Introduction
Background
Babesiosis is an intraerythrocytic parasitic infection caused by protozoa of the genus Babesia and transmitted through the bite of the Ixodes tick, the same vector responsible for transmission of Lyme disease. While most cases are tick-borne, transfusion and transplacental transmission have been reported. In the United States, babesiosis is usually an asymptomatic infection in healthy individuals. Several groups of patients become symptomatic, and, within these subpopulations, significant morbidity and mortality occur. The disease most severely affects patients who are elderly, immunocompromised, or asplenic. Among those symptomatically infected, the mortality rate is 10% in the United States and 50% in Europe.
Pathophysiology
Babesiosis is a zoonotic disease maintained by the interaction of tick vectors, transport hosts, and animal reservoirs. The primary vectors of the parasite are ticks of the genus Ixodes. In the United States, the black-legged tick, Ixodes scapularis (also known as Ixodes dammini) is the primary vector for the parasite; in Europe, Ixodes ricinus appears to be the primary tick vector. In each location, the Ixodes tick vector for Babesia is the same vector that locally transmits Borrelia burgdorferi, the agent implicated in Lyme disease.
Ixodes scapularis, tick vector for babesiosis. Courtesy of the Centers for Disease Control and Prevention.
The primary US animal reservoir is the white-footed mouse, Peromyscus leucopus. Additionally, white-tailed deer serve as transport hosts for the adult tick vector, I scapularis. In Europe, the primary animal reservoir is cattle.
The Ixodid ticks ingest Babesia during feeding from the host, multiply the protozoa in their gut wall, and concentrate it in their salivary glands. The tick inoculates a new host when feeding again. The parasite then infects red blood cells (RBCs) and differentiated and undifferentiated trophozoites are produced. The former produce 2-4 merozoites that disrupt the RBC and go on to invade other RBCs. This leads to hemolytic anemia, thrombocytopenia, and atypical lymphocyte formation. Alterations in RBC membranes cause decreased conformability and increased red cell adherence, which can lead to development of noncardiac pulmonary edema and acute respiratory distress syndrome (ARDS) among those severely affected.1
Frequency
United States
The first US case of babesiosis was reported on Nantucket Island in 1966. An increasing trend over the past 30 years may be the result of restocking of the deer population, curtailment of hunting, and an increase in outdoor recreational activities. Between 1968 and 1993, more than 450 cases of Babesia infections were confirmed in the United States. However, the actual prevalence of this disease is unknown because most infected patients are asymptomatic.
International
The first case of human babesiosis was reported in 1957 from the former Yugoslavia in an asplenic farmer. Approximately 40 cases have been reported since then, mostly in Ireland, the United Kingdom, and France. Sporadic case reports of babesiosis in Japan, Korea, China, Mexico, South Africa, and Egypt have also been documented.
Mortality/Morbidity
Babesiosis exists as a spectrum of disease in 3 distinct groups: (1) asymptomatic infection, (2) a mild/moderate viral-like syndrome, and (3) severe disease with a fulminant course resulting in death or persistent relapsing course.1
The US mortality rate is significant.
- Twenty-five percent of adults and 50% of children infected with babesiosis are asymptomatic and/or improve spontaneously without treatment.
- Fewer than 10% of patients with babesiosis have died in the United States, mostly composed of elderly or asplenic patients.
- Deaths have been reported from transfusion-transmitted babesiosis within the immunocompromised population in areas where Babesia infection is not endemic.2
- Approximately 20% of patients with babesiosis are co-infected with Lyme disease. These patients experience more severe symptoms for a longer duration than those with either disease alone.
In Europe, babesiosis is a life-threatening disease.
- Fifty-three percent of infected patients become comatose and die.
- Eighty-three percent of infected patients are asplenic.
Race
Babesiosis has no predilection for race.
Sex
The male-to-female ratio is about 1:1.
Age
Babesiosis affects all age groups with similar frequency; however, patients older than 50 years are at increased risk for severe infection and death.
Clinical
History
Patients report a history of travel to an endemic area between the months of May and September. This is the period during which the Ixodes tick is in its infectious nymph stage; however, most do not recall the tick bite. The incubation period is between 1 and 4 weeks. The signs and symptoms mimic malaria and range in severity from asymptomatic to septic shock.
- Symptoms
- Generalized weakness
- Fatigue
- Depression
- Fever
- Anorexia and weight loss
- CNS - Headache, photophobia, neck stiffness, altered sensorium
- Pulmonary - Cough, shortness of breath
- GI - Nausea, vomiting, abdominal pain
- Musculoskeletal - Arthralgia and myalgia
- Renal - Dark urine
Physical
Physical examination findings of babesiosis can include the following:
- Fever
- Rigors
- Diaphoresis
- Altered mental status
- Renal insufficiency/failure
- Pulmonary edema
- Hepatosplenomegaly
- Spontaneous splenic rupture3
- Jaundice
- Shock
Causes
More than 100 species of Babesia exist, but only a small number of species are known to be responsible for the majority of symptomatic disease. The causative agent of babesiosis varies according to geographic region.
- In the United States, human infection with Babesia species is primarily due to Babesia microti, found mostly in northeastern and midwestern states. A few cases have been reported in Missouri, California, and Washington and are found to be caused by Babesia -like agents named after their geographic location, MO1 (Missouri), CA-1 (California), and WA-1 (Washington).
- In Europe, the causative agent of babesiosis is typically Babesia divergens, though B microti and B microti -like agents have been identified.
- Several reported cases of infection via blood transfusions from donors who lived in or traveled to an endemic area have been documented. All of these cases have occurred in the United States with the exception of one patient in Canada (acquired from a donor who became infected while in the United States) and one in Japan. The rate of acquiring B microti from a unit of packed red cells has been estimated to be 1 in 600-1800 in endemic areas.
- Case reports of transplacental/perinatal transmission have been documented.
More on Babesiosis |
Overview: Babesiosis |
| Differential Diagnoses & Workup: Babesiosis |
| Treatment & Medication: Babesiosis |
| Follow-up: Babesiosis |
| Multimedia: Babesiosis |
| References |
| Further Reading |
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References
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Further Reading
Clinical guidelines
Infectious Diseases Society of America practice guidelines for clinical assessment, treatment and prevention of Lyme disease, human granulocytic anaplasmosis, and babesiosis. Wormser GP, Dattwyler RJ, Shapiro ED, Halperin JJ, Steere AC, Klempner MS, Krause PJ, Bakken JS, Strle F, Stanek G, Bockenstedt L, Fish D, Dumler JS, Nadelman RB. The clinical assessment, treatment, and prevention of lyme disease, human granulocytic anaplasmosis, and babesiosis: clinical practice guidelines by the Infectious Diseases Society of America. Clin Infect Dis 2006 Nov 1;43(9):1089-134. PubMed
Keywords
babesiosis, Babesia species, Ixodes tick, parasitic infection, intraerythrocytic parasitic infection, tick bite, hemolytic anemia, thrombocytopenia, atypical lymphocyte formation, acute respiratory distress syndrome, ARDS, Lyme disease, Ixodes scapularis, white-tailed deer, white-footed mouse, Peromyscus leucopus, adult tick vector




Overview: Babesiosis