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Acute conjunctivitis with episcleritis and anterior uveitis linked to adiaspiromycosis and freshwater sponges, Amazon region, Brazil, 2005.

Adiaspiromycosis, caused by the fungus Emmonsia sp., was first identified in Brazil during pathologic examination of lung tissue in a patient with pneumonia who died unexpectedly during treatment (1). Conidia of Emmonsia sp. are commonly present in the environment, mainly in soil and dust, and some studies have shown that pulmonary infection most often results from inhalation (2-4). Conidia, which also affect other mammals, including marsupials and rodents, do not cause infection; rather, disease is caused by the robust, multicellular immunologic response in tissue against the growing conidia, which results in noncaseating granulomas (2). Human pulmonary adiaspiromycosis has been reported in the literature from multiple countries, including Russia, the Czech Republic, Guatemala, Brazil, and the United States (1-4); disseminated infection may occur in immunocompromised persons. Diagnosis is most frequently made by experienced pathologists who microscopically exam tissue using various stains, including periodic acid-Shiff, which shows large, round, multiwalled structures with surrounding foreign-body-type mixed cellular reactions (3-5).

On October 26, 2006, local ophthalmologists notified the State Health Secretariat in Tocantins, located in the northern Amazon region of Brazil, of an unusual outbreak of conjunctivitis with ocular nodules of unknown etiology among children. Illness was identified in 17 children, 16 of whom were <15 years of age; all were residents of Araguatins (population = 29,336), a city located along the slow-moving Araguaia River. The disease had remained underdiagnosed and underreported in Araguatins until an ophthalmologic service was initiated in the neighboring city of Augustinopolis, where the initial case-patients were referred, examined, and subsequently reported to local health authorities. Shortly after the condition was reported to Brazil's Ministry of Health, a team of epidemiologists, laboratorians, and ophthalmologists began an investigation with the following objectives: 1) determine the magnitude of the problem, 2) identify the cause, and 3) implement prevention and control activities.



Because 16 (94%) of the 17 initial case-patients reported were 5-15 years of age, active searches were conducted in 40 of the 41 primary schools in Araguatins. Health workers were trained by ophthalmologists to identify children with clinical signs that were similar to the initial 17 case reports. Children with blurred vision, or any of the following, were referred for an ophthalmologic examination: conjunctival injection or inflammation, nodules on conjunctiva or sclera, or cornea with any discoloration or opacification.


We defined a case of confirmed ocular disease (COD) in a child with any of the following physical signs: conjunctival injection or inflammation, nodules on sclera, or conjunctival or corneal opacities with anterior uveitis identified during ophthalmologic examination (including by slit-lamp and microscopy). Patients with COD were interviewed by using a standardized semistructured questionnaire; parents served as proxies for young children. Information was collected about basic demographic characteristics, duration and type(s) of symptoms, source of drinking water, frequency and specific locations where children had exposure to the local freshwater river, and similar illness in family members.

Case-Control Study

We hypothesized that exposure to the Araguaia River played a role in the chain of events resulting in ocular disease. This hypothesis was tested by using an unmatched case-control study design, based on an estimated 90% of case-patients having prior ocular exposure to river water; and by using 80% power, an a level of 0.05, and a case:control ratio of 1:3, which yielded a study sample size of 62 case-patients and 186 controls. The 62 case-patients included in this study were randomly selected from a total of 91 children with COD identified and interviewed. Two separate control groups were selected for interviews. The first group (community controls) included 186 asymptomatic persons ranging from 5 to 20 years of age living in households systematically selected from randomly chosen residential blocks in the urban area of Araguatins municipality. A second control group (household controls) comprised all asymptomatic residents of case-patient households.

Statistical Analysis

In the univariate analysis of the case-control study data, categorical variables were tested by using a [chi square] test, and continuous variables were compared by using a Kruskall-Wallis or t test, as appropriate. The odds ratio (OR) was used as the measure of association, 95% confidence intervals (CIs) were calculated, and p<0.05 was considered significant. Using a stepwise backward elimination strategy to calculate the adjusted OR, an unconditional logistic regression model was used for the multivariate analysis.

Laboratory Methods

Serologic tests from children with COD included ELISA tests for onchocercosis (immunoglobulin [Ig] G), toxoplasmosis (IgM), and toxocariasis (IgG). Blood smears and aqueous humor from selected patients were examined microscopically for evidence of microfilaria. Biopsy samples from COD case-patients with scleral nodules or corneal abnormalities were fixed in formalin, stained with hemotoxylin and eosin, and periodic acid-Schiff, and examined microscopically. Soil samples were examined for helminth eggs and larvae. Water samples were collected from areas of the Araguaia River where case-patients reportedly swam. These samples were examined for 1) freshwater sponges, which were identified to species, and 2) silicious spicules (gemmoscleres) of these sponges; details of the methods and results of this sampling have been published (6,7).


In addition to the initial 17 COD case-patients who were examined by ophthalmologists and reported to the Ministry of Health, a total of 5,084 children 5-15 years of age (corresponding to 83% of this age group in the population) were examined at 40 schools by health workers. During these active searches, of 235 students triaged and referred for evaluation of possible ocular abnormalities, 64 (27%) were categorized by ophthalmologists as having COD and 103 (44%) had sequelae. In addition to the total 81 COD case-patients identified above by November 26, 2005, COD was diagnosed for an additional 18 by January 26, 2006, identified initially by local clinicians or through patient self-referral.

Of the 99 COD case-patients identified, 91 (92%) were interviewed, of whom 70 (77%) were male and the mean age ([+ or -]1 SD) was 11.0 [+ or -] 4.4 years. Ocular-related signs and symptoms were conjunctival hyperemia (89%), conjunctival nodule (70%), excessive tearing (63%), conjunctival pruritus (60%), photophobia (57%), ocular pain (42%), and blurred vision (40%); other reported symptoms included headache (37%) and generalized pruritus (16%). The number of COD case-patients peaked during the dry season (July-September) (Figure 1) when schools were closed and contact with the local river was most common. Of those interviewed, 88 (97%) resided in urban areas of Araguatins, and 3 (3%) resided in rural areas.

Ophthalmologists identified unilateral ocular lesions in 73 (80%) of interviewed COD case-patients; in 18 (20%) patients, the lesions were bilateral. Unilateral subconjunctival nodule(s) of sclera (Figure 2), some of which extended to the corneal limbus, were identified in 43 (47%) case-patients and were present bilaterally in 12 (13%). Unilateral corneal opacities (Figure 3) were observed in 32 (35%) case-patients, bilaterally in 18 (20%).

Neighborhoods most commonly affected in the city of Araguatins included Centro, where 61 (67%) of all case-patients resided (prevalence of 8 cases per 100,000 inhabitants), Vila Cidinha (6 per 100,000), and Nova Araguatins (3 per 100,000). Seventy-five (82%) case-patients attended an urban school in Araguatins, and 3 (3%) attended a rural school (Table 1); 13 (14%) of case-patients were not enrolled in a school.


Of the 62 COD case-patients randomly selected to participate in the case-control study, 48 (77%) were male. Case-patients were significantly younger (mean 11.4 [+ or -] 3.5 years) than household controls (mean 25 [+ or -] 17.8 years; p<0.001, Student t test), but age distribution was similar to that of community controls (13 [+ or -] 6.0 years; p = 0.4, Student t test). In univariate analysis, male sex was significantly associated with disease when case-patients were compared with 178 household controls (OR 4.7, 95% CI 2.3-9.8, p<0.001); and with 186 community controls (OR 4.5, 95% CI 2.2-9.4, p<0.001).

Environmental exposures most strongly associated with increased risk for disease, which was significant when compared with both household and community controls (Table 2), were swimming or diving in the Araguaia River and frequenting Cais beach on the bank of the Araguaia River. Fishing in the river was associated with disease but only when case-patients were compared with community controls. Factors not significantly associated with disease (using either control group) were drinking untreated river water, washing clothes in the river, contact with various types of domesticated animals, a history of exposure to ticks, or a history of allergies. Frequency of river contact was also significantly associated with disease (Table 3). According to multivariate analysis, factors most strongly associated with disease were being of male sex, frequenting the Cais beach area, and diving underwater in the Araguaia River (Table 4).



Among 32 case-patients treated with corticosteroid (oral and/or topical prednisone) by ophthalmologists, disease was resolved or cured in 25 (78%); 7 (22%) case-patients had more severe symptoms and were referred to the Sao Geraldo Hospital in Belo Horizonte, Minas Gerais State.

Among those with nodules, 14 had biopsy samples taken under sterile surgical conditions for diagnostic purposes. Microscopic examination of nodules identified microulcerations of corneal epithelium (Figure 4), and a mixed acute inflammatory response mainly consisting of leukocytes, with some eosinophils, and lymphohistocytic and diffuse neutrophilic infiltrates with edema. Twelve case-patients (13%) had a granuloma of the anterior chamber of the eye unilaterally; 1 case-patient had bilateral anterior chamber granulomas. In addition, in 2 biopsy samples, subconjunctival inflammation was present surrounding large, 200-600-micron, thick-walled, spherical foreign bodies (Figure 5) consistent with adiaconidia of Emmonsia sp. fungus, a cause of adiaspiromycosis.

Onchocerciasis, toxoplasmosis, toxocariasis, and microfilaria were discarded as possible etiologies for COD. All 17 samples tested for onchocerciasis were nonreactive for IgG, and no evidence of microfilaria was found in blood smears (n = 17), aqueous humor (n = 1), or biopsy samples of cutaneous nodules (n = 6) examined microscopically. All samples tested for toxoplasmosis (n = 46) were nonreactive for IgM antibodies. Serologic tests for detection of IgG for toxocariasis were reactive for 59 (88%) of 67 COD case-patients, 14 (74%) of 19 household controls, and 53 (64%) of 82 community controls; helminth eggs and larvae, including Toxocara spp., were found in 7 of 10 soil samples.


These results confirm the existence of an outbreak of conjunctivitis and severe ocular disease probably caused by adiaspiromycosis, mainly among school-aged children. Risk factors for COD identified in this investigation included diving underwater and frequenting a specific beach (Cais) on the Araguia River in the Amazon region of Brazil. The precise reasons eye contact with river water increased risk remain unclear. Perhaps exposure to freshwater sponge spicules caused an initial conjunctival irritation, as suggested in previous publications (6-8). However, the microscopic identification of probable adiaconidia of Emmonsia sp. fungus in the scleral biopsy samples from children with severe disease in this outbreak suggests that conjunctival irritation was most likely followed by conjunctival exposure to conidia of this fungus, perhaps in dust caused in part by dry environmental conditions, similar to the exposure of respiratory mucosa described in case reports of pulmonary adiaspiromycosis (1-5,9). Adiaspiromycosis causes an inflammatory and often granulomatous response in tissue because of the presence of nonbudding, thick-walled adiaconidia of Emmonsia sp. fungus (10). Disease is thought to result from exposure to conidia (through inhalation or mucosal contact with dust); these conidia subsequently cause a marked inflammatory response and enlarge to become adiaconidia ranging in diameter from 300 to 600-micorons (1-5,9,10).

Boys were at higher risk than girls most likely because boys had more facial and eye contact with the river water while swimming and diving. To minimize bias, we randomly selected asymptomatic controls among persons 5-25 years of age in the community, but some selection bias may have resulted because boys and adolescents were absent at the time of interview (only 42% of community-based controls were boys). The clinical characteristics of conjunctivitis in this outbreak were unusual for several reasons. First, unlike conjunctivitis caused by common bacterial or viral pathogens, neither purulent conjunctival discharge nor hemorrhage was reported, and family members of case-patient households were not commonly affected. In addition, disease was characterized by unusual, single or multiple, white, opaque scleral nodules, often with hyperemia or local edema, and in some cases with opacification (changes in the normally transparent characteristics of the cornea or superficially on scleral tissue) extending to the limbus, or angular corneal opacities and anterior uveitis with granulomas in the anterior chamber. We believe that the clinical improvement of nearly all patients treated with corticosteroids also argues strongly against a bacterial cause or fungal species other than Emmonsia because conidia of Emmonsia sp. enlarge and cause a localized inflammatory response but do not commonly have the potential to disseminate.

Characteristics of this outbreak are similar to those of an outbreak of anterior uveitis and granuloma previously reported in India, where the etiology was traced to trematodes (11). Although the thick-walled foreign body we observed microscopically on slides from 2 case-patients was initially suspected to be trematodes, the round, apparently spherical shape, thick walls, and vacuous central area with lack of organized, internal structures is most consistent with the adiaconidia of the Emmonsia sp. Morphologic appearance differs from that of the fungus Coccidiodes immitis, in which spores contain internal microsporules (10).


The natural history of this disease is unknown. However, we identified COD case-patients in several stages of disease, including patients with sequalae. Moreover, after obtaining school surveys, we identified [approximately equal to]5% of children with ocular abnormalities; COD was diagnosed in one third of children after an ophthalmologic exam. We educated the population about risks for eye contact with river water; active searches were conducted to identify all ill persons in the population and in neighboring cities, and health officials limited recreational access to the Araguaia River. These findings suggest that the extent of this problem may be more widespread in the Amazon region than is currently recognized.



We acknowledge the important contributions of the Araguaia River Study Group and the following groups and individuals, without whom this investigation would not have been possible: Agentes de Endemias, Agentes de Saude de Araguatins, Technicians from Municipal Health Secretariat/Araguatins, Ophthalmologists from the Augustinopolis Reference Hospital; technical staff from the State Secretariat of Health/Tocantins, and the national Secretariat of Health Surveillance; Ministry of Health; Victor Marques de Alencar, Henrique Leonel Lenzi and staff, Cecilia Volkmer-Ribeiro, Twiggy Cristina Alves Batista, Antonio Augusto Cruz, Norma Helen Medina, Pedro Paulo Chieffi, and Regina Maura Franco; the Field Epidemiology Training Program; and Vera Gattas.

We thank the United Nations Educational, Scientific, and Cultural Organization (Grant 914 BRA 2009) for salary support.

Ms Mendes is an epidemiologist who completed her Field Epidemiology Training Program with the Brazilian Ministry of Health (MoH) in 2007. She is currently working in Dengue Program Control at MoH. Her main research interests are infectious diseases of public health importance.


(1.) Nunes AS, Saldiva PH. Adiaspiromicose pulmonar (Pneumopatia por Emmonsia crescens). Jornal de Pneumologia. 1986;12:S94.

(2.) Moraes MA, Gomes MI, Vianna LMS. Pulmonary adiaspiromycosis: casual finding in a patient who died of yellow fever [in Portuguese] Rev Soc Bras Med Trop. 2001;34:83-5.

(3.) Sun Y, Bhuiya T, Wasil T, Macias A, Wasserman PG. Fine needle aspirations of pulmonary adiaspiromycosis: a case report. Acta Cytol. 2007;51:217-21.

(4.) England DM, Hochholzer L. Adiapiromycosis: an unusual fungal infection of the lung: report of 11 cases. Am J Surg Pathol. 1993;17:876-86. DOI: 10.1097/00000478-199309000-00003

(5.) Moraes MA, Gomes MI. Human adiaspiromycosis: cicatricial lesions in mediastinal lymph notes. Rev Soc Bras Med Trop. 2004;37:177-78.PMID: 15094906

(6.) Volkmer-Ribeiro C, Batista TCA. Levantamento de cauxi (Porifera, Demospongiae), provavel agente etiologico de doenca ocular em humanos, Araguatins, rio Araguaia, Estado do Tocantins, Brasil. Rev Bras Zool. 2007;24:133-43. DOI: 10.1590/S0101-81752007000100016

(7.) Volkmer-Ribeiro C, Lenzi HL, Orefice F, Pelajo-Machado M, Alencar LM, Fonseca CF, et al. Freshwater sponge spicules: a new agent of ocular pathology. Mem Inst Oswaldo Cruz, Rio de Janeiro. 2006;101:899-903.

(8.) Volkmer-Bibeiro C, Batista TCA, Melao MGG, Fonseca-Gessner AA. Anthropically dislodged assemblages of sponges (Porifer: Demospongiae) in the River Araguaia at Araguatins, Tocantins, Brazil. Acta Limnol Bras. 2008;20:169-75.

(9.) Nuorva K, Pitkanen R, Issakainen J, Huttunen NP, Juhola M. Pulmonary adiaspiromycosis in a two year old girl. J Clin Pathol. 1997;50:82-5. DOI: 10.1136/jcp.50.1.82

(10.) Emmons CW, Ashburn LL. The isolation of Haplosporangium parvum n. sp. and Coccidioides immitis from wild rodents. Their relationship to coccidioidomycosis. Public Health Rep. 1942;57: 1715-27.

(11.) Rathinam SR. KIM MD, Usha KM, Rao NA. Presumed trematode-induced granulomatous anterior uveitis: a newly recognized cause of intraocular inflammation in children from south India. Am J Ophthalmol. 2002;133:773-9. DOI: 10.1016/S0002-9394(02)01435-6


Medscape, LLC is pleased to provide online continuing medical education (CME) for this journal article, allowing clinicians the opportunity to earn CME credit. This activity has been planned and implemented in accordance with the Essential Areas and policies of the Accreditation Council for Continuing Medical Education through the joint sponsorship of Medscape, LLC and Emerging Infectious Diseases. Medscape, LLC is accredited by the Accreditation Council for Continuing Medical Education (ACCME) to provide continuing medical education for physicians. Medscape, LLC designates this educational activity for a maximum of 0.5 AMA PRA Category 1 Credits(tm). Physicians should only claim credit commensurate with the extent of their participation in the activity. All other clinicians completing this activity will be issued a certificate of participation. To participate in this journal CME activity: (1) review the learning objectives and author disclosures; (2) study the education content; (3) take the post-test and/or complete the evaluation at; (4) view/print certificate.

Learning Objectives

Upon completion of this activity, participants will be able to:

* Describe the mechanism of infection for adiaspiromycosis.

* Identify the age group most susceptible to ocular adiaspiromycosis.

* Describe presenting symptoms associated with ocular adiaspiromycosis.

* Describe the frequency of ocular lesions associated with adiaspiromycosis.

* Identify risk factors for ocular adiaspiromycosis.


Beverly Merritt, Technical Writer-Editor, Emerging Infectious Diseases. Disclosure: Beverly Merritt has disclosed no relevant financial relationships.

CME Author

Desiree Lie, MD, MSEd, Clinical Professor, Family Medicine, University of California, Orange; Director, Division of Faculty Development, UCI Medical Center, Orange, California. Disclosure: Desiree Lie, MD, MSEd, has disclosed no relevant financial relationships.


Disclosures: Tatiana M. Lanzieri, MD, MSc, has disclosed that she has been employed by GlaxoSmithKline since April 2008, but this study was conducted while she was working in the Brazilian Ministry of Health. Marcia O. Mendes, BSc, MSc; Mario A.P. Moraes, MD; Ernesto I.M. Renoiner, ND; Marta H.P. Dantas, ND, MSc; Carlos F. Fonseca, MD; Expedito J.A. Luna, MD; and Douglas L. Hatch, MD, MPH, have disclosed no relevant financial relationships.

DOI: 10.3201/eid1504.081281

Marcia O. Mendes, Mario A.P. Moraes, Ernesto I.M. Renoiner, Marta H.P. Dantas, Tatiania M. Lanzieri, Carlos F. Fonseca, Expedito J.A. Luna, and Douglas L. Hatch

Address for correspondence: Marcia O. Mendes, EPISUS, CGDT, SVS, Ministerio da Saude Esplanada dos Ministerios, Bloco G--Ed. Sede--Sala 122, Brasilia, Brazil, 70058-900; email:

Author affiliations: Ministry of Health, Brasilia, Brazil (M.O. Mendes, E.I.M. Renoiner, M.H.P. Dantas, T.M. Lanzieri, E.J.A. Luna); University of Brasilia, Brasilia (M.A.P. Moraes); Reference Hospital of Augustinopolis, Augustinopolis, Brazil (C.F. Fonseca); Centers for Disease Control and Prevention, Atlanta, Georgia, USA (D.L. Hatch); and Department of Public Health, Los Angeles, California, USA (D.L. Hatch)
Table 1. Prevalence of confirmed ocular disease in schools
surveyed, stratified by urban area, Araguatins, Brazil, 2005

 No. case-
School zone * identified No. students Prevalence, %

Urban 75 3,299 2.3
A 11 179 6.2
B 28 664 4.2
C 14 615 2.3
D 9 379 2.4
E 1 88 1.4
F 4 331 1.2
G 4 331 1.2
H 4 581 0.7

Rural 3 1,785 0.2
I 1 26 3.8
J 1 52 1.9
L 1 108 0.9

* Area where schools are located.

Table 2. Results of univariate analysis of case-control study on
relationship between various exposures to freshwater rivers and
confirmed ocular disease, Araguatins, Brazil, 2005 *

 Household control group,
 n = 178

 No. (%)
 exposed, No. (%)
Exposure n = 62 exposed OR 95% CI

Contacting river water 61 (98) 132 (74) 21.3 3.0-424.2
Diving underwater 49 (83) 67 (38) 8.1 3.7-18.4
Visiting Cais Beach 50 (81) 97 (55) 3.4 1.6-7.2
Fishing 30 (48) 74 (42) 1.3 0.7-2.4
Drinking untreated 23 (38) 62 (35) 1.1 0.6-2.2
 river water
Washing clothes in 6 (10) 43 (24) 0.3 0.1-0.9
 river water

 Community control group,
 n = 186

 No. (%)
 exposed, No. (%)
Exposure n = 62 exposed OR 95% CI

Contacting river water 61 (98) 145 (78) 17.2 2.5-344.8
Diving underwater 49 (83) 90 (49) 5.1 2.3-11.5
Visiting Cais Beach 50 (81) 52 (30) 10.1 4.7-21.9
Fishing 30 (48) 54 (29) 2.3 1.2-4.3
Drinking untreated 23 (38) 50 (27) 1.7 0.9-3.3
 river water
Washing clothes in 6 (10) 29 (16) 0.6 0.2-1.6
 river water

* OR, odds ratio; CI, confidence interval.

Table 3. Results of univariate analysis of case-control study on
relationship between frequency of exposure to Araguaia River and
odds of confirmed ocular disease, Araguatins, Brazil, 2005 *

 Household control group,
 No. (%) n = 178
 exposed, No. (%)
Frequency n = 62 exposed OR ([dagger])

Weekly 25 (40) 20 (11) 6.9
Once every 2 weeks 4 (7) 5 (3) 4.4
Vacations 25 (40) 109 (61) 1.3
Rarely ([section]) 8 (13) 44 (25) 1.0

 No. (%) Community control group, n = 186
 exposed, No. (%)
Frequency n = 62 exposed OR ([double dagger])

Weekly 25 (40) 13 (7) 10.8
Once every 2 weeks 4 (7) 7 (4) 3.2
Vacations 25 (40) 121 (65) 1.2
Rarely ([section]) 8 (13) 45 (24) 1.0

* OR, odds ratio.

([dagger]) 2 test for trend 25.7; p<0.0001.

([double dagger]) 2 test for trend 35.3; p<0.0001.

([section]) Fewer than 3x/year.

Table 4. Results of multivariate analysis of case-control data
showing independent effect of type of exposures to Araguaia River
and srisk for confirmed ocular disease, Araguatins, Brazil, 2005 *

 Household control group
Exposure to
Araguaia River aOR (95% CI) p value

Swimming 3.1 (0.4-26.8) 0.3
Diving underwater 4.6 (1.9-10.6) 0.0004
Visited Cais Beach 3.2 (1.4-7.1) 0.005
Male gender 3.4 (1.6-7.2) 0.001
Fishing in river -- --

 Community control group
Exposure to
Araguaia River aOR (95% CI) p value

Swimming 2.1 (0.2-19.4) 0.5
Diving underwater 2.7 (1.1-7.1) 0.04
Visited Cais Beach 9.9 (4.3-22.9) 0.00001
Male gender 4.7 (1.9-11.0) 0.0004
Fishing in river 1.2 (0.5-2.7) 0.6

* Unconditional logistic regression model used.
aOR, adjusted odds ratio; CI, confidence interval.
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Article Details
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Author:Mendes, Marcia O.; Moraes, Mario A.P.; Renoiner, Ernesto I.M.; Dantas, Marta H.P.; Lanzieri, Tatiani
Publication:Emerging Infectious Diseases
Geographic Code:3BRAZ
Date:Apr 1, 2009
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