Contents
Academic literature on the topic 'Staphylococcus aureus infections Mastitis Lipids Cattle Staphylococcus aureus'
Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles
Consult the lists of relevant articles, books, theses, conference reports, and other scholarly sources on the topic 'Staphylococcus aureus infections Mastitis Lipids Cattle Staphylococcus aureus.'
Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.
You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.
Journal articles on the topic "Staphylococcus aureus infections Mastitis Lipids Cattle Staphylococcus aureus"
1
BATRA, T. R. "EFFECT OF COMPLETE DRY COW TREATMENT ON MASTITIS CONTROL IN DAIRY CATTLE." Canadian Journal of Animal Science 68, no. 2 (June 1, 1988): 553–56. http://dx.doi.org/10.4141/cjas88-061.
Full textAbstract:
Data on 297 cows which received complete dry cow treatment and subsequently calved were used in this study. At drying-off, 7.7% of the quarters were infected. Among the mastitic pathogens, Staphylococcus aureus was isolated in 75% of the infected quarters. About 92% of the infected quarters were cured with dry cow treatment and 6% of the quarters had new infections during dry period. It appears that dry cow treatment is an effective means of eliminating Staphylococcus aureus infections. Key words: Mastitis, dry cow treatment, dairy cattle
2
Rajamanickam, Karthic, Jian Yang, Saravana Babu Chidambaram, and Meena Kishore Sakharkar. "Enhancing Drug Efficacy against Mastitis Pathogens—An In Vitro Pilot Study in Staphylococcus aureus and Staphylococcus epidermidis." Animals 10, no. 11 (November 15, 2020): 2117. http://dx.doi.org/10.3390/ani10112117.
Full textAbstract:
Background: Bovine mastitis is one of the major infectious diseases in dairy cattle, resulting in large economic loss due to decreased milk production and increased production cost to the dairy industry. Antibiotics are commonly used to prevent/treat bovine mastitis infections. However, increased antibiotic resistance and consumers’ concern regarding antibiotic overuse make it prudent and urgent to develop novel therapeutic protocols for this disease. Materials and methods: Potential druggable targets were found in 20 mastitis-causing pathogens and conserved and unique targets were identified. Bacterial strains Staphylococcus aureus (ATCC 29213, and two clinical isolates CI 1 and CI 2) and Staphylococcus epidermidis (ATCC 12228, and two clinical isolates CI 1 and CI 2) were used in the present study for validation of an effective drug combination. Results: In the current study, we identified the common and the unique druggable targets for twenty mastitis-causing pathogens using an integrative approach. Furthermore, we showed that phosphorylcholine, a drug for a unique target gamma-hemolysin component B in Staphylococcus aureus, and ceftiofur, the mostly used veterinary antibiotic that is FDA approved for treating mastitis infections, exhibit a synergistic effect against S. aureus and a strong additive effect against Staphylococcus epidermidis in vitro. Conclusion: Based on the data generated in this study, we propose that combination therapy with drugs that work synergistically against conserved and unique targets can help increase efficacy and lower the usage of antibiotics for treating bacterial infections. However, these data need further validations in animal models of infection.
3
Vlkova, H., V. Babak, I. Vrtkova, D. Cervinkova, D. Marosevic, M. Moravkova, and Z. Jaglic. "Epidemiology of intramammary infections with Staphylococcus aureus and mastitis streptococci in a dairy cattle herd with a history of recurrent clinical mastitis." Polish Journal of Veterinary Sciences 20, no. 1 (March 28, 2017): 133–39. http://dx.doi.org/10.1515/pjvs-2017-0017.
Full textAbstract:
AbstractThe aim of the present work was to examine a dairy herd with an anamnesis of recurrent clinical mastitis and decreased milk production. A total of 239 individual cow milk samples originating from asymptomatic cows were collected at four-month intervals and examined mainly for the presence of Staphylococcus aureus and mastitis streptococci using standard cultivation methods. In total, 29.7% and 9.2% samples were positive for S. aureus and mastitis streptococci, respectively. Unlike for mastitis streptococci, the prevalence of animals positive for S. aureus had an increasing trend (p<0.05; Chi-squared test for trend) with rising parity. Despite in vitro susceptibility of S. aureus to potentiated penicillins and cephalosporins, the persistence of S. aureus was observed in cows undergoing intramammary treatment with amoxicillin/clavulanic acid (a potentiated penicillin antibiotic). All isolates of S. aureus were biofilm-positive and had the same macrorestriction pattern. Furthermore, no dependence was observed between the occurrence of S. aureus in milk and previous cases of clinical mastitis, reproductive and periparturient disorders and administration of antibiotics. In contrast to S. aureus, the occurrence of mastitis streptococci in milk was linked with previous cases of clinical mastitis and intramammary administration of antibiotics.
4
Neamah, Ahmed Jasim, Hayder Naji Ayyez, Saba Falah Klaif, Yahia Ismail Khudhair, and Muthanna Hadi Hussain. "Molecular and phylogenetic study of Staphylococcus aureus isolated from human and cattle of Al-Qadisiyah Governorate, Iraq." Veterinary World 12, no. 9 (September 2019): 1378–82. http://dx.doi.org/10.14202/vetworld.2019.1378-1382.
Full textAbstract:
Aim: This study was designed to detect the prevalence of Staphylococcus aureus, to estimate the frequency of methicillin resistance gene (mecA), femA (specific gene for S. aureus), and lukS gene, and the prevalence of urinary tract infection (UTI) in human and bovine mastitis caused by S. aureus. Materials and Methods: A total of 102 cases of S. aureus were included in this study; 72 specimens were isolated from human with UTIs and 30 specimens were isolated from milk of cattle with acute mastitis. Diagnosis was done by VITEK 2 Compact after subculture and purification. All isolates were examined for the presence of mecA, femA, and lukS (Panton- Valentine leukocidin) using multiplex polymerase chain reaction. Results: Culture and biochemical evaluation of the samples revealed the presence of S. aureus, among which the genes mecA, femA, and lukS were positively detected in 68 (94.4%), 36 (50%), and 20 (27.7%) of S. aureus isolates from methicillin-resistant humans, respectively. In the same manner, the genes mecA, femA, and lukS were positively detected in 27 (90%), 14 (46.7%), and 11 (36.7%) of S. aureus isolates from methicillin-resistant cattle. Sequencing of partial order of femA gene isolated from human isolate and from cattle with mecA isolated from human revealed high sequence identity with the National Center for Biotechnology Information (NCBI)-Basic Local Alignment Search Tool. S. aureus isolates and the phylogenetic analysis showed that there was a significant genetic similarity (0.5 genetic change) between human and animals isolates, and then, the gene sequences were deposited into NCBI-Genbank accession numbers MG696860.1 for mecA and femA from human, MG696861.1 for mecA and femA from cattle, MK474469.1 for mecA and femA gene from human, and MG696862.1 for mecA and femA gene from cattle. Conclusion: The study represents the first report of genetic relationship between S. aureus from humans and cattle of Iraq. Therefore, it is essential to define the role of animals as an important source of the distribution of pathogen related to public health. The continuous monitoring of methicillin susceptibility pattern of S. aureus isolates that have high standards of infections might prevent methicillin-resistant S. aureus transmission in either direction between human and cattle, the risk of dairy milk on humans, or self-direction between the same species.
5
Hoekstra, Jurriaan, Victor P. M. G. Rutten, Theo J. G. M. Lam, Kok P. M. Van Kessel, Mirlin P. Spaninks, J. Arjan Stegeman, Lindert Benedictus, and Gerrit Koop. "Activation of a Bovine Mammary Epithelial Cell Line by Ruminant-Associated Staphylococcus aureus is Lineage Dependent." Microorganisms 7, no. 12 (December 12, 2019): 688. http://dx.doi.org/10.3390/microorganisms7120688.
Full textAbstract:
Bovine mastitis is a costly disease to the dairy industry and intramammary infections (IMI) with Staphylococcus aureus are a major cause of mastitis. Staphylococcus aureus strains responsible for mastitis in cattle predominantly belong to ruminant-associated clonal complexes (CCs). Recognition of pathogens by bovine mammary epithelial cells (bMEC) plays a key role in activation of immune responsiveness during IMI. However, it is still largely unknown to what extent the bMEC response differs according to S. aureus CC. The aim of this study was to determine whether ruminant-associated S. aureus CCs differentially activate bMEC. For this purpose, the immortalized bMEC line PS was stimulated with S. aureus mastitis isolates belonging to four different clonal complexes (CCs; CC133, CC479, CC151 and CC425) and interleukin 8 (IL-8) release was measured as indicator of activation. To validate our bMEC model, we first stimulated PS cells with genetically modified S. aureus strains lacking (protein A, wall teichoic acid (WTA) synthesis) or expressing (capsular polysaccharide (CP) type 5 or type 8) factors expected to affect S. aureus recognition by bMEC. The absence of functional WTA synthesis increased IL-8 release by bMEC in response to bacterial stimulation compared to wildtype. In addition, bMEC released more IL-8 after stimulation with S. aureus expressing CP type 5 compared to CP type 8 or a strain lacking CP expression. Among the S. aureus lineages, isolates belonging to CC133 induced a significantly stronger IL-8 release from bMEC than isolates from the other CCs, and the IL-8 response to CC479 was higher compared to CC151 and CC425. Transcription levels of IL-8, tumor necrosis factor alpha (TNFα), serum amyloid A3 (SAA3), Toll-like receptor (TLR)-2 and nuclear factor κB (NF-κB) in bMEC after bacterial stimulation tended to follow a similar pattern as IL-8 release, but there were no significant differences between the CCs. This study demonstrates a differential activation of bMEC by ruminant-associated CCs of S. aureus, which may have implications for the severity of mastitis during IMI by S. aureus belonging to these lineages.
6
Tesfaye, Kaleab, Zemichael Gizaw, and Aklilu Feleke Haile. "Prevalence of Mastitis and Phenotypic Characterization of Methicillin-Resistant Staphylococcus aureus in Lactating Dairy Cows of Selected Dairy Farms in and Around Adama Town, Central Ethiopia." Environmental Health Insights 15 (January 2021): 117863022110212. http://dx.doi.org/10.1177/11786302211021297.
Full textAbstract:
Background: The emergence of Methicillin resistant Staphylococcus aureus (MRSA) poses a serious public health threat. Strains of Staphylococcus aureus resistant to β-lactam antibiotics are known as MRSA. MRSA has gained attention as community pathogen. MRSA has been increasingly reported as emerging problem in veterinary medicine. However, little is known in Ethiopia. This study was, therefore, conducted to identify MRSA, to determine its drug susceptibility patterns, and mastitis infection in dairy cattle in and around Adama town, Central Ethiopia. Methods: A cross-sectional study was conducted to estimate the occurrence of MRSA in mastitic dairy cows in and around Adama town, central Ethiopia. A total of 384 lactating cows were included from the conveniently selected dairy farms in the study area. Approximately 10 ml of milk was aseptically collected from clinical and subclinical mastitic cows into sterile universal bottles after discarding the first 3 milking streams. Then, Staphylococcus aureus was isolated using the conventional bacteriological procedure. Resistance to methicillin was detected using the Kirby-Bauer disc diffusion antibiotic susceptibility method. Oxacillin disc was used to detect methicillin resistant Staphylococcus aureus strains. Antimicrobial susceptibility test was conducted against MRSA strains using streptomycin (S, 10 µg), amoxicillin (Am, 25 µg), kanamycin (k, 30 µg), nalidixic acid (NA, 30 µg), oxytetracycline (OT, 30 µg) sulphonamide (S, 300 µg) and ceftriazole (CRO, 30 µg). Results: The study found that the prevalence of mastitis was 121(31.5%). Among this 37(30.6%) were clinical mastitis and 84 (69.4%) of them were sub-clinical mastitis. Of 121 mastitis cases, Staphylococcus aureus was isolated in 37 (30.6%) of mastitic cow milk samples. The prevalence of mastitis was significantly affected by breed, age, floor type and hygienic status of the milkers ( P < .05). Moreover, 32.4% of Staphylococcus aureus isolates were resistant to oxacillin. A total of 75% percent of MRSA isolates were resistant to amoxicillin, 66.7% were resistant to oxytetracycline, and 50% were resistant to sulphonamide. However, 75% of MRSA isolates were susceptible to kanamycin, 58.3% were susceptible to streptomycin, and 50% were susceptible to nalidixic acid. Conclusion: The study revealed that relatively high number of strains are resistant to the antibiotics commonly used in the therapeutic protocol of many human and animal infections. Therefore, antimicrobial susceptibility test should be carried out at a regular basis and proper hygienic practices should be introduced at farm level. Creating public awareness about transmission, prevention and control of MRSA should also be considered.
7
DALLA POZZA, MARIA CRISTINA, ANTONIA RICCI, and GADDO VICENZONI. "Protein A gene polymorphism analysis in Staphylococcus aureus strains isolated from bovine subclinical mastitis." Journal of Dairy Research 66, no. 3 (August 1999): 449–53. http://dx.doi.org/10.1017/s0022029999003672.
Full textAbstract:
Mammary infections caused by Staphylococcus aureus are still one of the most serious problems in dairy farms all over the world (Sischo et al. 1993), and the epidemiology of the infection has not yet been completely elucidated (Aarestrup et al. 1995). Any effective modern approach to this disease must therefore be based on more comprehensive epidemiological studies, conducted with valid microbiological typing tools.A technique for use in epidemiological studies should identify many types, and should be inexpensive, quick and easy to perform, but above all reproducible. Among the available methods, phage typing has up to now been widely and successfully used in differentiating strains of Staph. aureus isolated from cattle with mastitis (Mackie et al. 1987; Fox et al. 1991), but it has some limitations, being a technically demanding method subject to considerable experimental as well as biological variation (Maslow et al. 1993). Moreover, in some studies the number of strains that could not be typed with available bacteriophage panels has been high (Carroll & Francis, 1985; Farah et al. 1988).Alternative methods have been investigated, and of these molecular techniques have been the most intensely studied (Aarestrup et al. 1995). In studies of human infections caused by Staph. aureus, analysis of the so-called X region of protein A gene polymorphism has been a useful epidemiological marker (Frénay et al. 1994). This gene is ∼2150 bp and harbours some functionally distinct regions: an FC-binding region, the so-called X region and, at the C terminus, a sequence required for cell wall attachment (Guss et al. 1984; Frénay et al. 1994). The X region polymorphism depends on the presence, within the region itself, of a varying number of 24 bp repeats, highlighted by the amplification of this highly polymorphic DNA region and its subsequent restriction fragment length polymorphism (RFLP) analysis (Frénay et al. 1994).Human epidemic (MRSA) and non-epidemic methicillin-resistant Staph. aureus (non-MRSA) strains, which both cause infections but have completely different infection patterns, have been successfully distinguished by analysis of this polymorphism (Frénay et al. 1994). However, protein A has been identified in only 93% of Staph. aureus strains isolated from bovine intramammary infections (Poutrel & Ducelliez, 1979; Johne & Jarp, 1988).The aim of the present study was to determine whether the gene for protein A of Staph. aureus (Spa) was present in Staph. aureus strains isolated from cases of subclinical bovine mastitis. This was carried out using the polymerase chain reaction (PCR), as suggested by Frénay et al. (1994). In addition, we have investigated the genetic polymorphism related to the X region of the gene, by means of PCR amplification and subsequent RFLP analysis. Finally we verified the stability of this region after in vitro subculture.
8
Kalashnikova, V. A. "Agr-typing of methicillin-susceptible Staphylococcus aureus (MSSA) isolated from non-human primates." Veterinary Science Today, no. 2 (June 16, 2020): 127–31. http://dx.doi.org/10.29326/2304-196x-2020-2-33-127-131.
Full textAbstract:
Staphylococcus aureus (S. aureus) is a microorganism that causes a great number of diseases in humans and animals, including sepsis, pneumonia, food toxicoinfections, wound abscess, etc. Numerous studies on genotyping S. aureus strains isolated from humans, food and mastitis in cattle and small ruminants have been carried out. The lack of information on the genotyping of methicillin-susceptible S. aureus detected in monkeys served as a stimulus to conduct a similar research, since staphylococcal infections in the primates are widespread. The present study is devoted to molecular genetic testing of S. aureus isolated from different biological samples taken from monkeys and is based on typing of agr polymorphic locus which acts as a regulator of pathogenic gene expression. As a result of PCR analysis of 301 S. aureus isolates it was established that most of S. aureus belonged to agr IV (55%), and agr I (34%) was the second most group. Data resulting from the study differ from the results of other researchers published in literary sources, who performed typing of salmonella isolated from people with agr I prevailing. In conducting the study, neither distinct correlation between microbial isolation source and agr complex groups, nor relationship between the diseases and S. aureus group specificity were detected. Prevalence ratio of each agr group is nearly similar in S. aureus isolated from rhesus macaques and crab-eating macaques. But in hamadryas baboons and green monkeys II and III groups of agr complex were not detected.
9
JOHLER, SOPHIA, FRANZISKA LAYER, and ROGER STEPHAN. "Comparison of Virulence and Antibiotic Resistance Genes of Food Poisoning Outbreak Isolates of Staphylococcus aureus with Isolates Obtained from Bovine Mastitis Milk and Pig Carcasses." Journal of Food Protection 74, no. 11 (November 1, 2011): 1852–59. http://dx.doi.org/10.4315/0362-028x.jfp-11-192.
Full textAbstract:
Staphylococcus aureus is the etiological agent in a variety of infections in humans and livestock and produces enterotoxins leading to staphylococcal food poisoning (SFP), one of the most prevalent foodborne intoxication diseases worldwide. Pork and bovine milk are considered possible sources of SFP because pig skin is often colonized by S. aureus and bovine mastitis caused by S. aureus is common, but conclusive data are limited. The objective of the present study was to compare S. aureus isolates associated with cases of SFP with isolates obtained from bovine mastitis milk and pig carcasses. DNA microarray analysis and spa gene typing were performed with 100 S. aureus isolates: 20 isolates related to outbreaks of SFP in humans, 39 isolates obtained from pig carcasses, and 41 isolates collected from bovine mastitis milk. No overlap in spa types was observed for SFP isolates (t008, t015, t018, t024, t056, t084, t279, t377, t383, t648, t733, t912, t1239, t1270, t4802, and t6969) and isolates gathered from milk or pork. The porcine isolates were assigned to t034, t208, t337, t524, t899, t1939, t2922, t2971, t4475, and t7006, and the bovine isolates belonged to t267, t524, t529, t1403, t2953, t7007, t7008, and t7013. Comparison of microarray profiles revealed similar virulence gene patterns for isolates collected from the same host (pigs or cattle) but few similarities between SFP isolate profiles and the profiles of isolates obtained from bovine mastitis milk and pig carcasses. Although only some bovine and porcine isolates possessed the β-lactamase gene blaZ (milk, 24%; pork, 28%), significantly higher numbers of SFP isolates contained blaZ (90%). Investigations of these isolates provided no evidence that pork or bovine mastitis milk represent common sources of SFP.
10
Donovan, David M., Shengli Dong, Wes Garrett, Geneviève M. Rousseau, Sylvain Moineau, and David G. Pritchard. "Peptidoglycan Hydrolase Fusions Maintain Their Parental Specificities." Applied and Environmental Microbiology 72, no. 4 (April 2006): 2988–96. http://dx.doi.org/10.1128/aem.72.4.2988-2996.2006.
Full textAbstract:
ABSTRACT The increased incidence of bacterial antibiotic resistance has led to a renewed search for novel antimicrobials. Avoiding the use of broad-range antimicrobials through the use of specific peptidoglycan hydrolases (endolysins) might reduce the incidence of antibiotic-resistant pathogens worldwide. Staphylococcus aureus and Streptococcus agalactiae are human pathogens and also cause mastitis in dairy cattle. The ultimate goal of this work is to create transgenic cattle that are resistant to mastitis through the expression of an antimicrobial protein(s) in their milk. Toward this end, two novel antimicrobials were produced. The (i) full-length and (ii) 182-amino-acid, C-terminally truncated S. agalactiae bacteriophage B30 endolysins were fused to the mature lysostaphin protein of Staphylococcus simulans. Both fusions display lytic specificity for streptococcal pathogens and S. aureus. The full lytic ability of the truncated B30 protein also suggests that the SH3b domain at the C terminus is dispensable. The fusions are active in a milk-like environment. They are also active against some lactic acid bacteria used to make cheese and yogurt, but their lytic activity is destroyed by pasteurization (63°C for 30 min). Immunohistochemical studies indicated that the fusion proteins can be expressed in cultured mammalian cells with no obvious deleterious effects on the cells, making it a strong candidate for use in future transgenic mice and cattle. Since the fusion peptidoglycan hydrolase also kills multiple human pathogens, it also may prove useful as a highly selective, multipathogen-targeting antimicrobial agent that could potentially reduce the use of broad-range antibiotics in fighting clinical infections.