Characterization of Klebsiella pneumoniae isolates from New Zealand sea lion ( Phocarctos hookeri) pups during and after the epidemics on Enderby Island, Auckland Islands

• Published in: Veterinary microbiology 2007-05, Vol.122 (1), p.178-184
• Main Authors: Castinel, Aurélie, Grinberg, Alex, Pattison, Rebecca, Duignan, Pádraig, Pomroy, Bill, Rogers, Lynn, Wilkinson, Ian
• Format: Article
• Language: English
• Subjects: Animal Diseases - epidemiology; Animal Diseases - microbiology; Animals; antibiotic resistance; bacterial infections; Bacteriology; beta-lactam antibiotics; Biological and medical sciences; breeding season; clonal variation; disease outbreaks; Disease Outbreaks - veterinary; Epidemics; epidemiological studies; etiology; Fundamental and applied biological sciences. Psychology; Klebsiella Infections - epidemiology; Klebsiella Infections - microbiology; Klebsiella Infections - veterinary; Klebsiella oxytoca; Klebsiella pneumoniae; Klebsiella pneumoniae - genetics; Marine; marine mammals; Microbiology; minimum inhibitory concentration; Miscellaneous; molecular genetics; mortality; New Zealand - epidemiology; New Zealand sea lion; Otariidae; pathogen identification; pathogenicity; PFGE; Phocarctos hookeri; Phylogeny; pulsed-field gel electrophoresis; pups; Sea Lions - microbiology; virulence; wild animals
• ISSN: 0378-1135; 1873-2542
• DOI: 10.1016/j.vetmic.2006.12.024

The 2001/2002 and 2002/2003 breeding seasons of New Zealand sea lions (NZSLs) on the Auckland Islands were marked by a high pup mortality caused by acute bacterial infections. As part of a health survey from 1998/1999 to 2004/2005, tissues and swabs of lesions had been collected at necropsy to identify the bacteria associated with pup mortality. Klebsiella pneumoniae was grown in pure culture from 83% of various organs and lesions in 2001/2002 and 76% in 2002/2003, and less frequently in the following seasons (56% in 2003/2004 and 49% in 2004/2005). Pup isolates of K. pneumoniae showed identical minimal inhibitory concentrations (MIC) of cefuroxime, neomycin, cephalotin, cephalexin and dihydrostreptomycin, suggesting clonal aetiology of the pathogen. Isolates also tested negative for production of extended-spectrum beta-lactamases (ESBLs), which was not in favour of an anthropogenetic origin of the epidemic strain. Pulsed-field gel electrophoresis (PFGE) of XbaI DNA macrorestriction fragments was performed on isolates of K. pneumoniae and Klebsiella oxytoca from 35 pups, thee NZSL adult females, and from three human patients for comparison. PFGE showed that pup isolates of K. pneumoniae were genetically indistinguishable but were neither related to K. pneumoniae from humans and from NZSL adults, nor to K. oxytoca from NZSLs. It is concluded that the 2001/2002 and 2002/2003 epidemics at Sandy Bay rookery were caused by a single K. pneumoniae clonal lineage, genetically different from the strain carried by adult NZSLs. An anthropogenic origin of the K. pneumoniae clone could not be confirmed, but further investigations are required to rule-out such occurrence.