ACE receptors are affected in severe 
acute respiratory distress syndrome related coronaviruses. ACE genes are directly related to the morbidity and mortality of those with 
cystic fibrosis. The thick, sticky 
mucus in the respiratory, and digestive systems, is seen in the 
inherited disease cystic fibrosis. Viral induced sticky 
mucus in the respiratory and digestive systems can also be appreciated as a response to viral pathogens where the cycle of 
mucus production 
in vivo induces the recruitment of more mucus production to the extent that cellular damage occurs within the lower respiratory track requiring 
intubation as a 
life saving measure. In the most severe cases mechanical 
intubation fails due to the fact that no control over the recruitment of mucus production was achieved at the onset. SARS 
pathology shows inflammatory exudation in the alveoli and 
interstitial tissue, with 
hyperplasia of 
fibrous tissue and 
fibrosis. Inherited 
cystic fibrosis pathology shows atelectasis, mucoid impaction, acute and chronic 
inflammation, 
bronchiectasis, 
cyst formation, and 
fibrosis widespread. A virally induced disorder in relations to ACE2 receptors can be treated successfully at the 
early onset with inherited cystic 
fibrosis disease mimicking techniques with the efforts of minimizing the activity and utilization of the ACE2 
receptor. 
Cystic fibrosis lung infections, and opportunistic pathogens contribute to chronic 
airway inflammation that is characterized by neutrophil / 
macrophage infiltration, 
cytokine release and 
ceramide accumulation. In terms of virally induced forms off ACE2 
receptor pathologies, as it related to 
coronavirus such as Covid 19, presumably 
ceramide precursors which aid in 
intracellular transport of the 
virus into the 
cell via 
inflammation and remodeling is present in alveolar tissues of the 
lung in patients with cystic fibrosis while the same 
pathology occurs in patients with virally induced forms of ACE2 pathology which to often progresses to SARS or 
ARDS.