Maternal-infant perinatal transmission of methicillin-resistant and methicillin-sensitive Staphylococcus aureus

David M Pinter1, Judy Mandel, Kristina G Hulten

  • 1Department of Pediatrics, Maimonides Medical Center, Brooklyn, New York, USA.

Insights

Perinatal transmission contributes to Staphylococcus aureus (SA) colonization in newborns, with methicillin-resistant SA (MRSA) confirmed between mothers and infants. Post-discharge colonization, not perinatal transmission, primarily drives early infant infections.

Area of Science:

  • Neonatal infections
  • Microbiology
  • Public Health

Background:

  • Staphylococcus aureus (SA), particularly methicillin-resistant SA (MRSA), is a growing concern in neonatal infections.
  • Understanding the transmission dynamics of SA from mother to infant during the perinatal period is crucial for infection control.

Purpose of the Study:

  • To investigate the contribution of perinatal maternal-infant transmission of SA to infant colonization and infection.
  • To molecularly confirm the transmission of MRSA between mothers and newborns.

Main Methods:

  • Collected cultures from mothers (nares, vagina) and infants (nares, skin) during the perinatal period.
  • Utilized pulsed field gel electrophoresis (PFGE) to analyze SA and MRSA isolates for genetic relatedness.
  • Monitored infants for staphylococcal infections for four weeks post-discharge.

Main Results:

  • Approximately 20% of maternal SA isolates were MRSA.
  • Perinatal transmission accounted for 20% of infant SA colonization.
  • Molecular evidence confirmed MRSA transmission from mother to infant in one case.
  • Most SA infections in the first four weeks of life originated from post-discharge colonization.

Conclusions:

  • Perinatal maternal-infant transmission plays a role in neonatal SA colonization, including MRSA.
  • Post-discharge colonization is a more significant factor in early-onset staphylococcal infections in term infants.
  • Molecular confirmation of perinatal MRSA transmission was achieved.

Related Concept Videos

Development of the Oral Microbiota01:28

Development of the Oral Microbiota

The establishment of the oral microbiome begins before birth, challenging the long-held belief that the fetal oral cavity is sterile. The presence of oral microbes such as Streptococcus and Fusobacterium in amniotic fluid suggests that microbial exposure may occur in utero, potentially through translocation from the maternal oral or gastrointestinal tract. This early colonization primes the neonatal immune system and sets the stage for subsequent microbial succession. Maternal health,...
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...
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...
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...
Development of Human Microbiota01:30

Development of Human Microbiota

The human microbiota begins developing at birth and undergoes continual change as we age. Infancy marks a critical period of microbial sensitivity, offering a “window of opportunity” during which beneficial microbes help mature the immune system. By age three, children typically develop a more stable and diverse microbial community. Newborns acquire microbes from their immediate environment; vaginal delivery favors maternal vaginal microbes, while cesarean births favor microbes from the skin...
Transmission of Pathogens01:24

Transmission of Pathogens

Pathogens spread from their reservoirs to susceptible hosts through three main routes: contact transmission, vehicle transmission, and vector transmission. Each route involves distinct mechanisms of transfer.Contact TransmissionThis category includes direct contact, indirect contact, and droplet transmission:Direct contact involves immediate physical interaction between individuals—such as a handshake—which can spread pathogens like Streptococcus pyogenes, the bacterium responsible for...