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Published on: August 12, 2020
Host Defense Proteins in Breast Milk and Neonatal Yeast Colonization
Brian D W Chow1, Juliann L Reardon2, Emily O Perry3
1Marshfield Clinic Research Foundation, Marshfield, WI, USA.
Insights
Breast milk contains proteins that may protect infants from yeast colonization. Lower levels of lysozyme and dermcidin in breast milk were associated with Candida colonization in neonates.
Area of Science:
- Neonatal immunology
- Microbial colonization
- Host-pathogen interactions
Background:
- Neonatal invasive candidiasis risk increases with colonization.
- Breast milk host defense proteins may influence infant yeast colonization.
Purpose of the Study:
- To evaluate breast milk host defense proteins in relation to infant yeast colonization.
- Investigate specific proteins like lactoferrin, lysozyme, and dermcidin.
Main Methods:
- Analyzed breast milk from 61 infants in a neonatal intensive care unit over 12 weeks.
- Measured levels of human lactoferrin, lysozyme, apolipoprotein J, mucin-1, dermcidin, and soluble CD14 using ELISA.
- Compared protein concentrations between colonized and uncolonized infants.
Main Results:
- Soluble CD14 was higher in colonized infants (1.8 μg/mL) vs. uncolonized (1.6 μg/mL).
- Lysozyme levels were significantly higher in uncolonized infants (483.0 ng/mL) compared to colonized (298.3 ng/mL).
- Dermcidin levels were also higher in uncolonized infants (19.4 ng/mL) versus colonized (8.7 ng/mL).
Conclusions:
- Neonatal Candida colonization is associated with lower levels of lysozyme and dermcidin in breast milk.
- Further research is required to validate these findings and understand the implications.
Background:
Colonization increases risk for invasive candidiasis in neonates. Breast milk host defense proteins may affect yeast colonization of infants.
Objective:
This study aimed to evaluate breast milk host defense proteins relative to yeast colonization in infants.
Methods:
Infants admitted for longer than 72 hours to the neonatal intensive care unit at Women & Infants Hospital in Providence, Rhode Island, were eligible. After consent, expressed breast milk and swabs from oral, rectal, and inguinal sites from infants were cultured weekly for 12 weeks, or until discharge, transfer, or death. Breast milk was tested for levels of human lactoferrin, lysozyme, apolipoprotein J, mucin-1, dermcidin, and soluble CD14 using commercial ELISA. Concentrations of these components were compared in breast milk received by infants who were colonized or not colonized with yeast.
Results:
From an original cohort of 130, 61 infants had samples available for this subanalysis. A convenience sample of stored breast milk was analyzed. Median lactoferrin, apolipoprotein J, and mucin-1 did not differ between colonized and uncolonized groups. Soluble CD14 was higher in the surface-colonized group (1.8 μg/mL, n = 12) compared with the surface-uncolonized group (1.6 μg/mL, n = 12, P = .02). Median lysozyme levels were higher in the surface-uncolonized group (483.0 ng/mL, n = 12) versus the surface-colonized group (298.3 ng/mL, n = 12, P = .04). Median dermcidin levels were higher in the surface-uncolonized group (19.4 ng/mL, n = 12) versus the surface-colonized group (8.7 ng/mL, n = 12, P = .04).
Conclusion:
This study shows an association between colonization with Candida in neonates and lower levels of lysozyme and dermcidin in received breast milk. Further study is needed to confirm these findings.
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