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BMC Veterinary Research

, 14:384 | Cite as

First report on nasal myiasis in an alpaca “Vicugna pacos” – a case report

  • Teresa Maria Punsmann
  • Lucie Marie Grimm
  • Carolin Reckmann
  • Cornelia Schwennen
  • Matthias Gerhard Wagener
  • Martin Ganter
Open Access
Case Report
  • 84 Downloads
Part of the following topical collections:
  1. Parasitology

Abstract

Background

An infestation of bot fly larvae causes myiasis which is known to cause respiratory symptoms in ruminants. There are reports of bot fly larvae in llamas, but to our knowledge there are no previous reports of nasal myiasis due to bot flies in alpacas (“Vicugna pacos”).

Case presentation

The following case report describes a neutered male alpaca showing sneezing and mild nasal discharge. Endoscopic examination of the upper respiratory tract revealed bot fly larvae in one nostril. After treatment with doramectin, there was no evidence of living bot fly larvae visible in the nostril.

Conclusion

Bot fly larvae should be considered as a potential cause of respiratory symptoms in alpacas. In the present case, a treatment with doramectin was successful.

Keywords

Alpaca New world camelids Bot flies Treatment Doramectin Germany 

Background

In New World camelids bot flies play a role causing parasite-induced respiratory symptoms [1]. However, case reports of myiasis due to bot flies in New World camelids are rare. All reports published to date deal with nasal bots in llamas. There are, in total, four described cases of bot fly larvae in llamas in the United States and South America [2, 3, 4]. The animals were presented because of respiratory symptoms like sneezing and nasal discharge, which were not responsive to antibiotic treatment. In cases where the causative species could be isolated, Oestrus ovis (sheep and goat bot fly) [3] and Cephenemyia spp. (deer bot flies) were identified [4]. In two cases, the species remained unknown [2].

Oestrus ovis is a common parasite in sheep and goats. The adult fly shoots larvae onto the area around the nostrils of the affected animals, whence the larvae move into the nasal cavity where they become mature. When they become the third instar larvae they fall to the ground and pupate in the environment [1]. Cephenemyia spp. larvae are shot by the flies directly into the nasal cavity where they remain until they reach the third larval stage. The third instar larvae is sneezed out into the environment where they pupate [1].

Cephenemyia spp. lead to worse reactions in New World camelids than in deer. In the nasal meatus a granulomatous swelling evolves [1, 4].

Knowledge about the life cycle of bot flies in llamas and alpacas is insufficient and further investigations are needed.

In Old World camelids myiasis can be caused by Cephalopina titillator [5]. Infections of New World camelids with this species have not been described.

As there are only few described cases of myiasis caused by bot flies in New World camelids recommendations for treatment are rare. In one llama [3] bot fly larvae were identified during necropsy after the animal had died due to haemorrhagic pneumonia. Therefore, no specific treatment was provided. The other affected animals were treated with ivermectin 0.2 mg/kg. In one llama the treatment had to be repeated and combined with local ivermectin administration in order to kill the larvae [2]. One llama, which had been successfully treated subcutaneously with ivermectin, died shortly afterwards due to unknown reasons [2]. To date a treatment with doramectin against bot fly larvae in New World camelids has not been described, while in sheep it is described as an effective drug against Oestrus ovis at a dosage of 200 μg/kg [6].

This case report gives the first clinical description of bot flies in an alpaca.

Case description

A five-year-old neutered male huacaya-alpaca showing sneezing for three weeks was presented to the Clinic for Swine, Small Ruminants and Forensic Medicine, University of Veterinary Medicine Hannover, Foundation, Germany. The alpaca was privately owned and kept on pasture together with four female alpacas. The sneezing was noticed for the first time by the owner about two to three weeks before presenting the animal to the clinic. He reported sneezing fits lasting up to two hours. Apart from that, the general condition of the animal was good. The four female alpacas did not show any symptoms to the author’s knowledge.

The alpaca had serous, clear nasal discharge coming out of both nostrils. During examination sneezing could be triggered by applying pressure to the bridge of the nose. The distending of the nostrils indicated that breathing was impeded (Fig. 1). Auscultation of the lung revealed physiologically mild respiratory sounds on both sides.
Fig. 1

The affected alpaca showing serous nasal discharge and impeded breathing

The analysis of blood samples and faeces showed mild anaemia, granulocytosis and lymphopenia (Table 1). Eosinophils were not increased above the upper reference limits [7]. Clinical chemistry revealed slight hyperproteinaemia, hyperalbuminaemia, hypercalcaemia and hypophosphataemia (Table 1). In the faecal sample a very low number of gastrointestinal nematode eggs was found.
Table 1

Haematology and clinical chemistry of the alpaca

 

Unit

Reference

Patient

Haematology

 Haemoglobin

g/L

127–166

124

 PCV

L/L

0.29–0.37

0.28

 MCHC

g/L

414–459

443

 Leucozytes

G/L

9.8–15.8

14.9

 Neutrophils

G/L

4.5–9.3

10.9

 Band neutrophils

G/L

0–0.1

0.07

 Lymphocytes

G/L

1.7–4.5

1.1

 Monocytes

G/L

0.1–0.7

0.4

 Eosinophils

G/L

1–3.6

2.2

 Basophils

G/L

0–0.3

0.2

 Neutrophils

%

44–70.5

73

 Band neutrophils

%

0–1

0.5

 Lymphocytes

%

15.2–31

7.5

 Monocytes

%

2–5.5

2.5

 Eosinophils

%

8–27

15

 Basophils

%

0–2

1.5

Clinical chemistry

   

 Total protein

g/L

59.9–69.1

74.3

 Albumin

g/L

31.3–38.6

46.7

 Creatinine

μmol/L

97–167

142

 Urea

mmol/L

5.2–9.7

4.9

 Calcium

mmol/L

2.2–2.5

2.7

 Phosphorus

mmol/L

1.6–3

1.5

References from [7]. Only small deviations from reference range were found in the alpaca affected by bot fly larvae

Endoscopic examination of the nose was carried out. Due to the tension of the alpaca, the examination was conducted under general anaesthesia (0.4 mg/kg xylazine [Xylavet 20 mg/ml®, CP-Pharma, Burgdorf, Germany], 4 mg/kg ketamine [Ketamidor 100 mg/ml®, WDT, Garbsen, Germany]) [1], [8] and local anaesthesia of the nostrils (Procainhydrochlorid, Epinephrin [Isocain ad us. vet.®, Selectavet, Dr. Otto Fischer GmbH, Weyarn/Holzolling, Germany]). The endoscope was inserted approximately 15 cm into the right ventral nasal meatus. At this position a soft tissue mass originating from the nasal mucosa was observed. There were no signs of an acute inflammation at this location. The mass filled out about a third of the lumen of the meatus and at least four living larvae were revealed in this tissue (Fig. 2). No larvae could be removed due to technical reasons. Examination of the left nostril was not carried out because bleeding and noticeable mucosal irritation occurred while examining the right nostril. Under general anaesthesia radiographs of the head were taken. No abnormal radiopaque structures could be found on the radiographs.
Fig. 2

Endoscopic picture of the right ventral meatus from the affected alpaca before treatment. A soft tissue mass with moving larvae was found

The alpaca was treated subcutaneously with doramectin by a dose of 0.2 mg/kg (Dectomax®, Lilly Deutschland GmbH, Elanco Animal Health, Bad Homburg, Germany).

Five days after treatment, sneezing could not be triggered any more by pressing on the bridge of the nose. Six days after treatment another endoscopic examination under local anaesthesia (Isocain ad us. vet.®) was carried out. Compared to the first examination, the soft tissue mass had notably decreased; there were no more larvae visible within the mass (Fig. 3).
Fig. 3

Endoscopic picture of the right ventral meatus from the affected alpaca after treatment. The soft tissue mass has decreased and no more larvae were found

In the endoscopy before the treatment with doramectin no larvae could be removed and, in addition, no larvae were sneezed out, so species of the bots could not be determined.

Discussion

To the authors’ knowledge the present case is the first report of respiratory symptoms due to bot fly larvae in an alpaca. To date it is mentioned, that Oestrus ovis and Cephenemyia spp. are ectoparasites alpacas are exposed to [9], but no clinical symptoms are outlined. Additionally, it is the first published successful treatment of bot flies in New World camelids using doramectin.

In order to determine the causative species which has caused the alterations of the mucosa we tried to remove the larvae endoscopically. The larvae could not be gripped successful and additionally bleeding and swelling of the mucosa occurred. In some of the reported cases respiratory distress leading to a tracheotomy was caused by trying to remove larvae from the nostrils [2, 4]. To avoid such a serious intervention the attempt to remove the larvae was interrupted. Moreover, no larvae were found in the stable, so the species could not be identified. Both bot fly species which have been found in llamas (Cephenemyia spp. and Oestrus ovis) occur in Germany. The Camel nasal bot fly (Cephalopina titillator) occurs in large parts of Africa, Asia, Australia and the Middle East. Central Europe is not the natural habitat of this species [10]. An indication as to the identity of the causative bot fly species may be seen in the fact that the neutered male alpaca did not have any contact to sheep, but as it was kept on pasture with contact to deer, the end host of Cephenemyia spp.. Another hint to the causal species in the present case is the severe swelling within the nostril. It is known that Cephenemyia spp. in New World camelids cause a severe reaction, with noticeable swelling and granulation tissue [1, 4]. If it was Oestrus ovis the button in the posterior spiracular plate would be located in the center of the plate [10, 11]. In the photographs taken during endoscopy the buttons seem to be located at the medial border of the plate. This finding supports the suspicion, that the bot fly causing the myiasis could be Cephenemyia spp..

The small deviations from the reference range found in the haematology and clinical chemistry are not associated with the occurrence of bot fly larvae according to the current state of knowledge.

The formerly described cases of bot flies fly larvae in llamas were treated with ivermectin [2, 4], but this treatment was not successful after one administration in all cases. As alternative therapy we decided to use doramectin, as doramectin is an effective drug against myiasis due to bot flies in sheep. In sheep a dosage of 200 μg/kg has a sufficient effect on Oestrus ovis [6]. As such a dosage has no negative effects on alpacas [1] the alpaca in the present case was treated subcutaneously with doramectin 200 μg/kg. A single treatment was successful, the sneezing stopped, no larvae could be found within the nostril and the swelling decreased.

Conclusion

This case report describes the first clinical finding of myiasis caused by bot flies in an alpaca. Additionally it is the first description of a successful treatment with doramectin. Bot fly larvae should be perceived as a differential diagnosis when an alpaca is presented with nonspecific respiratory symptoms, especially sneezing.

Notes

Acknowledgements

We would like to thank our animal keepers Tanja Bode and Thorsten Waßmann for helping during treatment and examination of the alpaca and our laboratory staff for their prompt and reliable work. Furthermore we would like to thank Frances Sherwood-Brock, English editorial office, University of Veterinary Medicine Hannover, Foundation, Germany, for proofreading the manuscript.

Funding

Not applicable.

Availability of data and materials

Not applicable.

Authors’ contributions

TP, LG, CS, MW and MG dealt with the case. TP drafted the manuscript. CR was involved in drafting the manuscript and revised it critically. All authors reviewed and approved the final manuscript.

Ethics approval and consent to participate

Not applicable.

Consent for publication

The owner of the alpaca gave written consent for publication.

Competing interests

The authors declare that they have no competing interests.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

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Copyright information

© The Author(s). 2018

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Authors and Affiliations

  1. 1.Clinic for Swine, Small Ruminants and Forensic MedicineUniversity of Veterinary Medicine Hannover, FoundationHannoverGermany

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