This study determined the activities of Bidens pilosa and Moringa oleifera leaf extracts on microbial count of ground beef during 6-day cold storage. Fresh ground beef sample was treated with butylated hydroxytoluene (BHT) (0.2 g/kg), M. oleifera (ML, 1 g/kg) and B. pilosa (BP, 1 g/kg) leaf extracts and compared with the control. The result of the phytochemical contents revealed that ML extract had higher phenolic and flavonoid contents than BP extract (p > 0.05). The antibacterial assay of the extracts revealed an appreciable broad-spectrum activity against tested bacteria with minimum inhibitory concentrations between 0.6 and 10.0 mg/mL. Addition of ML leaf extract to ground beef sample lowered total viable and lactic acid bacteria (p < 0.05) counts than control and BHT treatments at day 3 of storage. These results suggest that ML leaf extract could be used as potential sources of natural antimicrobial agent in meat products.Actividades antimicrobianas in vitro de extractos de hoja de Bidens pilosa y Moringa oleifera y sus efectos en la calidad de ternera triturada durante el almacenamiento en frío RESUMEN Este estudio determinó las actividades de los extractos de hoja de B. pilosa y M. oleifera en los recuentos microbianos de ternera triturada durante 6 días de almacenamiento en frío. Se trató con BHT una muestra fresca de ternera triturada (0,2 g/kg) y extractos de hoja M. oleifera (ML, 1 g/kg) y B. pilosa (BP, 1 g/kg), entonces estos fueron contrastados con la muestra control. Los resultados de los contenidos fitoquímicos revelaron que el extracto de ML tenía un mayor contenido fenólico y de flavonoides en comparación con el extracto de BP (p > 0,05). El ensayo antibacteriano de los extractos reveló una apreciable actividad de amplio espectro frente a las bacterias examinadas con concentraciones inhibitorias mínimas utilizando rangos entre 0,6 y 10,0 mg/mL. La adición de extracto de hoja de ML a la muestra de ternera triturada disminuyó el recuento total viable de bacteria ácido-láctica (p < 0,05) más que en la muestra control y los tratamientos de BHT en tercer día de almacenamiento. Estos resultados sugieren que el extracto de hoja de ML podría ser utilizado como fuente potencial de agente antimicrobiano natural en los productos cárnicos. ARTICLE HISTORY
The study aimed to compare the bacteriological quality of an urban and rural irrigation water source. Bacterial counts, characterization, identification and diversity of aerobic bacteria were determined. Escherichia coli isolated from both sites was subjected to antibiotic susceptibility testing, virulence gene (Stx1/Stx2 and eae) determination and (GTG) 5 Rep-PCR fingerprinting. Low mean monthly counts for aerobic spore formers, anaerobic spore formers and Staphylococcus aureus were noted although occasional spikes were observed. The most prevalent bacterial species at both sites were Bacillus spp., E. coli and Enterobacter spp.Additionally, E. coli and Bacillus spp. were most prevalent in winter and summer respectively. Resistance to at least one antibiotic was 84% (rural) and 83% (urban). Highest resistance at both sites was to cephalothin and ampicillin. Prevalence of E. coli possessing at least one virulence gene (Stx1/Stx2 and eae) was 15% (rural) and 42% (urban). All (rural) and 80% (urban) of E. coli possessing virulence genes showed antibiotic resistance. Complete genetic relatedness (100%) was shown by 47% of rural and 67% of urban E. coli isolates. 1Results from this study show that surface irrigation water sources regardless of geographical location and surrounding land-use practices can be reservoirs of similar bacterial pathogens.
Three Gram-staining-negative, rod-shaped, non-spore-forming, non-motile, oxidase-positive, yellow pigmented and aerobic bacterial isolates designated 8_R23573, 9_R23581 T and 10_R23577 were isolated from raw chicken at a broiler processing plant in Bloemfontein, South Africa. A polyphasic taxonomic approach was used to determine their exact taxonomic identities. Phylogenetic analysis of the 16S rRNA gene sequences showed that the three strains belonged to the genus Chryseobacterium, exhibiting the highest similarities to Chryseobacterium shigense DSM 17126 T (98.6-99.2 %) and Chryseobacterium luteum DSM 18605 T (98.3-98.7 %). The most abundant quinone was menaquinone MK-6 and the predominant cellular fatty acids were iso-15 : 0, iso-17 : 1v9c, iso-17 : 0 3-OH and summed feature 3 (iso-16 : 1v7c and/or iso-15 : 0 2-OH), which supported the affiliation of the strains to the genus Chryseobacterium. The DNA G+C contents of the strains were 36.9, 36.7 and 36.6 mol% respectively. The DNA-DNA hybridization results gave relatedness values ranging from 78.8 to 87.2 % among the three strains and 23.4 to 56.1 % to the two nearest phylogenetic neighbours C. shigense DSM 17126 T and C. luteum LMG 23785 T . On the basis of the data from this polyphasic study, the three strains are concluded to represent a novel species of the genus Chryseobacterium for which the name Chryseobacterium carnipullorum sp. nov. is proposed. The type strain is 9_R23581 T (5LMG 26732 T 5DSM 25581 T ).The genus Chryseobacterium belongs to the family Flavobacteriaceae (Bernardet et al., 2002;Bernardet, 2011). It was described by Vandamme et al. (1994) to accommodate six species formerly classified within the genus Flavobacterium, namely Chryseobacterium balustinum, Chryseobacterium gleum, Chryseobacterium indologenes, Chryseobacterium indoltheticum, Chryseobacterium meningosepticum and Chryseobacterium scophthalmum and was later amended (Kämpfer et al., 2009). The type species is C. gleum. Members of the genus Chryseobacterium include psychrotolerant and proteolytic spoilage micro-organisms that are widely distributed in food sources such as milk, fish, meat and poultry (Hugo et al., 2003;de Beer et al., 2005 de Beer et al., , 2006 and occur in a variety of ecological niches such as soil, water, sludge, plants, and human and fish clinical specimens (Hugo et al., 2003;Bernardet et al., 2005Bernardet et al., , 2011Hugo & Jooste, 2012).In 2006 the genus Chryseobacterium consisted of only 10 validly named species. Since then the genus has undergone significant and rapid expansion and, at the time of writing, it comprises 61 species with validly published names (Bernardet et al., 2006) and more continue to be described (Euzéby, 2012). This can be ascribed to the readily available and improved phenotypic, chemotaxonomic and molecular identification methods used in the polyphasic taxonomic approach.During the course of the characterization of chryseobacterial strains isolated from raw chicken in a previous study (de Beer, 2005) at a poultry processing plan...
Chryseobacterium species are isolated and taxonomically evaluated from a wide range of sources. While C. gleum and C. indologenes have been implicated in human disease, the potential pathogenicity of numerous other species have not been investigated. The aims were therefore to evaluate 37 Chryseobacterium species and Elizabethkingia meningoseptica from environmental, food, fish, water and clinical sources for production of haemolysis, growth at 37 °C, and production of virulence enzymes. The control of these strains were investigated by determination of antimicrobial and disinfectant resistance. All the species produced α- or β-haemolysis. In terms of growth at 37 °C and production of virulence enzymes, C. soldanellicola (environmental), C. oranimense (food) and C. koreense (natural mineral water) could be potential human pathogens. Chryseobacterium piscium might be pathogenic to fish. Trimethoprim could be the most effective antimicrobial for the treatment of a Chryseobacterium species infection, while the disinfectants that contain poly-dimethyl ammonium chloride or benzalkonium chloride could be regarded as the most effective for decontamination of surfaces contaminated with Chryseobacterium species.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
customersupport@researchsolutions.com
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.