Abstract

The creation of a genetic resource bank of avian species aims to prevent the decline and fragmentation of wild bird populations, which in turn lead to the loss of genetic diversity and, in more serious cases, the extinction of the most threatened species. In order for the collected genetic material to be stored in a bank and useful when necessary, it is essential to improve the technique ensuring its effectiveness. Thus, our study used feather follicle cells from the domestic gallus species to standardize the technique of cell culture and subsequent cryopreservation. This study aimed to establish a protocol, in vitro, of isolation and primary culture of somatic cells derived from the feather follicle, with the purpose of establishing a cell lineage, and evaluate its viability for the biobank formation. Developing feathers of gallus domesticus were collected at 12, 21 and 34 days of age. The feathers were morphologically analyzed and then we selected the region of the calamus due to the presence of pulp for cell culture and cryopreservation. The results showed that it is possible to find cells with distinct morphology; cells in elliptical shape with central nucleus also in elliptical shape, cells with shape and round nucleus, cells compatible with the fibers of the barbules, cell agglomerates and cells adhered to the bottom of the plate with fibroblastatoid shape. After 24 hours of culture there was the presence of primary culture with 80% of confluence and after cryopreservation the average viability after freezing was 68.8%, with cellular morphologies being maintained. Therefore, we proved the isolation of somatic cells from the follicle of bird’s feathers, suggesting that this is a source of great value, viable and effective for obtaining biological material for the elaboration of a biobank.

Highlights

  • It is well known that Earth's biodiversity is being degraded by several factors, such as urbanization, agribusiness, exploration of raw materials, illegal trade in wild animals, pollution, emerging diseases, invasive exotic animals and plants, and climate changes. (Wildt et al, 2010)

  • The 1rd passage cultures were marked by a high rate of proliferation and great difference in the morphology of the cells presenting floating cells with elliptical shape and central nucleus elliptical, rounded cells, cell clusters and cells compatible with the fibers of the barbules, in addition to cells adhered to the bottom of the plate with fibroblast format

  • Due to the lack of a bank of genetic resources of the Brazilian avian species, we have created a protocol of somatic cell culture, through a minimally invasive method, such as the cells present in the feather follicle

Read more

Summary

Introduction

It is well known that Earth's biodiversity is being degraded by several factors, such as urbanization, agribusiness, exploration of raw materials, illegal trade in wild animals, pollution, emerging diseases, invasive exotic animals and plants, and climate changes. (Wildt et al, 2010). These factors endanger the presence of thousands of animal species, especially species in or close to be in danger and genetically diverse, due to natural selection promoted by changes in the environment in which they are inserted. Conservation in situ, ideal as it seems still insufficient, due to the large number of the human population on earth, natural resources are increasingly needed and this ends up Copyright © The Author(s).

Objectives
Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call