scholarly journals Clustering of Staphylococcus aureus bovine mastitis strains from regions of Central-Eastern Poland based on their biochemical and genetic characteristics

2015 ◽  
Vol 18 (2) ◽  
pp. 333-342 ◽  
Author(s):  
E. Puacz ◽  
W.M. Ilczyszyn ◽  
M. Kosecka ◽  
A. Buda ◽  
W. Dudziak ◽  
...  

AbstractStaphylococcus aureusstrains were isolated from mastitic milk of cows with infected mammary glands. The animals were living in 12 different farms near Lublin, in Central-Eastern Poland. A biochemical identification method based on enzymatic assay was performed, followed by haemolytic and proteolytic tests. PCR-RFLP targeted on thegapgene allowed the genetic identification of strains at the species level and verified phenotypic identification results. A molecular typing method using triplex PCR was performed to recognize the genetic similarity of the analyzed strains. DNA microarray hybridization (StaphyType, Alere Technologies) was used for detection of antibiotic resistance and virulence associated markers. The results obtained indicate high genetic similarity in strains isolated from the same sites. High genetic similarities were also detected between strains isolated from cows from different farms of the same region. A slightly lower similarity was noted however, in strains from various regions indicating that the strains are herd specific and that the cow’s infections caused byS. aureuswere of a clonal character. In 21 representative isolates selected for DNA-microarray testing, only fosfomycin (fosB) and penicillin resistance markers (blaZ, blaI, blaR) were detected. The presence of genes coding for haemolysins (lukF, lukS, hlgA, hla, hld, hlb), proteases (aur, sspA, sspB, sspP), enterotoxins (entA, entD, entG, entI, entJ, entM, entN, entO, entR, entU, egc-cluster), adhesins (icaA, icaC, icaD, bbp, clfA, clfB, fib, fnbA, map, vwb) or immune evasion proteins (scn, chp, sak) was common and, with exceptions, matched triplex PCR-defined clusters.

2010 ◽  
Vol 8 (1) ◽  
pp. 82-90 ◽  
Author(s):  
Fernanda Delgado ◽  
Sílvia Ribeiro ◽  
Álvaro Alves ◽  
Eliseu Bettencourt ◽  
Sónia Dias

The morphological characterisation and data analysis of germplasm accessions of wild Portuguese Lavandula luisieri (Rozeira) Rivas-Martínez from the southern Beira Interior region of central eastern Portugal are described. The study, based on seeds and cultivated plants, was conducted in 2005, 2006 and 2008 among populations selected from four sites (I, II, III and IV). Quantitative and qualitative phenotypic data relating to a set of 35 morphological traits were analysed using canonical discriminant analysis. Genetic similarity among accessions was assessed using amplified fragment length polymorphism molecular markers. The traits contributing most to the variability among studied populations were related to plant density, leaf colour, seed weight and various spike and flower characteristics. Plant populations from each of the four test sites were statistically distinct, exhibiting unique characteristics when compared with one another; however, populations from Sites II, III and IV showed greater genetic similarity and differed substantially from the population of Site I. Altitude and temperature were found to be the most significant environmental variables influencing plant traits, yet the morphological variability of L. luisieri was also influenced by soil pH levels, suggesting that the expressed variability is not only a result of genetic characteristics but also of existing ecological conditions.


2021 ◽  
Author(s):  
Hye-Ri Jung ◽  
Young Ju Lee

Abstract Background: Staphylococcus aureus, a persistent and chronic mastitis-causing pathogen, produces various virulence factors, including enterotoxins. This study analyzed the genetic characteristics of bovine mastitis-related virulence factors to evaluate potential pathogenesis in S. aureus isolated from bulk tank milk.Results: Among 93 S. aureus isolates from 396 dairy farms in six factories operated by three dairy companies in Korea, 40 (43.0%) isolates carried at least one or more enterotoxin genes and there were significant differences between factories within the same company (p < 0.05). Moreover, S. aureus carrying enterotoxin genes showed a higher prevalence in all virulence genes tested in this study except for pvl and lukM, which were not detected in any isolate, than the isolates without enterotoxin genes. In particular, the prevalence of six genes (hla, hlb, lukED, fnbA, clfA, and clfB) was significantly higher in S. aureus carrying enterotoxin genes than isolates without enterotoxin genes (p < 0.05). The most common multilocus sequence type (ST) of 40 enterotoxin-producing isolates was ST188, and all isolates of ST188 harbored the see gene. However, none of the isolates of ST1 and ST72 carried the see gene, and all isolates of ST1 carried the seh gene.Conclusions: Although S. aureus isolated from bulk tank milk, not from mastitis, had a high prevalence of enterotoxins and virulence factors simultaneously, posing a public health threat. Moreover, high enterotoxins in bulk tank milk may be reflected by poor hygiene; therefore, it is important to develop strong monitoring and sanitation programs to ensure that dairy factories produce hygienic milk.


2014 ◽  
Vol 77 (7) ◽  
pp. 1232-1236 ◽  
Author(s):  
ANDREAS BAUMGARTNER ◽  
ISABEL NIEDERHAUSER ◽  
SOPHIA JOHLER

Staphylococcal food poisoning represents the most prevalent foodborne intoxication worldwide. Oral intake of staphylococcal enterotoxins from food can result in emesis and diarrhea and can be fatal in children and the elderly. Few data have been available on the characteristics and sources of Staphylococcus aureus strains isolated from ready-to-eat (RTE) foods. In this study, we used a DNA microarray to determine virulence and antimicrobial resistance gene profiles of S. aureus from RTE foods. A total of 267 S. aureus strains isolated from 244 RTE foods were investigated. The isolates originated from precooked foods (41% of isolates), meat and fish products (17%), cheese (13%), delicatessen salads (8%), sandwiches and canapés (8%), confectionery and bakery products (6%), and various other RTE foods (7%). Eleven samples (5%), of which 9 were raw milk cheeses, contained &gt;105 CFU/g, which is considered a health risk. Four S. aureus strains were associated with intoxications; three cases were linked to consumption of cheese and one case was linked to consumption of potato salad. DNA microarray results revealed that one-third of the tested strains had at least one major enterotoxin gene (sea through see). We also detected the toxic shock syndrome gene (18% of isolates) and various genes conferring antimicrobial resistance, including genes involved in resistance to beta-lactams (blaZ, 72% of isolates), methicillin (mecA, 1% of isolates), and vancomycin (vanB, 1% of isolates). S. aureus strains were most frequently assigned to clonal complex (CC) 30 (17% of isolates), CC8 (12%), CC15 (11%), and CC45 (10%), which are commonly detected in humans colonized or infected with S. aureus. Although a large proportion of the tested food items contained milk, we did not detect CC705, the most prevalent clonal complex among S. aureus isolates from bovine mastitis milk. Our results suggest that S. aureus isolates from RTE foods do not commonly originate from animals but more likely come from food handlers who contaminate foods.


2016 ◽  
Vol 4 (1) ◽  
Author(s):  
Danielle Mendes Silva ◽  
Mônica Pacheco da Silva ◽  
Pedro M. Pereira Vidigal ◽  
Rafael Mazioli Barcelos ◽  
Raphael Contelli Klein ◽  
...  

Here, we present the draft genome sequences of four Staphylococcus aureus strains isolated from mastitic milk collected from animals with subclinical manifestations. Three of them were typed as sequence type 126 (ST126), a genotype with no genome sequence available. ST126 is found in several herds of southern Brazil and is described as a bovine pathogen strongly associated with milk around the world.


Antibiotics ◽  
2021 ◽  
Vol 10 (5) ◽  
pp. 594
Author(s):  
Sydney E. Schnur ◽  
Raghavendra G. Amachawadi ◽  
Giovanna Baca ◽  
Sarah Sexton-Bowser ◽  
Davina H. Rhodes ◽  
...  

Antimicrobial resistance in bacterial pathogens associated with bovine mastitis and human foodborne illnesses from contaminated food and water have an impact on animal and human health. Phenolic compounds have antimicrobial properties and some specialty sorghum grains are high in phenolic compounds, and the grain extract may have the potential as a natural antimicrobial alternative. The study’s objective was to determine antimicrobial effects of sorghum phenolic extract on bacterial pathogens that cause bovine mastitis and human foodborne illnesses. Bacterial pathogens tested included Escherichia coli, Salmonella Typhimurium, Campylobacter jejuni, Campylobacter coli, Pseudomonas aeruginosa, Klebsiella pneumoniae, Klebsiella oxytoca, Staphylococcus aureus, and Enterococcus faecalis. Antibacterial activities of sorghum phenolic extracts were determined by agar-well diffusion assay. Sorghum phenolic extract was added to the wells in concentrations of 0, 100, 200, 500, 1000, or 4000 µg/mL. The control wells did not receive phenolic extract. Plates were incubated for 18–24 h, and the diameter of each zone of inhibition was measured. The results indicated that sorghum phenolic extract had inhibitory effects on Staphylococcus aureus, Enterococcus faecalis, Campylobacter jejuni, and Campylobacter coli.


Pathogens ◽  
2021 ◽  
Vol 10 (5) ◽  
pp. 506
Author(s):  
Xiaolong Wang ◽  
Yongliang Fan ◽  
Yifan He ◽  
Ziyin Han ◽  
Zaicheng Gong ◽  
...  

Staphylococcus aureus- induced mastitis is one of the most intractable problems for the dairy industry, which causes loss of milk yield and early slaughter of cows worldwide. Few studies have used a comprehensive approach based on the integrative analysis of miRNA and mRNA expression profiles to explore molecular mechanism in bovine mastitis caused by S. aureus. In this study, S. aureus (A1, B1 and C1) and sterile phosphate buffered saline (PBS) (A2, B2 and C2) were introduced to different udder quarters of three individual cows, and transcriptome sequencing and microarrays were utilized to detected miRNA and gene expression in mammary glands from the challenged and control groups. A total of 77 differentially expressed microRNAs (DE miRNAs) and 1625 differentially expressed genes (DEGs) were identified. Gene Ontology (GO) annotation and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis showed that multiple DEGs were enriched in significant terms and pathways associated with immunity and inflammation. Integrative analysis between DE miRNAs and DEGs proved that miR-664b, miR-23b-3p, miR-331-5p, miR-19b and miR-2431-3p were potential factors regulating the expression levels of CD14 Molecule (CD14), G protein subunit gamma 2 (GNG2), interleukin 17A (IL17A), collagen type IV alpha 1 chain (COL4A1), microtubule associated protein RP/EB family member 2 (MAPRE2), member of RAS oncogene family (RAP1B), LDOC1 regulator of NFKB signaling (LDOC1), low-density lipoprotein receptor (LDLR) and S100 calcium binding protein A9 (S100A9) in bovine mastitis caused by S. aureus. These findings could enhance the understanding of the underlying immune response in bovine mammary glands against S. aureus infection and provide a useful foundation for future application of the miRNA–mRNA-based genetic regulatory network in the breeding cows resistant to S. aureus.


2001 ◽  
Vol 155 (4) ◽  
pp. 339-344 ◽  
Author(s):  
Terhi Ali-Vehmas ◽  
Maija Vikerpuur ◽  
Satu Pyörälä ◽  
Faik Atroshi

2011 ◽  
Vol 14 (2) ◽  
pp. 285-286 ◽  
Author(s):  
J. Karakulska ◽  
A. Pobucewicz ◽  
P. Nawrotek ◽  
M. Muszyńska ◽  
A. Furowicz ◽  
...  

Molecular typing ofStaphylococcus aureusbased on PCR-RFLP ofcoagene and RAPD analysisThe aim of this study was molecular identification ofS. aureusstrains isolated from mastitic milk samples and establishing the genetic relationship between strains isolated from cows belonging to the same herd. In all 43 isolated strains thegapgene (930 bp) was amplified, which enabled their affiliation to theStaphylococcusgenus to be established. PCR-RFLP withAluI endonuclease of thegapgene as well asnuc(450 bp) andcoa(1130 bp) gene amplification allowed preciseS. aureusspecies identification. One hundred percent of the genetic relationship between strains was establishedviaRAPD-PCR and coa-typing.


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