First pathological report of parasitic gastric ulceration in Humboldt penguin (Spheniscus humboldti) along the coast of south-central Chile/Primera descripcion patologica de ulceras gastricas parasitarias en el pinguino de Humboldt (Spheniscus humboldti) en la costa centro-sur de Chile.
Specifically, the genus Contracaecum has been described in piscivorous birds, particularly different penguin species (Pazos et al., 2003; Fredes et al., 2006; Garbin et al., 2007). Several authors, including Portes-Santos (1984), Grabda (1991) and Fagerholm & Overstreet (2008), have studied the taxonomy of this parasite.
The life cycle of the genus Contracaecum is heteroxenous, and adult stages are located in the proventriculous of seabirds, which serve as definitive hosts (Melhorn et al., 1991). Gravid female parasites release eggs that are excreted into the water with bird feces. Third-stage larvae emerge and are ingested by crustaceans, which act as intermediate hosts. Fish may act as paratenic hosts. Thus, if fish consume infected invertebrates, the larvae does not continue to develop but remain encapsulated inside the intestinal wall, mesentery, liver, and other internal organs of the host. When fish are consumed by seabirds, fourth-stage larvae develops and eventually reach the adult stage (Fagerholm & Overstreet, 2008).
Many publications deal with gastric ulceration by Contracaecum in mammals and birds such as penguins, but no studies have described these symptoms in Humboldt penguins. Thus, the present work is the first description of gastric ulceration by C. pelagicum in S. humboldti.
Given the vulnerable condition of the Humboldt penguin (CONAMA, 2008), it is important to improve our knowledge of this disease. Therefore, prevalence and incidence studies are required to determine the real impact of parasitic ulcers on this population. Such knowledge would allow us to define adequate preventive or therapeutic strategies that would reduce mortality and strengthen the species recovery.
Description and discussion of cases
Three moribund Humboldt penguins were captured by the National Fishing Service (SERNAPESCA) along the shore of Talcahuano, in the Biobio Region, Chile (36[degrees]43'S, 73[degrees]07'W). A clinical evaluation of the birds showed them to be inattentive to surrounding stimuli, highly undernourished, weak, and suffering digestive alteration (diarrhea). Emergency clinical procedures were applied: penguins were rehydrated orally with glucosaline serum (30 mL [kg.sup.-1] +2 g HCI) and an oral vitamin B and E complex was administered (400 U.I.). In keeping with the indications of Wallace & Walsh (2005), an intramuscular antibiotic (Enrofloxacin 10 mg [kg.sup.-1]) and an oral antifungal (Itraconazole 10 mg [kg.sup.-1]) were administered. Despite these emergency measures, penguins died three hours after treatment. Postmortem evaluations were performed immediately.
The necropsy was done according to the protocol presented by Work (2000). A severe gastrointestinal parasitic condition was found. Anisakidae worms were present in the middle third of the esophagus, increasing their number towards the glandular portion of the stomach. Parasites observed in the esophageal tract had probably been regurgitated since no lesions were found in the esophageal mucosa. The stomachs of the birds showed severe blood congestion, as evidenced by the plethoric condition of the blood vessels superficially arranged on the greater curvature of the organ.
Multiple ulcerations with yellow-whitish borders and a caseous aspect were located exclusively in the glandular portion of the gastric mucosa (Fig. 1a). Nematodes of different sizes were found in most of the observed lesions in the Humboldt penguins. The affected areas varied from 0.6 to 2.3 cm in diameter.
In total, 23 specimens of nematode parasites were collected; one female, four males, and two juveniles from the first penguin; two female, five males, and two juveniles from the second penguin; and three females and four males from the third penguin. When examined under light microscopy, all were found to belong to the genus Contracaecum.
Studies describing gastric ulcers caused by Contracaecum have reported similar macroscopic lesions in the gastric mucosa of seabirds such as the white pelican (Pelecamus erythrorhynchu) and marine mammals such as the northern sea lion (Eumetopias jubata; Liu & Edward, 1971), South American sea lion (Otaria byronia; Cattan et al., 1976), and the sea bear (Callorhinus ursinus; Spraker et al., 2003). Although the distribution of the lesions differed, the authors agreed that most worms were found free in the stomach contents.
In penguins, gastric ulcerative processes caused by Contracaecum sp. have been described in the little penguin (Eudyptula minor; Obendorf & McColl, 1980) and the Magellanic penguin (Spheniscus magellanicus; Garbin et al., 2007). Penguins are fundamentally ichthyophagous and, therefore, they acquire the parasite through the ingestion of infected fish. Ulcerations in the esophageal and intestinal mucosa caused by Anisakidae are less frequent in S. magellanicus (Mann, 1992; Garbin et al., 2007).
The injured tissue was extracted, fixed in 10% buffered formalin, and sent to the Veterinary Anatomic Pathology Center (CAPAVET), Concepcion, Chile for histological analysis. Samples were embedded in paraffin. Sections of 5 [micro]m were stained with hematoxylin and eosin.
The histoarchitecture of the gastric mucosa was severely altered by a granulomatous reaction. The central area consisted of an acellular hyaline substance and presented calcium mineralization foci that replaced the mucosal glandular tissue and, in many cases, extended to the muscular tunica (Fig. 1b).
The origin of the hyaline substance is uncertain. However, Liu & Edward (1971) performed histochemical studies of ulcers caused by Contracaecum osculatum in the stomachs of northern sea lions and white pelicans, concluding that this substance was essentially made up of parasite secretions and cellular fragments from the host.
The inflammatory infiltration showed a great amount of neutrophils (heterophils), lymphocytes, plasma cells, bordered by multinucleated giant cells (foreign-body-type), and epithelioid cells aggregates. The injured area was surrounded by a severe desmoplastic reaction (Fig. 1c).
Our histological observations agreed with those described by Liu & Edward (1971), Obendorf & McColl (1980), and Garbin et al. (2007) for seabirds and by Cattan et al. (1976) and Spraker et al. (2003) for marine mammals.
Electron microscopy of worms
The collected parasites were stored in alcohol at 70% for taxonomic purposes and dehydrated in ascending grades of ethanol and finally rinsed in 100% ethanol, several times for 10-15 min according to Anderson (1951). Individual specimens were at first dehydrated by the critical point drying method, mounted in metal stubs, gold-palladium coated and examined in scanning electron microscope (JEOL JSM-6380LV) belonging to the Electron Microscopy Laboratory of the University of Concepcion, Chile.
The worm Contracaecum pelagicum was identified by the spatial distribution of tail papillae and the presence of bifurcated interlabia (Fig. 1d) according to the descriptions of Johnston & Mawson (1942), Portes-Santos (1984), and Fagerholm & Overstreet (2008). This identification agreed with the diagnostic characteristics established by Garbin et al. (2007).
C. pelagicum was described for the first time in the black-browed albatross (Diomedea melanophris) in Australia. It was subsequently redescribed on the Uruguayan coasts. Portes-Santos (1984), Fagerholm et al. (1996), and Garbin et al. (2007) identified this species in Sphenicus magellanicus along the coasts of Brazil, South Africa, and Argentina. Silva et al. (2005) reported the occurrence of C. pelagicum in the brown booby (Sula leucogaster, Sulidae, Pelecaniformes) off Sao Paulo, Brazil.
In Chile, studies of gastrointestinal parasitosis caused by nematodes of the Contracaecum genus have been carried out by Mann (1992) and Gonzalez-Acuna et al. (2008). However, these works were primarily taxonomic studies of the parasite specimens rather than studies of the tissular alterations they caused in the hosts.
In general, few publications have described the pathological alterations caused by the genus Contracaecum in marine birds. To date, no studies dealing with ulcers caused by this parasite in the Humboldt penguin have been published.
Tissular alterations by Contracaecum pelagicum should be common in the Humboldt penguin population since these birds are part of the life cycle of this parasite. S. humboldti acts as a definitive host when they ingest infected fishes. Herling et al. (2005) examined and compared the diet of the Humboldt penguin in northern and southern of Chile. In this study, fish were the dominant prey item, mainly anchovy (Engraulis rigens) and Inca scad (Trachurus murphyi). Both species have been catalogued as intermediate hosts and transmitters of Contracaecum to the penguins (Fagerholm & Overstreet, 2008). Therefore, this worm could play an important role in increasing the vulnerability of Humboldt penguins.
Previously described pathological alterations are enough to generate abdominal pain, general discomfort, reduction of hunting performance, and an insufficient rate of feeding, amongst others, in living penguins. These instances have to be considered debilitating factors and promoters of immunosuppression, hence, facilitators for infectious and non-infectious diseases in population.
For present cases, it is important to mention that the ulcerative lesions were not the cause of death, but the extreme undernourishment and dehydration determined the multisystem organ failure. It is linely that Contracaecum becomes a primary etiological agent causative of death if it pierce the stomach wall and induce peritonitis.
We think it's relevant to highlight the great number of questions generated while making this report and once it was finished. For example, how many Humboldt penguins die yearly by this parasitosis as primary disease? How many Humboldt penguins becomes "easy preys" for its natural predators due to weakness induced by this parasitosis? Are there important variations in the number of penguins affected by this disease throughout the year? seasonal dependence?. Does this parasitosis significantly affect the reproductive rate of S. humboldti?
[FIGURE 1 OMITTED]
We strongly believe that the effect of Contracaecum in Humboldt penguins is an important factor that would impede the success of any enterprise for protecting these birds. Thus, research related to the incidence and prevalence of this parasite and the real impact of gastric ulceration on the penguin population is necessary in order to apply environmental and therapeutic strategies leading to the recovery of the species.
Este trabajo fue financiado por Proyecto de la Universidad de Concepcion: DIUC-18.104.22.168.
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Received: 27 September 2011; Accepted: 23 March 2012
Francisco Yanez (1,2), Italo Fernandez (2,3), Victor Campos V. (2,4), Miguel Mansilla (1), Ariel Valenzuela (2), Hernan Gonzalez (1), Cristhian Rodriguez (1), Meyling Rivas (2), Katherine Alveal (2) & Ciro Oyarzun (2)
(1) Centro de Anatomia Patologica Veterinaria (CAPAVET), Concepcion, Chile
(2) Laboratorio de Piscicultura y Patologia Acuatica, Facultad de Ciencias Naturales y Oceanograficas Universidad de Concepcion, Concepcion, Chile
(3) Laboratorio de Parasitologia, Departamento de Microbiologia, Facultad de Ciencias Biologicas Universidad de Concepcion, Concepcion, Chile
(4) Laboratorio de Microbiologia ambiental, Departamento de Microbiologia, Facultad de Ciencias Biologicas Universidad de Concepcion, Concepcion, Chile
Corresponding author: Francisco Yanez (firstname.lastname@example.org)
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|Title Annotation:||articulo en ingles|
|Author:||Yanez, Francisco; Fernandez, Italo; Campos V., Victor; Mansilla, Miguel; Valenzuela, Ariel; Gonzalez|
|Publication:||Latin American Journal of Aquatic Research|
|Date:||Jul 1, 2012|
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