- Infectious Diseases of Livestock
- Part 3
- Leptospirosis
- GENERAL INTRODUCTION: SPIROCHAETES
- Swine dysentery
- Borrelia theileri infection
- Borrelia suilla infection
- Lyme disease in livestock
- Leptospirosis
- GENERAL INTRODUCTION: AEROBIC ⁄ MICRO-AEROPHILIC, MOTILE, HELICAL ⁄ VIBROID GRAM-NEGATIVE BACTERIA
- Genital campylobacteriosis in cattle
- Proliferative enteropathies of pigs
- Campylobacter jejuni infection
- GENERAL INTRODUCTION: GRAM-NEGATIVE AEROBIC OR CAPNOPHILIC RODS AND COCCI
- Moraxella spp. infections
- Bordetella bronchiseptica infections
- Pseudomonas spp. infections
- Glanders
- Melioidosis
- Brucella spp. infections
- Bovine brucellosis
- Brucella ovis infection
- Brucella melitensis infection
- Brucella suis infection
- Brucella infections in terrestrial wildlife
- GENERAL INTRODUCTION: FACULTATIVELY ANAEROBIC GRAM NEGATIVE RODS
- Klebsiella spp. infections
- Escherichia coli infections
- Salmonella spp. infections
- Bovine salmonellosis
- Ovine and caprine salmonellosis
- Porcine salmonellosis
- Equine salmonellosis
- Yersinia spp. infections
- Haemophilus and Histophilus spp. infections
- Haemophilus parasuis infection
- Histophilus somni disease complex in cattle
- Actinobacillus spp. infections
- infections
- Actinobacillus equuli infections
- Gram-negative pleomorphic infections: Actinobacillus seminis, Histophilus ovis and Histophilus somni
- Porcine pleuropneumonia
- Actinobacillus suis infections
- Pasteurella and Mannheimia spp. infections
- Pneumonic mannheimiosis and pasteurellosis of cattle
- Haemorrhagic septicaemia
- Pasteurellosis in sheep and goats
- Porcine pasteurellosis
- Progressive atrophic rhinitis
- GENERAL INTRODUCTION: ANAEROBIC GRAM-NEGATIVE, IRREGULAR RODS
- Fusobacterium necrophorum, Dichelobacter (Bacteroides) nodosus and Bacteroides spp. infections
- GENERAL INTRODUCTION: GRAM-POSITIVE COCCI
- Staphylococcus spp. infections
- Staphylococcus aureus infections
- Exudative epidermitis
- Other Staphylococcus spp. infections
- Streptococcus spp. infections
- Strangles
- Streptococcus suis infections
- Streptococcus porcinus infections
- Other Streptococcus spp. infections
- GENERAL INTRODUCTION: ENDOSPORE-FORMING GRAM-POSITIVE RODS AND COCCI
- Anthrax
- Clostridium perfringens group infections
- Clostridium perfringens type A infections
- Clostridium perfringens type B infections
- Clostridium perfringens type C infections
- Clostridium perfringens type D infections
- Malignant oedema⁄gas gangrene group of Clostridium spp.
- Clostridium chauvoei infections
- Clostridium novyi infections
- Clostridium septicum infections
- Other clostridial infections
- Tetanus
- Botulism
- GENERAL INTRODUCTION: REGULAR, NON-SPORING, GRAM-POSITIVE RODS
- Listeriosis
- Erysipelothrix rhusiopathiae infections
- GENERAL INTRODUCTION: IRREGULAR, NON-SPORING, GRAM-POSITIVE RODS
- Corynebacterium pseudotuberculosis infections
- Corynebacterium renale group infections
- Bolo disease
- Actinomyces bovis infections
- Trueperella pyogenes infections
- Actinobaculum suis infections
- Actinomyces hyovaginalis infections
- GENERAL INTRODUCTION: MYCOBACTERIA
- Tuberculosis
- Paratuberculosis
- GENERAL INTRODUCTION: ACTINOMYCETES
- Nocardiosis
- Rhodococcus equi infections
- Dermatophilosis
- GENERAL INTRODUCTION: MOLLICUTES
- Contagious bovine pleuropneumonia
- Contagious caprine pleuropneumonia
- Mycoplasmal pneumonia of pigs
- Mycoplasmal polyserositis and arthritis of pigs
- Mycoplasmal arthritis of pigs
- Bovine genital mycoplasmosis
- Neurotoxin-producing group of Clostridium spp.
- Contagious equine metritis
- Tyzzer's disease
- MYCOTIC AND ALGAL DISEASES: Mycoses
- MYCOTIC AND ALGAL DISEASES: Pneumocystosis
- MYCOTIC AND ALGAL DISEASES: Protothecosis and other algal diseases
- DISEASE COMPLEXES / UNKNOWN AETIOLOGY: Epivag
- DISEASE COMPLEXES / UNKNOWN AETIOLOGY: Ulcerative balanoposthitis and vulvovaginitis of sheep
- DISEASE COMPLEXES / UNKNOWN AETIOLOGY: Ill thrift
- Eperythrozoonosis
- Bovine haemobartonellosis
Leptospirosis
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Leptospirosis
Previous authors: P HUNTER
Current authors:
M H MOSELEY - Research fellow, BVSc, MPhil, PhD, School of Biological Sciences, University of Aberdeen, Aberdeen, AB24 2TZ, United Kingdom
K ALLAN - Veterinary Training Fellow, BSc (Hons), BVM&S, PhD, MRCVS, Graham Kerr Building, University of Glasgow, University Avenue, Glasgow, Lanarkshire, G12 8QQ, United Kingdom
P OBEREM - Self Employed, BVsc Hons, 11 Bruce Avenue, Mont Lorraine, Gauteng, South Africa
Introduction
Leptospirosis in livestock is caused by spirochaetes of the genus Leptospira and is characterised by fever, renal and hepatic failure and reproductive failure.2 In equids, leptospirosis may manifest as recurrent uveitis associated with an autoimmune response.122 Infection in livestock also may result in chronic renal infection and urinary shedding that persists for months to years following initial infection. Contact with livestock is an important risk factor for human leptospirosis,2, 144 a widespread but neglected zoonotic disease that is estimated to affect more than one million people and result in around 59 000 deaths worldwide each year.35
Leptospirosis was first recognized in humans in 1886 by Weil,194 who described it as an infectious disease characterized by icterus. The responsible organism was simultaneously isolated and reported in 1916 by two independent groups of researchers,105, 184 and shortly afterwards rats were shown to be a host of infection.104 Leptospira spp. are difficult organisms to culture, which presents challenges for the diagnosis of infection and has limited research into human and animal disease. However, the advent of molecular typing and, more recently, whole genome sequencing, has improved our knowledge of Leptospira taxonomy, virulence and transmission.
Aetiology
Leptospira spp. bacteria belong to the family Leptospiraceae. Leptospira spp. are thin (0.15µm), right-handed helical, motile organisms that are 10-20µm long with distinctive hooked ends.152 They are Gram-negative organisms with an inner membrane and peptidoglycan cell wall overlain by an outer membrane containing lipopolysaccharides (LPS).152 Leptospira LPS are structurally and immunologically similar to LPS from other Gram-negative organisms although they do not appear to exhibit the same endotoxicity.2, 3
Dark-field microscopy is used to visualise Leptospira, which aredifficult to visualise with conventional microscopy because they are so thin. Leptospira exhibit rapid darting movements in liquid media with flexing motions and rotation about their long axes.3 The characteristic motility of Leptospira is due to a periplasmic endoflagellum with polar insertions, which is unique to spirochaete bacteria.152 The motility of Leptospira allows them to move in viscous environments, which enables them to penetrate blood vessels and rapidly reach target organs through haematogenous dissemination.152
Based on genetic typing, 22 species of Leptospira have been identified, which are divided into three distinct phylogenetic clades (Figure 1).152 The genus comprises a clade of 10 pathogenic Leptospira species that have been associated with disease in humans and animals; a clade of five species with ‘intermediate’ pathogenicity traits that have been associated with mild clinical manifestations; and six saprophytic Leptospira species, which do not cause disease. Within the pathogenic Leptospira clade, four subgroups197 have been identified that are thought to correlate to the degree of virulence in humans.152 Subgroup I contains three species (L. interrogans, L. kirschneri, L. noguchii) that are most often associated with severe manifestations of leptospirosis. Subgroup II contains five species (L. borgpetersenii, L. mayottensis, L. santarosai, L. alexanderi, L. weilii) that are typically associated with milder disease and that show evidence of co-evolution with particular animal host species.152 Subgroups III and IV are represented by only one species each (L. alstoni and L. kmetyi respectively) and the virulence of these species remains unclear.
The smallest taxonomic unit of Leptospira is the serovar and more than 250 distinct serovars have been described to date. Nomenclature for Leptospira serovars has changed over the years but now follows a format agreed by the Committee on the Taxonomy of Leptospira in 2002, where the genus and species are stated and italicised followed by the serovar name, which is capitalised but not italicised (for example; Leptospira interrogans serovar Icterohaemorrhagiae) (http://www.leptosociety.org/resources). This nomenclature is also useful as it reflects both the phylogenetic and serological classifications of each serovar. Although the serogroup is not strictly included in serovar nomenclature, it is commonly stated in parentheses after the serovar name (e.g. L. interrogans serovar Copenhagenii (serogroup Icterohaemorrhagiae)).
Identifying new Leptospira serovars is a complicated and time-consuming process requiring specialist facilities.152 Cross-agglutination absorption tests and monoclonal and polyclonal agglutination testing are used to characterise serovars based on their serological profile, determined by structural heterogeneity in the carbohydrate component of the LPS.21, 88, 122 Related serovars are grouped into...
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