The Efficacy of a Trivalent Inactivated Vaccine Combined with the Live Gallinarum 9R Vaccine in Young Layers after Experimental Infections with Enteritidis, Typhimurium, and Infantis.

Worldwide, poultry infections by are the cause of significant economic losses, not only due to reduced production (due to fowl typhoid disease), but also considering the efforts and control measures that must be constantly applied, especially due to zoonotic serovars. Poultry is a common reservoir of and its transmission into the food chain is a risk for humans. The vaccination of layers plays an important role in the overall efforts to prevent infections.

Pathogenicity of Strains from Peru and the Selection of Candidate Strains for an Inactivated Vaccine.

Worldwide, is the aetiological agent of infectious coryza in poultry. Vaccines are the best means of control, helping reduce clinical signs and colonization of this bacterium. Most vaccines are based on international reference strains, or, lately, regional strains, but, generally, without any information regarding their virulence.

Serotyping of Avibacterium paragallinarum isolates from Peru.

This study appears to represent the first serotyping study of 24 isolates of Avibacterium paragallinarum obtained from different regions of Peru during 1998-2008. All isolates were characterized as beta-nicotinamide adenine dinucleotide dependent. According to the Page scheme, modified by Blackall, it was found that eight isolates were classified as serogroup A, seven isolates as serogroup B, and five isolates as serogroup C, while four isolates could not be serotyped.

Amplified 16S ribosomal DNA restriction analysis for identification of Avibacterium paragallinarum.

A molecular technique based on the restriction fragment length polymorphism of the 16S ribosomal genes amplified by a polymerase chain reaction (PCR), referred to as amplified 16S ribosomal DNA restriction analysis (ARDRA), was designed to identify 19 Avibacterium paragallinarum strains isolated from infraorbital sinus and nasal turbinate bone samples of broiler chickens, breeders, and laying hens from different regions of Peru. The 16S rDNA was amplified by PCR using a pair of bacterial universal primers and restriction analysis of 16S rDNA sequences was done to select endonucleases with the highest number of cutting points inside the 16S rDNA. The DNA patterns with DdeI and RsaI endonucleases were identical for the 19 A.