Daily Rhythms of Body Temperature in Acornys russatus: The Response to Chemical Signals Released by Acomys cahirinus

Two species of spiny mice of the genus Acomys—the golden spiny A. russaturs and the common spiny A. cuhirinus—are syrnpatnc in the and and hot parts of the Rift Valley in Israel. The coexistence of these two species is due to exclusion of A. russatus mice by A. cuhirinus mice from nocturnal activity. The aim of this research was to study if odor signals released by A. cahirinus mice can play a role in the exclusion of A. russatus mice. A. russatus mice with an implanted transmitter recording body temperature (T_b) were kept alone in a metabolic chamber under constant conditions of ambient temperature (27°C) and photoperiod (12 h light: 12 h dark). After 5 days of recording, chemical signals from an A. cuhirinus mouse were added through the air tube going into the metabolic chamber of the A. russatus mice. This treatment caused a shift of ∼ 2 h inT_b daily rhythm of the naive tested A. russutus mice, whereas no shift was observed in A. russatus mice that had been kept in the same room with the A. cahirinus mouse before measurements. These results strongly support the idea that chemical signals released by A. cahirinus mice can entrain the T_b rhythms of A. russatus mice. Therefore, it may be assumed that the exclusion of A. russatus mice from nocturnal activity by A. cuhirinus mice could be achieved through the odor released by the latter.     

Development of a new protein labeling system to map subunits and domains of macromolecular complexes for electron microscopy

Several gene fusion technologies have been successfully applied to label particular subunits or domains within macromolecular complexes to enable positional mapping of electron microscopy (EM) density maps, but exogenous fusion of a protein domain into the target polypeptide can cause unwanted structural and functional outcomes. Fab fragments from antibodies can be used as labeling reagents during EM visualization without gene manipulation of the target protein, but this method requires a panel of high-affinity antibodies that recognize a wide variety of epitopes. Linear peptide tags and their anti-tag antibodies can be used but they have a limited mapping ability as their placement is usually limited to the terminal regions of a protein. The PA dodecapeptide epitope tag (GVAMPGAEDDVV), forms a tight β-turn in the antigen binding pocket of its antibody (NZ-1). This capability allows for insertion of the PA tag into various surface-exposed loops within a multi-domain cell adhesion receptor, α_IIbβ₃ integrin. We confirmed that the purified PA-tagged integrin ectodomain fragments can form a stable complex with NZ-1 Fab. Negative stain EM of the various integrin-NZ-1 complexes revealed that a majority of the particles exhibited a clear density corresponding to the NZ-1 Fab; and the positions of the bound Fab were in good agreement with the predicted location of the inserted PA tag. The high-affinity and insertion-compatibility of the PA tag system allowed us to develop a new EM labeling methodology applicable to proteins for which good antibodies are not available.     

Do leaf domatia mediate intraguild predation and host plant resistance to Oligonychus aceris (Shimer) on Red Sunset Maple (Acer rubrum)?

The predatory mites Neoseiulus fallacis (Garman) (Acarina: Phytoseiidae) and Zetzellia mali (Ewing) (Acarina: Stigmaeidae) have the potential to suppress populations of Oligonychus aceris (Shimer) (Acarina: Tetranychidae) on maple cultivars under field conditions. Red Sunset red maples (Acer rubrum) are more resistant to O. aceris than ‘Autumn Blaze’ Freeman maple (Acer × fremanii). Examination of leaves indicated that the mite resistant Red Sunset trees had more leaf domatia than those from Autumn Blaze. Laboratory assays found that maple cultivars did not affect rates of O. aceris consumption by N. fallacis or Z. mali in a 24 h period. Each predator exhibited distinct preferences for O. aceris life stages. N. fallacis consumed significantly more protonymphs and adults of O. aceris, whereas Z. mali consumed more eggs. In contrast, maple cultivars significantly influenced rates of intraguild predation between phytoseiids and stigmaeids. Adult N. fallacis consumed more immature stages of Z. mali on Autumn Blaze than on Red Sunset maple, but adult Z. mali consumed the same numbers of N. fallacis nymphs on both cultivars. These findings provide a potential mechanism to explain the resistance of Red Sunset maples to O. aceris. On Red Sunset maples, where domatia provide Z. mali with refugia from predation by N. fallacis, both predators can contribute to the mortality of O. aceris. In contrast on Autumn Blaze maples Z. mali have no place to hide from N. fallacis, so the contribution of this stigmaeid to O. aceris mortality is greatly diminished. Thus, differential susceptibility of these cultivars to spider mites may be mediated by the capacity of leaf domatia to influence rates of intraguild predation among phytoseiid and stigmaeid predators.     

Predators induce egg retention in prey

To prevent predation on their eggs, prey often avoid patches occupied by predators. As a result, they need to delay oviposition until they reach predator-free patches. Because many species allocate energy to egg production in a continuous fashion, it is not clear what kind of mechanism prey use to delay oviposition. We used females of the phytoseiid mite Neoseiulus cucumeris to study these mechanisms. Females were placed in patches with pollen, a food source they use for egg production, and they were exposed to another phytoseiid mite, Iphiseius degenerans, which is an intraguild predator of N. cucumeris juveniles. We found that the oviposition of N. cucumeris females on patches with the predator was lower than on patches without the predator. Cues left by the intraguild predator were not sufficient to elicit such behaviour. Females of N. cucumeris reduced oviposition when exposed to the predator by retaining the egg inside their body, resulting in a lower developmental rate once these eggs were laid. Hence, females are capable of retaining eggs, but the development of these eggs continues inside the mother’s body. In this way, females gain some time to search for less risky oviposition sites.