Brochosome influence on parasitisation efficiency of Homalodisca coagulata (Say) (Hemiptera: Cicadellidae) egg masses by Gonatocerus ashmeadi Girault (Hymenoptera: Mymaridae)

Abstract. 1. Many cicadellid females in the tribe Proconiini (Hemiptera: Cicadellidae) cover their egg masses with specialised, usually rod‐shaped, brochosomes as the eggs are being laid. The brochosomes are produced in Golgi complexes in the Malpighian tubules of Cicadellidae. In contrast to the gravid females, adult males, pre‐reproductive adult females, and nymphal males and females produce specialised, usually spherically shaped brochosomes. Brochosomes are also used to cover the external surfaces of nymphs and newly moulted adult males and females. 2. The function of the brochosome covering the egg masses is unknown but various hypotheses have been suggested, including protecting the eggs against pathogens, predators, and parasitoids. Based on preliminary observations of Gonatocerus ashmeadi Girault (Hymenoptera: Mymaridae) parasitising the eggs of the cicadellid, Homalodisca coagulata (Say), it is speculated here that brochosomes covering an egg mass hinder parasitisation of eggs by G. ashmeadi. This hypothesis was tested by observing G. ashmeadi females foraging on leaves with H. coagulata egg masses heavily covered with rod‐shaped brochosomes vs. those lacking brochosomes. 3. Cox's proportional hazards model was used to evaluate the probability, per unit time, that a female G. ashmeadi displayed the sequence of behaviours that ended in successful oviposition as influenced by five variables: (a) presence or absence of brochosomes on an egg mass, (b) the leaf surface, upper or lower, being searched by the parasitoid (the egg masses are laid in the parenchyma on the lower leaf surface), (c) the parasitoid's previous ovipositional experience, (d) egg mass size, and (e) the parasitoid's age. 4. Brochosomes significantly decreased oviposition efficacy of G. ashmeadi females. Scanning electron microscopy showed that females exposed to brochosome‐covered egg masses had brochosomes adhering to their tarsi, legs, antennae, and eyes, all of which prompted extensive bouts of grooming.     

Separation and characteristics of inside-out and right side-out vesicles from a rat cardiac sarcolemma preparation

Purified cardiac sarcolemma (SL) vesicles are highly suitable to study various Ca2+-transport systems present in the SL. We describe in this paper the separation of the Inside-Out (IO) and Right side-Out (RO) oriented vesicle subpopulations from a purified rat heart SL preparation. The isolated subfractions were characterized with respect to the number of beta-adrenergic binding sites and the Ca2+-uptake and (Ca2+-Mg2+)-ATPase activities. It was found that the Ca2+-uptake and the (Ca2+-Mg2+)-ATPase activities reside in the IO fraction and are virtually absent in the RO fraction, confirming that the active Ca2+-uptake represents the outward directed sarcolemmal Ca2+-flux.     

High Reproducibility of Histological Characterization by Whole Virtual Slide Quantification; An Example Using Carotid Plaque Specimens

Objective

Tissue biobanks are an important source for discovery and validation studies aiming for new proteins that are causally related with disease development. There is an increasing demand for accurate and reproducible histological characterization, especially for subsequent analysis and interpretation of data in association studies. We assessed reproducibility of one semiquantative and two quantitative methods for histological tissue characterization. We introduce a new automated method for whole digital slide quantification. Carotid atherosclerotic plaques were used to test reproducibility.

Methods

50 atherosclerotic plaques that were obtained during carotid endarterectomy were analysed. For the semiquantitative analysis, 6 different plaque characteristics were scored in categories by two independent observers, and Cohen''s κ was used to test intra- and interobserver reproducibility. The computer-aided method (assessed by two independent observers) and automated method were tested on CD68 (for macrophages) and α smooth muscle actin (for smooth muscle cells) stainings. Agreement for these two methods (done on a continuous scale) was assessed by intraclass correlation coefficients (ICCs).

Results

For the semiquantitative analysis, κ values ranged from 0.55 to 0.69 for interobserver variability, and were slightly higher for intraobserver reproducibility in both observers. The computer-aided method yielded intra- and interobserver ICCs between 0.6 and 0.9. The new automated method performed most optimal regarding reproducibility, with ICCs ranging from 0.92 to 0.97.

Conclusions

The analysis of performance of three methods for histological slide characterization on carotid atherosclerotic plaques showed high precision and agreement in repeated measurements for the automated method for whole digital slide quantification. We suggest that this method can fulfill the need for reproducible histological quantification.     

Comparison of cyclic AMP-dependent phosphorylation of sarcolemma and sarcoplasmic reticulum from rat cardiac ventricle muscle

1. The phosphorylation by cAMP and protein kinase I of rat cardiac sarcolemma (SL) and sarcoplasmic reticulum (SR) isolated from the same homogenate, was compared. 2. In both fractions, the phosphate incorporation is strongly dependent on the ATP and the membrane protein concentration. 3. SDS-gel electrophoresis reveals that in the SL preparation a protein of Mr = 24,500 and a glycoprotein of Mr = 17,500 are mainly phosphorylated, while in the SR fraction the main phosphate incorporation is found in a protein having a Mr = 37,000. 4. Isoprenaline stimulates the phosphorylation of SL but not of SR. Propranolol abolished that stimulatory action of isoprenaline completely, suggesting that the beta-adrenoceptor is involved.