Interdisciplinary Perspectives on Infectious Diseases

Interdisciplinary Perspectives on Infectious Diseases / 2009 / Article
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Parasitic Diseases, Diagnostic Approaches, and Therapies

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Volume 2009 |Article ID 984568 |

Edouard Vannier, Peter J. Krause, "Update on Babesiosis", Interdisciplinary Perspectives on Infectious Diseases, vol. 2009, Article ID 984568, 9 pages, 2009.

Update on Babesiosis

Academic Editor: Louis M. Weiss
Received12 Mar 2009
Accepted14 May 2009
Published27 Aug 2009


Human babesiosis is an emerging tick-borne infectious disease caused by intraerythrocytic protozoan species of the genus Babesia with many clinical features similar to those of malaria. Over the last 50 years, the epidemiology of human babesiosis has changed from a few isolated cases to the establishment of endemic areas in the northeastern and midwestern United States. Episodic cases are reported in Europe, Asia, Africa, and South America. The severity of infection ranges from asymptomatic infection to fulminant disease resulting in death, although the majority of healthy adults experience a mild-to-moderate illness. People over the age of 50 years and immunocompromised individuals are at the highest risk of severe disease, including those with malignancy, HIV, lacking a spleen, or receiving immunosuppressive drugs. Asymptomatic carriers present a blood safety risk when they donate blood. Definitive diagnosis of babesial infection generally is made by microscopic identification of the organism on thin blood smear, amplification of Babesia DNA using PCR, and detection of Babesia antibody in acute and convalescent sera. Specific antimicrobial therapy consists of atovaquone and azithromycin or clindamycin and quinine. Exchange transfusion is used in severe cases. The use of multiple prevention strategies is recommended and consists of personal, residential, and community approaches.

1. Introduction

Human babesiosis is an emerging tick-borne infectious disease caused by an intraerythrocytic protozoan and has many clinical features similar to those of malaria. The parasite was first described in cattle by Babes in 1888 [1]. The first human case was described in 1957 [2]. Over the past 50 years, the epidemiology of the disease has changed from a few isolated cases to the establishment of endemic areas in southern New England, New York, New Jersey, and the northern Midwest [38]. Isolated cases are reported over a wide geographic range in Europe, Asia, Africa, and South America [917]. We will review the epidemiology, clinical characteristics, diagnosis, and treatment of infections caused by the four Babesia species that most commonly infect people: B. microti, B. duncani, B. divergens, and B. venatorum.

2. Epidemiology

2.1. United States
2.1.1. B. microti Infection

The most common cause of human babesiosis is Babesia microti, a Babesia of mice and other small rodents that is endemic in the United States [58]. Most cases occur along the northeastern seaboard. The first confirmed case was a normosplenic individual on Nantucket Island off the coast of Massachusetts [18]. Additional cases were soon identified and the disease became known as Nantucket fever. Other islands off the coast of southern New England subsequently became recognized as endemic areas, including Martha’s Vineyard, the Elizabeth Islands, Block Island, Shelter Island, the eastern part of Long Island, and Fire Island [19]. Endemic areas on the mainland include Cape Cod, the southwestern counties of Rhode Island, and southeastern Connecticut [6, 19, 20]. Babesiosis has been diagnosed in individuals from the Lower Hudson Valley (Westchester, Putnam, Dutchess, and Columbia counties) in New York State, and is endemic in New Jersey [2123]. B. microti is also the etiologic agent of babesiosis in the northern midwestern region of the United States, particularly in Wisconsin and Minnesota [2426]. A few isolated cases have been noted in Indiana [27, 28]. Human babesiosis due to B. microti recently has been reported from Europe while B. microti-like species have been described as the cause of infection in people living in Asia [13, 17, 29].

The distribution of B. microti overlaps with that of Borrelia burgdorferi, the agent of Lyme disease, as both organisms are transmitted by Ixodes scapularis in the United States [19, 30]. Although the geographic distribution of babesiosis appears to be restricted to certain foci within the areas of endemicity for B. burgdorferi, the endemic range is expanding. For this reason and because the number of reported cases has dramatically increased over the last two decades, babesiosis is recognized as an emerging infectious disease [8, 31, 32]. The increase in incidence has often been attributed to the expansion of the deer population because these vertebrates are the primary host for adult ticks, although they are not competent reservoirs for B. microti. Other factors include better awareness of the disease by local physicians, an encroachment of humans on wildlife habitat, and increasing travel of immunosuppressed individuals to endemic areas.

Although most B. microti infections are acquired by tick bites from May through October, at least 70 patients in the United States have acquired babesiosis by transfusion of contaminated blood products from asymptomatic donors [3336]. Blood products typically are fresh or frozen packed red blood cells, although one case has been attributed to platelet transfusion. Several cases of neonatal babesiosis have been reported, and these were acquired by tick bite, transfusion, or transplacental transmission [37, 38].

2.1.2. B. duncani Infection

B. duncani is the name given to the previously designated WA1 Babesia [3]. All nine documented cases of B. duncani infection have occurred on the west coast of the United States. Two people acquired the babesial infection by transfusion of blood products while the remaining cases were attributed to tick bites [39, 40]. One blood donor was asymptomatic at time of donation whereas the other reported a 10-day episode of nausea. Both recipients were immunologically at risk; one was an elderly man and the other was a premature infant. Among the five other symptomatic cases, one was a young normosplenic adult living in Washington State (index case) whereas four were splenectomized and lived in California [41, 42]. One of these four men died. Sequence analysis of the entire 18S rRNA gene indicated that the organisms causing babesial illness in the index case from Washington State and in the two cases acquired by blood transfusion were phylogenetically indistinguishable whereas the organisms acquired by three of the four splenectomized cases in California formed a separate but closely related phylogenetic group [3, 43]. The seroprevalence of B. duncani infection has been found to vary from 4% to 17% [41].

2.1.3. B. divergens-Like Infection

B. divergens-like organisms have been identified in three cases, two from the Midwest (Missouri and Kentucky) and one from Washington State [4, 44, 45]. All three patients had risk factors for severe babesial disease, namely, age greater than 50 years and splenectomy. Sequence analysis of the entire 18S rRNA gene indicated that the Missouri isolate (MO1) and the Kentucky isolate (KY) were identical to each other and to piroplasms found in eastern cottontail rabbits on Nantucket Island [46]. These isolates differed by a few bp in their 18S rRNA gene from the isolate of the Washington State patient and from the B. divergens organisms of European cattle. Because the piroplasms isolated from eastern cottontail rabbits are not infectious to cattle, the isolates obtained from the three US patients are now referred to as B. divergens-like organisms.

2.2. Europe
2.2.1. B. divergens Infection

About 40 cases of B. divergens infection have been documented in Europe, mostly from countries with extensive cattle industry such as France, Ireland, and Great Britain [4749]. Cases have sporadically been reported from Sweden, Switzerland, Spain, Portugal, and Croatia (index case). Nearly all patients were splenectomized prior to the onset of Babesia infection. Because cattle are the reservoir for B. divergens, persons at risk of contracting babesiosis are farmers or people vacationing in rural areas. Limited data suggest that infection with B. divergens can be asymptomatic in normosplenic individuals [47]. There are no reports of B. divergens infection acquired by blood transfusion [49].

2.2.2. B. venatorum (EU1) Infection

Because the advent of PCR allows for molecular characterization of babesial organisms, a new Babesia species has been identified in Europe. Originally referred to as EU1, the name “B. venatorum” was later proposed [12]. B. venatorum, together with B. odocoilei that infects white-tail deer in the United States, form a sister group to that of B. divergens. Three cases of infection with B. venatorum have been documented [12, 50]. All three were men beyond 50 years of age who had been splenectomized. Unlike B. divergens infections that are fulminant and often fatal, B. venatorum infections have varied from mild to severe but have not been fatal.

3. Clinical Characteristics

3.1. B. microti Infection

The severity of B. microti infection is variable, depending primarily on the immune status of the host. Several clinical syndromes have been described, including asymptomatic infection, mild-to-moderate viral-like illness, and severe disease with a fulminant course that sometimes results in death or a persistent relapsing illness. Concurrent infection with Lyme disease increases neither the number nor the duration of symptoms of babesiosis [30, 51]. It is unclear whether this is also true of concurrent babesiosis and human granulocytic anaplasmosis.

3.1.1. Asymptomatic Infection

Following transmission of the babesial parasite, the incubation period may last from 1 to 9 weeks [5, 8]. Many people who are infected with B. microti never experience symptoms, as suggested by the disparity between seroprevalence and the number of reported cases. The frequency of asymptomatic B. microti infection was derived from an epidemiologic study of babesiosis carried out on Block Island, Rhode Island [6]. About a third of babesial infections at this site were asymptomatic, including 19% (13 of 67) of adults and 40% (4 of 10) of children [6]. Asymptomatic infection may persist for months or years following resolution of symptomatic babesiosis [36]. It is uncertain whether patients experiencing asymptomatic babesial infection are at risk for any long-term complications. They may transmit the infection if they donate blood [33].

3.1.2. Mild-to-Moderate Illness

Most cases of B. microti infection consist of a mild to moderate viral-like illness. These cases typically begin with a gradual onset of malaise and fatigue followed by intermittent fever and one or more of the following: chills, sweats, headache, arthralgia, myalgia, anorexia, cough, and nausea (Table 1) [30, 5254]. Less commonly noted are gastrointestinal symptoms, weight loss, conjunctival injection, and emotional lability [5357]. On physical examination, fever is commonly observed and pallor, mild splenomegaly or hepatomegaly occasionally may be noted. The illness usually lasts for a week to months, occasionally with prolonged recovery that can last more than a year [30, 36, 53, 56, 57]. Parasitemia may continue even after the patient feels well and rarely may persist for more than two years after the initial episode [36].

SymptomPercentage of outpatients Percentage of inpatients Percentage of all patients


Outpatient cases are from Ruebush et al. [60] and Krause et al. [30]. Inpatient cases are from White et al. [54] and Hatcher et al. [52].
3.1.3. Severe Disease

Severe disease generally occurs in people with underlying immunosuppressive conditions that include HIV, malignancy, immunosuppressive medication, and splenectomy [50, 56, 5860]. On physical examination, jaundice, retinal infarcts, or ecchymoses and petechiae may be noted [55, 58, 61]. The most common complications of severe babesiosis include acute respiratory failure, congestive heart failure, DIC, liver and renal failure, and splenic rupture [52]. A mortality rate of 5% was noted in a retrospective study of 136 patients experiencing B. microti infection on Long Island, New York, only one of whom was known to be immunocompromised [7]. In another study, the mortality rate among patients hospitalized for babesiosis was 9% [52]. The mortality rate is even higher among immunocompromised hosts. In a recent case-control study of 14 patients who were highly immunocompromised, 21% died and the remainder experienced a prolonged, relapsing course of illness, sometimes lasting more than a year, despite multiple courses of standard antibabesial therapy [59]. People 50 years of age and older also are more likely to experience severe babesiosis [52, 54, 62].

3.2. B. duncani Infection

Although studies of infection in hamsters suggest that B. duncani is more pathogenic than B. microti, the small number of reported B. duncani cases does not allow firm conclusions [32]. Of the nine reported cases of B. duncani, one died, one experienced pulmonary edema and renal insufficiency, and the remainder had a relatively mild clinical course or were asymptomatic [3, 39, 40, 42, 63]. Parasitemia ranged from 1% to 54%. Symptoms of B. duncani are similar to those of B. microti and consist of fever, chills, headache, sweats, myalgia, nausea, vomiting, diarrhea, dark urine, and fatigue.

3.3. B. divergens Infection

Nearly all 40 cases of B. divergens infection reported in Europe had been splenectomized and suffered a severe form of babesiosis [4749]. Signs and symptoms begin 1 to 3 weeks after tick transmission and consist of high fever (40-41°C) with severe intravascular hemolysis that results in hemoglobinemia, hemoglobinuria, and jaundice. Headache, shaking chills, intense sweating, myalgia, and abdominal pain are common. More than half the cases experienced a rapid onset of renal failure and pulmonary edema. Ecchymoses, petechiae, congestive heart failure, and coma also have been reported. The illness generally is fulminant, lasting about a week and ending in death in more than a third of patients or in a prolonged convalescence.

3.4. B. venatorum (EU1) Infection

All three reported cases of B. venatorum infection had a history of Hodgkin’s disease and had been splenectomized [12, 50]. One experienced mild babesiosis, whereas two had moderate-to-severe illness. In these two patients, babesiosis was concurrent with a relapse of nodular lymphocyte-predominant Hodgkin’s lymphoma or with stage IIIA diffuse large B cell lymphoma. All three patients were admitted to the hospital and recovered after antibabesial therapy. One had a prolonged relapsing illness that eventually cleared. Peak parasitemia ranged from 1% to 30%. Symptoms included fever, dark urine, fatigue, chills, headache, confusion, jaundice, sweats, and shortness of breath.

4. Diagnosis

The diagnosis of babesiosis should be considered in patients who live or travel in areas that are endemic for babesiosis and who experience a viral-like illness in the late spring, summer, or autumn (Table 2). As the symptoms and signs are relatively nonspecific, laboratory testing is required for diagnosis. In some cases, physicians may choose to obtain screening laboratory testing such as a CBC, platelet count, and liver enzymes before ordering specific diagnostic tests. Most cases of babesiosis are accompanied by some degree of hemolytic anemia with an elevated reticulocyte count. Thrombocytopenia is common. The leukocyte count usually is normal to slightly decreased. Elevated serum liver enzymes occur in about half the patients. Proteinuria and an elevated blood urea nitrogen and serum creatinine also may be noted. Specific laboratory tests that are used for the diagnosis of babesiosis are described below. Specific tests for concurrent Lyme disease and human granulocytic anaplasmosis should be performed in patients presenting with clinical manifestations that suggest coinfection, such as an erythema migrans type rash or neutropenia.


– Residence in or travel to an area endemic for babesiosis
Ixodes tick bite
– History of recent blood transfusion from a donor living or traveling in a Babesia endemic area


– Fever, fatigue, chills, sweats, headache, myalgia, anorexia, cough, arthralgia, nausea
– Less common: emotional lability and depression, hyperesthesia, sore throat, abdominal pain, conjunctival injection, photophobia, weight loss

Signs on physical examination

– Fever
– Splenomegaly, hepatomegaly, pallor

Common laboratory diagnostic procedures

– Identification of Babesia on Giemsa stained peripheral blood smears
– Amplification of Babesia DNA in blood using polymerase chain reaction
– Four-fold rise in Babesia antibody in acute or convalescent sera or identification of serum Babesia IgM antibody

4.1. Microscopic Identification

Specific diagnosis of babesiosis can be made by microscopic identification of the organism using Giemsa stains of thin blood smears [64, Figure 1]. Thick blood smears also may be performed but the babesial organisms are small and may be difficult to visualize. B.  microti and other Babesia spp. are round, oval, or pear-shaped and have a blue cytoplasm with a red chromatin. The ring form is most common and can be mistaken for early stage ring forms of Plasmodium falciparum. Multiple thin blood smears should be examined when only a few erythrocytes are infected, particularly in the early stage of illness when most people seek medical attention. PCR and serology should be performed if only a few ring-like structures are observed. Parasitemia seldom exceeds 5% in normal hosts but may be as high as 85% in asplenic individuals [55]. B. divergens and related organisms often appear as paired piriforms in human red blood cells. Pairs of B. divergens and B. divergens-like organisms are located in a subcentral, central, or peripheral position [46]. B. venatorum are morphologically indistinguishable from B. divergens [12, 50]. The tetrad form, referred to as a Maltese cross, is pathognomonic of small Babesia spp. such as B. microti and B. duncani [3]. B. duncani display more tetrad forms than B. microti.

4.2. Polymerase Chain Reaction

The polymerase chain reaction (PCR) provides a highly sensitive and specific test for detecting Babesia DNA in blood and identifies the Babesia species [65, 66]. Rigorous precautions are required to avoid false positive results. PCR is recommended when parasites are not identified on blood smears but symptoms and history are suggestive of babesiosis. As with all Babesia specific tests, it should only be performed in laboratories that are experienced in such testing and meet the highest laboratory performance standards.

4.3. Serology

Babesial infection can be confirmed by serologic testing using the indirect immunofluorescent assay (IFA) [67, 68]. During the acute phase of B. microti illness, IgG titers usually exceed and decline to or less within 8 to 12 months. Thus, IgG titers of or greater usually signify active or recent infection [69]. The detection of IgM is indicative of recent infection [67]. Although seroconversion occurs in virtually all immunocompetent individuals infected with B. microti, the diagnosis of active babesial infection based on serologic findings alone is suspect. Serology usually is not considered in cases attributed to B. divergens because the illness becomes fulminant before antibody can be detected. Sera from patients infected with B. divergens-like organisms or B. venatorum cross-react with antigen from B. divergens [41, 42, 63]. Sera from patients infected with B. duncani or related organisms do not cross-react with B. microti antigen [41, 42]. Sera from patients infected with one of several Babesia species may cross-react with antigen from Plasmodium species, but titers are almost always low ( or lower).

4.4. Amplification of Babesia in Laboratory Animals

Babesia parasitemia can also be detected by injecting patient blood by the intravenous or intraperitoneal route into such laboratory animals as hamsters or gerbils [65]. This test is only available in a few research laboratories and is seldom useful for diagnosis. B. microti is easily detected in hamsters whereas B. duncani is often lethal in these animals [32]. This approach is not suited for rapid diagnosis, as Babesia usually do not appear in the blood of the laboratory animal until two to four weeks after inoculation.

5. Treatment

5.1. B. microti Infection
5.1.1. Mild-to-Moderate Disease

Most people infected with B. microti experience mild-to-moderate disease and can be successfully treated with a combination of atovaquone and azithromycin administered for 7 to 10 days [70, 71]. This combination was shown to be as effective as clindamycin and quinine, the first drug combination used in the treatment of babesiosis. The two regimens were directly compared in adults in a prospective, nonblinded randomized control trial [71]. While these drug combinations were similarly effective in clearing parasitemia and achieving resolution of symptoms, adverse effects were reported in 15% of subjects who received atovaquone and azithromycin compared with 72% of subjects who received clindamycin and quinine. The most common side effects associated with atovaquone and azithromycin were diarrhea and rash while those of clindamycin and quinine were tinnitus, hearing loss, and diarrhea. About a third of the subjects receiving clindamycin and quinine suffered from adverse reactions that were severe enough to require a decrease in dosage or discontinuing the medication. Only 2% of subjects taking atovaquone and azithromycin experienced such severe drug reactions. Although the atovaquone and azithromycin combination has not been studied in a controlled trial for pediatric use, cure has been achieved with use of this regimen in a child [72]. Clindamycin and quinine should be substituted for atovaquone and azithromycin when patients do not respond well to atovaquone and azithromycin.

5.1.2. Severe Disease

The combination of clindamycin (administered intravenously) and quinine given for 7 to 10 days is the treatment of choice for severe babesiosis. (Table 3) [70, 73]. Exchange red blood cell transfusion is indicated for all babesiosis patients experiencing heavy parasitemia ( 10%) or who have significant pulmonary, renal, or hepatic compromise [7477]. Partial or complete exchange transfusion rapidly decreases parasite burden and removes toxic byproducts of Babesia infection.


Atovaquone and azithromycin
AtovaquoneAdult: 750 mgEvery 12 hours
Child: 20 mg/kgEvery 12 hours
(maximum 750 mg/dose)
AzithromycinAdult: 500 to 1000 mgOn day 1
250 to 1000 mgOn subsequent days
Child: 10 mg/kgOn day 1
(maximum 500 mg/dose)
5 mg/kgOn subsequent days
(maximum 250 mg/dose)
Clindamycin and quinine
ClindamycinAdult: 600 mgEvery 8 hours
Child: 7–10 mg/kgEvery 6–8 hours
(maximum 600 mg/dose)
Intravenous administration
Adult: 300–600 mgEvery 6 hours
Child: 7–10 mg/kgEvery 6–8 hours
(maximum 600 mg/dose)
QuinineAdult: 650 mgEvery 6–8 hours
Child: 8 mg/kgEvery 8 hours
(maximum 650 mg/dose)

All antibiotics are administered by mouth unless otherwise specified. All doses are administered for 7 to 10 days except for persistent relapsing infection (see text). For immunocompromised patients experiencing babesiosis, successful outcome has been reported using atovaquone combined with higher doses of azithromycin (600–1000 mg per day) [78].
Complete or partial exchange transfusion should be considered for treatment of severe babesiosis.
5.1.3. Persistent Relapsing Disease

Babesial infection may persist and symptoms relapse in people with significant underlying immunosuppression despite standard combination antimicrobial therapy [59, 77]. Atovaquone-proguanil (250 mg–100 mg) was used to eradicate parasitemia in one such patient [77]. In a recent case-control study of chronic babesiosis in 14 highly immunocompromised patients, no single antimicrobial combination was uniformly superior to another in achieving resolution of infection [59]. Rather, cure was associated with duration of therapy for a minimum of six weeks and for at least two weeks after the last positive blood smear. Interestingly, the majority of case patients in the study had underlying B-cell lymphoma and had been treated with the anti-CD20 monoclonal antibody (Rituximab) prior to acute babesial infection, thereby dramatically impairing B-cell activity. It is important to recognize that a 7-to-10 day course of antibabesial therapy is sufficient for many immunocompromised patients. Thus, when acute babesiosis responds to a standard therapeutic course with resolution of symptoms and clearance of parasitemia on blood smear, no further treatment is required. Because immunosuppressed individuals are at increased risk for relapsing babesiosis, close clinical follow-up with repeat blood smears, Babesia PCR, and complete blood counts should be performed.

5.1.4. Asymptomatic Infection

In the unusual event that patients are identified with asymptomatic babesial infection, no treatment should be given unless parasitemia, as determined by blood smear or PCR, persists for longer than three months [70]. In this case, a one-week course of atovaquone and azithromycin should be considered. People who have positive serology, but negative blood smears and negative PCR should not be treated, as they likely have resolved the infection. Immunocompromised patients experiencing persistent asymptomatic parasitemia should have blood smears performed every month or two until they clear the infection.

5.2. B. duncani Infection

Recommended treatment consists of clindamycin and quinine [3, 39, 40, 42, 63]. Red cell exchange transfusion should be considered in the treatment of severe cases [41]. Renal insufficiency may require hemodialysis.

5.3. B. divergens and B. divergens-Like Infections

The morbidity and mortality rate of Babesia divergens infections are high and any such case should be considered a medical emergency [47, 49]. It is recommended that these infections be treated with exchange transfusion and clindamycin and quinine. One mild case of B. divergens infection was successfully treated with the combination of pentamidine and trimethoprim-sulfamethoxazole whereas another only required an abbreviated course of clindamycin and quinine (the quinine was stopped after 4 days) [79, 80]. In both cases, exchange transfusion was not needed. The Babesia divergens-like infections reported from Kentucky and Washington State were successfully treated with clindamycin and quinine or quinidine, but the case from Missouri died despite clindamycin and quinine therapy [4, 44, 45].

5.4. B. venatorum Infection

Of the three cases of B. venatorum infection, one cleared on clindamycin alone [12, 50]. The other two were given clindamycin and quinine. One of these patients was highly immunocompromised and relapsed after clindamycin and quinine was discontinued. He required a prolonged course of atovaquone and azithromycin followed by atovaquone alone for cure. In the third case, blood transfusion was given for massive hemolysis, and the infection eventually cleared following antimicrobial therapy.

6. Prevention

The use of multiple strategies is most likely to be effective for prevention of babesiosis. These include personal, residential, and community approaches [8188]. One obvious personal protective measure is to avoid areas where ticks, mice, and deer are known to thrive, especially from May through October [84]. Immunocompromised people who are at increased risk of severe babesiosis need to avoid such areas. Anyone who may contact foliage in endemic sites should wear clothing that covers the lower part of the body, tuck cuffs of the trousers into stockings, and spray or impregnate clothing with permethrin (Permanone) [86]. DEET-containing products should be applied to the skin if legs remain uncovered. After travel through a high-risk area, a tick check should be performed and attached ticks should be removed as soon as possible by use of tweezers [84]. No data is available on the use of prophylactic antimicrobials after a tick bite to prevent babesiosis nor has a human babesiosis vaccine been developed.

Property modifications can help reduce tick exposure. These include keeping grass mowed, removing leaf litter at the edge of lawns, sealing stonewalls to decrease the number of mice, using plantings that do not attract deer, and fencing to keep deer away [84]. Acaracides can be applied to property, rodents (Damminix or fipronil), or deer (four poster device) [82, 84, 88]. Elimination of the deer population may sharply reduce the risk of babesiosis and other tick-borne infections. Within 3–5 years after deer were eliminated on Great Island off Cape Cod, Massachusetts, the density of I. scapularis ticks fell precipitously [87]. Currently, the Red Cross and other blood donation agencies prohibit people with a history of babesiosis from donating blood in order to prevent transfusion-related cases. Additional measures such as screening blood donors for silent Babesia infection or inactivation of Babesia parasites in units of blood prior to transfusion have been considered but are not yet in use [89, 90].


This review has been made possible thanks to the generous support of The Gordon and Llura Gund Foundation.


  1. V. Babes, “Sur l'hemoglobinurie bacterienne du boeuf,” Comptes Rendus de l'Academie des Sciences, vol. 107, pp. 692–694, 1888. View at: Google Scholar
  2. Z. Skrabalo and Z. Deanovic, “Piroplasmosis in man; report of a case,” Documenta de Medicina Geographica et Tropica, vol. 9, no. 1, pp. 11–16, 1957. View at: Google Scholar
  3. P. A. Conrad, A. M. Kjemtrup, R. A. Carreno et al., “Description of Babesia duncani n.sp. (Apicomplexa: Babesiidae) from humans and its differentiation from other piroplasms,” International Journal for Parasitology, vol. 36, no. 7, pp. 779–789, 2006. View at: Publisher Site | Google Scholar
  4. B. L. Herwaldt, D. H. Persing, E. A. Précigout et al., “A fatal case of babesiosis in Missouri: Identification of another piroplasm that infects humans,” Annals of Internal Medicine, vol. 124, no. 7, pp. 643–650, 1996. View at: Google Scholar
  5. K.-P. Hunfeld, A. Hildebrandt, and J. S. Gray, “Babesiosis: recent insights into an ancient disease,” International Journal for Parasitology, vol. 38, no. 11, pp. 1219–1237, 2008. View at: Publisher Site | Google Scholar
  6. P. J. Krause, K. McKay, J. Gadbaw et al., “Increasing health burden of human babesiosis in endemic sites,” American Journal of Tropical Medicine and Hygiene, vol. 68, no. 4, pp. 431–436, 2003. View at: Google Scholar
  7. S. C. Meldrum, G. S. Birkhead, D. J. White, J. L. Benach, and D. L. Morse, “Human babesiosis in New York state: an epidemiological description of 136 cases,” Clinical Infectious Diseases, vol. 15, no. 6, pp. 1019–1023, 1992. View at: Google Scholar
  8. E. Vannier, B. E. Gewurz, and P. J. Krause, “Human Babesiosis,” Infectious Disease Clinics of North America, vol. 22, no. 3, pp. 469–488, 2008. View at: Publisher Site | Google Scholar
  9. J. B. Bush, M. Isaacson, A. S. Mohamed, F. T. Potgieter, and D. T. de Waal, “Human babesiosis—a preliminary report of 2 suspected cases in South Africa,” South African Medical Journal, vol. 78, no. 11, p. 699, 1990. View at: Google Scholar
  10. I. M. Foppa, P. J. Krause, A. Spielman et al., “Entomologic and serologic evidence of zoonotic transmission of Babesia microti, eastern Switzerland,” Emerging Infectious Diseases, vol. 8, no. 7, pp. 722–726, 2002. View at: Google Scholar
  11. A. Gorenflot, C. Bazin, and P. Ambroise-Thomas, “Human babesiosis. Treatment of severe forms,” La Presse Médicale, vol. 16, no. 22, p. 1099, 1987. View at: Google Scholar
  12. B. L. Herwaldt, S. Cacciò, F. Gherlinzoni et al., “Molecular characterization of a non-Babesia divergens organism causing zoonotic babesiosis in Europe,” Emerging Infectious Diseases, vol. 9, no. 8, pp. 942–948, 2003. View at: Google Scholar
  13. A. Hildebrandt, K.-P. Hunfeld, M. Baier et al., “First confirmed autochthonous case of human Babesia microti infection in Europe,” European Journal of Clinical Microbiology and Infectious Diseases, vol. 26, no. 8, pp. 595–601, 2007. View at: Publisher Site | Google Scholar
  14. J.-Y. Kim, S.-H. Cho, H.-N. Joo et al., “First case of human babesiosis in Korea: detection and characterization of a novel type of Babesia sp. (KO1) similar to ovine Babesia,” Journal of Clinical Microbiology, vol. 45, no. 6, pp. 2084–2087, 2007. View at: Publisher Site | Google Scholar
  15. A. Marathe, J. Tripathi, V. Handa, and V. Date, “Human babesiosis—a case report,” Indian Journal of Medical Microbiology, vol. 23, no. 4, pp. 267–269, 2005. View at: Google Scholar
  16. L. Rios, G. Alvarez, and S. Blair, “Serological and parasitological study and report of the first case of human babesiosis in Colombia,” Revista da Sociedade Brasileira de Medicina Tropical, vol. 36, no. 4, pp. 493–498, 2003. View at: Google Scholar
  17. C.-M. Shih, L.-P. Liu, W.-C. Chung, S.J. Ong, and C.-C. Wang, “Human babesiosis in Taiwan: asymptomatic infection with a Babesia microti-like organism in a Taiwanese woman,” Journal of Clinical Microbiology, vol. 35, no. 2, pp. 450–454, 1997. View at: Google Scholar
  18. K. A. Western, G. D. Benson, N. N. Gleason, G. R. Healy, and M. G. Schultz, “Babesiosis in a Massachusetts resident,” The New England Journal of Medicine, vol. 283, no. 16, pp. 854–856, 1970. View at: Google Scholar
  19. A. Spielman, M. L. Wilson, J. F. Levine, and J. Piesman, “Ecology of Ixodes dammini-borne human babesiosis and Lyme disease,” Annual Review of Entomology, vol. 30, pp. 439–460, 1985. View at: Google Scholar
  20. S. E. Rodgers and T. N. Mather, “Human Babesia microti incidence and Ixodes scapularis distribution, Rhode Island, 1998–2004,” Emerging Infectious Diseases, vol. 13, no. 4, pp. 633–635, 2007. View at: Google Scholar
  21. E. S. Eskow, P. J. Krause, A. Spielman, K. Freeman, and J. Aslanzadeh, “Southern extension of the range of human babesiosis in the Eastern United States,” Journal of Clinical Microbiology, vol. 37, no. 6, pp. 2051–2052, 1999. View at: Google Scholar
  22. S. J. Kogut, C. D. Thill, M. A. Prusinski et al., “Babesia microti, upstate New York,” Emerging Infectious Diseases, vol. 11, no. 3, pp. 476–478, 2005. View at: Google Scholar
  23. B. L. Herwaldt, P. C. McGovern, M. P. Gerwel, R. M. Easton, and R. R. MacGregor, “Endemic babesiosis in another eastern state: New Jersey,” Emerging Infectious Diseases, vol. 9, no. 2, pp. 184–188, 2003. View at: Google Scholar
  24. M. K. Froberg, D. Dannen, N. Bernier, W.-J. Shieh, J. Guarner, and S. Zaki, “Case report: spontaneous splenic rupture during acute parasitemia of Babesia microti,” Annals of Clinical and Laboratory Science, vol. 38, no. 4, pp. 390–392, 2008. View at: Google Scholar
  25. R. K. Pruthi, W. F. Marshall, J. C. Wiltsie, and D. H. Persing, “Human babesiosis,” Mayo Clinic Proceedings, vol. 70, no. 9, pp. 853–862, 1995. View at: Google Scholar
  26. R. W. Steketee, M. R. Eckman, and E. C. Burgess, “Babesiosis in Wisconsin. A new focus of disease transmission,” Journal of the American Medical Association, vol. 253, no. 18, pp. 2675–2678, 1985. View at: Publisher Site | Google Scholar
  27. K. H. Berman, D. E. Blue, D. S. Smith, P. Y. Kwo, and S. Liangpunsakul, “Fatal case of babesiosis in postliver transplant patient,” Transplantation, vol. 87, no. 3, pp. 452–453, 2009. View at: Publisher Site | Google Scholar
  28. D. Blue, V. Graves, L. McCarthy, J. Cruz, S. Gregurek, and D. Smith, “Fatal transfusion-transmitted Babesia microti in the Midwest,” Transfusion, vol. 49, no. 1, p. 8, 2009. View at: Publisher Site | Google Scholar
  29. Q. Wei, M. Tsuji, A. Zamoto et al., “Human babesiosis in Japan: isolation of Babesia microti-like parasites from an asymptomatic transfusion donor and from a rodent from an area where babesiosis is endemic,” Journal of Clinical Microbiology, vol. 39, no. 6, pp. 2178–2183, 2001. View at: Publisher Site | Google Scholar
  30. P. J. Krause, S. R. Telford III, A. Spielman et al., “Concurrent Lyme disease and babesiosis: evidence for increased severity and duration of illness,” Journal of the American Medical Association, vol. 275, no. 21, pp. 1657–1660, 1996. View at: Publisher Site | Google Scholar
  31. P. J. Krause, S. R. Telford III, R. Ryan et al., “Geographical and temporal distribution of babesial infection in Connecticut,” Journal of Clinical Microbiology, vol. 29, no. 1, pp. 1–4, 1991. View at: Google Scholar
  32. A. M. Kjemtrup and P. A. Conrad, “Human babesiosis: an emerging tick-borne disease,” International Journal for Parasitology, vol. 30, no. 12-13, pp. 1323–1337, 2000. View at: Publisher Site | Google Scholar
  33. D. A. Leiby, “Babesiosis and blood transfusion: flying under the radar,” Vox Sanguinis, vol. 90, no. 3, pp. 157–165, 2006. View at: Publisher Site | Google Scholar
  34. D. M. Gubernot, C. T. Lucey, K. C. Lee, G. B. Conley, L. G. Holness, and R. P. Wise, “Babesia infection through blood transfusions: reports received by the US Food and Drug Administration, 1997–2007,” Clinical Infectious Diseases, vol. 48, no. 1, pp. 25–30, 2009. View at: Publisher Site | Google Scholar
  35. J. V. Linden, S. J. Wong, F. K. Chu, G. B. Schmidt, and C. Bianco, “Transfusion-associated transmission of babesiosis in New York State,” Transfusion, vol. 40, no. 3, pp. 285–289, 2000. View at: Publisher Site | Google Scholar
  36. P. J. Krause, A. Spielman, S. R. Telford III et al., “Persistent parasitemia after acute babesiosis,” The New England Journal of Medicine, vol. 339, no. 3, pp. 160–165, 1998. View at: Publisher Site | Google Scholar
  37. D. Esernio-Jenssen, P. G. Scimeca, J. L. Benach, and M. J. Tenenbaum, “Transplacental/perinatal babesiosis,” Journal of Pediatrics, vol. 110, no. 4, pp. 570–572, 1987. View at: Google Scholar
  38. L. M. Fox, S. Wingerter, A. Ahmed et al., “Neonatal babesiosis: case report and review of the literature,” Pediatric Infectious Disease Journal, vol. 25, no. 2, pp. 169–173, 2006. View at: Publisher Site | Google Scholar
  39. B. L. Herwaldt, A. M. Kjemtrup, P. A. Conrad et al., “Transfusion-transmitted babesiosis in Washington state: first reported case caused by a WA1-type parasite,” Journal of Infectious Diseases, vol. 175, no. 5, pp. 1259–1262, 1997. View at: Google Scholar
  40. A. M. Kjemtrup, B. Lee, C. L. Fritz, C. Evans, M. Chervenak, and P. A. Conrad, “Investigation of transfusion transmission of a WA1-type babesial parasite to a premature infant in California,” Transfusion, vol. 42, no. 11, pp. 1482–1487, 2002. View at: Google Scholar
  41. D. H. Persing and P. A. Conrad, “Babesiosis: new insights from phylogenetic analysis,” Infectious Agents and Disease, vol. 4, no. 4, pp. 182–195, 1995. View at: Google Scholar
  42. R. E. Quick, B. L. Herwaldt, J. W. Thomford et al., “Babesiosis in Washington State: a new species of Babesia?” Annals of Internal Medicine, vol. 119, no. 4, pp. 284–290, 1993. View at: Google Scholar
  43. A. M. Kjemtrup, J. Thomford, T. Robinson, and P. A. Conrad, “Phylogenetic relationships of human and wildlife piroplasm isolates in the western United States inferred from the 18S nuclear small subunit RNA gene,” Parasitology, vol. 120, no. 5, pp. 487–493, 2000. View at: Publisher Site | Google Scholar
  44. J. F. Beattie, M. L. Michelson, and P. J. Holman, “Acute babesiosis caused by Babesia divergens in a resident of Kentucky,” The New England Journal of Medicine, vol. 347, no. 9, pp. 697–698, 2002. View at: Publisher Site | Google Scholar
  45. B. L. Herwaldt, G. de Bruyn, N. J. Pieniazek et al., “Babesia divergens-like Infection, Washington State,” Emerging Infectious Diseases, vol. 10, no. 4, pp. 622–629, 2004. View at: Google Scholar
  46. P. J. Holman, “Phylogenetic and biologic evidence that Babesia divergens is not endemic in the United States,” Annals of the New York Academy of Sciences, vol. 1081, pp. 518–525, 2006. View at: Publisher Site | Google Scholar
  47. A. Gorenflot, K. Moubri, E. Precigout, B. Carcy, and T. P. M. Schetters, “Human babesiosis,” Annals of Tropical Medicine and Parasitology, vol. 92, no. 4, pp. 489–501, 1998. View at: Publisher Site | Google Scholar
  48. A. Zintl, J. S. Gray, H. E. Skerrett, and G. Mulcahy, “Possible mechanisms underlying age-related resistance to bovine babesiosis,” Parasite Immunology, vol. 27, no. 4, pp. 115–120, 2005. View at: Publisher Site | Google Scholar
  49. A. Zintl, G. Mulcahy, H. E. Skerrett, S. M. Taylor, and J. S. Gray, “Babesia divergens, a bovine blood parasite of veterinary and zoonotic importance,” Clinical Microbiology Reviews, vol. 16, no. 4, pp. 622–636, 2003. View at: Publisher Site | Google Scholar
  50. K. Haselbarth, A. M. Tenter, V. Brade, G. Krieger, and K.-P. Hunfeld, “First case of human babesiosis in Germany—clinical presentation and molecular characterisation of the pathogen,” International Journal of Medical Microbiology, vol. 297, no. 3, pp. 197–204, 2007. View at: Publisher Site | Google Scholar
  51. P. J. Krause, K. McKay, C. A. Thompson et al., “Disease-specific diagnosis of coinfecting tickborne zoonoses: babesiosis, human granulocytic ehrlichiosis, and Lyme disease,” Clinical Infectious Diseases, vol. 34, no. 9, pp. 1184–1191, 2002. View at: Publisher Site | Google Scholar
  52. J. C. Hatcher, P. D. Greenberg, J. Antique, and V. E. Jimenez-Lucho, “Severe babesiosis in Long Island: review of 34 cases and their complications,” Clinical Infectious Diseases, vol. 32, no. 8, pp. 1117–1125, 2001. View at: Publisher Site | Google Scholar
  53. T. K. Ruebush II, D. D. Juranek, and E. S. Chisholm, “Human babesiosis on Nantucket Island. Evidence for self-limited and subclinical infections,” The New England Journal of Medicine, vol. 297, no. 15, pp. 825–827, 1977. View at: Google Scholar
  54. D. J. White, J. Talarico, H.-G. Chang, G. S. Birkhead, T. Heimberger, and D. L. Morse, “Human babesiosis in New York State: review of 139 hospitalized cases and analysis of prognostic factors,” Archives of Internal Medicine, vol. 158, no. 19, pp. 2149–2154, 1998. View at: Publisher Site | Google Scholar
  55. T. Sun, M. J. Tenenbaum, and J. Greenspan, “Morphologic and clinical observations in human infection with Babesia microti,” Journal of Infectious Diseases, vol. 148, no. 2, pp. 239–248, 1983. View at: Google Scholar
  56. H. O. Mathewson, A. E. Anderson, and G. W. Hazard, “Self-limited babesiosis in a splenectomized child,” Pediatric Infectious Disease, vol. 3, no. 2, pp. 148–149, 1984. View at: Google Scholar
  57. J. M. Ortiz and R. C. Eagle Jr., “Ocular findings in human babesiosis (Nantucket fever),” American Journal of Ophthalmology, vol. 93, no. 3, pp. 307–311, 1982. View at: Google Scholar
  58. F. Rosner, M. H. Zarrabi, J. L. Benach, and G. S. Habicht, “Babesiosis in splenectomized adults. Review of 22 reported cases,” American Journal of Medicine, vol. 76, no. 4, pp. 696–701, 1984. View at: Google Scholar
  59. P. J. Krause, B. E. Gewurz, D. Hill et al., “Persistent and relapsing babesiosis in immunocompromised patients,” Clinical Infectious Diseases, vol. 46, no. 3, pp. 370–376, 2008. View at: Publisher Site | Google Scholar
  60. T. K. Ruebush II, P. B. Cassaday, and H. J. Marsh, “Human babesiosis on Nantucket Island: clinical features,” Annals of Internal Medicine, vol. 86, no. 1, pp. 6–9, 1977. View at: Google Scholar
  61. C. P. Stowell, J. A. Gelfand, J.-A. O. Shepard, and A. Kratz, “Case 17-2007: a 25-year-old woman with relapsing fevers and recent onset of dyspnea,” The New England Journal of Medicine, vol. 356, no. 22, pp. 2313–2319, 2007. View at: Publisher Site | Google Scholar
  62. J. L. Benach and G. S. Habicht, “Clinical characteristics of human babesiosis,” Journal of Infectious Diseases, vol. 144, no. 5, p. 481, 1981. View at: Google Scholar
  63. D. H. Persing, B. L. Herwaldt, C. Glaser et al., “Infection with a Babesia-like organism in Northern California,” The New England Journal of Medicine, vol. 332, no. 5, pp. 298–303, 1995. View at: Publisher Site | Google Scholar
  64. G. R. Healy and T. K. Ruebush II, “Morphology of Babesia microti in human blood smears,” American Journal of Clinical Pathology, vol. 73, no. 1, pp. 107–109, 1980. View at: Google Scholar
  65. P. J. Krause, S. R. Telford III, A. Spielman et al., “Comparison of PCR with blood smear and inoculation of small animals for diagnosis of Babesia microti parasitemia,” Journal of Clinical Microbiology, vol. 34, no. 11, pp. 2791–2794, 1996. View at: Google Scholar
  66. D. H. Persing, D. Mathiesen, W. F. Marshall et al., “Detection of Babesia microti by polymerase chain reaction,” Journal of Clinical Microbiology, vol. 30, no. 8, pp. 2097–2103, 1992. View at: Google Scholar
  67. P. J. Krause, R. Ryan, S. R. Telford III, D. Persing, and A. Spielman, “Efficacy of immunoglobulin M serodiagnostic test for rapid diagnosis of acute babesiosis,” Journal of Clinical Microbiology, vol. 34, no. 8, pp. 2014–2016, 1996. View at: Google Scholar
  68. P. J. Krause, S. R. Telford III, R. Ryan et al., “Diagnosis of babesiosis: evaluation of a serologic test for the detection of Babesia microti antibody,” Journal of Infectious Diseases, vol. 169, no. 4, pp. 923–926, 1994. View at: Google Scholar
  69. T. K. Ruebush II, A. J. Sulzer, and G. R. Healy, “Development and persistence of antibody in persons infected with Babesia microti,” American Journal of Tropical Medicine and Hygiene, vol. 30, no. 1, pp. 291–292, 1981. View at: Google Scholar
  70. G. P. Wormser, R. J. Dattwyler, E. D. Shapiro et al., “The clinical assessments treatment, and prevention of lyme disease, human granulocytic anaplasmosis, and babesiosis: clinical practice guidelines by the Infectious Diseases Society of America,” Clinical Infectious Diseases, vol. 43, no. 9, pp. 1089–1134, 2006. View at: Publisher Site | Google Scholar
  71. P. J. Krause, T. Lepore, V. K. Sikand et al., “Atovaquone and azithromycin for the treatment of babesiosis,” The New England Journal of Medicine, vol. 343, no. 20, pp. 1454–1458, 2000. View at: Publisher Site | Google Scholar
  72. M. Raju, J. C. Salazar, H. Leopold, and P. J. Krause, “Atovaquone and azithromycin treatment for babesiosis in an infant,” Pediatric Infectious Disease Journal, vol. 26, no. 2, pp. 181–183, 2007. View at: Publisher Site | Google Scholar
  73. M. Wittner, K. S. Rowin, H. B. Tanowitz et al., “Successful chemotherapy of transfusion babesiosis,” Annals of Internal Medicine, vol. 96, no. 5, pp. 601–604, 1982. View at: Google Scholar
  74. K. M. Cahill, J. L. Benach, L. M. Reich et al., “Red cell exchange: treatment of babesiosis in a splenectomized patient,” Transfusion, vol. 21, no. 2, pp. 193–198, 1981. View at: Google Scholar
  75. G. A. Jacoby, J. V. Hunt, K. S. Kosinski et al., “Treatment of transfusion-transmitted babesiosis by exchange transfusion,” The New England Journal of Medicine, vol. 303, no. 19, pp. 1098–1100, 1980. View at: Google Scholar
  76. V. I. Powell and K. Grima, “Exchange transfusion for malaria and babesia infection,” Transfusion Medicine Reviews, vol. 16, no. 3, pp. 239–250, 2002. View at: Google Scholar
  77. J. M. Vyas, S. R. Telford, and G. K. Robbins, “Treatment of refractory Babesia microti infection with atovaquone-proguanil in an HIV-infected patient: case report,” Clinical Infectious Diseases, vol. 45, no. 12, pp. 1588–1590, 2007. View at: Publisher Site | Google Scholar
  78. L. M. Weiss, M. Wittner, and H. B. Tanowitz, “The treatment of babesiosis,” The New England Journal of Medicine, vol. 344, no. 10, p. 773, 2001. View at: Google Scholar
  79. D. Raoult, L. Soulayrol, B. Toga, H. Dumon, and P. Casanova, “Babesiosis, pentamidine, and cotrimoxazole,” Annals of Internal Medicine, vol. 107, no. 6, p. 944, 1987. View at: Google Scholar
  80. E. Denes, J. P. Rogez, M. L. Darde, and P. Weinbreck, “Management of Babesia divergens babesiosis without a complete course of quinine treatment,” European Journal of Clinical Microbiology and Infectious Diseases, vol. 18, no. 9, pp. 672–673, 1999. View at: Publisher Site | Google Scholar
  81. E. B. Hayes and J. Piesman, “How can we prevent Lyme disease?” The New England Journal of Medicine, vol. 348, no. 24, pp. 2424–2430, 2003. View at: Publisher Site | Google Scholar
  82. T. N. Mather, J. M. C. Ribeiro, and A. Spielman, “Lyme disease and babesiosis: acaricide focused on potentially infected ticks,” American Journal of Tropical Medicine and Hygiene, vol. 36, no. 3, pp. 609–614, 1987. View at: Google Scholar
  83. G. R. Needham, “Evaluation of five popular methods for tick removal,” Pediatrics, vol. 75, no. 6, pp. 997–1002, 1985. View at: Google Scholar
  84. K. C. Stafford III, Tick Management Handbook: An Integrated Guide for Homeowners, Pest Control Operators, and Public Health Officials for the Prevention of Tick-Associated Disease, The Connecticut Agricultural Experimental Station, New Haven, Conn, USA, 2007.
  85. J. I. Tsao, J. T. Wootton, J. Bunikis, M. G. Luna, D. Fish, and A. G. Barbour, “An ecological approach to preventing human infection: vaccinating wild mouse reservoirs intervenes in the Lyme disease cycle,” Proceedings of the National Academy of Sciences of the United States of America, vol. 101, no. 52, pp. 18159–18164, 2004. View at: Publisher Site | Google Scholar
  86. M. Vazquez, C. Muehlenbein, M. Cartter, E. B. Hayes, S. Ertel, and E. D. Shapiro, “Effectiveness of personal protective measures to prevent lyme disease,” Emerging Infectious Diseases, vol. 14, no. 2, pp. 210–216, 2008. View at: Google Scholar
  87. M. L. Wilson, S. R. Telford III, J. Piesman, and A. Spielman, “Reduced abundance of immature Ixodes dammini (Acari: Ixodidae) following elimination of deer,” Journal of Medical Entomology, vol. 25, no. 4, pp. 224–228, 1988. View at: Google Scholar
  88. D. Fish and J. E. Childs, “Community-Based Prevention of Lyme Disease and Other Tick-Borne Diseases Through Topical Application of Acaricide to White-Tailed Deer: Background and Rationale,” Vector-Borne and Zoonotic Diseases, vol. 9, no. 4, pp. 357–364, 2009. View at: Google Scholar
  89. P. Grellier, R. Santus, E. Mouray et al., “Photosensitized inactivation of Plasmodium falciparum- and Babesia divergens-infected erythrocytes in whole blood by lipophilic pheophorbide derivatives,” Vox Sanguinis, vol. 72, no. 4, pp. 211–220, 1997. View at: Google Scholar
  90. B. Zavizion, M. Pereira, M. de Melo Jorge et al., “Inactivation of protozoan parasites in red blood cells using INACTINE PEN110 chemistry,” Transfusion, vol. 44, no. 5, pp. 731–738, 2004. View at: Publisher Site | Google Scholar

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