Nucleotide sequence analysis of a DNA region involved in capsular polysaccharide biosynthesis reveals the molecular basis of the nontypeability of two Actinobacillus pleuropneumoniae isolates. (November 2016)

• Record Type: Journal Article
• Authors: Ito, Hiroya; Ogawa, Torata; Fukamizu, Dai; Morinaga, Yuiko; Kusumoto, Masahiro
• Is Part Of: Journal of veterinary diagnostic investigation. Volume 28:Number 6(2016:Nov.)
• Page Start: 632
• Page End: 637
• Publication Date: 2016-11
• Subjects: Actinobacillus pleuropneumoniae -- insertion sequence ISApl1 -- nontypeable; Veterinary medicine -- Diagnosis -- Periodicals; 636.0896075
• DOI: 10.1177/1040638716656026
• Languages: English
• ISSNs: 1040-6387

Abstract

The aim of our study was to reveal the molecular basis of the serologic nontypeability of 2 Actinobacillus pleuropneumoniae field isolates. Nine field strains of A. pleuropneumoniae, the causative agent of porcine pleuropneumonia, were isolated from pigs raised on the same farm and sent to our diagnostic laboratory for serotyping. Seven of the 9 strains were identified as serovar 15 strains by immunodiffusion tests. However, 2 strains, designated FH24-2 and FH24-5, could not be serotyped with antiserum prepared against serovars 1–15. Strain FH24-5 showed positive results in 2 serovar 15–specific PCR tests, whereas strain FH24-2 was only positive in 1 of the 2 PCR tests. The nucleotide sequence analysis of gene clusters involved in capsular polysaccharide biosynthesis of the 2 nontypeable strains revealed that both had been rendered nontypeable by the action of IS Apl1, a transposable element of A. pleuropneumoniae belonging to the IS 30 family. The results showed that IS Apl1 of A. pleuropneumoniae can interfere with both the serologic and molecular typing methods, and that nucleotide sequence analysis across the capsular gene clusters is the best means of determining the cause of serologic nontypeability in A. pleuropneumoniae .