BIRMINGHAM, Ala. - In contrast to the general belief that the airways of an infant are sterile until after birth, University of Alabama at Birmingham researchers and colleagues have found that the infant airway is already colonized with bacteria or bacterial DNA when a baby is born -- and this is true for infants born as early as 24 weeks gestation.
How microbes get into the airways and the purpose of this pre-birth colonization are still unclear, but the pattern of colonization appears to have an important link to later severe neonatal lung disease.
An early microbial imbalance, or dysbiosis, is predictive for the development of bronchopulmonary dysplasia, or BPD, a chronic lung disease of prematurity. The extremely low birth-weight, or ELBW, infants in this study had an average birth weight of 1 pound, 8 ounces. Researchers found that the ELBW infants who went on to develop life-threatening BPD showed abnormal microbial colonization patterns at birth, as compared to pre-term infants who did not get BPD.
"Right at birth, your respiratory microbiome can possibly predict your risk for BPD," said Charitharth Vivek Lal, M.D., assistant professor in the UAB Pediatrics Division of Neonatology and the lead investigator of this study.
The study also suggests that the 'healthy' pattern of colonization seen in the BPD-resistant ELBW infants -- with increased abundance of Lactobacillus -- is protective.
"We speculate that the early airway microbiome may prime the developing pulmonary immune system, and dysbiosis in its development may set the stage for subsequent lung disease," the researchers say in their paper in Scientific Reports, one of the Nature Publishing Group journals. "Should a disordered airway microbiome prove to be involved in the pathogenesis of disease, it will be of immediate interest to attempt to develop novel therapeutic interventions."
Lal says this is the first unbiased airway microbiome analysis to be done immediately at birth -- all the early saline aspirates from the tracheas of the newborns were collected at or within six hours of delivery.
It is also the only infant airway microbiome analysis to be validated at a second medical center. After the first group of 23 ELBW infants and 10 full-term infants were studied at the Regional Neonatal Intensive Care Unit, UAB Women & Infants Center, samples from a second group of 14 ELBW infants were studied in collaboration with Vineet Bhandari, M.D., at Drexel University College of Medicine, Philadelphia.
About half of the ELBW infants at both sites, all of them extremely pre-term, later developed BPD. The differences in the microbiomes between infants who were BPD-resistant and BPD-predisposed were similar for infants in both Birmingham and Philadelphia.
Extremely premature infants are at risk for BPD, which is the most common lung pathology of these tiny infants and a significant cause of morbidity, mortality and health care expenditures. Adults and children who had BPD as infants have lungs that failed to develop properly and are more prone to worse lung function, asthma, lung infections and pulmonary hypertension.
The researchers also looked at the airway microbiomes of 18 ELBW infants with established BPD and found that their microbiomes had a decreased diversity of types of microbes, and the pattern was very different from those of ELBW infants shortly after birth or full-term infants at birth.
As to specific groups of microbes, the phylum Proteobacteria, which includes bacteria like E. coli, appeared to be involved in BPD pathology, and the genus Lactobaccillus, part of the phylum Firmicutes, appeared to be involved in disease protection.
Lal and colleagues found decreased Lactobacillus abundance in the airway microbiomes of 10 infants born to mothers who had chorioamnionitis -- an infection of the membranes of the placenta and an independent risk factor for BPD -- as well as decreased Lactobacillus abundance at birth in the airways of the BPD-predisposed, ELBW infants, as compared to BPD-resistant infants. Research elsewhere has suggested a beneficial role for Lactobacillus against airway diseases and for lung development.
"I predict that researchers will study the use of respiratory probiotics, and the role of the gut-lung microbiome axis in the future," Lal said.
For five ELBW infants who later developed BPD, the researchers collected periodic airway microbiome samples from birth through 9 weeks and saw extremely similar patterns of change in the microbiomes over time.
As for the source of the microbes, Lal and colleagues wrote, "As it is commonly believed that colonization of neonates originates in the birth canal, we were surprised to find that the airway microbiome of vaginally delivered and caesarean section-delivered neonates were similar, which suggests that the microbial DNA in the airways is probably transplacentally derived, consistent with reports that the placenta has a rich microbiome."
The researchers speculate that this transmission of bacteria or bacterial DNA to the in-utero infant could be via blood or amniotic fluid.
Besides Lal, co-authors of the paper, "The Airway Microbiome at Birth," are Colm Travers, Tamas Jilling, Brian Halloran, Waldemar A. Carlo, Jordan Keeley, Gabriel Rezonzew and Namasivayam Ambalavanan, all of the UAB Department of Pediatrics Division of Neonatology; Zubair H. Aghai, Department of Pediatrics, Thomas Jefferson University, Philadelphia; Peter Eipers and Casey Morrow, UAB Department of Cell, Developmental and Integrative Biology; Ranjit Kumar, UAB Center for Clinical and Translational Sciences; and Vineet Bhandari, Department of Pediatrics, Drexel University College of Medicine.
The Regional Neonatal Intensive Care Unit at the UAB Women & Infants Center offers the only Level IV NICU in Alabama and is a part of one of the largest neonatal services in the nation.
Waldemar A. Carlo, M.D., holds the Edwin M. Dixon Endowed Chair in Neonatology at UAB. Namasivayam Ambalavanan, M.D., is the director of the Translational Research in Normal and Disordered Development Program at UAB.