Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Staphylococcal Skin Infections01:29

Staphylococcal Skin Infections

Staphylococcus aureus is a Gram-positive coccus that resides harmlessly on the skin and mucous membranes of healthy individuals. When the skin barrier is breached, it can shift from a commensal to an opportunistic pathogen. This transition is facilitated by surface adhesins, such as clumping factor B and S. aureus surface protein G (SasG), which bind to structural proteins, including loricrin and cytokeratin, in the damaged epidermis. Protein A, another key factor, binds the Fc region of...
Mechanism of Antibiotic Resistance in MRSA01:25

Mechanism of Antibiotic Resistance in MRSA

Antibiotic resistance in bacteria arises when microorganisms evolve the ability to withstand drugs designed to kill them or inhibit their growth, rendering once-effective treatments useless. This phenomenon, driven by genetic change and selection under antibiotic exposure, poses a profound threat to modern medicine. Mechanisms include drug-inactivating enzymes (e.g., β-lactamases), efflux pumps that eject antibiotics, mutations altering antibiotic targets, decreased drug uptake, and acquisition...
Clinical Significance of Antibiotic Resistance01:25

Clinical Significance of Antibiotic Resistance

Methicillin-resistant Staphylococcus aureus (MRSA) presents a critical public health threat, arising from its capacity to resist β-lactam antibiotics due to acquisition of the mecA gene within the staphylococcal cassette chromosome mec (SCCmec). This gene encodes penicillin-binding protein 2a (PBP2a), which impairs binding efficacy of methicillin and other β-lactams. MRSA has evolved into distinct clonal lineages impacting humans and animals alike, reinforcing its significance within the One...
Defense Against Bacterial Pathogens01:31

Defense Against Bacterial Pathogens

The human immune system is a complex network of cells, tissues, and organs that work together to defend the body against bacterial infections. It consists of various immune cells, each playing a specific role in the defense mechanism.
Phagocytes
Phagocytes are the frontline soldiers of the immune system. They include neutrophils and macrophages. Neutrophils are the most abundant type of white blood cell and are quickly mobilized to the site of infection. Macrophages are larger cells that patrol...
Colonisation of Pathogens01:25

Colonisation of Pathogens

Pathogen colonization of host tissues is a critical step in the development of infectious diseases. Various pathogenic microorganisms, including bacteria, fungi, viruses, and protozoa, have evolved complex strategies to attach to, invade, and persist within host environments. These mechanisms enable pathogens to establish infections, evade immune responses, and resist antimicrobial treatments.Attachment to Host CellsIn bacteria, colonization typically begins with adherence to host epithelial...
The Skin Microbiota01:27

The Skin Microbiota

The human skin serves as a complex ecosystem inhabited by a diverse community of microorganisms, including bacteria, fungi, and viruses. This microbiome plays a critical role in maintaining skin health and defending against pathogenic invaders. The composition of microbial communities varies significantly across different regions of the body, influenced primarily by the local levels of moisture and sebum.Regional Variation in Skin MicrobiotaCutibacterium acnes predominantly colonizes sebaceous...

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Association between community medicine rotation duration and general medicine in-training examination scores among second-year resident physicians in Japan: a nationwide cross-sectional study.

BMC medical education·2026
Same author

An Exploratory Study of the Effects of a High School-University Collaborative Program on Learning Motivation and Professional Understanding among Students Aspiring to Enter Medical School.

Juntendo medical journal·2026
Same author

Exploring the Feasibility of an Examiner-Worn Neck-Mounted Camera for Objective Structured Clinical Examination Assessment: Pilot Feasibility Study.

JMIR medical education·2026
Same author

Background characteristics and burnout of Japanese resident physicians who did and did not share voluntary clinical cases.

Scientific reports·2026
Same author

Association of Protocol Design-Related Factors With Enrollment Duration in Clinical Trials.

Clinical and translational science·2026
Same author

Association between resident physicians from foreign medical schools and general medicine in-training examination scores: a nationwide cross-sectional study in Japan.

BMC medical education·2026

Related Experiment Video

Updated: May 15, 2026

Staphylococcus aureus Growth using Human Hemoglobin as an Iron Source
06:37

Staphylococcus aureus Growth using Human Hemoglobin as an Iron Source

Published on: February 7, 2013

Beta-hemolysin promotes skin colonization by Staphylococcus aureus.

Yuki Katayama1, Tadashi Baba, Miwa Sekine

  • 1Department of Bacteriology, Juntendo University School of Medicine, Tokyo, Japan.

Journal of Bacteriology
|January 8, 2013
PubMed
Summary
This summary is machine-generated.

Staphylococcus aureus colonization of skin is enhanced by beta-hemolysin (Hlb). This toxin damages skin cells, increasing bacterial colonization efficiency and contributing to invasive infections.

More Related Videos

Improved Enzyme Protection Assay to Study Staphylococcus aureus Internalization and Intracellular Efficacy of Antimicrobial Compounds
06:36

Improved Enzyme Protection Assay to Study Staphylococcus aureus Internalization and Intracellular Efficacy of Antimicrobial Compounds

Published on: September 8, 2021

Related Experiment Videos

Last Updated: May 15, 2026

Staphylococcus aureus Growth using Human Hemoglobin as an Iron Source
06:37

Staphylococcus aureus Growth using Human Hemoglobin as an Iron Source

Published on: February 7, 2013

Improved Enzyme Protection Assay to Study Staphylococcus aureus Internalization and Intracellular Efficacy of Antimicrobial Compounds
06:36

Improved Enzyme Protection Assay to Study Staphylococcus aureus Internalization and Intracellular Efficacy of Antimicrobial Compounds

Published on: September 8, 2021

Area of Science:

  • Microbiology
  • Dermatology
  • Infectious Diseases

Background:

  • Staphylococcus aureus colonization is common in inflammatory skin diseases.
  • This colonization can lead to epidermal damage and invasive infections.
  • A virulent community-acquired methicillin-resistant S. aureus (CA-MRSA) strain, MW2, lacks beta-hemolysin (Hlb) due to prophage integration.

Purpose of the Study:

  • Investigate the mechanism of skin colonization by CA-MRSA strain MW2.
  • Determine the role of beta-hemolysin (Hlb) in S. aureus skin colonization.
  • Elucidate how Hlb contributes to epidermal damage and infection.

Main Methods:

  • Utilized a murine ear colonization model with CA-MRSA strain MW2.
  • Performed genome sequencing on Hlb-producing colonies derived from MW2.
  • Constructed MW2-derivative strains with and without the Hlb gene for comparative colonization tests.
  • Assessed the cytotoxicity of Hlb toxin on human primary keratinocytes.

Main Results:

  • CA-MRSA strain MW2 derivatives spontaneously produced Hlb via precise prophage excision.
  • Hlb-producing mutants exhibited over 50-fold greater colonization efficiency on murine ears compared to Hlb-deficient mutants.
  • Hlb toxin demonstrated elevated cytotoxicity towards human primary keratinocytes.

Conclusions:

  • Staphylococcus aureus beta-hemolysin (Hlb) plays a significant role in skin colonization.
  • Hlb contributes to skin colonization by damaging keratinocytes.
  • Hlb's role in keratinocyte damage is crucial for S. aureus skin colonization and potential invasive infections.