The Onderstepoort Journal of Veterinary Research (OJVR), is the official publication of the Onderstepoort Veterinary Institute. It publishes scientific papers reporting original research on diseases and disease vectors of livestock and wildlife with a focus on Africa, but with results of more than local interest.

Meat products have been implicated in many listeriosis outbreaks globally, however there is a dearth of information on the diversity of L. monocytogenes isolates circulating in food products in South Africa. The aim of this study was to investigate the population structure of L. monocytogenes isolated in the meat value chain within the South African market. Based on whole-genome sequence analysis, a total of 217 isolates were classified into two main lineage groupings namely lineages I (n = 97; 44.7%) and II (n = 120; 55.3%). The lineage groups were further differentiated into IIa (n = 95, 43.8%), IVb (n = 69, 31.8%), IIb (n = 28, 12.9%), and IIc (n = 25, 11.5%) sero-groups. The most abundant sequence types (STs) were ST204 (n = 32, 14.7%), ST2 (n = 30, 13.8%), ST1 (n = 25, 11.5%), ST9 (n = 24, 11.1%), and ST321 (n = 21, 9.7%). In addition, 14 clonal complex (CCs) were identified with over-representation of CC1, CC3, and CC121 in “Processed Meat-Beef”, “RTE-Poultry”, and “Raw-Lamb” meat categories, respectively. Listeria pathogenic islands were present in 7.4% (LIPI-1), 21.7% (LIPI-3), and 1.8% (LIPI-4) of the isolates. Mutation leading to premature stop codons was detected in inlA virulence genes across isolates identified as ST121 and ST321. The findings of this study demonstrated a high-level of genomic diversity among L. monocytogenes isolates recovered across the meat value chain control points in South Africa.

Listeria monocytogenes is a highly fatal foodborne causative agent that has been implicated in numerous outbreaks and related deaths of listeriosis in the world. In this study, six L. monocytogenes isolated from ready-to-eat (RTE) meat products were analysed using Whole Genome Sequencing (WGS) to identify virulence and resistance genes, prophage sequences, PCR-serogroups, and sequence types (STs). The WGS identified four different STs (ST1, ST121, ST204, and ST876) that belonged to serogroup 4b (lineage I) and 1/2a (lineage II). Core genome, and average nucleotide identity (ANI) phylogenetic analyses showed that the majority of strains from serogroup 4b (lineage I) clustered together. However, two isolates that belong to serogroup 1/2a (lineage II) grouped far from each other and the other strains. Examination of reference-guided scaffolds for the presence of prophages using the PHAge Search Tool Enhanced Release (PHASTER) software identified 24 diverse prophages, which were either intact or incomplete/questionable. The National Center for Biotechnology Information- Nucleotide Basic Local Alignment Search Tool (NCBI-BLASTn) revealed that Listeria monocytogenes strains in this study shared some known major virulence genes that are encoded in Listeria pathogenicity islands 1 and 3. In general, the resistance profiles for all the isolates were similar and encoded for multidrug, heavy metal, antibiotic, and sanitizer resistance genes. All the isolates in this study possessed genes that code for resistance to common food processing antiseptics such as Benzalkonium chloride.

The objective of the review was to assess the potential of indigenous browse trees as sustainable feed supplement in the form of silage for captive wild ungulates. Several attempts to use silage as feed in zoos in temperate regions have been conducted with success. Information on silage from the indigenous browse trees preferred by wild ungulates in southern Africa is scanty. The use of silage from the browse trees is of interest as it has potential to reduce or replace expensive feed sources (pellets, fruits and farm produce) currently offered in southern African zoos, game farms and reserves, especially during the cold-dry season. Considerable leaf biomass from the indigenous browse trees can be produced for silage making. High nutrient content and minerals from indigenous browsable trees are highly recognised. Indigenous browse trees have low water-soluble carbohydrates (WSC) that render them undesirable for fermentation. Techniques such as wilting browse leaves, mixing cereal crops with browse leaves, and use of additives such as urea and enzymes have been studied extensively to increase WSC of silage from the indigenous browse trees. Anti-nutritional factors from the indigenous browse preferred by the wild ungulates have also been studied extensively. Indigenous browse silages are a potential feed resource for the captive wild ungulates. If the browse trees are used to make silage, they are likely to improve performance of wild ungulates in captivity, especially during the cold-dry season when browse is scarce. Research is needed to assess the feasibility of sustainable production and the effective use of silage from indigenous browse trees in southern Africa. Improving intake and nutrient utilisation and reducing the concentrations of anti-nutritional compounds in silage from the indigenous browse trees of southern Africa should be the focus for animal nutrition research that need further investigation.