Comparison of immunoblot analysis of emergent multidrug-resistant Salmonella typhimurium definitive phage type 104 with a non-multidrug-resistant definitive phage type 104 strain.

BACKGROUND AND PURPOSE: The emergent multidrug-resistant (MDR) Salmonella typhimurium definitive phage type 104 (DT104) is a public and veterinary health problem not only due to its wide host range and potential for enhanced virulence, but also the difficulty associated with its control. There is thus a need to investigate possible antigens of MDR DT104. METHODS: Using standard protocols, whole cell lysates, outer membrane extracts and cell-free ultracentrifuge supernatants of selected isolates of MDR DT104 were prepared, electrophoretically separated and tested for their antigen-antibody reactivity in comparison with a non-MDR DT104 strain. RESULTS: Protein antigens of both strain types were recognized by antibodies in chick serum in a similar manner for all methods of antigen preparation used. CONCLUSIONS: This study did not find differences between the antibody recognition of MDR DT104 and that of the non-MDR DT104 strain tested. This observation should strengthen the quest for the possible use of vaccines to control this emergent strain in poultry.

Characterization of biofilm-forming abilities of antibiotic-resistant Salmonella typhimurium DT104 on hydrophobic abiotic surfaces.

BACKGROUND AND PURPOSE: Salmonella typhimurium DT104 strain has emerged as a global human and veterinary public health concern because of its antibiotic resistance and extensive host range. Although it is thought to be more virulent, to date, factors relevant to its virulence have not been fully elucidated. Thus, understanding how this strain forms biofilms on hydrophobic surfaces will add to current knowledge on its possible virulence mechanism. METHODS: Biofilm-forming abilities of clinical isolates of S. typhimurium DT104 from human and animal sources on hydrophobic inanimate surfaces were assessed by absorbance at 600 nm of crystal violet-bound cells recovered from 96-well tissue culture plates after growth in a nutrient-rich growth medium and various adjusted media; and scanning electron microscopy based on standard procedures. RESULTS: In the nutrient-rich growth medium, Luria-Bertani (LB), biofilms were formed in small quantities, preferentially on polystyrene (p<0.05), and followed different time courses. Significantly lower amounts of biofilms were formed on polystyrene when a nutrient-deficient growth medium (adherence test medium) was used. Inclusion of D-(+)-mannose in LB at a concentration of 100 mM significantly (p<0.05) inhibited biofilm formation on polystyrene. D-(+)-glucose relatively enhanced biofilm formation but D-(-)-mannitol only insignificantly influenced the process. The action of mannose on polyvinly chloride (PVC) was insignificant, suggesting that its action may be surface-dependent. Additionally, glucose significantly reduced biofilm growths of 2 of the isolates and only that of the PVC-loving strain T980021 on polystyrene and PVC, respectively. At the concentration tested, unlike xylose, both D-mannose and D-glucose significantly (p<0.05) inhibited bacterial growth, providing a possible mechanism for their inhibitory action on biofilm formation by S. typhimurium. While stress of starvation resulted in significant reduction in biofilm formation on polystyrene in all but the PVC-loving strain T980021, high osmolarity had little effect on the quantity of biofilm formed on polystyrene. The extent of primary attachment to polystyrene as well as their capacity to form biofilm did not correlate with their cell surface hydrophobicity and exopolysaccharide production. CONCLUSIONS: D-(+)-mannose inhibits biofilm formation by S. typhimurium DT104 on polystyrene but not on PVC. There was also a general lack of correlation between the ability of S. typhimurium DT104 to form biofilm and its physicochemical surface characteristics.

Spatio-temporal dynamics of African swine fever outbreaks in Nigeria, 2002-2007.

African swine fever (ASF) was first introduced into Nigeria through Lagos state in 1997. The disease rapidly spread to Ogun state in 1998 and extended to the Niger Delta (Delta, Rivers and Akwa Ibom states) in the same year. In 1998, Kaduna, Plateau and Benue states all north of the country experienced ASF for the first time. Poor farm biosecurity, bad abattoir practices and extensive/free range pig farming systems led to extensive spread of the diseases to about 16 Nigerian states excluding the far northwest and north east. A total of 1036 field samples collected over a 6-year period covering 19 Nigerian states were analysed during the period under review; 805 samples were PCR positive and 231 negative. Positive samples were detected in all three surveillance phases and from all agroecological zones across the country. For the first time since its incursion, ASF was identified in some states; Bauchi, Adamawa Taraba and Gombe with chances of control very slim and further spread of the virus northward envisaged. Outbreaks of the disease are now a perennial problem with an increasing disease burden in areas where high numbers of pigs are produced in the country. The National Veterinary Research Institute (NVRI), Vom, since 2002 investigated ASF based on tissue submissions and reports made by individuals, private & commercial farms and agricultural bodies. We present an analysis of geographical and temporal distribution of ASF in the country from 2002 to 2007 and a review of historic outbreaks since the first incursion. Risk factors and prospects for control are discussed.