Prevalence, organ distribution and antimicrobial susceptibility profile of Salmonella isolated from chickens purchased from markets in selected districts of West Shoa, Ethiopia
Abstract:Salmonella is one of the major causes of heavy losses in chicken and foodborne diseases worldwide. The current study was conducted from November 2015 to May 2016 to estimate the prevalence of Salmonella and determine the antimicrobial susceptibility of isolates in chickens. Chickens (n=205) were purchased from local markets of five selected districts of West Shoa Zone, Central Ethiopia. Following clinical examination, chicken were euthanized and 2-3 ml of blood sample was collected immediately. Then after pos… Show more
“…The sample-level prevalence of Salmonella was 6.4% in the current study, which is higher than similar studies in Adama and Modjo towns (2.8%), Central Ethiopia (4.7%), and in and around Modjo and Central Oromia [ 2 , 5 , 23 ]. However, it is lower than the 19% prevalence reported from West Showa, Ethiopia [ 24 ] (Sarba et al). Such variation could be due to factors such as differences in detection methods employed, farm biosecurity level, and hygienic practices in the farms.…”
Poultry and poultry products are the common sources of Salmonella,which is one of the serious food-borne bacterial diseases in humans. Little is known about the status of Salmonella and their antimicrobial susceptibility in poultry farms in Addis Ababa. This study was conducted to estimate the prevalence and antimicrobial susceptibility of Salmonella isolates and to investigate possible risk factors for the occurrence of Salmonella in poultry farms in Addis Ababa. We recruited 58 poultry farms, from which 471 poultry-related samples and 44 stool samples from in-contact humans were collected. The isolates were tested for their susceptibility to 11 antimicrobials using the Kirby–Bauer disk diffusion assay. The farm-level prevalence of Salmonella was 36.2% and the sample-level prevalence was 6.4% for samples taken from poultry farms and 4.5% in human stool samples who have contact with poultry. On-farm waste disposal practices and chicken being purchased from different multiplication farms were significantly associated with Salmonella positivity of the farms (p<0.05). Eleven (34.4%) Salmonella isolates were resistant to streptomycin, and nine (28.1%) were resistant to tetracycline. Thirteen (40.6%) Salmonella isolates were resistant to two or more antimicrobials tested in this study, whereas resistance to 3 or more antimicrobials was detected in seven (21.9%) isolates. In conclusion, a high prevalence of Salmonella and a high rate of resistance to multiple antimicrobials were detected in poultry farms in Addis Ababa. Hence, implementation of strong biosecurity measures and rational use of antimicrobials are recommended.
“…The sample-level prevalence of Salmonella was 6.4% in the current study, which is higher than similar studies in Adama and Modjo towns (2.8%), Central Ethiopia (4.7%), and in and around Modjo and Central Oromia [ 2 , 5 , 23 ]. However, it is lower than the 19% prevalence reported from West Showa, Ethiopia [ 24 ] (Sarba et al). Such variation could be due to factors such as differences in detection methods employed, farm biosecurity level, and hygienic practices in the farms.…”
Poultry and poultry products are the common sources of Salmonella,which is one of the serious food-borne bacterial diseases in humans. Little is known about the status of Salmonella and their antimicrobial susceptibility in poultry farms in Addis Ababa. This study was conducted to estimate the prevalence and antimicrobial susceptibility of Salmonella isolates and to investigate possible risk factors for the occurrence of Salmonella in poultry farms in Addis Ababa. We recruited 58 poultry farms, from which 471 poultry-related samples and 44 stool samples from in-contact humans were collected. The isolates were tested for their susceptibility to 11 antimicrobials using the Kirby–Bauer disk diffusion assay. The farm-level prevalence of Salmonella was 36.2% and the sample-level prevalence was 6.4% for samples taken from poultry farms and 4.5% in human stool samples who have contact with poultry. On-farm waste disposal practices and chicken being purchased from different multiplication farms were significantly associated with Salmonella positivity of the farms (p<0.05). Eleven (34.4%) Salmonella isolates were resistant to streptomycin, and nine (28.1%) were resistant to tetracycline. Thirteen (40.6%) Salmonella isolates were resistant to two or more antimicrobials tested in this study, whereas resistance to 3 or more antimicrobials was detected in seven (21.9%) isolates. In conclusion, a high prevalence of Salmonella and a high rate of resistance to multiple antimicrobials were detected in poultry farms in Addis Ababa. Hence, implementation of strong biosecurity measures and rational use of antimicrobials are recommended.
“…The worldwide increase of food‐borne infections with antibiotic resistant pathogens is of growing concern and is designated by the World Health Organization (WHO) as an emerging public health problem (CDC, 2006 ; Dagnew et al., 2020 ; Lynch et al., 2006 ; Much et al., 2007 ). Different studies revealed that Salmonella serotypes isolated from foods of animal origin have multidrug resistance with resistance to ≥3 antimicrobial classes (Molla et al., 2003 ; Sarba et al., 2020 ). Globally, Salmonella exhibits extensive resistance profiles, which have been associated with higher rates of morbidity and mortality and costs associated with disease (Angulo et al., 2004 ).…”
BackgroundSalmonellosis is one of the most common food‐borne diseases in industrialised and developing countries. In recent year, an increase in antimicrobial resistance among different Salmonella serotypes has been observed.ObjectiveA cross‐sectional study was conducted to assess the prevalence and antimicrobial susceptibility of Salmonella isolated from local chicken eggs in four selected towns in Ethiopia.MethodsA total of 115 eggs were examined to detect Salmonella by using standard microbiological methods. The susceptibilities of the isolates to nine antimicrobials were tested by the Kirby–Bauer disk diffusion method.ResultThe study revealed that of the 115 eggs examined, 22 (19.1%) were positive for Salmonella of which 14 (12.2%) and 8 (7%) of the isolates were from shells and contents, respectively. The occurrence of Salmonella in egg shells and content and between different altitudes did not differ significantly (p > 0.05). Most isolates were resistant to more than three antimicrobials with a high resistance to kanamycin, ampicillin, nalidixic acid, cotrimoxazole, oxytetracycline and chloramphenicol.ConclusionThe results indicate the potential importance of local chicken eggs as source of multiple antimicrobial‐resistant salmonellae and the need for proper cooking before consumption. Further studies are required to describe the epidemiology of Salmonella in various agroclimatic zones of Ethiopia.
“…In Ethiopia, β-lactam antibiotics, i.e., ampicillin, amoxicillin and penicillin are the most widely used class of medicines to treat respiratory tract infections, prostatitis, urinary tract infections, skin, and soft tissue infections of sensitive bacteria in poultry production [11][12][13]. High level of antibiotic residues were detected in meat and milk in studies conducted in Addis Ababa, Bishoftu, and Adama major cities in the country by microbiological or screening methods [14].…”
ABSTRACT. A simple analytical method for the extraction and determination of three β-lactam antibiotics in chicken tissues and feather samples was developed and validated using solid phase extraction (SPE) and liquid chromatography-ultraviolet, LC-UV, detection. The analytes were extracted with strong anion exchange (SAX) cartridges for the extract clean-up and enrichment before introduction into the LC system. The validation was carried out based on the recommendations from Commission Decision 2002/657/EC. Under optimised conditions, the proposed method offers correlation coefficients of r2 ≥ 0.9991 for all the studied analytes in both matrices. Percent recovery results were found to vary between 79.7-101.8% and 94.2-101.6% for chicken feathers and tissues, respectively, with the relative standard deviation, RSD < 8.4%. The limits of detection (LOD) were in the range of 0.1-0.13 µg kg-1 and 0.1-0.15 µg kg-1 while the limits of quantification (LOQ) were in the range of 0.3-0.38 µg kg-1 and 0.3-4.5 µg kg-1 in chicken feathers and tissues, respectively. The proposed method offers good sensitivity and selectivity and all the results demonstrating that the method would be widely used for determination of β-lactam antibiotics and other trace level antibiotics residues having similar physical and chemical properties in the matrices of varying origins.
KEY WORDS: Chicken tissues, Chicken feathers, β-Lactams, Solid phase extraction, LC-UV
Bull. Chem. Soc. Ethiop. 2022, 36(3), 503-519.
DOI: https://dx.doi.org/10.4314/bcse.v36i3.2
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