Babesiosis pathophysiology: Difference between revisions
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Note that unlike the ''[[Plasmodium]]'' parasites that cause malaria, ''Babesia'' species lack an exo-erythrotic phase, so the liver is usually not affected. | Note that unlike the ''[[Plasmodium]]'' parasites that cause malaria, ''Babesia'' species lack an exo-erythrotic phase, so the liver is usually not affected. | ||
==Pathophysiology== | |||
===Pathogenesis=== | |||
The Babesia microti life cycle involves two hosts, which include a rodent, primarily the white-footed mouse, Peromyscus leucopus, and a tick in the genus Ixodes. | |||
# During a blood meal, a Babesia-infected tick introduces sporozoites into the mouse host. | |||
# Sporozoites enter erythrocytes and undergo asexual reproduction (budding). | |||
# In the blood, some parasites differentiate into male and female gametes, although these cannot be distinguished by light microscopy. | |||
# The definitive host is the tick. Once ingested by an appropriate tick | |||
# Gametes unite and undergo a sporogonic cycle resulting in sporozoites. | |||
# Humans enter the cycle when bitten by infected ticks. During a blood meal, a Babesia-infected tick introduces sporozoites into the human host. | |||
# Sporozoites enter erythrocytes and undergo asexual replication (budding). | |||
# Multiplication of the blood-stage parasites is responsible for the clinical manifestations of the disease. | |||
# Humans usually are dead-end hosts. However, human-to-human transmission is well recognized to occur via contaminated blood transfusions. | |||
===Life Cycle=== | ===Life Cycle=== | ||
Revision as of 15:34, 20 November 2012
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Babesiosis Microchapters |
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Diagnosis |
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Treatment |
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Case Studies |
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Babesiosis pathophysiology On the Web |
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American Roentgen Ray Society Images of Babesiosis pathophysiology |
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Risk calculators and risk factors for Babesiosis pathophysiology |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
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Overview
Babesia parasites reproduce in red blood cells, where they can be seen as cross-shaped inclusions (4 merozoites asexually budding but attached together forming a structure looking like a "Maltese Cross") and cause hemolytic anemia, quite similar to malaria.
Note that unlike the Plasmodium parasites that cause malaria, Babesia species lack an exo-erythrotic phase, so the liver is usually not affected.
Pathophysiology
Pathogenesis
The Babesia microti life cycle involves two hosts, which include a rodent, primarily the white-footed mouse, Peromyscus leucopus, and a tick in the genus Ixodes.
- During a blood meal, a Babesia-infected tick introduces sporozoites into the mouse host.
- Sporozoites enter erythrocytes and undergo asexual reproduction (budding).
- In the blood, some parasites differentiate into male and female gametes, although these cannot be distinguished by light microscopy.
- The definitive host is the tick. Once ingested by an appropriate tick
- Gametes unite and undergo a sporogonic cycle resulting in sporozoites.
- Humans enter the cycle when bitten by infected ticks. During a blood meal, a Babesia-infected tick introduces sporozoites into the human host.
- Sporozoites enter erythrocytes and undergo asexual replication (budding).
- Multiplication of the blood-stage parasites is responsible for the clinical manifestations of the disease.
- Humans usually are dead-end hosts. However, human-to-human transmission is well recognized to occur via contaminated blood transfusions.
Life Cycle
Images
