N. fowleri invades the
central nervous system via the nose, specifically through the
olfactory mucosa of the nasal tissues. This usually occurs as the result of the introduction of water that has been contaminated with
N. fowleri into the nose during activities such as swimming, bathing or
nasal irrigation. The amoeba follows the
olfactory nerve fibers through the cribriform plate of the
ethmoid bone into the skull. There, it migrates to the
olfactory bulbs and subsequently other regions of the brain, where it feeds on the
nerve tissue. The organism then begins to consume cells of the brain, piecemeal through
trogocytosis, by means of an
amoebostome, a unique actin-rich sucking apparatus extended from its cell surface. It then becomes
pathogenic, causing primary amoebic meningoencephalitis (PAM or PAME). Additionally, the cytokines may act on the
vascular organ of the lamina terminalis, leading to upregulation of
prostaglandin E2 contributing to hyperthermia. Further, the release of cytokines,
exotoxins released by the pathogens, and an increase in
intracranial pressure stimulate the
nociceptors in the
meninges Specifically, the olfactory nerve and bulbs become necrotic and hemorrhagic. Spinal flexion leads to
nuchal rigidity, or stiff neck, due to the stretching of the inflamed meninges. The increase in intracranial pressure stimulates the
area postrema to create nausea sensations, which may lead to
brain herniation and damage to the
reticular formation. Ultimately, the increase in cerebrospinal fluid from inflammation of the meninges increases intracranial pressure to an extent that leads to the destruction of the central nervous system. Although the exact pathophysiology behind the seizures caused by PAM is unknown, it is speculated that the seizures arise from altered meningeal permeability caused by increased intracranial pressure. ==Pathogenesis==