Association between transmission rate and disease severity for Actinobacillus pleuropneumoniae infection in pigs

• Published in: Veterinary research (Paris) Vol. 44; no. 1; p. 2
• Main Authors: Tobias, Tijs J, Bouma, Annemarie, Daemen, Angeline J J M, Wagenaar, Jaap A, Stegeman, Arjan, Klinkenberg, Don
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 11-01-2013; BioMed Central; BMC
• Subjects: Actinobacillus Infections - microbiology; Actinobacillus Infections - transmission; Actinobacillus Infections - veterinary; Actinobacillus pleuropneumoniae - pathogenicity; Actinobacillus pleuropneumoniae - physiology; Analysis; Animal experimentation; Animals; bacteria; design; Disease transmission; Epidemics; epidemiology; Feces - microbiology; herd; Infection; influenza; Medical research; Medicine, Experimental; Nasal Mucosa - microbiology; Palatine Tonsil - microbiology; parahaemolyticus; Polymerase Chain Reaction - veterinary; Pork industry; Random Allocation; serotype 9; strain; Swine; Swine Diseases - microbiology; Swine Diseases - transmission; virulence
• ISSN: 1297-9716; 0928-4249; 1297-9716
• DOI: 10.1186/1297-9716-44-2

A better understanding of the variation in infectivity and its relation with clinical signs may help to improve measures to control and prevent (clinical) outbreaks of diseases. Here we investigated the role of disease severity on infectivity and transmission of Actinobacillus pleuropneumoniae, a bacterium causing respiratory problems in pig farms. We carried out transmission experiments with 10 pairs of caesarean-derived, colostrum-deprived pigs. In each pair, one pig was inoculated intranasally with 5×10(6) CFUs of A. pleuropneumoniae strain 1536 and housed together with a contact pig. Clinical signs were scored and the course of infection was observed by bacterial examination and qPCR analysis of tonsillar brush and nasal swab samples. In 6 out of 10 pairs transmission to contact pigs was observed, but disease scores in contact infected pigs were low compared to the score in inoculated pigs. Whereas disease score was positively associated with bacterial load in inoculated pigs and bacterial load with the transmission rate, the disease score had a negative association with transmission. These findings indicate that in pigs with equal bacterial load, those with higher clinical scores transmit A. pleuropneumoniae less efficiently. Finally, the correlation between disease score in inoculated pigs and in positive contact pigs was low. Although translation of experimental work towards farm level has limitations, our results suggest that clinical outbreaks of A. pleuropneumoniae are unlikely to be caused only by spread of the pathogen by clinically diseased pigs, but may rather be the result of development of clinical signs in already infected pigs.