This study was performed to investigate the bacterial diversity isolated from the twospotted spider mite and to interpret their correlation between insect bacteria and acaricide resistance. Twospotted spider mite, Tetranychus urticae was used the resistance strains, which developed over eight years to the six acaricides such as abamectin, acequinocyl, bifenozate, etoxazole, fenpropathrin, and pyridaben, respectively. After cultivating the bacteria from body maceration, bacterial colony was selected and identified through 16S rRNA gene sequences. We are identified six genus from Pyridaben resistant strain, five genus from acequinocyl, three genus from abamectin, bifenozate, etoxazole, and two genus from fenpropathrin. However, we could not found correlation between bacterial density and diversity (phylotypes) among these resistant strains. By analyzing the diversity of population microorganisms, fenpropathrin was showed 40% of Cs value (Similarity coefficient) with susceptible strain, however, abamectin and pyridaben were perfectly different (0%) with susceptible strain. It remains to be learned about how microorganisms co-evolutionary developed with their host insect correlating to the resistance and how microorganisms play role in acaricide resistant mite.
Tobacco whitefly-Bemisia tabaci is considered one of the most important pests in tropical and subtropical agriculture, as well as in production systems in glasshouses in temperate zones. Principle research on the identity of B. tabaci began with the recognition of more than one biotype differing in life history parameters, host plant associations, plant-related damage and insecticide resistance. Our laboratory strains of B. tabaci were identified and classified as biotype B and Q, through mtCOI PCR. Also, they were tested for their host plant preference and reaction to different insecticide. Biotype Q prefers to feed on red pepper and tomato, was less susceptible to tested insecticides, for instance acetamipirid, spinosad and thiamethoxam, than the biotype B (feed on tomato alone). There has been a report on the presence of gut bacteria in B. argentifolii (= B. tabaci biotype B) and its influence on the host insect processes. Hence, as a further pursuit, we examined our laboratory B. tabaci biotypes B and Q for their gut bacteria, whether these two biotypes are differed with each other. Gut bacterial strains isolated by standard surface sterilization method was identified through 16S rRNA gene sequence. Gut bacterial strains of B. tabaci biotypes B and Q and their close relatives retrieved from the public database (NCBI) indicated that the biotype B was less diversified only with four genera viz., Bacillus, Micrococcus, Pseudomonas and Staphylococcus, whereas the biotype Q diversified with six such as Bacillus, Janibacter, Micrococcus, Staphylococcus, Stenotrophomonas, and Streptomyces. Results of the present investigation suggesting that there may be a relationship with gut bacterial strains and susceptibility to insecticides and host plant preference of B. tabaci biotype B and Q.