We documented bronchopneumonia in seven mountain goat (
All-age pneumonia epizootics followed in subsequent years by sporadic or recurring summer lamb mortalities are a significant source of mortality and population declines in bighorn sheep (Ovis canadensis) throughout western North America (Cassirer et al. 2018). Clinical signs in pneumonic lambs include coughing, nasal discharge, head shaking, ear drooping, and lethargy (Cassirer et al. 2013). Organisms most commonly detected in the lungs of pneumonic lambs include Mycoplasma ovipneumoniae, diverse Pasteurellaceae spp., and obligate anaerobic bacterial species (Besser et al. 2008).
In parts of their range, mountain goats (Oreamnos americanus) are sympatric with bighorn sheep. They may also contact domestic livestock on public grazing allotments or private land. Mountain goats are potential hosts for respiratory pathogens that are of concern for bighorn sheep (Lowrey et al. 2018). A single adult goat mortality related to Pasteurella pneumonia has been reported (Brandborg 1955). We report the diagnosis of bronchopneumonia and the detection of M. ovipneumoniae by real-time (RT)-PCR from upper and lower respiratory tract samples of seven dead kids from the East Humboldt Range (EHR), coordinates 40°55′16″N, 115°7′7″W, and the adjacent Ruby Mountains (RM), coordinates 40°37′19″N, 115°28′30″W in Elko County, Nevada US.
In the winter of 2009–10, an all-age pneumonia epizootic with consistent detection of M. ovipneumoniae in the upper and lower respiratory tracts was documented in bighorn sheep (McAdoo et al. 2010). The Nevada Department of Wildlife (NDOW) estimated that 10% (population estimated at 220) and 13% (population estimated at 130) of sympatric mountain goat populations also died during this epizootic in the RM and EHR, respectively (Cox et al. 2017). During the disease event, one adult mountain goat carcass was recovered, and gross necropsy results documented bronchopneumonia. Due to advanced autolysis, no samples were collected for analysis. A total of 75 goats were captured by helicopter net gunning during (n=3) and after (n=72) the outbreak for marking and sample collection for pathogen surveillance. Nasal and pharyngeal swabs and blood samples were collected from goats in both mountain ranges and submitted to the Washington Animal Disease Diagnostic Laboratory for detection of M. ovipneumoniae by RTPCR, identification of Pasteurellaceae spp. by bacterial culture as described by Roug et al. (2017), and M. ovipneumoniae–specific antibodies by enzyme-linked immunosorbent assay (Ziegler et al. 2014), respectively. The laboratory detected M. ovipneumoniae from nasal swabs of 12 goats and M. ovipneumoniae–specific serum antibodies in 68 goats. Pharyngeal bacterial cultures yielded Bibersteinia trehalosi in 77% (58/75) and Mannheimia haemolytica in 61% (46/75) of the animals sampled during this period. In 2015, RT-PCR targeting lktA, the gene encoding leukotoxin A (Walsh et al. 2016), was performed on the B. trehalosi (n=14) and Mannheimia haemolytica (n=8) pharyngeal isolates, detecting this gene in four and eight isolates, respectively (Table 1). Aerial surveys and ground observations conducted from 2011 to 2015 indicated decreased annual kid recruitment in both the RM and EHR populations (Cox et al. 2017; Blanchong et al. 2018), as has been documented for bighorn lambs following pneumonia epizootics (Cassirer et al. 2018).
Table 1.
Diagnostic summaries for Pasteurellaceae spp. (Bibersteinia trehalosi and Mannheimia haemolytica), lktA (the gene encoding leukotoxin A), and Mycoplasma ovipneumoniae (Mo) detected in mountain goats (Oreamnos americanus) sampled between 2010 and 2015 in the East Humboldt Range (EHR) and Ruby Mountains (RM) by the Nevada Department of Wildlife during an investigation of an outbreak of respiratory disease. Samples were tested by the Washington Animal Disease Diagnostic Laboratory (Pullman, Washington, USA)a
Between January 2011 and August 2015, seven mountain goat kids (two from the RM and five from EHR), approximately 56–217 d of age, were presented to NDOW for necropsy. In 2011, one kid from the RM was found dead in January, and another alive in August that died 36 h after surrender to NDOW. The five kid mortalities from the EHR were collected in the summers of 2014 and 2015, coincident with weekly ground field observations to document kid behavior, signs of respiratory disease, and timing of kid mortalities (Cox et al. 2017; Blanchong et al. 2018). Clinical signs observed included coughing, head shaking, extension of the neck, nasal discharge, and lethargy (Blanchong et al. 2018). In July–August 2014 and August 2015, kids exhibiting severe clinical signs of respiratory disease were opportunistically collected; two immediately after natural death and three following euthanasia by gunshot. Whole carcasses were packed in ice and transported to NDOW for necropsy within 24 h.
Table 2.
Histopathology findings by the Washington Animal Disease Diagnostics Laboratory (Pullman Washington, USA) for seven mountain goat (Oreamnos americanus) kids collected in 2011–15 following a bighorn sheep (Ovis canadensis) pneumonia epizootic in the Ruby Mountains and East Humboldt Range, Nevada, USA. Except for kid 917, all were recovered and submitted for necropsy to the Nevada Department of Wildlife within 24 h of death
Gross necropsy lesions (Fig. 1), histopathology (Fig. 1 and Table 2), and culture results (Table 3) for all kids were consistent with acute to chronic suppurative bronchopneumonia, including varying degrees of bronchiolar mucosal hyperplasia and bronchiolar lymphatic tissue hyperplasia. Five of the seven kids had histologic lesions consistent with acute secondary septicemia. There was no histologic evidence of predisposing immunosuppression, and all kids were negative for bovine virus diarrhea virus by immunohistochemistry or PCR. Mycoplasma ovipneumoniae was detected in all kids tested by RTPCR in both the upper (nasal, sinus, tonsil, and tympanic bullae) and lower (lung) respiratory tract. The M. ovipneumoniae strain detected in the mountain goats (adults and kids) shared the 16S-23S intergenic spacer region DNA sequence previously detected in sympatric bighorn sheep during and after the 2009–10 pneumonia outbreak (Besser et al. 2012). As with other reports of pathogens recovered from the respiratory tract of pneumonic bighorn lambs (Besser et al. 2008; Grigg et al. 2017; Wood et al. 2017), M. ovipneumoniae was a consistently detected respiratory pathogen in the lungs of these pneumonic kids. However, the Pasteurellaceae spp. isolated from the pneumonic lung tissue of the kids were largely discordant with those detected in the pharyngeal cultures from the goats sampled during the same period (Table 1) and also with those detected in some studies of pneumonic bighorn lambs (Grigg et al. 2017; Wood et al. 2017). However, it is likely that additional Pasteurellaceae spp. were present but not detected by culture (Butler et al. 2017). Four kids had additional organs submitted for aerobic culture, and in three, pathogenic bacteria were recovered, supporting the histologic finding of septicemia.
Table 3.
Bacterial culture and real-time PCR findings of the Washington Animal Disease Diagnostics Laboratory (Pullman, Washington, USA) for seven mountain goat (Oreamnos americanus) kids collected in 2011–15 following a bighorn sheep (Ovis canadensis) pneumonia epizootic in the Ruby Mountains and East Humboldt Range, Nevada, USA. Mycoplasma ovipneumoniae (Mo) was detected by real-time PCR in the lungs and upper respiratory tract (nose, tonsil, sinus, or middle ear [bulla]) of all seven kids tested. The PCR detections of lktA, the gene encoding leukotoxin A, conducted on upper respiratory tract or lung Pasteurellaceae isolates are indicated. Bacterial culture results conducted on nonrespiratory tissues (other tissues) are identified
To our knowledge, respiratory disease as a cause of kid mortality has not been previously documented in mountain goats. Histopathology, bacterial culture, and agent-specific, as well as leukotoxin PCR assays, coupled with direct animal observations and decreasing recruitment, strongly suggest that mountain goat kids can have a similar clinical presentation, etiology, and population response as bighorn lambs following an all-age pneumonia epizootic (Besser et al. 2008; Wood et al. 2017). However, further research is needed to define the population impacts and epidemiology of respiratory disease in this species. Where mountain goats are sympatric with domestic or wild members of the Caprinae subfamily, wildlife managers should consider mountain goats to be susceptible to and potentially carriers of, important respiratory pathogens that may lead to population-limiting disease.
Funding for this project was provided by the Elko Bighorns Unlimited, Nevada Bighorns Unlimited, the Nevada Department of Wildlife Heritage Trust Fund, the Rocky Mountain Goat Alliance, and Iowa State University. Without the hard work of our field technicians, Joe Hoffmann, Wade McCammond, and Cole Bleke, this work would not have been possible. We are grateful to Washington Animal Disease Diagnostic Laboratory anatomic pathologist Kyle Taylor and Nevada Department of Wildlife personnel, Shane Talley, Tyler Nall, and especially, Chris Morris, for their dedication and support.