In this study we report on the structural diversity of adipokinetic hormones (AKHs) in the evolutionarily oldest group of social insects, the termites (Isoptera). Using molecular methods combined with in silico bioinformatic analysis, we studied and compared the sequences coding for these neuropeptides in thirteen species of five families of Isoptera. There are three types of AKH octapeptides in termites: Empusa pennata adipokinetic hormone (Emppe-AKH; pQVNFTPNWamide), Microhodotermes viator corpus cardiacum peptide (Micvi-CC; pQINFTPNWamide) and Periplaneta americana cardioaccelerating hormone (Peram-CAH-I; pQVNFSPNWamide). Of these the Peram-CAH-I was the most frequently bioactive form detected in representatives of four out of the six families studied. The complete AKH preprohormones in the termites studied shared at least an 84% amino acid similarity. In agreement with current phylogenetic scenarios of termites as an internal monophyletic clade nested within cockroaches (Blattaria) in the proximity of the family Blattidae, our phylogenetic analysis of the AKH precursor sequences (in the absence of data for the Cryptocercidae) placed the Blattidae (Periplaneta americana) as a sister group of termites and the AKHs of other cockroach families (Blattellidae and Blaberidae) were more divergent from those of termites. Representatives of the basal termite families Mastotermitidae and Archotermopsidae (but also one rhinotermitid genus Prorhinotermes) occurred separately from the phylogenetically advanced lineage (Rhinotermitidae and Termitidae), and Neotermes (Kalotermitidae) was sister to all other termites included., Veronika Jedličková, Pavel Jedlička, Barbora Špuláková., and Obsahuje bibliografii
1_The respiratory metabolism of different polyphenic forms of the pea aphid, including wingless and winged asexual females (virginoparae), sexual females (oviparae) and winged or wingless adult males, was investigated using a micro-respirographic method. The records revealed sub-nanoliter amounts per min of O2 consumption or CO2 output. Respiratory metabolism of individuals was monitored for 3 to7 h after removal of the aphid from the food plant. Most of the recordings were for relatively large (3.5 mg), wingless asexual females (virginoparae). These aphids exhibited a continuous and very regular respiratory gas exchange (example: specimen of 3.5 mg body mass consumed 180 nl of O2 per min; released simultaneously 300 nl CO2 per min; = standard metabolic rate of 3085 µl O2 / g / h; R.Q. = 1.66). This continuous pattern of respiration occurred only when the aphids were kept at relatively high humidity. By contrast, aphids of various seasonal forms exhibited discontinuous respiratory gas exchange when kept in relatively dry air (atmospheric, room conditions). These patterns can be briefly described as follows: (a) Short and rather small micro-cycles of CO2 emission, manifested usually by the sudden expiration of 60–120 nl of CO2 once every 5 min; (b) Larger bursts of 240–480 nl of CO2 with a periodicity of one hour; (c) Enormously large, discontinuous bursts of 10–14 µl CO2, duration 10–30 min, repeated with a periodicity of several hours. There was no constant pattern of diffusive CO2 emission (DGC). The aphids exhibited a pattern of CO2 release that was appropriate for the external conditions, such as temperature and humidity, and internal physiological conditions such as metabolic activity, availability of reserve substances (carbohydrate, lipid) and water. Certain stages (wingless virginoparae) exhaled volumes of CO2 greatly in excess of their O2 consumption (R.Q. over 1.5)., 2_Sudden exhalations of CO2 from the body were a consequence of a bulk production and outflow of CO2 and not due to the diffusion of CO2 previously accumulated within the tracheal system. Due to their generally high metabolic activity (1142 to 6780 µl O2 / g / h), aphid tissue and organs produced relatively large amounts of metabolically formed carbonic acid. The resulting respiratory acidaemia was moderated by outbursts of gaseous CO2, liberated from liquid carbonate buffers by a regulatory mechanism based on enzymatic hydration and neutralization of carbonic acid by discontinuous formation of gaseous CO2., Karel Sláma, Pavel Jedlička., and Obsahuje seznam literatury