Community structure and antifungal activity of actinobacteria in a fungus-growing termite

1. Fungus-growing termites cultivate the fungal mutualist Termitomyces as their main food source; however, how fungus-growing termites protect Termitomyces from threats is still unclear. In this study, we investigated the actinobacterial communities in Odontotermes formosanus individuals and their fungal combs.
2. Moreover, the antifungal activities of the isolated actinobacteria were tested. 16 S rRNA gene sequencing results indicated that the actinobacteria in O. formosanus and its fungal combs belong to 5 classes, 17 orders, 40 families, and 84 genera.
3. The relative abundance of Coriobacteriia in the nymphs, young workers, old workers, and soldiers was higher than that in the queens and fungal combs, and the relative abundance of class Actinobacteria in the queens and the fungal combs was higher than that in the nymphs, young workers, old workers, and soldiers.
4. Based on antifungal bioassays, 3 strains of Amycolatopsis and 2 strains of Streptomyces isolated from old workers had strong inhibitory activity against Xylaria angulosa but weak inhibitory activity against Termitomyces sp.
5. These results indicated that the actinobacteria of O. formosanus may contribute to protecting termite fungal food via their asymmetric antifungal activities.

     

Aquaporin water channel in the salivary glands of the Formosan subterranean termite Coptotermes formosanus is predominant in workers and absent in soldiers

Termite society is unique because the worker caste fetches and carries free water, utilizing it as a solvent for nest construction and gallery building and to maintain wetness for their nestmates. Such water management in a social organization relies largely upon the function of the workers in the colony, as well as on the individuals controlling the location and movement of water inside their bodies. The movement of water via aquaporins (AQPs; water channels) into and out of cells is a key feature of the numerous physiological functions related to whole‐insect water balance. In the present study, the homologue of the water‐specific Drosophila AQP [Drosophila integral protein (DRIP)] is characterized in workers of the Formosan subterranean termite Coptotermes formosanus Shiraki (Isoptera: Rhinotermitidae), a highly active wood decomposer. Immunoblot analysis of DRIP‐type AQP using an antibody from the silkworm Bombyx mori reveals that the Coptotermes DRIP (formerly cloned as ‘CfAQP1’) with a molecular mass of approximately 25.7 kDa is expressed predominantly in the salivary (labial) gland of the workers. The Coptotermes DRIP is present at the basal plasma membrane of the parietal cells, as demonstrated by immunocytochemistry. By contrast, there is no DRIP detected within the salivary glands of soldier termites, and neither caste expresses DRIP in their labial gland reservoir (water sac), a tissue that is suggested to have a function as a water sink. The AQP present in the salivary glands is of physiological importance with respect to salivation, aiding in the secretion of cellulolytic enzymes for wood ingestion by the workers of the subterranean termite.     

Chroniodiplogaster formosiana sp. n. (Rhabditida: Diplogastridae) from Chinese populations of Odontotermes formosanus Shiraki (Isoptera: Termitidae)

Chroniodiplogaster formosiana sp. n. (Rhabditida: Diplogastridae) is described from a population of Odontotermes formosanus Shiraki (Isoptera: Termitidae) collected from dead (unidentified) wood at Dinghu Park, China. Characters of C. formosiana which separate it from C. aerivora (Cobb) are a longer tail, the presence of four micropapillae (quadriform condition), and the adjacent position of the second and third macropapillae on the male tail. The diplogasterid Pristionchus uniformis Fedorko & Stanuszek, which is transferred to Chroniodiplogaster, can be distinguished from both C. formosiana and C. aerivora by the position of its excretory pore. Variable results in experimental infection trials suggest that some still unknown factor or factors are important in the infection process. Further studies are necessary to better define these factors before C. formosiana can be considered as a biological control agent of the Formosan termite.     

Differential fluctuation in virulence and VOC profiles among different cultures of entomopathogenic fungi

Insect-passaged cultures of entomopathogenic fungi grown on potato dextrose agar media have been shown to have altered virulence and profiles of volatile compounds. The present study demonstrated the pathogenic status of FS₀ (in vitro) and FS₁ and FS₂ (insect-passaged cultures grown on PDA) cultures of Metarhizium anisopliae (strains 406 and 02049) and Beauveria bassiana by a non-choice assay, in which filter paper was inoculated with fungal spores at a concentration of 1 × 10⁷ spores/ml. The FS₁ and FS₂ cultures of M. anisopliae strain 02049 and B. bassiana produced conidia with high virulence, and the volatile profiles of these conidia comprised relatively lower percentages of branched-alkanes than conidia from the FS₀ cultures. In contrast, the conidia from an FS₀ culture of M. anisopliae strain 406 had somewhat elevated virulence levels, but their volatile profile had <2% branched-alkanes. The FS₁ and FS₂ cultures of M. anisopliae strain 406 did not gain virulence, and these cultures showed a decline in virulence along with major alteration of their volatile profiles. Their volatile profiles mainly comprised branched-alkanes. The volatile profiles of the FS₁ and FS₂ cultures lacked n-tetradecane, which was an important component of all the virulent cultures. Four compounds, 2-phenylpropenal, 2,5,5-trimethyl-1-hexene, n-tetradecane and 2,6-dimethylheptadecane, were detected only from the virulent cultures, suggesting that low LT₅₀ values were probably due to the production of these compounds. This is the first report to characterize volatiles from FS₀, FS₁ and FS₂ cultures of entomopathogenic fungi; its utility in different aspects opens an interesting area for further investigations.     

Evaluation of DNA Fingerprinting, Aggression Tests, and Morphometry as Tools for Colony Delineation of the Formosan Subterranean Termite

Multilocus DNA fingerprinting, aggression tests, and morphometry were compared to evaluate their potential for the delineation of colonies of Coptotermes formosanus Shiraki (Isoptera; Rhinotermitidae) in Hawaii. DNA fingerprinting segregates the termites from all collection sites and allows the assignment of all individuals to their original collection site. The genetic similarity of termites from different collection sites approaches the population's genetic background similarity, consequently collection sites represent independent colonies. Aggression between colonies is comparatively low and does not provide reliable colony delineation. Morphometry allows a 79% classification rate of termites to their colony of origin. No correlation among genetic similarities, aggression levels, and morphometric distances is found. Of the three investigated methods, we conclude that the genetic approach is the most useful tool for colony delineation in C. formosanus.