The evolution of size of the uropygial gland: mutualistic feather mites and uropygial secretion reduce bacterial loads of eggshells and hatching failures of European birds

Potentially, pathogenic bacteria are one of the main infective agents against which a battery of chemical and physical barriers has evolved in animals. Among these are the secretions by the exocrine uropygial gland in birds. The antimicrobial properties of uropygial secretions may prevent colonization and growth of microorganisms on feathers, skin and eggshells. However, uropygial gland secretions also favour the proliferation of feather mites that feed on secretions and microorganisms living on feathers that would otherwise reach eggshells during incubation if not consumed by feather mites. Therefore, at the interspecific level, uropygial gland size (as an index of volume of uropygial secretion) should be positively related to eggshell bacterial load (i.e. the risk of egg infection), whereas eggshell bacterial loads may be negatively related to abundance of feather mites eating bacteria. Here, we explore these previously untested predictions in a comparative framework using information on eggshell bacterial loads, uropygial gland size, diversity and abundance of feather mites and hatching success of 22 species of birds. The size of the uropygial gland was positively related to eggshell bacterial loads (mesophilic bacteria and Enterobacteriaceae), and bird species with higher diversity and abundance of feather mites harboured lower bacterial density on their eggshells (Enterococcus and Staphylococcus), in accordance with the hypothesis. Importantly, eggshell bacterial loads of mesophilic bacteria, Enterococcus and Enterobacteriaceae were negatively associated with hatching success, allowing us to interpret these interspecific relationships in a functional scenario, where both uropygial glands and mutualistic feather mites independently reduce the negative effects of pathogenic bacteria on avian fitness.

[1]  A. Møller,et al.  Goshawk prey have more bacteria than non-prey. , 2012, The Journal of animal ecology.

[2]  A. Møller,et al.  Innate humoural immunity is related to eggshell bacterial load of European birds: a comparative analysis , 2011, Naturwissenschaften.

[3]  M. Martínez-Bueno,et al.  Brood parasitism is associated with increased bacterial contamination of host eggs: bacterial loads of host and parasitic eggs , 2011 .

[4]  A. MØller,et al.  Migratory divides and their consequences for dispersal, population size and parasite–host interactions , 2011, Journal of evolutionary biology.

[5]  Juan Manuel Peralta-Sánchez Las bacterias como agentes modeladores de las estrategias vitales en aves , 2011 .

[6]  S. Merino,et al.  Do secretions from the uropygial gland of birds attract biting midges and black flies? , 2011, Parasitology Research.

[7]  M. Firestone,et al.  Microbial and environmental effects on avian egg viability: do tropical mechanisms act in a temperate environment? , 2011, Ecology.

[8]  Wilfried Thuiller,et al.  Consequences of climate change on the tree of life in Europe , 2011, Nature.

[9]  Z. Barta,et al.  Seasonality in the uropygial gland size and feather mite abundance in house sparrows Passer domesticus: natural covariation and an experiment , 2010 .

[10]  L. Garamszegi,et al.  Effects of sample size and intraspecific variation in phylogenetic comparative studies: a meta‐analytic review , 2010, Biological reviews of the Cambridge Philosophical Society.

[11]  A. Møller,et al.  Predators and microorganisms of prey: goshawks prefer prey with small uropygial glands , 2010 .

[12]  Rob Knight,et al.  Effect of storage conditions on the assessment of bacterial community structure in soil and human-associated samples. , 2010, FEMS microbiology letters.

[13]  A. Møller,et al.  Ectoparasites, uropygial glands and hatching success in birds , 2010, Oecologia.

[14]  J. Soler,et al.  Sibling Competition and Conspicuousness of Nestling Gapes in Altricial Birds: A Comparative Study , 2010, PloS one.

[15]  M. Martín-Vivaldi,et al.  Antibiotic-Producing Bacteria as a Possible Defence of Birds against Pathogenic Microorganisms , 2010 .

[16]  A. Møller,et al.  Number and colour composition of nest lining feathers predict eggshell bacterial community in barn swallow nests: an experimental study , 2010 .

[17]  M. Martín-Vivaldi,et al.  Antimicrobial chemicals in hoopoe preen secretions are produced by symbiotic bacteria , 2010, Proceedings of the Royal Society B: Biological Sciences.

[18]  A. Møller,et al.  Feather micro‐organisms and uropygial antimicrobial defences in a colonial passerine bird , 2009 .

[19]  M. Martínez-Bueno,et al.  Seasonal, sexual and developmental differences in hoopoe Upupa epops preen gland morphology and secretions: evidence for a role of bacteria , 2009 .

[20]  Eoin L. Brodie,et al.  Avian Incubation Inhibits Growth and Diversification of Bacterial Assemblages on Eggs , 2009, PloS one.

[21]  M. Martínez-Bueno,et al.  Symbiotic association between hoopoes and antibiotic- producing bacteria that live in their uropygial gland , 2008 .

[22]  T. Piersma,et al.  Seasonally Changing Preen-Wax Composition: Red Knots' (Calidris Canutus) Flexible Defense Against Feather-Degrading Bacteria , 2008 .

[23]  J. S. Monrós,et al.  Feather mites and birds: an interaction mediated by uropygial gland size? , 2008, Journal of evolutionary biology.

[24]  C. Wilson,et al.  The effects of exposure and microbes on hatchability of eggs in open‐cup and cavity nests , 2007 .

[25]  A. Møller,et al.  Prevalence of avian influenza and host ecology , 2007, Proceedings of the Royal Society B: Biological Sciences.

[26]  M. Brown,et al.  Feather mites are positively associated with daily survival in cliff swallows , 2006 .

[27]  M. Martín-Vivaldi,et al.  Relative importance of factors affecting nestling immune response differs between junior and senior nestlings within broods of hoopoes Upupa epops , 2006 .

[28]  T. Piersma,et al.  Seasonal shifts in uropygial gland secretions in Red Knots : a flexible defense against feather-degrading bacteria? , 2006 .

[29]  I. Galván,et al.  Feather mite abundance increases with uropygial gland size and plumage yellowness in Great Tits Parus major , 2006 .

[30]  S. Beissinger,et al.  Incubation reduces microbial growth on eggshells and the opportunity for trans-shell infection. , 2005, Ecology letters.

[31]  V G Narushin,et al.  Egg geometry calculation using the measurements of length and breadth. , 2005, Poultry science.

[32]  J. M. Ichida,et al.  GLOGER'S RULE, FEATHER-DEGRADING BACTERIA, AND COLOR VARIATION AMONG SONG SPARROWS , 2004 .

[33]  A. Møller,et al.  Genetic similarity and hatching success in birds , 2004, Proceedings of the Royal Society of London. Series B: Biological Sciences.

[34]  G. Hill,et al.  Chemical warfare? Effects of uropygial oil on feather‐degrading bacteria , 2003 .

[35]  S. Beissinger,et al.  Trans–shell infection by pathogenic micro–organisms reduces the shelf life of non–incubated bird's eggs: a constraint on the onset of incubation? , 2003, Proceedings of the Royal Society of London. Series B: Biological Sciences.

[36]  S. Merino,et al.  BENEFICIAL EFFECTS OF CLOACAL BACTERIA ON GROWTH AND FLEDGING SIZE IN NESTLING PIED FLYCATCHERS (FICEDULA HYPOLEUCA) IN SPAIN , 2003 .

[37]  M. Pagel,et al.  Phylogenetic Analysis and Comparative Data: A Test and Review of Evidence , 2002, The American Naturalist.

[38]  J. S. Sinninghe Damsté,et al.  Sandpipers (Scolopacidae) switch from monoester to diester preen waxes during courtship and incubation, but why? , 2002, Proceedings of the Royal Society of London. Series B: Biological Sciences.

[39]  J. Tella,et al.  Feather mites on birds: costs of parasitism or conditional outcomes? , 2001 .

[40]  C. Borror Nonparametric Statistical Methods, 2nd, Ed. , 2001 .

[41]  R. Jovani,et al.  Resemblance within flocks and individual differences in feather mite abundance on long-tailed tits, Aegithalos caudatus (L.) , 2000 .

[42]  M. Pagel Inferring the historical patterns of biological evolution , 1999, Nature.

[43]  S. V. Mironov,et al.  Origin and Evolution of Feather Mites (Astigmata) , 1999, Experimental & Applied Acarology.

[44]  W. Holzapfel,et al.  Enterococci at the crossroads of food safety? , 1999, International journal of food microbiology.

[45]  D. Singleton,et al.  Bacteria in old house wrent nests , 1998 .

[46]  A. Møller,et al.  Host immune defence and migration in birds , 1998, Evolutionary Ecology.

[47]  A. Møller,et al.  Condition, disease and immune defence , 1998 .

[48]  M. Pagel Inferring evolutionary processes from phylogenies , 1997 .

[49]  J. Tella,et al.  Feather mites on group-living Red-billed Choughs : a non-parasitic interaction ? , 1997 .

[50]  B. Gottstein Immunity to parasites: How parasitic infections are controlled (2nd edn) , 1997 .

[51]  J. Saunders,et al.  Aerobic Bacterial Flora of Addled Raptor Eggs in Saskatchewan , 1997, Journal of wildlife diseases.

[52]  T. F. Hansen,et al.  Phylogenies and the Comparative Method: A General Approach to Incorporating Phylogenetic Information into the Analysis of Interspecific Data , 1997, The American Naturalist.

[53]  A. Møller,et al.  PARASITE VIRULENCE AND HOST IMMUNE DEFENSE: HOST IMMUNE RESPONSE IS RELATED TO NEST REUSE IN BIRDS , 1996, Evolution; international journal of organic evolution.

[54]  D. Wakelin Immunity to Parasites: How Parasitic Infections are Controlled , 1996 .

[55]  A. Møller Egg Predation as a Selective Factor for Nest Design: An Experiment , 1987 .

[56]  D. Brooks,et al.  Evolutionary biology of parasites. , 1981, Monographs in population biology.

[57]  G. Moreno-Rueda House Sparrows Passer domesticus with larger uropygial glands show reduced feather wear , 2011 .

[58]  J. Walker,et al.  Bacterial Pathogenesis , 2008, Methods in Molecular Biology™.

[59]  J. Playfair,et al.  Comprar Infection and Immunity | Gregory Bancroft | 9780199206735 | Oxford University Press , 2008 .

[60]  A. Roulin,et al.  Experimental Support for the Makeup Hypothesis in Nestling Tawny Owls (strix Aluco) , 2008 .

[61]  T. Piersma,et al.  Seasonally changing preen wax composition: red knots’ flexible defense against feather-degrading bacteria? , 2006 .

[62]  S. Beissinger,et al.  Microbial infection affects egg viability and incubation behavior in a tropical passerine , 2005 .

[63]  G. Garrity Bergey's Manual of systematic bacteriology , 2001 .

[64]  A. Bandyopadhyay,et al.  Influence of fowl uropygial gland and its secretory lipid components on the growth of skin surface fungi of fowl. , 1999, Indian journal of experimental biology.

[65]  A. Bandyopadhyay,et al.  Influence of fowl uropygial gland and its secretory lipid components on growth of skin surface bacteria of fowl. , 1996, Indian journal of experimental biology.

[66]  J. Bruce,et al.  Trans-shell transmission , 1994 .

[67]  M. Pagel,et al.  The comparative method in evolutionary biology , 1991 .

[68]  H. Stolp,et al.  Microbial Ecology: Organisms, Habitats, Activities , 1989 .

[69]  J. Jacob,et al.  Chapter 4 – THE UROPYGIAL GLAND , 1982 .