Transcript Bacillus

Bacillus
Saprophytic
B.cereus
B.subtilis
B.megaterium
B.Circulans
Pathogenic
B.anthracis
B.anthracis
It is aerobic G+ve, large ,square-ended 
(rectangular)bacilli with oval central spores, non
motile, capsulated, arranged singly or in short chains,
the organism grows well on blood agar. Hemolysis is
uncommon with B.anthracis but common with
saprophytic bacilli. If the colonies are looked under
microscopic lens. They will appear as apiece of curled
hair. The colony is composed of continuous chain of
bacilli. The colony is described as "Medusa- head", this
character is useful for DX & identification of the
colony. By G.stain, some spores will be seen in
between the vegetative cells and these spores appear
as empty spaces with out stain. The spores usually
ْresist boiling & some chemicals & dry heat of 140C
but they are destroyed by autoclaving (moist heat) for
15 min.
Biochemical reaction
Glucose , sucorose & maltose are 
fermented with production of acid
only. The bacilli are catalase+ve and
reduce nitrates to nitrites.
Antigens
C.W Ag 
Capsular Ag. 
Somatic Ag 
Types of anthrax
There are three clinical types of anthrax 
based on the route of infection
1-Skin or coetaneous anthrax (Malignant 
pustule)
2- Respiratory or pulmonary anthrax (wool 
sorters' disease)
3- Intestinal anthrax (rare) in primitive or 
poor society. Eat meat of infected
animals 

Pathogenesis
Anthrax is a zoonosis. The portal of entry is the 
respiratory tract, a cut in skin or the mouth when
spores enter the human body, they lodge in one place
& starts to germinate they will produce toxins &
enzymes till hemorrhage & oedema are produced .
In susceptible persons, the bacilli resist Φ & spread to
lymphatic to the blood where they multiply freely in
blood & tissues. While in resistant people, there is
more leukocyte response with Φ and decapsulation of
the microorganisms.
Once the organism looses its capsule, it will die easily
because it looses its virulence.



Clinical findings
Skin anthrax: a papule first develops within 12-36 hrs 
after entry of the organisms or spores through a
scratch. This papule rapidly changes into a vesicle,
then a pustule, and finally a necrotic ulcer from which
the infection may disseminate. Giving rise to
septicemia.
Respiratory anthrax:: In inhalation anthrax , early 
manifestations may be mediastinitis, sepsis,
meningitis, or hemorrhagic pulmonary edema.
Hemorrhagic pneumonia with shock is a terminal
event.
Intestinal anthrax:: Ingestion of spores cause severe 
enteritis accompanied by bloody diarrhea with high
fatality.
Hence, all types of anthrax, if not treated in time, 
progress to septicemia and death occurs from
overwhelming infection.
Lab DX
Specimens: Pus, Blood, swabs, fluid, sputum
Smear 
Culture: 
1-Medusa head 
2-fir tree appearance 
3-curled hair 
Animal inoculation 
Serodiagnosis 

Treatment
B.anthracis

Pencillin, ciprofloxacin, erythromycin,
tetracycline
Other Bacillus spp: 
Vancomycin, ciprofloxacin 
