Relevant bibliographies by topics / Staphylococcal disease

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Staphylococcal disease'

Author: Grafiati
Published: 4 June 2021
Last updated: 16 February 2022

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Journal articles on the topic "Staphylococcal disease"

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Homsombat, Theeyathart, Sukolrat Boonyayatra, Nattakarn Awaiwanont, and Duangporn Pichpol. "Effect of Temperature on the Expression of Classical Enterotoxin Genes among Staphylococci Associated with Bovine Mastitis." Pathogens 10, no. 8 (August 2, 2021): 975. http://dx.doi.org/10.3390/pathogens10080975.

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Staphylococcal food poisoning (SFP), caused by the contamination of staphylococcal enterotoxins, is a common foodborne disease worldwide. The aims of this study were: (1) to investigate classical staphylococcal enterotoxin genes, sea, seb, sec, sed, and see, among Staphylococcus aureus and coagulase-negative staphylococci (CNS) associated with bovine mastitis; (2) to determine the effect of temperature on the expression of classical staphylococcal enterotoxin genes in staphylococci in milk. The detection of classical staphylococcal enterotoxin genes was performed using S. aureus (n = 51) and CNS (n = 47). The expression of classical enterotoxin genes, including sea, seb, sec, and see, was determined during the growth of staphylococci in milk subjected to ultra-high-temperature processing at two different temperatures: 8 °C and room temperature. Classical staphylococcal enterotoxin genes were expressed more frequently in S. aureus (35.30%) than in CNS (12.77%). The sec gene was most frequently detected in S. aureus (29.41%) and CNS (6.38%). Moreover, the expression of sea and sec was significantly higher at room temperature than at 8 °C after 16 h of incubation (p < 0.05). These results emphasize the importance of maintaining the storage temperature of milk below 8 °C to reduce the risk of SFP.
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Speziale, Pietro, and Giampiero Pietrocola. "Monoclonal Antibodies Targeting Surface-Exposed and Secreted Proteins from Staphylococci." Vaccines 9, no. 5 (May 4, 2021): 459. http://dx.doi.org/10.3390/vaccines9050459.

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Staphylococci (specifically Staphylococcus aureus and Staphylococcus epidermidis) are the causative agents of diseases ranging from superficial skin and soft tissue infections to severe conditions such as fatal pneumonia, bacteremia, sepsis and endocarditis. The widespread and indiscriminate use of antibiotics has led to serious problems of resistance to staphylococcal disease and has generated a renewed interest in alternative therapeutic agents such as vaccines and antibodies. Staphylococci express a large repertoire of surface and secreted virulence factors, which provide mechanisms (adhesion, invasion and biofilm development among others) for both bacterial survival in the host and evasion from innate and adaptive immunity. Consequently, the development of antibodies that target specific antigens would provide an effective protective strategy against staphylococcal infections. In this review, we report an update on efforts to develop anti-staphylococci monoclonal antibodies (and their derivatives: minibodies, antibody–antibiotic conjugates) and the mechanism by which such antibodies can help fight infections. We also provide an overview of mAbs used in clinical trials and highlight their therapeutic potential in various infectious contexts.
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Edslev, Sofie Marie, Caroline Meyer Olesen, Line Brok Nørreslet, Anna Cäcilia Ingham, Søren Iversen, Berit Lilje, Maja-Lisa Clausen, et al. "Staphylococcal Communities on Skin Are Associated with Atopic Dermatitis and Disease Severity." Microorganisms 9, no. 2 (February 19, 2021): 432. http://dx.doi.org/10.3390/microorganisms9020432.

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The skin microbiota of atopic dermatitis (AD) patients is characterized by increased Staphylococcus aureus colonization, which exacerbates disease symptoms and has been linked to reduced bacterial diversity. Skin bacterial communities in AD patients have mostly been described at family and genus levels, while species-level characterization has been limited. In this study, we investigated the role of the bacteria belonging to the Staphylococcus genus using targeted sequencing of the tuf gene with genus-specific primers. We compared staphylococcal communities on lesional and non-lesional skin of AD patients, as well as AD patients with healthy controls, and determined the absolute abundance of bacteria present at each site. We observed that the staphylococcal community, bacterial alpha diversity, and bacterial densities were similar on lesional and non-lesional skin, whereas AD severity was associated with significant changes in staphylococcal composition. Increased S. aureus, Staphylococcus capitis, and Staphylococcus lugdunensis abundances were correlated with increased severity. Conversely, Staphylococcus hominis abundance was negatively correlated with severity. Furthermore, S. hominis relative abundance was reduced on AD skin compared to healthy skin. In conclusion, various staphylococcal species appear to be important for skin health.
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Mourenza, Álvaro, José A. Gil, Luis M. Mateos, and Michal Letek. "Novel Treatments and Preventative Strategies Against Food-Poisoning Caused by Staphylococcal Species." Pathogens 10, no. 2 (January 20, 2021): 91. http://dx.doi.org/10.3390/pathogens10020091.

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Staphylococcal infections are a widespread cause of disease in humans. In particular, S. aureus is a major causative agent of infection in clinical medicine. In addition, these bacteria can produce a high number of staphylococcal enterotoxins (SE) that may cause food intoxications. Apart from S. aureus, many coagulase-negative Staphylococcus spp. could be the source of food contamination. Thus, there is an active research work focused on developing novel preventative interventions based on food supplements to reduce the impact of staphylococcal food poisoning. Interestingly, many plant-derived compounds, such as polyphenols, flavonoids, or terpenoids, show significant antimicrobial activity against staphylococci, and therefore these compounds could be crucial to reduce the incidence of food intoxication in humans. Here, we reviewed the most promising strategies developed to prevent staphylococcal food poisoning.
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White, Mark. "Disease Facts: Staphylococcal dermatitis." Livestock 15, no. 2 (March 2010): 45–46. http://dx.doi.org/10.1111/j.2044-3870.2010.tb00276.x.

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Kadariya, Jhalka, Tara C. Smith, and Dipendra Thapaliya. "Staphylococcus aureusand Staphylococcal Food-Borne Disease: An Ongoing Challenge in Public Health." BioMed Research International 2014 (2014): 1–9. http://dx.doi.org/10.1155/2014/827965.

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Staphylococcal food-borne disease (SFD) is one of the most common food-borne diseases worldwide resulting from the contamination of food by preformedS. aureusenterotoxins. It is one of the most common causes of reported food-borne diseases in the United States. Although several Staphylococcal enterotoxins (SEs) have been identified, SEA, a highly heat-stable SE, is the most common cause of SFD worldwide. Outbreak investigations have found that improper food handling practices in the retail industry account for the majority of SFD outbreaks. However, several studies have documented prevalence ofS. aureusin many food products including raw retail meat indicating that consumers are at potential risk ofS. aureuscolonization and subsequent infection. Presence of pathogens in food products imposes potential hazard for consumers and causes grave economic loss and loss in human productivity via food-borne disease. Symptoms of SFD include nausea, vomiting, and abdominal cramps with or without diarrhea. Preventive measures include safe food handling and processing practice, maintaining cold chain, adequate cleaning and disinfection of equipment, prevention of cross-contamination in home and kitchen, and prevention of contamination from farm to fork. This paper provides a brief overview of SFD, contributing factors, risk that it imposes to the consumers, current research gaps, and preventive measures.
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Dollani, Lorena C., and Kalyani S. Marathe. "Impetigo/Staphylococcal Scalded Skin Disease." Pediatrics in Review 41, no. 4 (April 2020): 210–12. http://dx.doi.org/10.1542/pir.2018-0206.

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Foster, Aiden P. "Staphylococcal skin disease in livestock." Veterinary Dermatology 23, no. 4 (July 24, 2012): 342—e63. http://dx.doi.org/10.1111/j.1365-3164.2012.01093.x.

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Kirby, William M. M. "THERAPEUTIC ASPECTS OF STAPHYLOCOCCAL DISEASE." Annals of the New York Academy of Sciences 128, no. 1 (December 16, 2006): 443–50. http://dx.doi.org/10.1111/j.1749-6632.1965.tb11653.x.

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Arbuthnott, J. P., D. C. Coleman, and Joyce S. de Azavedo. "Staphylococcal toxins in human disease." Journal of Applied Bacteriology 69 (January 1990): 101S—107S. http://dx.doi.org/10.1111/j.1365-2672.1990.tb01802.x.

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Dissertations / Theses on the topic "Staphylococcal disease"

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Nutbeam-Tuffs, Stephen William. "Functional characterisation of superantigens in Staphylococcus aureus disease pathogenesis." Thesis, University of Edinburgh, 2016. http://hdl.handle.net/1842/25519.

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Bacterial superantigens (SAgs) are virulence factors that induce nonspecific T-cell proliferation contributing to host immune avoidance, and occasionally severe life-threatening toxinoses such as toxic shock syndrome. In the current study, the multiple functions of 3 superantigens named staphylococcal enterotoxin-like toxins X, Y and Z are investigated. SElX and SElZ were non-emetic in a musk shrew model of emesis. SElX is structurally and phylogenetically related to staphylococcal superantigen-like proteins (SSls) which are non-mitogenic but exhibit a variety of immune modulatory properties. We carried out protein and gene expression analysis of mutants of different S. aureus gene regulators and demonstrated that selx expression is controlled by saeRS, a two-component regulator linked to the bacterial response to phagocytic signals. Considering the co-regulation of SElX with known mediators of innate immune evasion we investigated a potential role for SElX in both humoral and cellular innate immune modulation and discovered that SElX strongly binds to human, bovine, murine, and laprine neutrophils and interferes with IgG-mediated phagocytosis, independently of Fcγ receptor signalling. Bacterial survival assays with neutrophils demonstrated that the deletion of selx significantly reduced the ability of S. aureus to resist neutrophil killing. Site-directed mutagenesis in the conserved sialic acid-binding motif of SElX abolished its neutrophil binding capacity, which is consistent with a critical role for glycosylated receptors in this interaction. Importantly, the sialic-acid binding mutants of SElX retained the ability to induce T-cell proliferation demonstrating that the distinct functions of SElX are mechanistically independent. Affinity precipitation experiments identified potential glycoprotein receptors for SElX and the interaction with protein ICAM-3, an important ligand for MAC-1 integrins, was validated suggesting SElX may interfere with cell signalling. Taken together, we present the first example of a bi-functional SAg that can manipulate two distinct arms of the human immune system and contribute to S. aureus survival during infection.
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Passalacqua, Edward F. "X-ray crystallographic studies of toxic shock syndrome toxin-1 and related superantigens." Thesis, University of Bath, 1995. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.295442.

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Lindberg, Hanna. "Engineering of Affibody molecules targeting the Alzheimer’s-related amyloid β peptide." Doctoral thesis, KTH, Proteinteknologi, 2015. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-173864.

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Röhrbein, Jan Hendrik [Verfasser]. "The influence of the staphylococcal Extracellular Adherence Protein on T cells functions in vitro in the context of the psoriasiform skin disease / Jan Hendrik Röhrbein." Ulm : Universität Ulm. Medizinische Fakultät, 2013. http://d-nb.info/1037395018/34.

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Matar, Suzan. "Characterization of staphylococcal small colony variants and their pathogenic role in biomaterial-related infections with special reference to Staphylococcus epidermidis." Thesis, University of Nottingham, 2004. http://eprints.nottingham.ac.uk/12135/.

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There are many surgical implanted devices in current use and all are prone to biomaterial-related infections (BRI) associated with staphylococcal biofilm formation. BRI are usually associated with S. epidermidis or S. Aureus and are characterized by treatment failure and chronicity resulting in reoperation, removal of the implant, and loss of function or death. Staphylococcal small colony variants (SCVs) may be generated by exposure to sublethal concentrations of antibiotics or nutrient limitation which may occur in biofilms. Although the characteristics of S. aureus SCVs have been well studied, little information on SCVs of S. epidermidis and their potential role in BRI is currently available. This study was designed to investigate the biochemical and phenotypic characteristics of S. epidermidis SCVs to further identify characteristics which may contribute to their ability to cause these increasingly important infections. Exposure to two to four times the gentamicin MIC led to the emergence of stable S. epidermidis SCVs, and the ability to produce SCVs was strain dependent. These variants were isogenic by PFGE and less immunogenic by western blotting, and SDS-PAGE analysis of whole cell preparations and cell wall fractions showed altered protein profiles when compared to wild type strains. S epidermidis SCVs were resistant to aminoglycosides such as amikacin and/or netilmicin and they were thiamine and/or menadione auxotrophs. Chemiluminescence assays showed a decreased ATP content reflecting the deficiency in electron transport systems which results in a growth rate – all characteristics similar to those of S. aureus SCVs. Analysis of virulence factor production indicated that S. epidermidis SCVs showed increased lipolytic and proteolytic activity when compared to those of S. aureus. Some S. epidermidis SCVs showed phase variation in exopolysaccharide production which enabled them to be more adherent to uncoated plastic -a property that may also be important for the later stages of development of biofilms. Invasion assays demonstrated that some S. epidermidis and S. aureus SCVs were internalised by HUVECs by a receptor-mediated mechanism which differed from that of the wild type strains. Interaction of staphylococci with HUVECs induced cytokine production but SCVs stimulated production of IL1, IL-6 and IL-8 at lower concentrations than their related wild type parents in the first 6 hours of co-incubation. SCVs were also less damaging to the HUVEC cell line after 24 hours when compared to wild type strains. This study supports the suggestion that a switch to the S. epidermidis SCV phenotype could be a mechanism exploited by the wild type strains to facilitate their survival inside the host. The chronicity and increased antibiotic resistance associated with BRI could in part, be explained by the characteristics of SCVs identified in this study. In particular the ability to survive intracellularly combined with reduced immunogenicity and resulting decreased cytokine production, may contribute to persistence of infection. Although SCVs are resistant to some antibiotics, surviving intracellularly may further protect staphylococci from other drugs which are unable to enter mammalian cells. Resistance may be further enhanced for some strains in biofilms where enhanced polysaccharide production may also limit antibiotic access.
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Ek, Moira. "Bacterial Display of a Tau-Binding Affibody Construct:Towards Affinity Maturation." Thesis, KTH, Skolan för kemi, bioteknologi och hälsa (CBH), 2020. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-278580.

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Aggregation of microtubule-associated protein tau is involved in the pathology of several neurodegenerative diseases, including Alzheimer’s disease. The affibody TP4 has been shown to inhibit this aggregation process, and its target-binding positions were previously grafted onto a dimeric affibody scaffold, creating the sequestrin seqTP4. This project constitutes a part of the affinity maturation process of seqTP4, using two different bacterial display methods. An error-prone PCR library was first expressed on Staphylococcus carnosus cells for selection of variants with improved tau-binding properties, resulting in a library of 1.4×107 transformants. Flow cytometric tests indicated difficulties in the setup due to nonspecific interactions, and whereas several different approaches to alleviate the problems were investigated, two cell sorting attempts were ultimately unsuccessful. Subcloning of seqTP4 and the library to an Escherichia coli surface display vector resulted in functional surface expression of seqTP4 on E. coli JK321 and BL21 cells, and a BL21 library size of 1.6×109 transformants. An initial flow cytometric test of this library indicates the presence of improved tau-binding variants, paving the way for future cell sorting.
Aggregering av mikrotubuli-associerat protein tau är involverad i patologin av flera neurodegenerativa sjukdomar, däribland Alzheimers sjukdom. Affibodymolekylen TP4 har visat sig inhibera denna aggregeringsprocess, och överföring av dess målbindande positioner till ett dimeriskt affibodyprotein har tidigare gett upphov till seqTP4, en så kallad sequestrin. Detta projekt utgör ett led i processen att affinitetsmaturera seqTP4, med hjälp av två olika metoder för presentation av proteiner på ytan av bakterieceller. Ett error-prone PCR-bibliotek uttrycktes först på ytan av Staphylococcus carnosus-celler för selektion av varianter med ökad affinitet för tau, vilket resulterade i ett bibliotek av 1.4×107 transformanter. Flödescytometriska tester tydde på svårigheter i detta upplägg på grund av ospecifika interaktioner, och emedan flera olika angreppssätt för att förmildra dessa problem undersöktes, misslyckades slutligen två cellsorteringsförsök. Omkloning av seqTP4 och biblioteket till en vektor för ytpresentation på Escherichia coli resulterade i funktionellt ytuttryck av seqTP4 på E. coli JK321- och BL21-celler, och ett BL21-bibliotek bestående av 1.6×109 transformanter. Ett första flödescytometriskt test av detta bibliotek tyder på närvaron av varianter med förbättrad förmåga att binda tau, och vägen ligger nu relativt öppen för cellsortering.
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Lawal, Opeyemi U. "Evolutionary genomics of Staphylococcus saprophyticus: origin and disease signatures of pathogenic clones." Doctoral thesis, Universidade Nova de Lisboa, Instituto de Tecnologia Química e Biológica António Xavier, 2020. http://hdl.handle.net/10362/96280.

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"Staphylococcus saprophyticus is the second only to Escherichia coli as the leading cause of uncomplicated urinary tract infection (UTI), and it is associated with 10-20% of this type of infection in young women. Besides being a uropathogen, S. saprophyticus is also known to be a common coloniser of the gut, vagina, perineum, and the rectum of humans. Moreover, it colonises food producing animals such as pigs, and is a frequent contaminant of meat and fermented food products. Although the source(s) of S. saprophyticus causing UTI in humans are considered to be endogenous, increased contact with animal production settings and consumption of contaminated meat products have been hypothesised to increase the risk of human colonisation and infection with this bacterium.(...)"
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Brant, Jamet Ann. "Devleopment of an in vitro model of peritonitis complicating continuous ambulatory peritoneal dialysis." Thesis, University of Brighton, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.337400.

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McGregor, Neil Roland. "An Investigation Of The Association Between Toxin-Producing Staphylococcus Biochemical Changes And Jaw Muscle Pain." University of Sydney, 1999. http://hdl.handle.net/2123/4697.

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Doctor of Philosophy
This work was digitised and made available on open access by the University of Sydney, Faculty of Dentistry and Sydney eScholarship . It may only be used for the purposes of research and study. Where possible, the Faculty will try to notify the author of this work. If you have any inquiries or issues regarding this work being made available please contact the Sydney eScholarship Repository Coordinator - ses@library.usyd.edu.au
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Thorberg, Britt-Marie. "Coagulase-negative staphylococci in bovine sub-clinical mastitis /." Uppsala : Dept. of Biomedical Sciences and Veterinary Public Health, Swedish University of Agricultural Sciences, 2008. http://epsilon.slu.se/10971614.pdf.

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Books on the topic "Staphylococcal disease"

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Mittag, Hans-Christian. Toxic shock syndrome and the other staphylococcal toxicoses. Stuttgart: New York, 1988.

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Mittag, Hans-Christian. Toxic shock syndrome and the other staphylococcal toxicoses. Stuttgart: Schattauer, 1988.

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Crossley, Kent B., Kimberly K. Jefferson, Gordon L. Archer, and Vance G. Fowler, eds. Staphylococci in Human Disease. Oxford, UK: Wiley-Blackwell, 2009. http://dx.doi.org/10.1002/9781444308464.

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Honeyman, Allen L., Herman Friedman, and Mauro Bendinelli, eds. Staphylococcus aureus Infection and Disease. Boston, MA: Springer US, 2001. http://dx.doi.org/10.1007/b111097.

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Freeman-Cook, Lisa. Staphylococcus aureus infections. Edited by Freeman-Cook Kevin D, Alcamo I. Edward, and Heymann David L. Philadelphia: Chelsea House Publishers, 2006.

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Georg, Peters. Role of clindamycin in the therapy of staphylococcal diseases. Erlangen: Pharmacia & Upjohn, 1996.

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Ireland. Food Safety Advisory Committee. Cryptosporidiosis staphylococcal food poisoning food borne illness enterohaemorrhagic E Coli (EHEC/VTEC). Dublin: Stationery Office, 1992.

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Parker, James N., and Philip M. Parker. Staphylococcus aureus: A medical dictionary, bibliography, and annotated research guide to internet references. San Diego, CA: ICON Health Publications, 2004.

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European Congress of Clinical Microbiology and Infectious Diseases (7th 1995 Vienna). Infections by multiresistant staphylococci: 7th European Congress of Clinical Microbiology and Infectious Diseases, Vienna, March 26-30, 1995. Edited by Kayser F. H and Carbon C. Basel: Karger, 1996.

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B, Crossley Kent, and Archer Gordon 1943-, eds. The staphylococci in human disease. New York: Churchill Livingstone, 1997.

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Book chapters on the topic "Staphylococcal disease"

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Leung, Alexander K. C., Cham Pion Kao, Andrew L. Wong, Alexander K. C. Leung, Thomas Kolter, Ute Schepers, Konrad Sandhoff, et al. "Staphylococcal Food Poisoning." In Encyclopedia of Molecular Mechanisms of Disease, 1974–75. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-29676-8_1664.

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Graber, Christopher J., and Dennis R. Schaberg. "Staphylococcal and Enterococcal Infections." In Infectious Disease in the Aging, 327–45. Totowa, NJ: Humana Press, 2009. http://dx.doi.org/10.1007/978-1-60327-534-7_21.

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Leung, Alexander K. C., Cham Pion Kao, Andrew L. Wong, Alexander K. C. Leung, Thomas Kolter, Ute Schepers, Konrad Sandhoff, et al. "Staphylococcal Scalded Skin Syndrome." In Encyclopedia of Molecular Mechanisms of Disease, 1975–76. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-29676-8_1665.

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Leung, Alexander K. C., Cham Pion Kao, Andrew L. Wong, Alexander K. C. Leung, Thomas Kolter, Ute Schepers, Konrad Sandhoff, et al. "Staphylococcal Toxic Shock Syndrome." In Encyclopedia of Molecular Mechanisms of Disease, 1976. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-29676-8_7029.

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Alves, Maria Almerinda Vieira Fernandes Ri. "Staphylococcal Infections and Kidney Disease." In Tropical Nephrology, 223–30. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-44500-3_17.

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Bergdoll, Merlin S. "The Staphylococcal Toxins in Human Disease." In Infectious Agents and Pathogenesis, 169–85. Boston, MA: Springer US, 1996. http://dx.doi.org/10.1007/978-1-4899-0313-6_9.

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Bachert, C., P. Gevaert, Nan Zhang, T. van Zele, and Claudina Perez-Novo. "Role of Staphylococcal Superantigens in Airway Disease." In Superantigens and Superallergens, 214–36. Basel: KARGER, 2007. http://dx.doi.org/10.1159/000100897.

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Varaldo, P. E., and G. Satta. "Staphylococcal Diseases." In Laboratory Diagnosis of Infectious Diseases, 473–82. New York, NY: Springer New York, 1988. http://dx.doi.org/10.1007/978-1-4612-3898-0_49.

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Thapaliya, Dipendra. "Staphylococcus." In Handbook of Foodborne Diseases, 215–22. Boca Raton : Taylor & Francis, [2019] | Series: Food microbiology series | “A CRC title, part of the Taylor & Francis imprint, a member of the Taylor & Francis Group, the academic division of T&F Informa plc.”: CRC Press, 2018. http://dx.doi.org/10.1201/b22030-20.

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Wood, Sara. "Methicillin-Resistant Staphylococcus aureus." In Vulvar Disease, 301–2. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-319-61621-6_46.

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Conference papers on the topic "Staphylococcal disease"

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Warheit-Niemi, H., D. O'Dwyer, and B. B. Moore. "Staphylococcal Pneumonia Impacts Disease Outcome in Pulmonary Fibrosis." In American Thoracic Society 2019 International Conference, May 17-22, 2019 - Dallas, TX. American Thoracic Society, 2019. http://dx.doi.org/10.1164/ajrccm-conference.2019.199.1_meetingabstracts.a4598.

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Leanse, Leon G., Xueping Sharon Goh, Ji-Xin Cheng, David C. Hooper, and Tianhong Dai. "Dual-wavelength photo-killing of methicillin resistant staphylococcus aureus." In Photonic Diagnosis, Monitoring, Prevention, and Treatment of Infections and Inflammatory Diseases 2021, edited by Tianhong Dai, Mei X. Wu, and Jürgen Popp. SPIE, 2021. http://dx.doi.org/10.1117/12.2577202.

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Dong, Pu-Ting, Haroon T. Mohammad, Xiaoyu Wang, Jie Hui, Lijia Liang, Junjie Li, Mohamed N. Seleem, and Ji-Xin Cheng. "Staphyloxanthin photobleaching sensitizes methicillin-resistant Staphylococcus aureus to reactive oxygen species attack." In Photonic Diagnosis and Treatment of Infections and Inflammatory Diseases, edited by Tianhong Dai. SPIE, 2018. http://dx.doi.org/10.1117/12.2291248.

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Hui, Jie, Pu-Ting Dong, Lijia Liang, Taraknath Mandal, Junjie Li, Erlinda R. Ulloa, Yuewei Zhan, et al. "Inhibiting staphylococcus aureus antibiotic resistance via photo-disassembly of membrane microdomains." In Photonic Diagnosis, Monitoring, Prevention, and Treatment of Infections and Inflammatory Diseases 2020, edited by Tianhong Dai, Mei X. Wu, and Jürgen Popp. SPIE, 2020. http://dx.doi.org/10.1117/12.2543045.

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Gal, Olivier, Chakib Belafdil, Emmanuelle Schultz, Valentin Genuer, Max Maurin, Pierre R. Marcoux, Damien Decq, and Sophie Morales. "Elastic light scattering for clinical pathogens identification: application to early screening of Staphylococcus aureus on specific medium." In Photonic Diagnosis and Treatment of Infections and Inflammatory Diseases, edited by Tianhong Dai. SPIE, 2018. http://dx.doi.org/10.1117/12.2287698.

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Welling, Mick, Danny M. van Willigen, Silvia J. Spa, Tessa Buckle, Fijs W. B. van Leeuwen, Meta Roestenberg, and Matthias N. van Oosterom. "Multi-modal radioactive and fluorescent tracking of Staphylococcus aureus infections in mice (Conference Presentation)." In Photonic Diagnosis, Monitoring, Prevention, and Treatment of Infections and Inflammatory Diseases 2019, edited by Tianhong Dai, Mei X. Wu, and Jürgen Popp. SPIE, 2019. http://dx.doi.org/10.1117/12.2509858.

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Iancu, Irina Mihaela, Laura Adriana Bucur, Verginica Schröder, and Manuela Rossemary Apetroaei. "TESTING THE BIOLOGICAL ACTIVITY OF LYTHRI HERBA EXTRACT FOR APPLICATIONS IN MEDICAL BIOTECHNOLOGIES." In GEOLINKS Conference Proceedings. Saima Consult Ltd, 2021. http://dx.doi.org/10.32008/geolinks2021/b1/v3/26.

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Abstract:
"Nowadays we are witnessing an increased interest in phytotherapy and implicitly for herbal products that have lower side effects. One medicinal plant whose popularity has decreased significantly in recent years is Lythrum salicaria L., loosestrife, known in Romanian traditional medicine for its beneficial effects against gastrointestinal diseases. The aim of this study is to evaluate the biological activity of three different extracts (aqueous, alcoholic, acetonic) from the flower tips of Lythrum salicaria L. using the BSLA (Brine Shrimp Lethality Assay) test and the antimicrobial activity of the extracts on two reference bacterial strains which are important for the medical field (Staphylococcus aureus and Escherichia coli) through the diffusimetric method. We demonstrated the fact that the Lythri herba plant product extracts (aqueous, alcoholic, and acetonic) lack acute toxicity, as well as the moderate antibacterial effect on the Gram-positive reference strain, Staphylococcus aureus, thus highlighting the possibility of using the plant in biomedical applications."
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Khairullah, Aswin, Sri Sudjarwo, Mustofa Effendi, Sancaka Ramandinianto, and Katty Priscilia Riwu. "Livestock-Associated Methicillin-Resistant Staphylococcus Aureus (LA-MRSA) CC398: An Emerging Infectious Disease." In Proceedings of the 1st International Conference on Education, Humanities, Health and Agriculture, ICEHHA 2021, 3-4 June 2021, Ruteng, Flores, Indonesia. EAI, 2021. http://dx.doi.org/10.4108/eai.3-6-2021.2310716.

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Alvarez, Crysthal, Alma Hernandez, Natanael Cuando-Espitia, and Guillermo Aguilar. "Growth inhibition of Staphylococcus Aureus by a combined treatment of ZnO nanoparticles and femtosecond laser light." In Photonic Diagnosis, Monitoring, Prevention, and Treatment of Infections and Inflammatory Diseases 2019, edited by Tianhong Dai, Mei X. Wu, and Jürgen Popp. SPIE, 2019. http://dx.doi.org/10.1117/12.2510263.

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Chang, Ching-Wen, and Meng-Hsuan Lin. "0168 Quantification of viable staphylococcus aureus and viable bacteria in workplaces by propidium monoazide with qpcr." In Eliminating Occupational Disease: Translating Research into Action, EPICOH 2017, EPICOH 2017, 28–31 August 2017, Edinburgh, UK. BMJ Publishing Group Ltd, 2017. http://dx.doi.org/10.1136/oemed-2017-104636.136.

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