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Distance from construction site and risk for coccidioidomycosis, Arizona, USA.

The fungal infection coccidioidomycosis, which is also called Valley fever, is caused by Coccidioides spp. and is acquired through inhalation of airborne spores. Of the estimated 150,000 infections that occur annually, [approximately equal to] 60% occur in Arizona, USA. In Arizona, Maricopa County has been the center of a coccidioidal epidemic for years (1). Coccidioidomycosis is the second most commonly reported infectious disease in Arizona (2), although reported cases are likely an underestimate of the true number of cases. Respiratory illness develops in persons with symptomatic infection. The severity of illness varies from person to person; some patients require prolonged medical evaluation, time away from work or school, treatment, or hospitalization (2,3). In 2007, estimated hospital-related charges for coccidioidomycosis totaled $89 million in Arizona (3). It has been estimated that 3% of the nonimmune population residing in Coccidioides spp .-endemic areas is infected annually (4); thus, even if up to 60% of the infected population is asymptomatic, the potential number of patients who may lose the ability to perform daily activities, work, or go to school because of illness is substantial.

Once a person is infected with coccidioidomycosis, the immune system mounts a complex reaction to control the infection; this reaction eventually results in the presence of cell-mediated and humoral immunity (5,6). The cell-mediated immunity is measured by using a delayed-type hypersensitivity (DTH) skin test (5) or an in vitro assay of cellular immunity to Coccidioides spp.

In areas of the US Southwest where Coccidioides spp. are endemic, the fungi grow in the top 18 inches of soil. Climate and soil conditions in the area foster growth of the fungi, and after rainfall, the fungi proliferate in the mold form with arthroconidia. As the weather dries, arthroconidia break off and become airborne spores when the soil is disrupted (7). Situations and activities that increase exposure to dust increase the risk for coccidioidomycosis in humans (7); these situations and activities include, but are not limited to, dust storms, earthquakes, construction work, outdoor occupations or activities, and military maneuvers (7). Little data exist to quantify the effects of construction activities on the local epidemiology of coccidioidomycosis. Measures to control construction-associated dust have been codified into law, but no data exist to demonstrate the efficacy of these mandatory, dust-control measures in eliminating airborne arthroconidia or associated coccidioidal infections.

In late 2011, our institution embarked on the construction of a new medical facility at the site of a previously undisturbed native desert area in Maricopa County (hereafter referred to as campus A). This construction project required a year-long process of excavation and hauling of large amounts of desert soil. With the current study, we sought to quantify and compare the rate of acquisition of coccidioidomycosis among employees working at an existing facility on campus A with that among employees working at another campus 13 miles away (hereafter referred to as campus B).


After approval was given by the Mayo Clinic Institutional Review Board, all employees at the 2 campuses were invited by email to participate in the study. Employees were included if they were [greater than or equal to] 18 years of age, spent [right arrow] 95% of their work time on a single campus (A or B), and were self-reported to be immunocompetent. Exclusion criteria included the following: presence of any immunosuppressive illness or medication (including seropositivity for HIV; history of hematologic malignancy; and receipt of cancer chemotherapy, antirejection medication, inhibitors of tumor necrosis factor, or other immunosuppressants); a history of anergy to tests of DTH, unless subsequent skin test reactivity had been demonstrated; a history of coccidioidal illness (diagnosed by a physician or confirmed by skin testing or serologic, microbiologic, or pathologic evidence); a history of positive results for coccidioidal serology or coccidioidal skin test; current use of an oral or intravenous antifungal drug (azole or amphotericin) that could prevent coccidioidomycosis; or current pregnancy (because of a theoretical decrease in cellular immunity).

During January 22-February 13, 2012, employees who provided verbal consent completed a questionnaire to ascertain whether they met inclusion criteria and to provide additional information, such as demographic information (sex, race/ethnicity, duration of residence in the Coccidioides spp.-endemic area, and residential zip code); the types of regular outdoor activities they participated in; and any perception they might have that construction was occurring near their area of employment or residence. A 10-mL blood sample was collected from each participant and assayed for cellular immunity to Coccidioides spp. All campus A participants were recruited and had a blood sample collected before excavation and construction began. Campus B participants were recruited and tested within 2 weeks of construction onset. Twelve to 13 months later, during January 29-March 27, 2013, we again collected and assayed blood samples from participants and administered a second questionnaire. Data were eliminated from analysis if a participant's employment site changed from 1 campus to the other after enrollment.

We used a whole-blood CD69 lymphocyte-activation assay to determine whether study participants were infected with Coccidioides fungi; the assay methods used were similar to previously described methods (8-10). In brief, we incubated 0.5 mL of whole peripheral blood with 5 pg of coccidioidin filtrate (provided by Mitch Magee, Arizona State University, Tempe, AZ, USA) for 24 h at 37[degrees]C in a humidified incubator containing 5% C[O.sub.2]. Phytohemagglutinin lectin (5 pg) was used as a positive stimulatory control, and 10 mL of phosphate-buffered saline (PBS) was added to the control tubes. After the 24-h incubation, we lysed the erythrocytes by using BD FACS lysing solution (Becton, Dickinson and Company, Franklin Lakes, NJ, USA) according to the manufacturer's instructions. We resuspended the resultant peripheral blood mononuclear cell (PBMC) pellet in 200 mL of PBS and then added 20 mL each of fluorescein-conjugated anti-CD3 and phycoerythrin-conjugated anti-CD69 antibodies (Becton, Dickinson and Company). The antibodies and PBMCs were gently mixed, incubated for 30 min at room temperature, and then washed twice with 3 mL of PBS. The final PBMC pellet was resuspended in 500 mL of PBS and analyzed on a Becton Dickinson CyAn flow cytometer. Before each flow cytometry run, the instrument was calibrated according to the manufacturer's protocol. Isotype controls for fluorescein isothiocyanate-labeled and phycoerythrin-labeled CD3 and CD69 antibodies were used to establish a CD3-positive cell gate. From that CD3-positive population, we quantified CD69-positive cell populations.

For the initial assay in 2012, we classified test results for all participants into 3 groups: definite negative (mean fluorescence intensity of CD69 above control; range 0%-5.9%), possibly negative (intermediate mean fluorescence intensity; range 6.1%-8.1%), and definite positive (mean fluorescence intensity; range 9.4%-33.1%). On the basis of results from healthy controls with known or no known history of definite coccidioidomycosis, we used 6.1% as a cutoff for differentiating between study participants with a positive or a negative test result for coccidioidomycosis. For participants eligible for the second test in 2013, a similar process was undertaken.

The percentage of employees who converted from a negative to a positive test result was calculated for each study site and compared by using the [chi square] test or the Fisher exact test, as applicable. For other employee characteristics, categorical variables were reported in numbers and percentages and compared by using the [chi square] test or the Fisher exact test; for the ages of participants, we reported the medians and compared them by using the Wilcoxon rank sum test.

After reviewing the results of our study, we conducted a logistic regression analysis, using only information collected in the initial questionnaire, to explore possible factors associated with conversion of cellular immunity. The univariate analysis was performed first, and any variables with p<0.30 were considered in the model-selection process. We used the backward elimination procedure to identify the variables, and any variable with p < 0.15 was retained in the model. Since the comparison between employees from different campuses was of interest, campus location was retained in the model. These liberal criteria were used for the exploratory purposes of our analysis. For the final model, adjusted odds ratios (ORs), 95% CIs, and p values were reported. All analyses were conducted by using SAS 9.2 (SAS Institute Inc., Cary, NC, USA). All tests were 2-sided; p < 0.05 was considered statistically significant.

With regard to the construction, the medical institution's Construction Safety and Infection Control policy required that the contractor develop a plan for using every appropriate precaution to avoid or limit dust in the air and in adjacent buildings during construction. The plan included precautions compliant with the Maricopa County Air Quality Department specifications to limit dust pollution (11), including a dust control permit (11). Trained county inspectors made periodic unannounced inspections of the construction site.

Construction commenced in late January 2012, and most of the excavation and movement of dirt was completed within 1 year. During that time, 15 unannounced inspections were conducted, and no violations of dust control regulations were documented. In total, 154,600 cubic yards of soil was excavated to a depth of 33 feet; pockets for concrete and steel caissons were excavated another 40-90 feet. The top 18 inches of soil was removed in the first 4 months. All excavated soil was initially moved to on-site stockpiles, but from the fourth month onward, 80% of the stockpiled soil was hauled off site; the balance of soil was re-used on the construction site for backfill or for building up new parking lots or an electric substation. It is not known when the movement of topsoil was completed or how much of the original top 18 inches of soil was in the soil that was re-used.


In January 2012, campus A employees were recruited and enrolled in the study during the 2 weeks before onset of the construction site excavation; campus B employees were enrolled 2 weeks later. A total of 316 employees met inclusion criteria: 176 from campus A and 140 from campus B. Of these employees, 20 (11.4%, 95% CI 6.7%-12.1%) from campus A and 19 (13.6%, 95% CI 7.9%-19.2%) from campus B were excluded because test results for the CD69 lymphocyte-activation assay were positive, indicating previous coccidioidal infection and current immunity (p = 0.55).

The flow of study participation, from the beginning to the end of the study, is summarized in Figure 1. After an initial positive test result, making participants ineligible for the second test a year later, the most common reasons for exclusion were employee attrition, change of employment campus, or medical leave (n = 16 for campus A; n = 14 for campus B). A year after the study was initiated, campus A had 140 eligible employees available for participation, of whom 120 (85.7%) continued in the study, and campus B had 107, of whom 90 (84.1%) continued.

At the 1-year follow-up, 3 (2.5%) of 120 participants from campus A who had previously negative test results had lymphocyte proliferation evidence of newly acquired coccidioidal infection, compared with 8 (8.9%) of 90 participants from campus B (p = 0.04). Figure 2 shows test results for representative study participants from each campus who showed immunologic conversion from negative for coccidioidal infection in 2012 to positive in 2013.

Table 1 summarizes the demographics, perceptions of risk for coccidioidomycosis, and outdoor activities of the study population. Campus B employees were older and more likely to regularly walk outdoors than were campus A employees. At the 1-year follow-up, there was a disproportionate drop in male participants on campus B and an increase in the proportion of participants on campus B who reported construction activity near their homes. Table 2 summarizes the comparison of demographic characteristics and risk factors for coccidioidomycosis among participants who did and those who did not show immunologic conversion after 1 year. Campus location and walking outdoors for recreation were associated with conversion of cellular immunity. Participant variables, including age, participation in other (or any) outdoor activities, and residential zip code, were assessed by logistic regression, and did not correlate with conversion of cellular immunity (data not shown).

The final model, which evaluated factors associated with the conversion of cellular immunity, showed that participants on campus A, compared with those on campus B, had a lower odds of acquiring coccidioidal infection (adjusted OR 0.42, 95% CI 0.15-1.19; p = 0.10). Regularly taking walks outdoors was associated with increased odds of acquisition (adjusted OR 3.39, 95% CI 0.74-15.49; p = 0.11).

During the 1-year study period, 1 participant had a clinical episode consistent with new coccidioidal infection. This otherwise healthy 54-year-old woman experienced an insidious onset of heart palpitations, dyspnea, cough, profound fatigue, and new back pain; chest imaging showed a 12-mm solid pulmonary nodule with satellite lesions that were not present in a radiograph from 4 years earlier. The results of coccidioidal serologic testing were positive by enzyme immunoassay for IgG and indeterminate for IgM; immunodiffusion was indeterminate for IgM. This participant received a clinical diagnosis of probable coccidioidomycosis; she recovered clinically and had negative coccidioidal serology results within 6 months, without antifungal treatment. Results of her enrollment and follow-up lymphocyte activation studies were negative. During the study period, short-term (<2 weeks' duration) antifungal treatments were administered to 2 other study participants (1 from each campus) for noncoccidioidal illnesses.


Coccidioidomycosis is a respiratory illness with a variety of clinical manifestations. Approximately two thirds of infected persons are asymptomatic; the remainder show signs and symptoms of systemic and respiratory illness that range from mild to severe and life threatening.

Once a person is infected with Coccidioides fungi, the immune system mounts a complex reaction to control the infection; this reaction eventually results in the presence of cell-mediated and humoral immunity (5,6). Persons who recover uneventfully from coccidioidomycosis become immune and are unlikely to have subsequent coccidioidal infections. Such immunity can be assessed (regardless of the presence or absence of symptomatic illness) with a DTH skin test (5) or an in vitro assay of cellular immunity to Coccidioides spp., such as the assay described in this report. Because the DTH skin test is not commercially available, we elected to use a lymphocyte activation assay to identify any study participants with such immunity (10). As reported by Ampel et al. (10,12), this assay detects the activation marker CD69 on the surface of CD3+ T cells, correlates well with skin test reactivity, and indicates previous (or current) exposure to Coccidioides spp. Although Johnson et al. (13) later used T27K, a coccidioidal antigen preparation, we elected to use coccidioidin filtrate, which has historically been shown to be a good coccidioidal preparation for DTH testing and to be an even better preparation for determining cellular immunity in vitro (14). We chose to use the lymphocyte activation assay rather than standard serologic testing to measure cellular immunity for 3 reasons: 1) serology, while often adequately sensitive for evaluation of clinical illness, is not 100% sensitive (15); 2) serologic sensitivity depends on the time from onset of symptoms and may be undetectable in early or resolved illness (15,16); and 3) in the absence of clinical illness, it may be difficult to distinguish true-positive from false-positive serologic testing results (17). Up to 60% of infections may be asymptomatic, so we wanted an assay that would measure asymptomatic infection.

Coccidioides fungi naturally reside in the top 18 inches of soil in areas where Coccidioides spp. are endemic. However, even within such areas, soil sampling studies aimed at isolating the fungus by culture or by molecular amplification have shown the distribution of Coccidioides fungi to be spotty and erratic, even where the fungi are highly prevalent (18,19). We did not undertake soil sampling studies before construction began, and it is certainly possible that, unbeknownst to us, the soil of the 2 campuses assessed in this study had different concentrations of Coccidioides fungi, and, more specifically, that the soil at the campus A construction site did not have a high level of fungal organisms.

Where present, Coccidioides fungi naturally reside in the top layers of soil; thus, activities that disrupt the soil and create dust, increasing the airborne dissemination of Coccidioides spores, are recognized as risk factors for an increased likelihood of coccidioidal acquisition. Persons engaged in construction, agriculture, archeological digs, and other soil-disrupting activities within areas where Coccidioides fungi are endemic have experienced increased dust exposure and subsequent coccidioidal infection (20-23). In addition, 2 reports have implicated construction as a risk for development of coccidioidomycosis among persons in the surrounding community (24,25).

In 2002, the onset of construction of a mental hospital adjacent to the Pleasant Valley State Prison in California was temporally associated with 127 new cases of coccidioidomycosis among prisoners over the subsequent 15 months; these 127 new cases compared with only 7 cases from the same institution in the preceding year (24). In other, more limited observations, dust control at military bases by natural means (i.e., rainfall) or by artificial measures (e.g., planting lawns or oiling down unpaved roads and airstrips) has been associated with a temporary reduction of airborne dust and with the subsequent rate of coccidioidal infection (25). However, the observations in both of these reports took place over 2 sequential years, and neither study controlled for year-to-year variations in weather (e.g., rainfall, temperature, or wind) or for background cases of coccidioidomycosis within the same area.

In planning this study, we hypothesized that the dust generated from the construction on campus A would result in an increase in the acquisition of coccidioidomycosis among employees at campus A, compared with the acquisition of coccidioidomycosis among employees on campus B, 13 miles away. Knowing that dust-suppression measures would be used at the construction site, we were uncertain about what magnitude of difference to expect in infection rates. However, our findings did not show that the rate of newly acquired coccidioidomycosis was higher among study participants from campus A than among participants from campus B. In fact, the 2.5% rate of newly acquired coccidioidomycosis cases on campus A is essentially the same as the 3% rate of infection previously estimated for residents of Coccidioides spp.-endemic areas (4). Whether the construction and/or the concurrent dust control measures had any effect on the acquisition of infection is not known.

Our findings showed an overall 1-year risk of coccidioidal acquisition of 5.2% (11/210 persons; 95% CI 2.2%-8.3%) among the study participants; this rate is similar to a previous acquisition estimate of 3% per year (4). Rather than finding an increase of coccidioidomycosis among participants on campus A, we instead observed a statistically significantly higher rate of acquisition at the control site, campus B, which is not in an area of known higher risk for coccidioidomycosis and which had no construction being conducted on or in the vicinity of its grounds.

Several factors can affect any person's risk for contact with arthroconidia and subsequent coccidioidal infection (e.g., recreational and other outdoor activities, exposure to dust storms, home or work location close to construction, or prevalent wind patterns). Thus, we examined demographic information provided by study participants to ascertain any risk factors among those with newly identified coccidioidomycosis. We observed an increased risk for coccidioidal acquisition not only among study participants who worked on campus B, but also a trend to significance in risk for participants at both campuses who regularly walked outdoors; no other risk factors emerged. Although walking is a common form of exercise, whether regularly walking outdoors represents a unique risk factor is not clear. In addition, this variable trended to statistical significance by virtue of a larger cohort participating in the activity; it is possible that this activity is merely an indirect marker of time spent outdoors. We also observed that the participants on each campus tended to reside in separate groups of zip codes, with only some overlap, but no particular residential zip codes were associated with a higher likelihood of infection (data not shown).

This study has several limitations. The study participants were predominantly female and white, reflecting the employee population on the 2 campuses, a factor that may limit the generalizability of our findings. In addition, the CD69 lymphocyte-activation assay has been shown to correlate with helper T cell, subtype 1 ([T.sub.H]1) cytokines, but not with [T.sub.H]2 cytokines. Therefore, if any participants had coccidioidomycosis that did not resolve because of a [T.sub.H]2 immune response, we may not have been able to detect the infection because of inadequate lymphocyte activation (i.e., a false-negative test result) (9). This scenario may explain the situation of the employee from campus A who had protracted, probable, symptomatic coccidioidal infection and an atypical serologic pattern, but who had a negative test result on the second CD69 lymphocyte-activation assay. Alternatively, since CD69 is a nonspecific marker of lymphocyte activation, an immune response to another infectious agent would have elevated a participant's baseline CD69 level, making it difficult to determine whether their PBMCs were responding to coccidioidin or another infection or both.

In summary, by using the CD69 lymphocyte-activation assay, we determined that employees working adjacent to a large construction project involving the excavation of previously undisturbed native desert soil and the use of active dust-control measures, compared with co-workers at another site 13 miles away, did not have an increased risk for acquisition of coccidioidomycosis. That the control group of employees on the second campus had a statistically higher rate of negative to positive assay conversion at 1 year is a finding that merits further study.



We gratefully acknowledge the helpful comments and review of Christopher J. Hilgemann, who oversaw the construction project.

Dr Blair is a consultant in infectious diseases at Mayo Clinic, Scottsdale, Arizona, and a professor of medicine in the Mayo Clinic College of Medicine. Her research interests include the study of coccidioidomycosis in healthy and immunosuppressed hosts.


(1.) Sunenshine RH, Anderson S, Erhart L, Vossbrink A, Kelly PC, Engelthaler D, et al. Public health surveillance for coccidioidomycosis in Arizona. Ann N Y Acad Sci. 2007;1111:96-102. http://dx.doi. org/10.1196/annals.1406.045

(2.) Arizona Department of Health Services. Summary of selected reportable diseases, January-December, 2012 [cited 2013 Oct 4].

(3.) Tsang CA, Anderson SM, Imholte SB, Erhart LM, Chen S, Park BJ, et al. Enhanced surveillance of coccidioidomycosis, Arizona, USA, 2007-2008. Emerg Infect Dis. 2010;16:1738-44. http://dx.doi. org/10.3201/eid1611.100475

(4.) Dodge RR, Lebowitz MD, Barbee R, Burrows B. Estimates of C. immitis infection by skin test reactivity in an endemic community. Am J Public Health. 1985;75:863-5. AJPH.75.8.863

(5.) Cox RA, Magee DM. Coccidioidomycosis: host response and vaccine development. Clin Microbiol Rev. 2004;17:804-39.

(6.) Ampel NM. The complex immunology of human coccidioidomycosis. Ann N Y Acad Sci. 2007;1111:245-58. http://dx.doi. org/10.1196/annals.1406.032

(7.) Laniado-Laborin R. Expanding understanding of epidemiology of coccidioidomycosis in the Western Hemisphere. Ann N Y Acad Sci. 2007;1111:19-34.

(8.) Richards JO, Ampel NM, Galgiani JN, Lake DF. Dendritic cells pulsed with Coccidioides immitis lysate induce antigen-specific naive T cell activation. J Infect Dis. 2001;184:1220-4. http://dx.doi. org/10.1086/323664

(9.) Richards JO, Ampel NM, Lake DF. Reversal of coccidioidal anergy in vitro by dendritic cells from patients with disseminated coccidioidomycosis. J Immunol. 2002;169:2020-5. http://dx.doi. org/10.4049/jimmunol.169.4.2020

(10.) Ampel NM, Kramer LA, Li L, Carroll DS, Kerekes KM, Johnson SM, et al. In vitro whole-blood analysis of cellular immunity in patients with active coccidioidomycosis by using the antigen preparation T27K. Clin Diagn Lab Immunol. 2002;9:1039-43.

(11.) Maricopa County Air Quality Department dust abatement handbook: June 2013 [cited 2013 Oct 18]. aq/divisions/compliance/dust/docs/pdf/.

(12.) Ampel NM, Hector RF, Lindan CP, Rutherford GW. An archived lot of coccidioidin induces specific coccidioidal delayed-type hypersensitivity and correlates with in vitro assays of coccidioidal cellular immune response. Mycopathologia. 2006;161:67-72. http://dx.doi. org/10.1007/s11046-005-0218-8

(13.) Johnson SM, Kerekes KM, Lunetta JM, Pappagianis D. Characteristics of the protective subcellular coccidioidal T27K vaccine. Ann N Y Acad Sci. 2007;1n1:275-89. annals.1406.016

(14.) Ampel NM, Bejarano GC, Salas SD, Galgiani JN. In vitro assessment of cellular immunity in human coccidioidomycosis: relationship between dermal hypersensitivity, lymphocyte transformation, and lymphokine production by peripheral blood mononuclear cells from healthy adults. J Infect Dis. 1992;165:710-5. http://dx.doi. org/10.1093/infdis/165.4.710

(15.) Blair JE, Coakley B, Santelli AC, Hentz JG, Wengenack NL. Serologic testing for symptomatic coccidioidomycosis in immunocompetent and immunosuppressed hosts. Mycopathologia. 2006;162:317-24.

(16.) Pappagianis D, Zimmer BL. Serology of coccidioidomycosis. Clin Microbiol Rev. 1990;3:247-68.

(17.) Blair JE, Mendoza N, Force S, Chang YH, Grys TE. Clinical specificity of the enzyme 18 test for coccidioidomycosis varies according to the reason for its performance. Clin Vaccine Immunol. 2013;20:95-8.

(18.) Lauer A, Baal JD, Baal JC, Verma M, Chen JM. Detection of Coccidioides immitis in Kern County, California, by multiplex PCR. Mycologia. 2012;104:62-9.

(19.) Egeberg RO, Ely AF. Coccidioides immitis in the soil of the southern San Joaquin Valley. Am J Med Sci. 1956;231:151-4. http://dx.doi. org/10.1097/00000441-195602000-00005

(20.) Cummings KC, McDowell A, Wheeler C, McNary J, Das R, Vugia DJ, et al. Point-source outbreak of coccidioidomycosis in construction workers. Epidemiol Infect. 2010;138:507-11.

(21.) Petersen LR, Marshall SL, Barton C, Hajjeh RA, Lindsley MD, Warnock DW, et al. Coccidioidomycosis among workers at archeological site, northeastern Utah. Emerg Infect Dis. 2004;10:637-42.

(22.) Centers for Disease Control and Prevention (CDC). Coccidioidomycosis in travelers returning from Mexico: Pennsylvania, 2000. MMWR Morb Mortal Wkly Rep. 2000;49:1004-6.

(23.) Schmelzer LL, Tabershaw IR. Exposure factors in occupational coccidioidomycosis. Am J Public Health Nations Health. 1968;58:107-13.

(24.) Pappagianis D; Coccidioidomycosis Serology Laboratory. Coccidioidomycosis in California state correctional institutions. Ann N Y Acad Sci. 2007;1111:103-11. annals.1406.011

(25.) Smith CE, Beard RR, Rosenberger HG, Whiting EG. Effect of season and dust control on coccidioidomycosis. J Am Med Assoc. 1946;132:833-8. 90011003

Author affiliations: Mayo Clinic Hospital, Phoenix, Arizona, USA (J.E. Blair); Mayo Clinic, Scottsdale, Arizona (Y.-H. H. Chang, B.E. Heinrich); and Arizona State University, Phoenix (Y Ruiz, S. Duffy, D.F. Lake)

Address for correspondence: Janis E. Blair, Division of Infectious Diseases, Mayo Clinic Hospital, 5777 E Mayo Blvd, Phoenix, AZ 85054, USA; email:

(1) Preliminary findings from this study were presented at the 57th Annual Meeting of the Coccidioidomycosis Study Group, Pasadena, California, USA, April 6, 2013.

Table 1. Characteristics of participants, at enrollment and 1
year later, in a study of distance from a construction site as a
risk factor for coccidioidomycosis, Arizona, UsA, 2012-2013 *

                                              At enrollment,
                                                n = 316

Characteristic                             Campus A ([dagger])

  M                                          28/176 (15.9)
  F                                          148/176 (84.1)

Median age, y (range)                          47 (21-75)

  White                                      144/176 (81.8)
  Hispanic                                    13/176 (7.4)
  Other                                      19/176 (10.8)
Indoor work location                         168/176 (95.5)

Work near a construction site                77/168 (45.8)

Live near a construction site                18/170 (10.6)

New home construction, remodeling,                 NA
landscaping in home or neighborhood
since enrollment ([paragraph])

Regular weekly participation in outdoor
activities (#)
  Running                                    26/176 (14.8)
  Hiking                                     52/176 (29.5)
  Walking                                    107/176 (60.8)
  Yard work                                  53/176 (30.1)

Received diagnosis of coccidioidomycosis           NA
during study period

Initiated antifungal therapy after                 NA

                                             At enrollment,
                                                n = 316

Characteristic                             Campus B ([dagger])

  M                                          20/140 (14.3)
  F                                          120/140 (85.7)

Median age, y (range)                          53 (18-76)

  White                                      119/140 (85.0)
  Hispanic                                    10/140 (7.1)
  Other                                       11/140 (7.9)
Indoor work location                         137/140 (97.9)

Work near a construction site                 2/140 (1.4)

Live near a construction site                 6/135 (4.4)

New home construction, remodeling,                 NA
landscaping in home or neighborhood
since enrollment ([paragraph])

Regular weekly participation in outdoor
activities (#)
  Running                                    23/140 (16.4)
  Hiking                                     39/140 (27.9)
  Walking                                    110/140 (78.6)
  Yard work                                  53/140 (37.9)

Received diagnosis of coccidioidomycosis           NA
during study period

Initiated antifungal therapy after                 NA

                                                At enrollment,
                                                   n = 316

Characteristic                                     p value

  M                                        0.691 ([double dagger])

Median age, y (range)                          0.04 ([section])

  White                                     0.66 ([double dagger])
Indoor work location                        0.35 ([double dagger])

Work near a construction site              <0.001 ([double dagger])

Live near a construction site              0.048 ([double dagger])

New home construction, remodeling,                    NA
landscaping in home or neighborhood
since enrollment ([paragraph])

Regular weekly participation in outdoor
activities (#)
  Running                                   0.69 ([double dagger])
  Hiking                                    0.74 ([double dagger])
  Walking                                  0.007 ([double dagger])
  Yard work                                 0.15 ([double dagger])

Received diagnosis of coccidioidomycosis              NA
during study period

Initiated antifungal therapy after                    NA

                                           At 1 -year follow-up,
                                                 n = 210

Characteristic                              Campus A ([dagger])

  M                                            22/120 (18.3)
  F                                            98/120 (81.7)

Median age, y (range)                           49 (23-72)

  White                                       101/120 (84.2)
  Hispanic                                      7/120 (5.8)
  Other                                        12/120 (10.0)
Indoor work location                          117/119 (98.3)

Work near a construction site                  86/114 (75.4)

Live near a construction site                  17/120 (14.2)

New home construction, remodeling,             28/116 (24.1)
landscaping in home or neighborhood
since enrollment ([paragraph])

Regular weekly participation in outdoor
activities (#)
  Running                                      18/120 (15.0)
  Hiking                                       34/120 (28.3)
  Walking                                      72/120 (60.0)
  Yard work                                    37/120 (30.8)

Received diagnosis of coccidioidomycosis        1/117 (0.9)
during study period

Initiated antifungal therapy after              1/120 (0.9)

                                           At 1 -year follow-up,
                                                 n = 210

Characteristic                              Campus B ([dagger])

  M                                             7/90 (7.8)
  F                                            83/90 (92.2)

Median age, y (range)                           53 (25-76)

  White                                        75/89 (84.3)
  Hispanic                                      7/89 (7.9)
  Other                                         7/89 (7.9)
Indoor work location                           89/90 (98.9)

Work near a construction site                   4/89 (4.5)

Live near a construction site                   8/88 (9.1)

New home construction, remodeling,             19/88 (21.6)
landscaping in home or neighborhood
since enrollment ([paragraph])

Regular weekly participation in outdoor
activities (#)
  Running                                       9/90 (10.0)
  Hiking                                       20/90 (22.2)
  Walking                                      71/90 (78.9)
  Yard work                                    33/90 (36.7)

Received diagnosis of coccidioidomycosis             0
during study period

Initiated antifungal therapy after              1/90 (1.1)

                                             At 1 -year follow-up,
                                                    n = 210

Characteristic                                     p value

Sex                                        0.03 ([double dagger])

Median age, y (range)                         0.04 ([section])

Race/ethnicity                             0.75 ([double dagger])
Indoor work location                       0.67 ([double dagger])

Work near a construction site              <0.001 ([double dagger])

Live near a construction site              0.27 ([double dagger])

New home construction, remodeling,         0.67 ([double dagger])
landscaping in home or neighborhood
since enrollment ([paragraph])

Regular weekly participation in outdoor
activities (#)
  Running                                  0.28 ([double dagger])
  Hiking                                   0.32 ([double dagger])
  Walking                                  0.004 ([double dagger])
  Yard work                                0.37 ([double dagger])

Received diagnosis of coccidioidomycosis          >0.99 **
during study period

Initiated antifungal therapy after                >0.99 **

* Campus A was adjacent to and campus B was 13 miles away from the
construction site, which required extensive excavation of soil
inhabited by Coccidioides fungi, NA, not available.

([dagger]) (Values are no. with characteristic/no. total (%),
except as noted for age.

([double dagger]) By [chi square] test.

([section]) By Wilcoxon rank sum test.

([paragraph]) Work that took place within the past year.

(#) Other activities that were evaluated but did not differ
significantly between campuses were jogging, gardening,
landscaping, golfing, playing team sports, swimming, and biking.

** By Fisher exact test

Table 2. Characteristics of participants, by cellular immunity
conversion status at 1 -year follow up, in a study of distance
from a construction site as a risk factor for coccidioidomycosis,
Arizona, USA, 2012-2013*

                                                  Cellular immunity
                                                  status ([dagger])

Characteristic                                    Negative, n = 199

  M                                                 27/199 (13.6)
  F                                                 172/199 (86.4)
Median age, y (range)                              50.0 (23.0-76.0)

  White                                             165/198 (83.3)
  Hispanic                                           14/198 (7.1)
  Other                                              19/198 (9.6)

Work near a construction site                       87/192 (45.3)

Live near a construction site                       23/198 (11.6)

New home construction, remodeling, landscaping      40/198 (20.2)
in home or neighborhood since enrollments

Regular weekly participation in outdoor
activities ([paragraph])
  Running                                           26/199 (13.1)
  Hiking                                            51/199 (25.6)
  Walking                                           133/199 (66.8)
  Yard work                                         64/199 (32.2)

Employment site
  Campus A                                          117/199 (58.8)
  Campus B                                          82/199 (41.2)

                                                  Cellular immunity
                                                  status ([dagger])

Characteristic                                     Positive, n = 11

  M                                                  2/11 (18.2)
  F                                                  9/11 (81.8)
Median age, y (range)                              52.0 (26.0-71.0)

  White                                              11/11 (100)
  Hispanic                                                0
  Other                                                   0

Work near a construction site                        3/11 (27.3)

Live near a construction site                        2/10 (20.0)

New home construction, remodeling, landscaping        1/9 (11.1)
in home or neighborhood since enrollments

Regular weekly participation in outdoor
activities ([paragraph])
  Running                                             1/11 (9.1)
  Hiking                                             3/11 (27.3)
  Walking                                            10/11 (90.9)
  Yard work                                          6 /II (54.6)

Employment site
  Campus A                                           3/11 (27.3)
  Campus B                                           8/11 (72.7)

                                                      p value
Characteristic                                    ([double dagger])

Sex                                                     0.65
Median age, y (range)                                   0.88

Race/ethnicity                                          0.66

Work near a construction site                           0.35

Live near a construction site                           0.34

New home construction, remodeling, landscaping          0.69
in home or neighborhood since enrollments

Regular weekly participation in outdoor
activities ([paragraph])
  Running                                               >0.99
  Hiking                                                >0.99
  Walking                                               0.18
  Yard work                                             0.19

Employment site                                         0.06
  Campus A
  Campus B

* A CD69 lymphocyte-activation test was used to determine if the
cellular immunity status of participants had converted from
negative to positive.

([dagger]) Values are no. with characteristic/no. total (%),
except as noted for age.

([double dagger]) For age, the Wilcoxon rank sum test was used;
for other variables, the Fisher exact test was used.

([section]) Work that took place within the past year.

([paragraph]) Other activities that were evaluated but that did
not differ significantly between participants who did and did not
convert from negative to positive cellular immunity status were
jogging, gardening, landscaping, golfing, playing team sports,
swimming, and biking.
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Title Annotation:RESEARCH
Author:Blair, Janis E.; Chang, Yu-Hui H.; Ruiz, Yvette; Duffy, Stacy; Heinrich, Beth E.; Lake, Douglas F.
Publication:Emerging Infectious Diseases
Geographic Code:1U8AZ
Date:Sep 1, 2014
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