The beneficial sexually transmitted microbe hypothesis of avian copulation

Several hypotheses have been proposed to explain why femalebirds either copulate repeatedly with a single mate or copulatewith multiple partners even though only a single copulationmay be sufficient to fertilize an entire clutch. We hypothesizethat females may directly benefit from high frequencies of copulationand multiple copulation partners if they receive a cloacal inoculationof beneficial sexually transmitted microbes (STMs) that caneither protect them against future encounters with pathogensand/or serve as therapy against present infections. Experimentsin domestic animal production, wildlife rehabilitation, andclinical medicine indicate that inoculations of beneficial microbesderived from the indigenous microflora of hosts can lead tonutritional benefits, resistance to colonization by pathogens,the elimination of infection, and improved immune system functioningin recipients. Our hypothesis predicts greater copulatory rateswhen the probability of the transmission of beneficial microbesexceeds that of pathogens and when the positive effects of beneficialmicrobes on host fitness exceed the negative effects of pathogens.Patterns of copulatory behavior in birds suggest the potentialutility of our hypothesis. We discuss our hypothesis in thecontext of observed patterns of copulation in birds and proposesome ways to directly test our hypothesis. Information on the probabilitiesof transmission during copulation of beneficial and pathogenic microbesand their relative potencies in birds are needed to directlytest the predictions of our hypothesis.     

Cell Tracking Using Photoconvertible Proteins During Zebrafish Development

Embryogenesis is a dynamic process that is best studied by using techniques that allow the documentation of developmental changes in vivo. The use of genetically-encoded fluorescent proteins has proven a valuable strategy for elucidating dynamic morphogenetic processes as they occur in the intact organism. During the past decade, the development of photoactivatable and photoconvertible fluorescent proteins has opened the possibility to investigate the fate of discrete subpopulations of tagged proteins¹. Unlike photoactivatable proteins, photoconvertible fluorescent proteins (PCFPs) are readily tracked and imaged in their native emission state prior to photoconversion, making it easier to identify and select regions by optical inspection. PCFPs, such as Kaede², KikGR³, Dendra⁴ and EosFP⁵, can be shifted from green to red upon exposure to UV or blue light due to a His-Tyr-Gly tripeptide sequence which forms a green chromophore that can be photoconverted to a red one by a light-catalyzed β-elimination and subsequent extension of a π-conjugated system³. PCFPs and their monomeric variants are useful tools for tracking cells^6-10 and studying protein dynamics^11-14, respectively. During recent years, PCFPs have been expressed in different animal model, such as zebrafish⁶, chicken^7,8 and mouse^9,10 for cell fate tracking. Here we report a protocol for cell-specific photoconversion of PCFPs in the living zebrafish embryo and further tracking of photoconverted proteins at later developmental stages. This methodology allows studying, in a tissue-specific manner, cell biological events underlying morphogenesis in the zebrafish animal model.     

SUMO fosters assembly and functionality of the MutSγ complex to facilitate meiotic crossing over

1. Download : Download high-res image (134KB)
2. Download : Download full-size image

     

Artificial fertilization and induction of triploidy and meiogynogenesis in the European sea bass, Dicentrarchus labrax L.

The European sea bass, Dicentrarchus labrax L., was successfully subjected to chromosome manipulation. Triploidy was induced by cold-shocking eggs at 0–2°C for 20 min starting 5 min after fertilization in order to prevent the extrusion of the second polar body. Meiogynogenesis was also obtained by fertilizing eggs with UV-irradiated sperm (3300 and 6600 erg m⁻²) and subsequently doubling the chromosome set by meiotic block as above. The commercial advantages of culturing triploid and gynogenetic sea bass are discussed.