almost 30% of the hatchlings vertically acquire symbiotic Burkholderia via symbiont-contaminated egg surfaces. The mixed strategy of symbiont transmission found in the oriental chinch bug might be an intermediate stage in evolution from environmental acquisition to strict vertical transmission in insects.
Mating behavior of the scarab beetle Dasylepida ishigakiensis was observed in a sugar cane field in Miyako Is., Okinawa, Japan. In field observations of tethered females on 6 February 2002, calling behaviors were observed only within 30 min of sunset time (18:25-18:55, JST), when light intensity decreased from ca. 500 lx to 1 lx. Mating was strongly affected by temperature: adults appeared and subsequent mating occurred when the temperature at 18:00 was higher than 18°C. Females appeared from the soil, flew to settle on sugar cane leaves and commenced rhythmical abdominal expansion and contraction. Males were attracted to the calling females from leeward, landed on or near the calling female, and immediately mounted. After genital connection, the male raised his legs and suspended himself with his genitalia. Mating lasted for ca 2 h. Most mated D. ishigakiensis females neither appeared from the soil nor attracted males until the end of March, so are considered monogamous. In contrast, males appeared from the soil after mating on evenings warmer than 18°C and probably repeat mating if females are available.
Insecticide resistance is a serious concern in modern agriculture, and an understanding of the underlying evolutionary processes is pivotal to prevent the problem. The bean bug Riptortus pedestris, a notorious pest of leguminous crops, acquires a specific Burkholderia symbiont from the environment every generation, and harbors the symbiont in the midgut crypts. The symbiont's natural role is to promote insect development but the insect host can also obtain resistance against the insecticide fenitrothion (MEP) by acquiring MEP-degrading Burkholderia from the environment. To understand the developing process of the symbiont-mediated MEP resistance in response to the application of the insecticide, we investigated here in parallel the soil bacterial dynamics and the infected gut symbionts under different MEP-spraying conditions by culture-dependent and culture-independent analyses, in conjunction with stinkbug rearing experiments. We demonstrate that MEP application did not affect the total bacterial soil population but significantly decreased its diversity while it dramatically increased the proportion of MEP-degrading bacteria, mostly Burkholderia. Moreover, we found that the infection of stinkbug hosts with MEP-degrading Burkholderia is highly specific and efficient, and is established after only a few times of insecticide spraying at least in a field soil with spraying history, suggesting that insecticide resistance could evolve in a pest bug population more quickly than was thought before.
Precopulatory behavior of the white grub beetle, Dasylepida ishigakiensis, was observed under laboratory conditions to determine the environmental factors controlling mating behavior, which is synchronized among individuals at dusk in the field. When light intensity was gradually decreased, both females and males sequentially started moving their antennae, legs and abdomen, then walking, and females rhythmically extruded their abdomen while males opened the elytra to fly. Pheromone release by females was suggested in a wind tunnel assay in which males oriented themselves to both intact and crushed bodies of females, but not of males. When illumination was suddenly turned off, precopulatory behavior of females and males was similarly induced but the frequencies of calling and flying behaviors were significantly reduced as compared with those observed when light intensity was gradually reduced. This result may suggest that gradual darkening is an important factor for their synchronized appearance from the soil and subsequent mating behaviors, including pheromone release in females and orientation flight in males. These behaviors were significantly suppressed at low temperatures below 18°C. This result supports our previous conclusion that temperature is the primary factor controlling the emergence and mating activity of sexually mature beetles in the field.
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