The importance of airway and lung microbiome in the critically ill
by Ignacio Martin-Loeches, Robert Dickson, Antoni Torres,
Håkan Hanberger, Jeffrey Lipman, Massimo Antonelli, Gennaro de Pascale,
Fernando Bozza, Jean Louis Vincent, Srinivas Murthy, Michael Bauer, John
Marshall, Catia Cilloniz and Lieuwe D. Bos
Critical Care volume 24,
Article number: 537 (2020)
During critical illness, there are a multitude of forces
such as antibiotic use, mechanical ventilation, diet changes and inflammatory
responses that could bring the microbiome out of balance. This so-called
dysbiosis of the microbiome seems to be involved in immunological responses and
may influence outcomes even in individuals who are not as vulnerable as a
critically ill ICU population. It is therefore probable that dysbiosis of the
microbiome is a consequence of critical illness and may, subsequently, shape an
inadequate response to these circumstances.
Bronchoscopic studies have revealed that the carina
represents the densest site of bacterial DNA along healthy airways, with a
tapering density with further bifurcations. This likely reflects the influence
of micro-aspiration as the primary route of microbial immigration in healthy
adults. Though bacterial DNA density grows extremely sparse at smaller airways,
bacterial signal is still consistently detectable in bronchoalveolar lavage
fluid, likely reflecting the fact that lavage via a wedged bronchoscope samples
an enormous surface area of small airways and alveoli. The dogma of lung
sterility also violated numerous observations that long predated
culture-independent microbiology.
The body’s resident microbial consortia (gut and/or
respiratory microbiota) affect normal host inflammatory and immune response
mechanisms. Disruptions in these host-pathogen interactions have been
associated with infection and altered innate immunity.
In this narrative review, we will focus on the rationale and
current evidence for a pathogenic role of the lung microbiome in the
exacerbation of complications of critical illness, such as acute respiratory
distress syndrome and ventilator-associated pneumonia.
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