Se describe un brote de sarna Knemidocoptic causada por Knemidocoptes pilae en periquitos australianos enjaulados (Melopsittacus undulatus), del parque público de L'Eliana (Valencia, España). Cinco individuos (5 de 70) muestran una malformación severa del pico, afectados por rhamphotheca, rhinotheca, y gnathotheca y una ligera desviación lateral de la mandíbula, que no impide, sin embargo, la alimentación o el aseo.An outbreak of knemidocoptic mange caused by Knemidocoptes pilae is described in caged Australian budgerigars (Melopsittacus undulatus) in a public park in L´Eliana (Valencia, Spain). Five individuals (5 out of 70) displayed severe malformation of the beak, with the rhamphotheca, rhinotheca, and gnathotheca affected and a slight lateral deviation of the jawbone, which did not, however, impede feeding or grooming.peerReviewe

Alarcón Elbal, Pedro María

Calero Bernal, Rafael

Carmona Salido, Víctor Jesús

Lucientes Curdi, Javier

Marín Sánchez-Murillo, José

TURKISH JOURNAL OF VETERINARY AND ANIMAL SCIENCES

Dehesa. Repositorio Institucional de la Universidad de Extremadura

344http://journals.tubitak.gov.tr/veterinary/Turkish Journal of Veterinary and Animal Sciences Turk J Vet Anim Sci(2014) 38: 344-346© TÜBİTAKdoi:10.3906/vet-1311-36Severe beak deformity in Melopsittacus undulatus caused by Knemidocoptes pilaePedro María ALARCÓN ELBAL1,*, Víctor Jesús CARMONA SALIDO1, José Marín SÁNCHEZ-MURILLO2,Rafael CALERO BERNAL3, Javier LUCIENTES CURDI11Animal Pathology Department, Veterinary Faculty, University of Zaragoza, Zaragoza, Spain2Parasitology Department, Regional Animal Health Laboratory, Government of Extremadura, Badajoz, Spain3Parasitology Section, Animal Health Department, Veterinary Faculty, University of Extremadura, Cáceres, Spain* Correspondence: pedro.alarcon@uv.es1. IntroductionBeak deformities with overgrowth or shortening of the maxilla that usually prevent their correct alignment are rarely observed phenomena (1); they are associated with a weakening in the individual that can threaten its survival and are thus a factor of vital importance in wild birds (2).  Although there is a higher incidence of these deformities in the families Icteridae and Mimidae (1), at least a further 28 have been found to have abnormal beaks, including Psittacidae (3,4).These anomalies have a varied aetiology, amongst which are trauma, abnormal wear of the rhamphotheca (5), nutritional deficiencies (vitamins and calcium metabolism), tumours (4), and infectious diseases (6), especially those caused by mange mites, in particular by the Knemidocoptes species, which are easily transmitted by direct contact between caged birds, and in many cases affect other parts of the body such as the legs (3,7,8).   2. Case history In a public park in L´Eliana (Valencia, Spain) (39°33′53.87″N 0°32′00.77″W), 5 Australian budgerigars (Melopsittacus undulatus) were observed to have differing degrees of beak malformations. The birds were housed in a pagoda-type bird cage (Figure 1A–C) with another 65 budgerigars and 2 cockatiels (Nymphicus hollandicus). The affected birds were captured using a net. Particularly notable was a mutated pearl green female weighing approximately 35 g with a very obvious scaly hyperkeratosis on the beak, both on the rhamphotheca (horny covering) and on the rhinotheca and gnatotheca (upper and lower maxillae), presenting a striking overgrowth as well as a slight lateral deviation of the jawbone (Figure 1). To confirm suspected knemidocoptic mange and in order to discover the aetiology of the deformity in the birds affected, we proceeded to perform deep scraping of the surface of the beak of both maxillae with the aid of a scalpel blade, and subsequently rinsing with Amman’s lactophenol. Microscope examination of the scraping revealed an abundance of mites, which were identified using identification keys. (9).3. Results and discussionParasitisation by Knemidocoptes pilae Lavoipierre & Griffiths, 1951 (Acari: Knemidokoptidae) (Figure 1D) is identified as the origin of the deformations found. Generally, the presence of beak malformations in birds, whatever the cause may be, is not frequent (less than 2%) (2,10). The lesions observed were only located on the beak, which coincides with previous findings in Turkey (3). However, K. pilae mange can also cause proliferative spongiform lesions in areas without feathers, such as the legs, nostrils, face, and around the eyes (8). Cases of “scaly leg” caused by K. pilae have been described in India (11) and in Brazil where, as well as an overgrowth of the beak very similar to that described by Abstract: An outbreak of knemidocoptic mange caused by Knemidocoptes pilae is described in caged Australian budgerigars (Melopsittacus undulatus) in a public park in L´Eliana (Valencia, Spain). Five individuals (5 out of 70) displayed severe malformation of the beak, with the rhamphotheca, rhinotheca, and gnathotheca affected and a slight lateral deviation of the jawbone, which did not, however, impede feeding or grooming.Key words: Knemidocoptes pilae, mange, Melopsittacus undulatus, abnormal beak growth, SpainReceived: 09.11.2013              Accepted: 27.12.2013             Published Online: 21.04.2014              Printed: 20.05.2014Case Report345ALARCÓN-ELBAL et al. / Turk J Vet Anim Scius, there were also obvious alterations around the nostrils (7). Likewise, in Turkey, an outbreak of mite infestation was described in a group of 30 budgerigars, causing pruritus and proliferative spongiform lesions of differing degrees of severity, with lesions mostly on the face and beak, although also on the legs and, to a minor degree, around the eyes (3). The pathogenic effect arises from the mechanical (burrowing into tissues) and chemical action (metabolites from their excretions) of the mites. As a general rule, knemidocoptic mange is transmitted by direct contact and it mainly affects young individuals with nutritional deficiencies, with high levels of stress or poor conditions of hygiene (3), although the disease is also associated with immunodepression and degree of consanguinity (12). The pathogen may also enter the bird cage via contact with free-living birds that are attracted to the surrounds by the bird feeders or the caged birds themselves.  Deformed beaks prevent correct grooming (10), which is the first line of defence against ectoparasites (13); however, the plumage of the individuals studied was in optimum condition and they had normal eating habits. Some birds are able to adapt to the malformation and survive by changing their habits (1).To control the outbreak, all the birds with lesions and all those that have been in direct contact with symptomatic individuals should be isolated and treated with macrocyclic lactones. For small birds such as M. undulatus, some authors advocate oral treatment with ivermectin (14); the dose should be calculated by means of interspecies extrapolation using allometric models, and topical treatment (15) or treatment with moxidectin spot-on solution, which achieves equally satisfactory results (3). The private character of this aviary did not allow us to take action ourselves. In this sense, we recommend the employees of the aviary follow these guidelines: separation of affected birds and treatment topically of all individuals (including apparently healthy ones) with ivermectin (1%, Ivomec® Inyectable Porcinos, Merial Laboratorios, Barcelona, Spain) twice with a 10-day interval.Infection by Knemidocoptes species mites is a frequent problem in poultry farming that also occurs in recreational aviculture and its consequences can lead to the death of infested birds. Given that poor hygiene and crowding are the main causes of infestations with this mite, it is essential to carry out basic preventive measures, in particular disinfection and cleaning the birdcage, watching for symptoms, and treating individuals with anti-parasitic products.  Figure 1. (A) Birdcage. (B) Several affected individuals. (C) Detail of one bird affected; changes can be appreciated in all structures of the beak. (D) K. pilae present in the lesions studied.  346ALARCÓN-ELBAL et al. / Turk J Vet Anim SciReferences1. Verea C, Verea JM. Deformidad del pico en el azulejo de jardín Thraupis episcopus (Passeriformes: Thraupidae) de Venezuela. Revista Brasileira de Ornitologia 2010; 18: 64–67 (in Spanish).2. Sogge MK, Paxton EH. A summary of observed physical deformities in the Willow Flycatcher: 1996–2000. Flagstaff, Arizona: Forest and Rangeland Ecosystem Science Center. 2000.3. Toparlak M, Tüzer E, Gargili A, Gülanber A. Therapy of knemidocoptic mange in budgerigars with spot-on application of moxidectin. Turk J Vet Anim Sci 1999; 23: 173–174.4. Owen HC, Doneley RJT, Schmidt RE, Patterson-Kane JC. Keratoacanthoma causing beak deformity in a budgerigar (Melopsittacus undulatus). Avian Pathology 2007; 36: 499–502.5. Olsen GH. Oral biology and beak disorders of birds. The Veterinary Clinics: Exotic Animal Practice 2003; 6: 505–521.6. Mans C, Guzman DS. What is your diagnosis? Fungal rhinosinusitis, with almost complete destruction of the premaxilla and deformation of the upper beak. Journal of Avian Medicine and Surgery 2007; 21: 235–238.7. Amaral V, Birgel EH. Nota sobre a presença de Cnemidocoptes pilae Lavoipierre & Griffins, 1951 (Acarina: Sarcoptiformes) em Melopsittacus undulatus (Aves, Psittacidae) no Brasil. Arquivos do Instituto Biológico de Sâo Paulo 1964; 31: 53–55 (in Portuguese).8. Hochleitner M. Diagnosis and treatment of avian skin diseases. Waltham Focus 1992; 4: 23–30.9. Fain A, Elsen A. Les acariens de la famille Knemidokoptidae, producteurs de la gale chez les oiseaux (Sarcoptiformes). Acta Zoologica Antverpiensia 1967; 45: 3–145 (in French).10. Sharp MS, Neill RL. Physical deformities in a population of wintering black birds. Condor 1979; 81: 427–430.11. Rao SR, Ghafoor MA, Narsapur VS. Cnemidocoptes pilae (Lavoipierre and Griffiths 1951) a causative agent of scaly leg in budgerigar (Melopsittacus undulatus) in India together with the description of the larval forms. Indian Veterinary Journal 1967; 44: 206–208.12. Godoy SN. In: Cubas ZS, Silva JC, Catão-Dias JL. Tratado de Animais Selvagens. São Paulo: Roca, 2006. Seção 4, Cap 16, p. 222 (in Portuguese).13. Clayton DH, Moyer BR, Bush SE, Jones TG, Gardiner DW, Rhodes BB, Goller F. Adaptive significance of avian beak morphology for ectoparasite control. Proceedings of the Royal Society of Biology 2005; 272: 811–817.14. Pachaly JR. In: Cubas ZS, Silva JC, Catão-Dias JL. Tratado de Animais Selvagens. São Paulo: Roca, 2006. Seção 8, Cap 64. p 1070–1071 (in Portuguese).15. Bichard SJ, Sherding RG. Clínica de Pequenos Animais. 2 ed. São Paulo: Roca, 2003. p 1561 (in Portuguese).

Severe beak deformity in Melopsittacus undulatus caused by Knemidocoptes pilae

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