Immunologically, the most
significant surface
proteins include
hemagglutinin (H) and
neuraminidase (N).
Hemagglutinin and
neuraminidase are critical
for virulence, and they
are major targets for the
neutralizing antibodies of
acquired immunity to
influenza. Hemagglutinin
binds to respiratory
epithelial cells, allowing
cellular infection.
Neuraminidase cleaves
the bond that holds newly
replicated virions to the
cell surface, permitting
the infection to spread.
Uncomplicated influenza illness
typically resolves after 3—7
days for the majority of persons,
although cough and malaise can
persist for >2 weeks. However,
influenza virus infections can
cause primary influenza viral
pneumonia; exacerbate
underlying medical conditions
(e.g., pulmonary or cardiac
disease), lead to secondary
bacterial pneumonia, sinusitis,
or otitis media; or contribute to
coinfections with other viral or
bacterial pathogens. Influenza
virus infection also has been
uncommonly associated with
encephalopathy, transverse
myelitis, myositis, myocarditis,
pericarditis, and Reye syndrome
Measles
Prodrome of fever
(as high as 105),
malaise, cough,
coryza, and
conjunctivitis (the
three c’s), a
pathognomic
exanthema (koplik
spots), followed by a
The cause of measles is
the measles virus, a
single-stranded, negative-
sense enveloped RNA
virus of the genus
Morbillivirus
within the
family Paramyxoviridae.
Patient is contagious from 4
days before the rash appears
until 4 days after the rash
appears. Some
immunocompromised patients
do not develop the rash. Acute
encephalitis can occur. Otitis
media, bronchopneumonia,
laryngotracheobronchitis, and
