scholarly journals Feather-Degrading Bacteria do not Affect Feathers on Captive Birds

The Auk ◽  
2005 ◽  
Vol 122 (1) ◽  
pp. 222-230 ◽  
Author(s):  
Daniel A. Cristol ◽  
Jessica L. Armstrong ◽  
Justine M. Whitaker ◽  
Mark H. Forsyth

Abstract Attention has recently been focused on microbes that occur in the plumage of wild birds and can degrade feathers under laboratory conditions and in poultry-waste composters. In particular, Bacillus licheniformis, a soil bacterium, was found in the plumage of many birds netted in eastern North America, and poultry feathers were rapidly broken down when incubated in a suspension of this bacterium (Burtt and Ichida 1999). If feather-degrading microbes affect wild birds under normal conditions, they may have played an important role in the evolution of molt, plumage color, and sanitation behavior, such as sunning and preening. We performed the first test on whether a feather-degrading bacterium can degrade feathers of live birds housed outdoors under seminatural conditions. We found no evidence that B. licheniformis degraded wing feathers of Northern Cardinals (Cardinalis cardinalis) when applied twice (with a two-week interval) during the winter, despite the fact that it degraded Northern Cardinal feathers when incubated in our laboratory. In a second experiment, we found no evidence that B. licheniformis degraded feathers of European Starlings (Sturnus vulgaris) when applied twice (with a one-week interval) during the summer, despite the fact that birds were housed in humid conditions that should have favored the growth of B. licheniformis. Las Bacterias que Degradan Plumas no Afectan las Plumas de Aves en Cautiverio

2012 ◽  
Vol 43 (6) ◽  
pp. 496-502 ◽  
Author(s):  
Jinelle H. Sperry ◽  
Douglas G. Barron ◽  
Patrick J. Weatherhead

2020 ◽  
Vol 10 (10) ◽  
pp. 3541-3548
Author(s):  
Simon Yung Wa Sin ◽  
Lily Lu ◽  
Scott V. Edwards

Northern cardinals (Cardinalis cardinalis) are common, mid-sized passerines widely distributed in North America. As an iconic species with strong sexual dichromatism, it has been the focus of extensive ecological and evolutionary research, yet genomic studies investigating the evolution of genotype–phenotype association of plumage coloration and dichromatism are lacking. Here we present a new, highly-contiguous assembly for C. cardinalis. We generated a 1.1 Gb assembly comprised of 4,762 scaffolds, with a scaffold N50 of 3.6 Mb, a contig N50 of 114.4 kb and a longest scaffold of 19.7 Mb. We identified 93.5% complete and single-copy orthologs from an Aves dataset using BUSCO, demonstrating high completeness of the genome assembly. We annotated the genomic region comprising the CYP2J19 gene, which plays a pivotal role in the red coloration in birds. Comparative analyses demonstrated non-exonic regions unique to the CYP2J19 gene in passerines and a long insertion upstream of the gene in C. cardinalis. Transcription factor binding motifs discovered in the unique insertion region in C. cardinalis suggest potential androgen-regulated mechanisms underlying sexual dichromatism. Pairwise Sequential Markovian Coalescent (PSMC) analysis of the genome reveals fluctuations in historic effective population size between 100,000–250,000 in the last 2 millions years, with declines concordant with the beginning of the Pleistocene epoch and Last Glacial Period. This draft genome of C. cardinalis provides an important resource for future studies of ecological, evolutionary, and functional genomics in cardinals and other birds.


1997 ◽  
Vol 36 (1) ◽  
pp. 215-220 ◽  
Author(s):  
M. F. Coughlin ◽  
B. K. Kinkle ◽  
A. Tepper ◽  
P. L. Bishop

An azo dye-degrading strain, originally named TBX65, was isolated from the mixed liquor of the Mill Creek waste water treatment plant in Cincinnati, Ohio. Strain TBX65 has the unusual ability to aerobically reduce the azo bond of several azo dyes and is able to use some of these dyes as growth substrate. Subsequent investigations have revealed that TBX65 is actually composed of several strains including two azo dye-degrading strains, MC1 and MI2. Strain MI2 is able to use the azo dyes AO7 and AO8 as its sole source of carbon, energy, and nitrogen. In contrast, MC1 can aerobically reduce the azo bond of these dyes but only in the presence of an exogenous source of carbon and nitrogen. Both MC1 and MI2 are Gram negative, rod-shaped bacteria that form yellow colonies. Sequencing and phylogenetic analysis of the 16S rRNA gene of MC1 indicates that it is a strain of Sphingomonas. Based on this phylogenetic analysis, the most closely related strain to MC1 is strain C7, a previously described azo dye-degrading bacterium isolated from biofilms growing in our laboratories. A strain-specific fluorescent antibody has been developed for strains MC1 and MI2, and is being used to determine the survival and azo dye-degrading ability of these strains in biofilms generated in a rotating drum bioreactor.


2005 ◽  
Vol 245 (1) ◽  
pp. 145-153 ◽  
Author(s):  
Kengo Inoue ◽  
Hiroshi Habe ◽  
Hisakazu Yamane ◽  
Toshio Omori ◽  
Hideaki Nojiri

Sign in / Sign up

Export Citation Format

Share Document