Differential Thermotolerance Adaptation between Species of Coccidioides
by
, , , , , ,
Heather L. Mead
1, 
Paris S. Hamm
2,
Isaac N. Shaffer
3,
Marcus de Melo Teixeira
4,
Christopher S. Wendel
5,
Nathan P. Wiederhold
6
,
George R. Thompson III
7
,
Raquel Muñiz-Salazar
8,
Laura Rosio Castañón-Olivares
9,
Paul Keim
1,
Carmel Plude
10,
Joel Terriquez
10,
John N. Galgiani
11,
Marc J. Orbach
11,12,† and
Bridget M. Barker
1,11,*,†
1
Pathogen and Microbiome Institute, Northern Arizona University, Flagstaff, AZ 86011, USA
2
Department of Biology, University of New Mexico, Albuquerque, NM 87131, USA
3
School of Informatics, Computers, and Cyber Systems, Northern Arizona University, Flagstaff, AZ 86011, USA
4
Faculty of Medicine, University of Brasilia, Brasilia 70000-000, Brazil
5
Department of Medicine, University of Arizona, Tucson, AZ 85721, USA
6
Department of Pathology and Laboratory Medicine, University of Texas Health Science Center at San Antonio, San Antonio, TX 77030, USA
7
Departments of Internal Medicine Division of Infectious Diseases, and Medical Microbiology and Immunology, University of California-Davis, Sacramento, CA 95616, USA
8
Laboratorio de Epidemiología y Ecología Molecular, Escuela Ciencias de la Salud, Universidad Autónoma de Baja California, Unidad Valle Dorado, Ensenada 22890, Mexico
9
Department of Microbiology and Parasitology, Universidad Nacional Autónoma de Mexico, Ciudad de México 04510, Mexico
10
Northern Arizona Healthcare, Flagstaff, AZ 86001, USA
11
Valley Fever Center for Excellence, University of Arizona, Tucson, AZ 85721, USA
12
School of Plant Sciences, University of Arizona, Tucson, AZ 85721, USA
*
Author to whom correspondence should be addressed.
†
These authors contributed equally to this work.
J. Fungi 2020, 6(4), 366; https://doi.org/10.3390/jof6040366
Submission received: 17 October 2020
/
Revised: 24 November 2020
/
Accepted: 5 December 2020
/
Published: 14 December 2020
(This article belongs to the Special Issue Coccidioides and Coccidioidomycosis 2020)
Abstract
:Coccidioidomycosis, or Valley fever, is caused by two species of dimorphic fungi. Based on molecular phylogenetic evidence, the genus Coccidioides contains two reciprocally monophyletic species: C. immitis and C. posadasii. However, phenotypic variation between species has not been deeply investigated. We therefore explored differences in growth rate under various conditions. A collection of 39 C. posadasii and 46 C. immitis isolates, representing the full geographical range of the two species, was screened for mycelial growth rate at 37 °C and 28 °C on solid media. The radial growth rate was measured for 16 days on yeast extract agar. A linear mixed effect model was used to compare the growth rate of C. posadasii and C. immitis at 37 °C and 28 °C, respectively. C. posadasii grew significantly faster at 37 °C, when compared to C. immitis; whereas both species had similar growth rates at 28 °C. These results indicate thermotolerance differs between these two species. As the ecological niche has not been well-described for Coccidioides spp., and disease variability between species has not been shown, the evolutionary pressure underlying the adaptation is unclear. However, this research reveals the first significant phenotypic difference between the two species that directly applies to ecological research.
1. Introduction
Coccidioidomycosis, or Valley fever, is an environmentally acquired disease caused by inhalation of arthroconidia of dimorphic fungi belonging to the genus Coccidioides. In the environment, the fungi grow as filamentous mycelia, alternate cells of which autolyze and become fragile, leaving intact asexual arthroconidia that may disperse via wind or soil disruption. If inhaled by a susceptible host, an arthroconidium switches to a host-associated lifecycle and develops into a specialized infectious structure called a spherule. Subsequently, the host’s immune system either represses spherule replication or the host succumbs to the illness [1,2]. It is thought that symptomatic infection occurs in approximately 40% of human patients, who exhibit a broad spectrum of clinical symptoms, ranging from acute self-limited pneumonia, fibrocavitary chronic pulmonary infection, or hematogenous spread to extrapulmonary locations (i.e., disseminated infection) [3]. By one estimate, there are 146,000 new symptomatic U.S. coccidioidal infections each year [4] although the reported cases are substantially lower [5].
Coccidioidomycosis is caused by two species, C. immitis and C. posadasii. Genetic analysis of multiple molecular markers has defined two monophyletic clades [6]. Subsequent population genetic/genomic studies revealed that C. immitis is composed of at least two populations in the western U.S., and C. posadasii is composed of three populations widely dispersed across the American continents [7,8,9,10]. Given the high number of autapomorphic mutations between Coccidioides species and among isolates within species, variation in phenotypes is predicted [11]. However, minimal work characterizing phenotypic differences has been undertaken. A previous study demonstrated that C. immitis in vitro spherules grew in a synchronous pattern where C. posadasii isolates did not [12]. Differences in pathogenesis and other disease-associated phenotypic characteristics among strains have been reported, although only one study had species information [13,14,15,16,17,18]. The publication that defined the novel species C. posadasii also found species-specific variance in growth rate on media containing 0.136 M NaCl, suggesting that C. immitis is more salt tolerant than C. posadasii, but due to overlap in the phenotype, and evaluation of only 10 isolates of each species, it was not statistically meaningful [6]. These data supported observations published in the 1950–1960s, which proposed that salinity of the soil may be a factor in determining the distribution of C. immitis in Californian soil [19,20,21]. In contrast, a correlation of C. posadasii with saline soils was not observed in Arizona, where other associations were observed [22,23,24,25,26]. Importantly, recent modeling analysis predicts the future expansion of Coccidioides species in response to changing climate dynamics [27]. Therefore, a robust investigation of abiotic tolerances that may either limit or enhance distribution of Coccidioides is needed [1,28,29]. Such vital information could provide clues regarding the ecological niche, geographical range limits, or host-specific adaptations of the two species of Coccidioides.
The division of Coccidioides into two species has been challenged by clinicians because of the lack of apparent difference in disease manifestation caused by the two pathogens, but recent work suggests that there might be differences in dissemination patterns between the species [1,2,30]. Unfortunately, diagnosis and treatment of coccidioidomycosis does not require clinicians to identify to species. The current diagnostic methods, AccuProbe® [31], CocciDx [32], and CocciENV [33], do not distinguish between the two species. Molecular-based technologies exist to differentiate the two species, but these have not been adapted to clinical use [34,35]. However, genotyping the causative agent would allow correlation of clinical presentations and outcomes associated with species. Severe disease and death typically occurs in high risk group patients; however, seemingly healthy individuals can succumb as well, without a known host immunologic or pathogen genotypic explanation [36]. Currently, the range of disease manifestations is suggested to be primarily due to host factors [37,38]. There are data supporting variation of virulence among individual isolates, but there is limited research on the subject [1,13,16,17,39]. A reasonable hypothesis would acknowledge that both host and pathogen genetics play a role in disease outcome and should be further investigated [40,41,42,43]. Coccidioides, like other human fungal pathogens, can grow at 37 °C—mammalian body temperature—which contributes to establishing host infection [44,45].
Thermotolerance is an intrinsic characteristic of an organism that allows for tolerance of excessively high temperatures. Heat acclimation can shape natural populations for a wide range of microorganisms, and is a physiological adaptation to heat stress imposed by the colonization of new habitats, global climate change and encountering new hosts [46,47,48,49,50,51,52,53,54]. This “preadaptation” is particularly important to pathogenic fungi that can grow in high temperatures, which allows colonization of mammalian tissues [55,56]. For example, Coccidioides is adapted to grow at high temperatures in the environment (i.e., North and South American deserts), and is able to colonize a wide range of endothermic hosts throughout the Americas [57,58,59,60,61]. C. immitis is endemic to the California Central Valley; whereas C. posadasii is widely distributed, but has highest prevalence in the Sonoran Desert. The annual mean temperature varies between the endemic areas, with the California Central Valley having more mild temperatures compared to the Sonoran Desert, which led us to hypothesize that C. posadasii is more thermotolerant than C. immitis. Therefore, we investigated the growth rate of both species at 37 °C and 28 °C, so that we might elucidate species-specific phenotypic variation. Here we demonstrate thermotolerance dissimilarity of the two species by analyzing growth rates of 85 isolates at these two temperatures.
2. Materials and Methods
Strains and Media. 39 C. posadasii strains and 46 C. immitis strains used in this study are primarily human patient isolates archived by various institutions, as detailed in Table 1 [6,8,28,62]. These strains represent both the full geographic range of the two species, and the proposed geographically distinct sub-populations [6,8]. Strains were grown on 2xGYE media (2% glucose, 1% yeast extract, 1.5% agar w/v) to supply initial plugs to inoculate plates for growth analysis, as this is the most common media used in Coccidioides laboratories. Yeast Extract (YE) media (0.5% yeast extract, 1.5% agar w/v) was used for growth experiments. Flagstaff Medical Center isolates were collected under IRB No. 764,034 through Northern Arizona Healthcare as part of the Northern Arizona University Biobank.
Growth Conditions and Measurements. Colonies were started by spreading approximately 106 arthroconidia over the entire surface of a 2xGYE plate to create a lawn of mycelium to be transferred to initiate the thermotolerance experiment; this allowed measurement of colonial growth and not spore germination differences. After five days of growth at 25 °C, 7 mm diameter mycelial plugs were subcultured to the center of YE plates using a transfer tool (Transfertube® Disposable Harvesters, Spectrum® Laboratories, a Repligen Brand, CA, USA). Three replicates of each strain were plated for each experiment. All plates (100 mm × 15 mm BD Falcon 1015, Corning Life Sciences, MA, USA) were sealed with gas permeable seals (TimeMed Time®Tape, PDC Healthcare, CA, USA or Shrink Seals, Scientific Device Laboratory, IL, USA) for safety. Plates were placed in temperature-controlled incubators at either 28 °C or 37 °C in the dark under ambient humidity (30–50% RH) and CO2 (0.1%) conditions. Plate stacks were rotated from top to bottom and repositioned in the incubator with each measurement timepoint to reduce effects of environmental variation within the incubators. For measurement of radial growth, the diameter of each colony was measured in mm at 5, 7, 9, 12, 14, and 16 days post-subculture. The initial experiment occurred at University of Arizona (UA) in 2004, and subsequent testing with a new set of isolates occurred at Northern Arizona University (NAU) in 2019. Details for strains tested at each institution are listed in Table 1 and all raw measurement data are available in File S1.
Statistical Analysis. To estimate the mean growth rate for each species over the two-week period a mixed effect linear model for each temperature was constructed using the lme4 package in R version 3.6.2 [63,64]. Initially, data sets were divided by institution to conduct an analysis of variance; however, after concluding that species-specific growth rate was not strongly impacted by collection site the data sets were combined (Table S1). In the temperature specific models, the factors “day” and “species” were assumed to be fixed linear effects, and individual isolate response for each day was considered to be a normally distributed random effect as appropriate in a longitudinal study. Thus, the response variable of colony diameter was modeled with fixed effects and a random effect to determine if growth rates varied between strains at either 28 °C or 37 °C. Shapiro-Wilk test (p-value < 0.001) shows that residuals are not normally distributed. However, the large sample size and overall residual structure support that a linear model is the most appropriate for this data set. In addition, bootstrapping using the boot package in R [65,66] was used to estimate 95% confidence intervals (CIs) for growth rates and other fixed effects (nsim = 2000). All bootstrap parameters were similar and support model estimates. A comparison between bootstrapped CIs and CIs constructed using the linear model can be found in Table S2.
3. Results
To define variability of one phenotypic trait between two Coccidioides species, we examined the ability of Coccidioides spp. to grow in filamentous form at 37 °C and 28 °C on YE agar. In this study, we surveyed 85 strains of Coccidioides, representing isolates from the entire geographical range (Figure 1). Initial investigations occurred at the University of Arizona, and subsequent studies occurred at Northern Arizona University (Table 1).
We observed that mean growth rates varied between institutions; however, overall species-specific temperature behavior was comparable. Therefore, data sets were combined (Figure S1, Table S1). Using a mixed effect linear model, we showed a significant species-specific difference for growth of the mycelial phase of the fungus based on temperature (Figure 2 and Table 2). Table 2 summarizes the estimated growth rate for each species, 95% confidence interval (CI), and p-value for each temperature specific model. Both species grew faster at 28 °C than 37 °C. Although C. immitis isolates had a larger mean diameter than C. posadasii on all days tested at 28 °C (Table S3), the overall rate of increase was not statistically significant (p-value = 0.072, Table 2). This was in contrast to growth at 37 °C. At this temperature, C. posadasii strains exhibited larger mean diameters, which reached double the diameter of C. immitis by day 16 (Table S4). At this temperature, the overall growth rate of C. posadasii was 1mm/day faster than C. immitis (Figure 2 and Table 2). This difference was statistically significant (p-value < 0.001, Table 2). These findings were consistent for all days tested and represent differential phenotypes for both species. Thus, our analysis indicates that high temperature is the important variable between species growth rate on solid media. This phenotypic difference supports the molecular phylogenetic species designation and may reflect adaptation of C. immitis to cooler environments, or possibly specific hosts.
Summary of temperature specific linear models, for 28 °C and 37 °C, respectively. Colony growth estimates for each species per day (slope), 95% confidence intervals (CI) and p values. At 28 °C, C. immitis grows 3.73 mm/day which is 0.26 mm faster per day than C. posadasii. The difference in slope is not significant (p = 0.072) based on α = 0.05. However, the p-value trends towards significance. At 37 °C, C. immitis grows 0.64mm/day which is 1.18mm slower than C. posadasii. The difference in slope (CI, 0.98–1.38 mm/day) is statistically significant (p < 0.001).
4. Discussion
Although many studies have looked at genetic variation among isolates of both species of Coccidioides, few studies have compared phenotypic differences. Observed genetic diversity between and within species makes it reasonable to hypothesize that phenotypic variation exists. We propose that a methodical documentation of phenotypic variation is a necessary first step to determine the ecological or clinical relevance of these traits. In this study, we have identified a definitive phenotypic difference with a congruent analysis at two institutions for a diverse set of isolates. A total of 85 isolates covering the geographic range of both species show that C. posadasii isolates grow at a significantly faster rate (p < 0.001, Figure 2 and Table 2) than C. immitis isolates in the mycelial form at 37 °C on YE agar. Additionally, C. immitis grows slightly faster than C. posadasii at 28 °C on YE agar although the difference in growth rate is not significant (p-value = 0.072, Figure 2 and Table 2). We note that growth rate may be influenced by nutrition source, and the results are limited to the media utilized for the current study.
Functionally, this phenotype is similar to a classic temperature sensitive (ts) conditional mutant, such that C. immitis exhibits normal growth at permissive temperature, and significantly slower growth under stressful conditions. It is possible that C. immitis could be restored to normal growth at 37 °C by gene replacement with appropriate C. posadasii alleles if candidate genes were identified. Currently, molecular techniques for genetic manipulations of Coccidioides are limited and need to be improved. Several genes and pathways have been described in Aspergillus fumigatus related to thermotolerance [54]. For example, the observed phenotype could be due to mutations in a heat shock protein (Hsp). Hsps are activated in response to changes in temperature and regulate cellular processes associated with morphogenesis, antifungal resistance, and virulence by triggering a wide array of cellular signaling pathways [53,67]. Hsps are activated by a heat shock transcription factor (Hsf) that acts as a thermosensor, regulating the Hsps at specific growth temperatures [68]. Several studies have shown that Coccidioides up-regulates heat shock proteins Hsp20 and Hsp9/12 at high temperature during the parasitic lifecycle while down-regulating Hsp30 and Hsp90 [69,70,71,72]. Further investigation of Hsps and Hsfs in Coccidioides could elucidate mechanisms of the species-specific thermotolerant behavior observed in this study. Alternatively, many classical ts mutants occur in genes required for normal cellular growth and are due to single amino acid changes that affect protein function or stability at the restrictive temperature. For example, a number of colonial temperature sensitive (cot) mutants have been identified in Neurospora crassa. The N. crassa cot-1 mutant has been studied in greatest detail, and the ts defect is due to a SNP causing a single amino acid change in a Ser/Thr protein kinase required for normal hyphal extension, thus resulting in restricted growth at normally permissive temperatures above 32 °C [73,74]. Finally, recent work in Saccharomyces indicates that mitochondrial genotypes are associated with heat tolerance [75]. The mitochondrial genomes of the two species of Coccidioides are also distinct, and thus mitochondrial function is another potential mechanism controlling thermotolerance in Coccidioides [76].
The source of the genotypic variation driving the observed phenotype may be attributable to a stochastic event, such as a founder effect or population bottleneck 10–12 MYA, which is the estimated time that the two species have been separated [6,77]. Alternatively, the observed pattern may be due to selection pressure from a specific environment, host, or directly associated with virulence. In fact, the observed differential thermotolerance as tested in this investigation relates to the saprobic phase of the lifecycle and likely reflects adaptation to specific environments. A pattern of alternating wet–dry conditions has been related to Valley fever incidence across the southwestern U.S. [5,78,79,80,81,82]. It has been proposed that fungal growth occurs during brief periods of heavy moisture during monsoon and winter rainy seasons in the Southwest, which are followed by prolific conidia production when warm temperatures and low rainfall desiccate soils and increase dispersal via dust (i.e., the “grow and blow” hypothesis) [27,79,83]. Additionally, during high temperature periods, it is hypothesized that the surface soil is partially sterilized and many competitors are removed, but Coccidioides spores remain viable [26]. Another hypothesis is that C. posadasii may be better adapted to growth in the high soil temperatures observed in the southwestern deserts compared to the California endemic C. immitis. Maricopa, Pinal, and Pima counties harbor the highest coccidioidomycosis case rates in Arizona due to C. posadasii, and according to the National Centers for Environmental Information [84], the annual mean temperature (1901–2000) were 20.7 °C, 19.8 °C, and 19.2 °C, respectively. On the other hand, Fresno, King and Kern counties, which harbor the highest coccidioidomycosis case rates in California due to C. immitis, had annual mean temperatures of 12.4 °C, 16.9 °C, and 15.8 °C, respectively. The difference in 100-year average annual mean temperature between highly endemic areas of Arizona and California supports our hypothesis that C. posadasii is more adapted during saprobic growth to higher temperatures compared to C. immitis. Alternatively, a preferred host species may vary in normal body temperature, in accordance with the endozoan small mammal reservoir hypothesis proposed by Barker and Taylor [85]. Interestingly, a decline in mean human body temperature (~1.6%) has recently been reported [86]. Whether this impacts coccidioidomycosis rates is unknown.
Published literature to date suggests that disease outcomes are related primarily to host-specific factors [37,38,87], and certainly, host genetic background can impact disease progression. We propose that pathogen-specific variation may also contribute to capricious disease outcomes in coccidioidomycosis patients. Currently, species-specific virulence is not well-documented in Coccidioides research, but has been suggested [1,13]. This is in part due to the use of a few characterized laboratory strains of Coccidioides for most hypothesis testing, primarily strains Silveira, C735 and RS [70,87,88,89,90,91]. Therefore, connecting phenotypic dissimilarity to established genetic variation using genome-wide association studies could provide novel insight into unique characteristics of these genetically distinct pathogens.
5. Conclusions
In summary, we have identified a significant phenotypic difference between C. immitis and C. posadasii. Although growth rate on YE media at two temperatures is the only characteristic we explicitly tested, there are certain to be more phenotypic differences between species, and possibly between populations. This, coupled with the recent availability of the genome sequence of multiple strains for both fungal species, may allow comparative genomic approaches to elucidate candidate genes for thermotolerance regulation in Coccidioides and closely related Onygenales [7].
Supplementary Materials
The following are available online at https://www.mdpi.com/2309-608X/6/4/366/s1, Figure S1. Growth of C. immitis and C. posadasii on YE media at NAU and UA. Seven mm diameter plugs were sub-cultured onto yeast extract plates and radial growth was documented over sixteen days. (A) Radial growth measurements at 28 °C and 37 °C for 85 isolates in triplicate, at both institutions. (B) Representative samples of phenotypic variation observed between species on day sixteen for both NAU and UA experiments. Table S1. Analysis of variance. Impact of institution collection site was investigated for each temperature specific model. The factors “day”, “species”, and “lab” were assumed to be fixed linear effects, and individual isolate response for each day was considered to be a normally distributed random effect as appropriate in a longitudinal study. The Factor “Lab” location adds variation to the data sets but does not alter overall findings. Species specific behavior based on temperature pattern remain. Table S2. Comparison Linear Model and Bootstrap Values. Comparison of linear model and bootstrap 95% confidence intervals for 28 °C and 37 °C data sets. Bootstrapping conducted using the boot package in R. S1 File. Final Raw Data for Temperature Differences at 37 °C and 28 °C. Measurements (diameter in mm) for each isolate on each plate were recorded on days 5, 7, 9, 12, 14, and 16. Three replicates were completed for each strain for both temperature conditions. Strain details are listed in Table 1. Table S3. Mean Colony Diameter at 28 °C. Mean diameter and standard deviation for C. posadasii and C. immitis at 28 °C. Welch’s t-test was used to compare difference in means. Mean is significantly different on all days tested. Significance is reduced on day 16. Table S4. Mean Colony Diameter at 37 °C. Mean diameter and standard deviation for C. posadasii and C. immitis at 37 °C. Welch’s t-test was used to compare difference in means at each time point. Mean is significantly different on all days tested.
Author Contributions
H.L.M., P.S.H., M.d.M.T., C.S.W., M.J.O. and B.M.B. prepared the initial draft of the manuscript. B.M.B., M.J.O., and J.N.G. developed the concept, provided funding, and were responsible for approving the final draft of the manuscript. M.d.M.T., H.L.M., P.S.H. assisted with creation of figures and writing final manuscript. I.N.S, H.L.M., and C.S.W. developed statistical models. H.L.M., P.S.H., B.M.B., performed experiments and collected data. N.P.W., G.R.T.III, R.M.-S., L.R.C.-O., P.K., C.P., J.T., J.N.G., provided isolates. All authors have read and agreed to the published version of the manuscript.
Funding
This work was funded through an ADCRC grant (Project #6017) NIH grant 1 PO 1AI061310-01, and the US Department of Veterans Affairs. BMB was supported by NSF IGERT fellowship in Genomics NSF-DGE 0114420 at the University of Arizona, and current support by Arizona Department of Health Services ABRC New Investigator grant 16-162415. This work was funded in part by a University of New Mexico (UNM) Graduate and Professional Student Association High Priority Grant to PSH and to HLM through the Grants in Community, Culture, and Environment by The Center for Ecosystem Science and Society and the McAllister Program in Community, Culture, and Environment at Northern Arizona University. Flagstaff Medical Center isolates were collected under IBR No. 764034 through Northern Arizona Healthcare as part of the Northern Arizona University Biobank. Funding for this biobank was provided by the Flinn Foundation of Arizona seed grant #1978 to P. Keim and J. Terriquez.
Acknowledgments
We are indebted to J. Taylor at UC Berkeley and G. Koenig at Roche Molecular Systems for assistance with obtaining several strains for phenotypic analysis. Special appreciation goes to E. Kellner, H. Paes and E. Temporini for their helpful suggestions.
Conflicts of Interest
The authors declare no conflict of interest.
References
- Cox, R.A.; Magee, D.M. Coccidioidomycosis: Host Response and Vaccine Development. Clin. Microbiol. Rev. 2004, 17, 804–839. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Lewis, E.R.G.; Bowers, J.R.; Barker, B.M. Dust Devil: The Life and Times of the Fungus That Causes Valley Fever. PLoS Pathog. 2015, 11, e1004762. [Google Scholar] [CrossRef] [PubMed]
- Galgiani, J.N.; Ampel, N.M.; Catanzaro, A.; Johnson, R.H.; Stevens, D.A.; Williams, P.L. Practice Guidelines for the Treatment of Coccidioidomycosis. Clin. Infect. Dis. 2000, 30, 658–661. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Freedman, M.B.; Jackson, B.R.; Benedict, R.; McCotter, O.; Benedict, K. Preliminary Estimates of Annual Burden of Coccidioidomycosis in the United States, 2010–2014. In Coccidioidomycosis Study Group 61st Annual Meeting in collaboration with the 7th International Coccidioidomycosis Symposium; Group CS, Ed.; Coccidioidomycosis Study Group: Palo Alto, CA, USA, 2017; p. 32. [Google Scholar]
- Centers for Disease Control and Prevention (CDC). Increase in reported coccidioidomycosis—United States, 1998–2011. MMWR Morb. Mortal Wkly. Rep. 2013, 62, 217–221. [Google Scholar]
- Fisher, M.C.; Koenig, G.L.; White, T.J.; Taylor, J.W. Molecular and Phenotypic Description of Coccidioides posadasii sp. nov., Previously Recognized as the Non-California Population of Coccidioides immitis. Mycologia 2002, 94, 73–84. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Engelthaler, D.M.; Roe, C.C.; Hepp, C.M.; Teixeira, M.; Driebe, E.M.; Schupp, J.M.; Gade, L.; Waddell, V.; Komatsu, K.; Arathoon, E.; et al. Local Population Structure and Patterns of Western Hemisphere Dispersal for Coccidioides spp., the Fungal Cause of Valley Fever. mBio 2016, 7, e00550-16. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Teixeira, M.M.; Barker, B.M. Use of Population Genetics to Assess the Ecology, Evolution, and Population Structure of Coccidioides. Emerg. Infect. Dis. 2016, 22, 1022–1030. [Google Scholar] [CrossRef] [Green Version]
- Maxwell, C.S.; Mattox, K.; Turissini, D.A.; Teixeira, M.M.; Barker, B.M.; Matute, D.R. Gene exchange between two divergent species of the fungal human pathogen, Coccidioides. Evolution 2019, 73, 42–58. [Google Scholar] [CrossRef] [Green Version]
- Teixeira, M.M.; Alvarado, P.; Roe, C.C.; Thompson, G.R., 3rd; Patane, J.S.L.; Sahl, J.W.; Keim, P.; Galgiani, J.N.; Litvintseva, A.P.; Matute, D.R.; et al. Population Structure and Genetic Diversity among Isolates of Coccidioides posadasii in Venezuela and Surrounding Regions. mBio 2019, 10. [Google Scholar] [CrossRef] [Green Version]
- Neafsey, D.E.; Barker, B.M.; Sharpton, T.J.; Stajich, J.E.; Park, D.J.; Whiston, E.; Hung, C.-Y.; Mcmahan, C.; White, J.; Sykes, S.; et al. Population genomic sequencing of Coccidioides fungi reveals recent hybridization and transposon control. Genome Res. 2010, 20, 938–946. [Google Scholar] [CrossRef] [Green Version]
- Mead, H.L.; Teixeira, M.D.M.; Galgiani, J.N.; Barker, B.M. Characterizing in vitro spherule morphogenesis of multiple strains of both species of Coccidioides. Med. Mycol. 2019, 57, 478–488. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Lewis, E.R.G.; David, V.R.; Doyle, A.L.; Rajabi, K.; Kiefer, J.A.; Pirrotte, P.; Barker, B.M. Differences in Host Innate Responses among Coccidioides Isolates in a Murine Model of Pulmonary Coccidioidomycosis. Eukaryot. Cell 2015, 14, 1043–1053. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Friedman, L.; Smith, C.E. The comparison of four strains of Coccidioides immitis with diverse histories. Mycopathol. Mycol. Appl. 1957, 8, 47–53. [Google Scholar] [CrossRef] [PubMed]
- Berman, R.J.; Friedman, L.; Pappagianis, D.; Smith, C.E. Survival of Coccidioides immitis Under Controlled Conditions of Temperature and Humidity. Am. J. Public Health Nations Health 1956, 46, 1317–1324. [Google Scholar]
- Friedman, L.; Smith, C.E.; Roessler, W.G.; Berman, R. The virulence and infectivity of twenty-seven strains of Coccidioides immitis. Am. J. Epidemiol. 1956, 64, 198–210. [Google Scholar] [CrossRef]
- Friedman, L.; Smith, C.E.; Gordon, L.E. The Assay of Virulence of Coccidioides in White Mice. J. Infect. Dis. 1955, 97, 311–316. [Google Scholar] [CrossRef]
- Huppert, M.; Walker, L.J. The selective and differential effects of cycloheximide on many strains of Coccidioides immitis. Am. J. Clin. Pathol. 1958, 29, 291–295. [Google Scholar] [CrossRef]
- Egeberg, R.O.; Elconin, A.E.; Egeberg, M.C. Effect of Salinity and Temperature on Coccidioides Immitis and Three Antagonistic Soil Saprophytes. J. Bacteriol. 1964, 88, 473–476. [Google Scholar] [CrossRef] [Green Version]
- Egeberg, R.O.; Ely, A.F. Coccidioides immitis in the soil of the southern San Joaquin Valley. Am. J. Med. Sci. 1956, 231, 151–154. [Google Scholar] [CrossRef]
- Elconin, A.F.; Egeberg, R.O.; Egeberg, M.C. Significance of soil salinity on the ecology of Coccidioides immitis. J. Bacteriol. 1964, 87, 500–503. [Google Scholar] [CrossRef] [Green Version]
- Emmons, C.W.; Ashburn, L.L. The Isolation of Haplosporangium parvum n. sp. and Coccidioides immitis from Wild Rodents. Their Relationship to Coccidioidomycosis. Public Health Rep. 1942, 57, 1715. [Google Scholar] [CrossRef]
- Emmons, C.W. Isolation of Coccidioides from Soil and Rodents. Public Health Rep. 1942, 57, 109. [Google Scholar] [CrossRef]
- Maddy, K.T. The geographic distribution of Coccidioides immitis and possible ecologic implications. Ariz. Med. 1958, 15, 178–188. [Google Scholar] [PubMed]
- Maddy KT, C.H. Establishment of Coccidiodies immitis in Negative Soil Following Burial of Infected Animal Tissues. In Proceedings of the Second Symposium on Coccidioidomycosis, Phoenix, AZ, USA, 8–10 December 1965; pp. 309–312. [Google Scholar]
- Maddy, K.T. Observations on Coccidioides immitis found growing naturally in soil. Ariz. Med. 1965, 22, 281–288. [Google Scholar] [PubMed]
- Gorris, M.E.; Treseder, K.K.; Zender, C.; Randerson, J.T. Expansion of Coccidioidomycosis Endemic Regions in the United States in Response to Climate Change. GeoHealth 2019, 3, 308–327. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Barker, B.M.; Tabor, J.A.; Shubitz, L.F.; Perrill, R.; Orbach, M.J. Detection and phylogenetic analysis of Coccidioides posadasii in Arizona soil samples. Fungal Ecol. 2012, 5, 163–176. [Google Scholar] [CrossRef]
- Barker, B.M.; Litvintseva, A.P.; Riquelme, M.; Vargas-Gastelum, L. Coccidioides ecology and genomics. Med. Mycol. 2019, 57 (Suppl. 1), S21–S29. [Google Scholar] [CrossRef]
- Luna-Isaac, J.A.; Muñiz-Salazar, R.; Baptista-Rosas, R.C.; Enríquez-Paredes, L.M.; Castañón-Olivares, L.R.; Contreras-Pérez, C.; Bazán-Mora, E.; González, G.M.; González-Martínez, M.R. Genetic analysis of the endemic fungal pathogens Coccidioides posadasii and Coccidioides immitis in Mexico. Med. Mycol. 2014, 52, 156–166. [Google Scholar] [CrossRef]
- McGinnis, M.R.; Smith, M.B.; Hinson, E. Use of the Coccidioides posadasii Deltachs5 strain for quality control in the ACCUPROBE culture identification test for Coccidioides immitis. J. Clin. Microbiol. 2006, 44, 4250–4251. [Google Scholar] [CrossRef] [Green Version]
- Litvintseva, A.P.; Marsden-Haug, N.; Hurst, S.; Hill, H.; Gade, L.; Driebe, E.M.; Ralston, C.; Roe, C.; Barker, B.M.; Goldoft, M.; et al. Valley Fever: Finding New Places for an Old Disease: Coccidioides immitis Found in Washington State Soil Associated with Recent Human Infection. Clin. Infect. Dis. 2014, 60, e1–e3. [Google Scholar] [CrossRef] [Green Version]
- Bowers, J.R.; Parise, K.L.; Kelley, E.J.; Lemmer, D.; Schupp, J.M.; Driebe, E.M.; Engelthaler, D.M.; Keim, P.; Barker, B.M. Direct detection of Coccidioides from Arizona soils using CocciENV, a highly sensitive and specific real-time PCR assay. Med. Mycol. 2019, 57, 246–255. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Sheff, K.; York, E.; Driebe, E.; Barker, B.M.; Rounsley, S.; Waddell, V.; Beckstrom-Sternberg, S.; Beckstrom-Sternberg, J.S.; Keim, P.; Engelthaler, D. Development of a rapid, cost-effective TaqMan Real-Time PCR Assay for identification and differentiation of Coccidioides immitis and Coccidioides posadasii. Med. Mycol. 2009, 48, 1–4. [Google Scholar] [CrossRef]
- Hamm, P.S.; Hutchison, M.I.; Leonard, P.; Melman, S.; Natvig, D.O. First Analysis of Human Coccidioides Isolates from New Mexico and the Southwest Four Corners Region: Implications for the Distributions of C. posadasii and C. immitis and Human Groups at Risk. J. Fungi 2019, 5, 74. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Catanzaro, A.; Drutz, D.J. Pulmonary Coccidioidomycosis. Coccidioidomycosis 1980, 32, 147–161. [Google Scholar]
- Odio, C.D.; Marciano, B.E.; Galgiani, J.N.; Holland, S.M. Risk Factors for Disseminated Coccidioidomycosis, United States. Emerg. Infect. Dis. 2017, 23, 308–311. [Google Scholar] [CrossRef]
- Galgiani, J. How does genetics influence valley fever? Research underway now to answer this question. Southwest J. Pulm. Crit. Care 2014, 9, 230–237. [Google Scholar] [CrossRef]
- Shubitz, L.F.; Powell, A.D.; Butkiewicz, C.D.; Lewis, M.L.; Trinh, H.T.; Frelinger, A.J.; Orbach, M.J.; Galgiani, J.N. A Chronic Murine Disease Model of Coccidioidomycosis Using Coccidioides posadasii, Strain 1038. J. Infect. Dis. 2020. [Google Scholar] [CrossRef]
- Davis, K.M. All Yersinia Are Not Created Equal: Phenotypic Adaptation to Distinct Niches Within Mammalian Tissues. Front. Cell. Infect. Microbiol. 2018, 8, 261. [Google Scholar] [CrossRef]
- Phan, H.T.; Rybak, K.; Furuki, E.; Breen, S.; Solomon, P.S.; Oliver, R.P.; Tan, K.-C. Differential effector gene expression underpins epistasis in a plant fungal disease. Plant J. 2016, 87, 343–354. [Google Scholar] [CrossRef]
- Abdelsamed, H.; Peters, J.; Byrne, G.I. Genetic variation in Chlamydia trachomatis and their hosts: Impact on disease severity and tissue tropism. Future Microbiol. 2013, 8, 1129–1146. [Google Scholar] [CrossRef] [Green Version]
- Freguja, R.; Gianesin, K.; Zanchetta, M.; De Rossi, A. Cross-talk between virus and host innate immunity in pediatric HIV-1 infection and disease progression. New Microbiol. 2012, 35, 249–257. [Google Scholar] [PubMed]
- Gauthier, G.M. Fungal Dimorphism and Virulence: Molecular Mechanisms for Temperature Adaptation, Immune Evasion, and In Vivo Survival. Mediat. Inflamm. 2017, 2017, 1–8. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Sil, A.; Andrianopoulos, A. Thermally Dimorphic Human Fungal Pathogens—Polyphyletic Pathogens with a Convergent Pathogenicity Trait. Cold Spring Harb. Perspect. Med. 2015, 5, a019794. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Perini, L.; Mogrovejo, D.C.; Tomazin, R.; Gostinčar, C.; Brill, F.H.H.; Gunde-Cimerman, N. Phenotypes Associated with Pathogenicity: Their Expression in Arctic Fungal Isolates. Microorganisms 2019, 7, 600. [Google Scholar] [CrossRef] [Green Version]
- Williams-Rhaesa, A.M.; Awuku, N.K.; Lipscomb, G.L.; Poole, F.L.; Rubinstein, G.M.; Conway, J.M.; Kelly, R.M.; Adams, M.W.W. Native xylose-inducible promoter expands the genetic tools for the biomass-degrading, extremely thermophilic bacterium Caldicellulosiruptor bescii. Extremophiles 2018, 22, 629–638. [Google Scholar] [CrossRef]
- Besten, H.M.D.; Wells-Bennik, M.H.; Zwietering, M.H. Natural Diversity in Heat Resistance of Bacteria and Bacterial Spores: Impact on Food Safety and Quality. Annu. Rev. Food Sci. Technol. 2018, 9, 383–410. [Google Scholar] [CrossRef]
- Barzkar, N.; Homaei, A.; Hemmati, R.; Patel, S. Thermostable marine microbial proteases for industrial applications: Scopes and risks. Extremophiles 2018, 22, 335–346. [Google Scholar] [CrossRef]
- Choi, D.-H.; Park, E.-H.; Kim, M.-D. Isolation of thermotolerant yeast Pichia kudriavzevii from nuruk. Food Sci. Biotechnol. 2017, 26, 1357–1362. [Google Scholar] [CrossRef]
- Kamthan, A.; Kamthan, M.; Datta, A. Expression of C-5 sterol desaturase from an edible mushroom in fisson yeast enhances its ethanol and thermotolerance. PLoS ONE 2017, 12, e0173381. [Google Scholar] [CrossRef]
- Matsushita, K.; Azuma, Y.; Kosaka, T.; Yakushi, T.; Hoshida, H.; Akada, R.; Yamada, M. Genomic analyses of thermotolerant microorganisms used for high-temperature fermentations. Biosci. Biotechnol. Biochem. 2015, 80, 655–668. [Google Scholar] [CrossRef] [Green Version]
- Reidy, M.; Sharma, R.; Shastry, S.; Roberts, B.-L.; Albino-Flores, I.; Wickner, S.; Masison, D.C. Hsp40s Specify Functions of Hsp104 and Hsp90 Protein Chaperone Machines. PLoS Genet. 2014, 10, e1004720. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Bhabhra, R.; Askew, D.S. Thermotolerance and virulence of Aspergillus fumigatus: Role of the fungal nucleolus. Med. Mycol. 2005, 43, 87–93. [Google Scholar] [CrossRef] [PubMed]
- Robert, V.A.; Casadevall, A. Vertebrate Endothermy Restricts Most Fungi as Potential Pathogens. J. Infect. Dis. 2009, 200, 1623–1626. [Google Scholar] [CrossRef] [PubMed]
- Casadevall, A.; Steenbergen, J.N.; Nosanchuk, J.D. ‘Ready made’ virulence and ‘dual use’ virulence factors in pathogenic environmental fungi—The Cryptococcus neoformans paradigm. Curr. Opin. Microbiol. 2003, 6, 332–337. [Google Scholar] [CrossRef]
- Denham, S.T.; Wambaugh, M.A.; Brown, J.C.S. How Environmental Fungi Cause a Range of Clinical Outcomes in Susceptible Hosts. J. Mol. Biol. 2019, 431, 2982–3009. [Google Scholar] [CrossRef]
- Reyes-Montes, M.D.R.; Pérez-Huitrón, M.A.; Ocaña-Monroy, J.L.; Frías-De-León, M.G.; Martínez-Herrera, E.; Arenas, R.; Duarte-Escalante, E. The habitat of Coccidioides spp. and the role of animals as reservoirs and disseminators in nature. BMC Infect. Dis. 2016, 16, 550. [Google Scholar]
- Shubitz, L.F. Comparative Aspects of Coccidioidomycosis in Animals and Humans. Ann. N. Y. Acad. Sci. 2007, 1111, 395–403. [Google Scholar] [CrossRef]
- Eulalio, K.D.; De Macedo, R.L.; Cavalcanti, M.D.A.S.; Martins, L.M.S.; Lazéra, M.D.S.; Wanke, B. Coccidioides immitis isolated from armadillos (Dasypus novemcinctus) in the state of Piauí, northeast Brazil. Mycopathologia 2001, 149, 57–61. [Google Scholar]
- Swatek, F.E.; Plunkett, O.A. Experimental Infections of Wild Rodents and Animals other than Mammals. In Proceedings of the First Symposium on Coccidiodomycosis; Ajello, L., Ed.; University of Arizona Press: Phoenix, AZ, USA, 1957; pp. 161–167. [Google Scholar]
- Burt, A.; Carter, D.A.; Koenig, G.L.; White, T.J.; Taylor, J.W. Molecular markers reveal cryptic sex in the human pathogen Coccidioides immitis. Proc. Natl. Acad. Sci. USA 1996, 93, 770–773. [Google Scholar] [CrossRef] [Green Version]
- Bates, D.; Machler, M.; Bolker, B.M.; Walker, S.C. Fitting Linear Mixed-Effects Models Using lme4. J. Stat. Softw. 2015, 67, 1–48. [Google Scholar] [CrossRef]
- R Core Team. R: A Language and Environment for Statistical Computing; R Core Team: Vienna, Australia, 2020. [Google Scholar]
- Canty, A.R.; Ripley, B.D. Boot: Bootstrap R (S-Plus) Functions, R package version 1.3-24; Cambridge University Press: Cambridge, UK, 2019. [Google Scholar]
- Davison, A.C.; Hinkley, D.V. Bootstrap Methods and Their Application; Cambridge University Press: Cambridge, UK; New York, NY, USA, 1997. [Google Scholar]
- Tiwari, S.; Thakur, R.; Shankar, J. Role of Heat-Shock Proteins in Cellular Function and in the Biology of Fungi. Biotechnol. Res. Int. 2015, 2015, 132635. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Brown, A.J.P.; Leach, M.D.; Nicholls, S. The relevance of heat shock regulation in fungal pathogens of humans. Virulence 2010, 1, 330–332. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Viriyakosol, S.; Singhania, A.; Fierer, J.; Goldberg, J.; Kirkland, T.N.; Woelk, C.H. Gene expression in human fungal pathogen Coccidioides immitis changes as arthroconidia differentiate into spherules and mature. BMC Microbiol. 2013, 13, 121. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Whiston, E.; Wise, H.Z.; Sharpton, T.J.; Jui, G.; Cole, G.T.; Taylor, J.W. Comparative Transcriptomics of the Saprobic and Parasitic Growth Phases in Coccidioides spp. PLoS ONE 2012, 7, e41034. [Google Scholar] [CrossRef] [Green Version]
- Mead, H.L.; Roe, C.C.; Keppler, E.A.H.; Van Dyke, M.C.C.; Laux, K.L.; Funke, A.; Miller, K.J.; Bean, H.D.; Sahl, J.W.; Barker, B.M. Defining Critical Genes During Spherule Remodeling and Endospore Development in the Fungal Pathogen, Coccidioides posadasii. Front. Genet. 2020, 11, 483. [Google Scholar] [CrossRef]
- Narra, H.P.; Shubitz, L.F.; Mandel, M.A.; Trinh, H.T.; Griffin, K.; Buntzman, A.S.; Frelinger, J.A.; Galgiani, J.N.; Orbach, M.J. A Coccidioides posadasii CPS1 Deletion Mutant Is Avirulent and Protects Mice from Lethal Infection. Infect. Immun. 2016, 84, 3007–3016. [Google Scholar] [CrossRef] [Green Version]
- Gorovits, R.; Propheta, O.; Kolot, M.; Dombradi, V.; Yarden, O. A Mutation within the Catalytic Domain of COT1 Kinase Confers Changes in the Presence of Two COT1 Isoforms and in Ser/Thr Protein Kinase and Phosphatase Activities in Neurospora crassa. Fungal Genet. Biol. 1999, 27, 264–274. [Google Scholar] [CrossRef] [Green Version]
- Yarden, O.; Plamann, M.; Ebbole, D.J.; Yanofsky, C. cot-1, a gene required for hyphal elongation in Neurospora crassa, encodes a protein kinase. EMBO J. 1992, 11, 2159–2166. [Google Scholar] [CrossRef]
- Li, X.C.; Peris, D.; Hittinger, C.T.; Sia, E.A.; Fay, J.C. Mitochondria-encoded genes contribute to evolution of heat and cold tolerance in yeast. Sci. Adv. 2019, 5, eaav1848. [Google Scholar] [CrossRef] [Green Version]
- Teixeira, M.d.M.; Lang, B.F.; Daniel, R.; Matute, D.R.; Stajich, J.E.; Barker, B. Structural characterization and evolutionary analyses of the Coccidioides immitis and Coccidioides posadasii mitochondrial genomes. bioRxiv 2020. [Google Scholar] [CrossRef]
- Fisher, M.C.; Koenig, G.L.; White, T.J.; San-Blas, G.; Negroni, R.; Alvarez, I.G.; Wanke, B.; Taylor, J.W. Biogeographic range expansion into South America by Coccidioides immitis mirrors New World patterns of human migration. Proc. Natl. Acad. Sci. USA 2001, 10, 4558–4562. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Park, B.J.; Sigel, K.; Vaz, V.; Komatsu, K.; McRill, C.; Phelan, M.; Colman, T.; Comrie, A.C.; Warnock, D.W.; Galgiani, J.N.; et al. An Epidemic of Coccidioidomycosis in Arizona Associated with Climatic Changes, 1998–2001. J. Infect. Dis. 2005, 191, 1981–1987. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Kolivras, K.N.; Comrie, A.C. Modeling valley fever (coccidioidomycosis) incidence on the basis of climate conditions. Int. J. Biometeorol. 2003, 47, 87–101. [Google Scholar] [CrossRef] [PubMed]
- Gorris, M.E.; Cat, L.A.; Zender, C.; Treseder, K.K.; Randerson, J.T. Coccidioidomycosis Dynamics in Relation to Climate in the Southwestern United States. GeoHealth 2018, 2, 6–24. [Google Scholar] [CrossRef]
- Coopersmith, E.J.; Bell, J.E.; Benedict, K.; Shriber, J.; McCotter, O.; Cosh, M.H. Relating coccidioidomycosis (valley fever) incidence to soil moisture conditions. GeoHealth 2017, 1, 51–63. [Google Scholar] [CrossRef]
- Comrie, A.C. Climate Factors Influencing Coccidioidomycosis Seasonality and Outbreaks. Environ. Health Perspect. 2005, 113, 688–692. [Google Scholar] [CrossRef]
- Maddy, K.T.; Coccozza, J. The Probable Geographic Distribution of Coccidioides Immitis in Mexico. Bol. Oficina Sanit. Panam. 1964, 57, 44–54. [Google Scholar]
- NOAA. National Centers for Environmental information. In Climate at a Glance: County Mapping; NOAA: Asheville, NC, USA, 2020. [Google Scholar]
- Taylor, J.W.; Barker, B.M. The endozoan, small-mammal reservoir hypothesis and the life cycle of Coccidioides species. Med. Mycol. 2019, 57, S16–S20. [Google Scholar] [CrossRef]
- Protsiv, M.; Ley, C.; Lankester, J.; Hastie, T.; Parsonnet, J. Decreasing human body temperature in the United States since the industrial revolution. Elife 2020, 9. [Google Scholar] [CrossRef]
- Sampaio, E.P.; Hsu, A.P.; Pechacek, J.; Bax, H.I.; Dias, D.L.; Paulson, M.L.; Chandrasekaran, P.; Rosen, L.B.; Carvalho, D.S.; Ding, L.; et al. Signal transducer and activator of transcription 1 (STAT1) gain-of-function mutations and disseminated coccidioidomycosis and histoplasmosis. J. Allergy Clin. Immunol. 2013, 131, 1624–1634. [Google Scholar] [CrossRef]
- González, Á.; Hung, C.-Y.; Cole, G.T. Coccidioides releases a soluble factor that suppresses nitric oxide production by murine primary macrophages. Microb. Pathog. 2011, 50, 100–108. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Hung, C.Y.; Zhang, H.; Castro-Lopez, N.; Ostroff, G.R.; Khoshlenar, P.; Abraham, A.; Cole, G.T.; Negron, A.; Forsthuber, T.; Peng, T.; et al. Glucan-Chitin Particles Enhance Th17 Response and Improve Protective Efficacy of a Multivalent Antigen (rCpa1) against Pulmonary Coccidioides posadasii Infection. Infect. Immun. 2018, 86. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Kirkland, T.N.; Fierer, J. Coccidioides immitis and posadasii; A review of their biology, genomics, pathogenesis, and host immunity. Virulence 2018, 9, 1426–1435. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Viriyakosol, S.; Kapoor, M.; Okamoto, S.; Covel, J.; Soltow, Q.A.; Trzoss, M.; Shaw, K.J.; Fierer, J. APX001 and Other Gwt1 Inhibitor Prodrugs Are Effective in Experimental Coccidioides immitis Pneumonia. Antimicrob. Agents Chemother. 2018, 63, e01715-18. [Google Scholar] [CrossRef] [Green Version]
Figure 1.
Temperature impacts growth ability of C. immitis isolates compared to C. posadasii on YE media. Seven mm diameter plugs were sub-cultured onto yeast extract plates and radial growth was documented over 16 days. (A) Radial growth measurements at 37 °C for 46 C. posadasii and 39 C. immitis isolates in triplicate. (B) Radial growth measurements at 28 °C for 46 C. posadasii and 39 C. immitis isolates in triplicate. (C) Representative of phenotypic variation observed for C. immitis on day 16. (D) Representative of phenotypic variation observed for C. posadasii on day 16.
Figure 1.
Temperature impacts growth ability of C. immitis isolates compared to C. posadasii on YE media. Seven mm diameter plugs were sub-cultured onto yeast extract plates and radial growth was documented over 16 days. (A) Radial growth measurements at 37 °C for 46 C. posadasii and 39 C. immitis isolates in triplicate. (B) Radial growth measurements at 28 °C for 46 C. posadasii and 39 C. immitis isolates in triplicate. (C) Representative of phenotypic variation observed for C. immitis on day 16. (D) Representative of phenotypic variation observed for C. posadasii on day 16.
Figure 2.
Radial growth rate of 85 isolates of Coccidioides demonstrates species-specific response to temperature. Each line represents the mean diameter (y-axis) for each isolate in triplicate (46 C. immitis and 39 C. posadasii) at a given time point (x-axis). Dark lines represent mean growth rate of each species. Radial growth was measured at day 5, 7, 9, 12, 14 and 16. There is a significant difference in growth rate (slope) in response to higher temperature between species of Coccidioides. The radial growth rate of C. immitis is decreased at a higher temperature 37 °C (slope37 = 0.64 mm/day; 95% C.I. 0.51–0.78) compared to C. posadasii (slope37 = 1.82 mm/day; 95% C.I. 1.49–2.16). Both species appear to tolerate 28 °C and grow at a similar rate (C. immitis slope28 = 3.73 mm/day; 95% C.I. 3.53–3.92, C. posadasii, slope28 = 3.47 mm/day; 95% C.I. 2.98–3.90).
Figure 2.
Radial growth rate of 85 isolates of Coccidioides demonstrates species-specific response to temperature. Each line represents the mean diameter (y-axis) for each isolate in triplicate (46 C. immitis and 39 C. posadasii) at a given time point (x-axis). Dark lines represent mean growth rate of each species. Radial growth was measured at day 5, 7, 9, 12, 14 and 16. There is a significant difference in growth rate (slope) in response to higher temperature between species of Coccidioides. The radial growth rate of C. immitis is decreased at a higher temperature 37 °C (slope37 = 0.64 mm/day; 95% C.I. 0.51–0.78) compared to C. posadasii (slope37 = 1.82 mm/day; 95% C.I. 1.49–2.16). Both species appear to tolerate 28 °C and grow at a similar rate (C. immitis slope28 = 3.73 mm/day; 95% C.I. 3.53–3.92, C. posadasii, slope28 = 3.47 mm/day; 95% C.I. 2.98–3.90).
Table 1.
Strain information.
| ID | Species | NCBI Accession | Geographic Origin a | Source | Testing Institution b |
|---|---|---|---|---|---|
| CA22 | C. immitis | NA | California | University of Texas Health Science Center (UTHSC) | NAU |
| 500 | C. posadasii | NA | Soil, Tucson, AZ | University of Arizona (UA) | UA |
| IL1 | C. posadasii | NA | Illinois | UTHSC | NAU |
| CA23 | C. immitis | NA | California | UTHSC | NAU |
| HS-I-000718 | C. posadasii | NA | Arizona | Flagstaff Medical Center (FMC) | NAU |
| GT164 | C. posadasii | NA | Texas | University of California Davis (UCD) | NAU |
| GT163 | C. immitis | NA | California | UCD | NAU |
| HS-I-000588 | C. posadasii | NA | Arizona | FMC | NAU |
| CA28 | C. immitis | NA | California | UTHSC | NAU |
| TX4 | C. posadasii | NA | Texas | UTHSC | NAU |
| HS-I-000235 | C. posadasii | NA | Arizona | FMC | NAU |
| TX1 | C. posadasii | NA | Texas | UTHSC | NAU |
| HS-I-000778 | C. posadasii | NA | Arizona | FMC | NAU |
| GT147 | C. immitis | NA | California | UCD | NAU |
| HS-I-000234 | C. posadasii | NA | Texas | FMC | NAU |
| CA30 | C. immitis | NA | California | UTHSC | NAU |
| HS-I-000547 | C. posadasii | NA | Arizona | FMC | NAU |
| HS-I-000233 | C. posadasii | NA | Arizona | FMC | NAU |
| GT166 | C. posadasii | NA | Texas | UCD | NAU |
| CA24 | C. immitis | NA | California | UTHSC | NAU |
| CA29 | C. immitis | NA | California | UTHSC | NAU |
| M211 | C. posadasii | NA | Central Mexico | Unidad de Micologia, UNAM | NAU |
| GT158 | C. posadasii | NA | Arizona | UCD | NAU |
| CA15 | C. immitis | NA | California | UTHSC | NAU |
| CA27 | C. immitis | NA | California | UTHSC | NAU |
| TX3 | C. posadasii | NA | Texas | UTHSC | NAU |
| CA20 | C. immitis | NA | California | UTHSC | NAU |
| RS | C. immitis | AAEC00000000.3 | California | Common Laboratory Strain | NAU |
| Silveira | C. posadasii | ABAI00000000.2 | California | Common Laboratory Strain | NAU |
| RMSCC2378 | C. posadasii | NA | Argentina | R. Negroni | UA |
| RMSCC2377 | C. posadasii | NA | Argentina | R. Negroni | UA |
| RMSCC2379 | C. posadasii | NA | Argentina | R. Negroni | UA |
| RMSCC3698 | C. immitis | NA | Barstow, California | Naval Hospital | UA |
| RMSCC3490 c | C. posadasii | SRR3468073 | Coahuila, Mexico | I. Gutierrez | UA |
| RMSCC3505 | C. immitis | NA | Coahuila, Mexico | I. Gutierrez | UA |
| RMSCC3506 c | C. posadasii | SRR3468053 | Coahuila, Mexico | I. Gutierrez | UA |
| RMSCC3472 | C. posadasii | NA | Michoacán, Mexico | I. Gutierrez | UA |
| RMSCC3474 | C. immitis | NA | Michoacán, Mexico | I. Gutierrez | UA |
| RMSCC3475 | C. immitis | NA | Michoacán, Mexico | I. Gutierrez | UA |
| RMSCC3476 c | C. immitis | SRR3468020 | Michoacán, Mexico | I. Gutierrez | UA |
| RMSCC3478 | C. posadasii | NA | Michoacán, Mexico | I. Gutierrez | UA |
| RMSCC3479 c | C. immitis | SRR3468018 | Michoacán, Mexico | I. Gutierrez | UA |
| RMSCC3377 | C. immitis | NA | Monterey, California | UCD | UA |
| RMSCC2343 c | C. posadasii | SRR3468064 | Nuevo Leon, Mexico | R. Diaz | UA |
| RMSCC2346 c | C. posadasii | SRR3468065 | Nuevo Leon, Mexico | R. Diaz | UA |
| RMSCC3738 | C. posadasii | NA | Piaui, Brazil | B. Wanke | UA |
| RMSCC3740 | C. posadasii | NA | Piaui, Brazil | B. Wanke | UA |
| RMSCC2127 | C. posadasii | NA | Texas | UTHSC | UA |
| RMSCC2133 | C. posadasii | GCA_000150185.1 | Texas | UTHSC | UA |
| RMSCC2234 | C. posadasii | NA | Texas | UTHSC | UA |
| RMSCC2102 | C. immitis | NA | San Diego, California | University of California San Diego (UCSD) Medical Center | UA |
| RMSCC2394 | C. immitis | GCA_000149895.1 | San Diego, California | UCSD Medical Center | UA |
| RMSCC2395 | C. immitis | NA | San Diego, California | UCSD Medical Center | UA |
| RMSCC3693 | C. immitis | NA | San Diego, California | Naval Hospital | UA |
| RMSCC3703 | C. immitis | GCA_000150085.1 | San Diego, California | UCSD Medical Center | UA |
| RMSCC3705 | C. immitis | NA | San Diego, California | UCSD Medical Center | UA |
| RMSCC3706 c | C. immitis | SRR3468019 | San Diego, California | UCSD Medical Center | UA |
| RMSCC2006 | C. immitis | NA | San Joaquin Valley | Kern County Public Health (KCPH) | UA |
| RMSCC2009 c | C. immitis | SRR3468015 | San Joaquin Valley | KCPH | UA |
| RMSCC2010 | C. immitis | NA | San Joaquin Valley | KCPH | UA and NAU |
| RMSCC2011 | C. immitis | NA | San Joaquin Valley | KCPH | UA |
| RMSCC2012 c | C. immitis | SRR3468016 | San Joaquin Valley | KCPH | UA |
| RMSCC2014 | C. immitis | NA | San Joaquin Valley | KCPH | UA |
| RMSCC2015 c | C. immitis | SRR3468027 | San Joaquin Valley | KCPH | UA |
| RMSCC2017 c | C. immitis | SRR3468038 | San Joaquin Valley | KCPH | UA |
| RMSCC2268 c | C. immitis | SRR3468049 | San Joaquin Valley | KCPH | UA |
| RMSCC2269 c | C. immitis | SRR3468060 | San Joaquin Valley | KCPH | UA |
| RMSCC2271 | C. immitis | NA | San Joaquin Valley | KCPH | UA |
| RMSCC2273 c | C. immitis | SRR3468071 | San Joaquin Valley | KCPH | UA |
| RMSCC2274 | C. immitis | NA | San Joaquin Valley | KCPH | UA |
| RMSCC2275 | C. immitis | NA | San Joaquin Valley | KCPH | UA |
| RMSCC2276 | C. immitis | NA | San Joaquin Valley | KCPH | UA |
| RMSCC2277 c | C. immitis | SRR3468079 | San Joaquin Valley | KCPH | UA |
| RMSCC2278 | C. immitis | NA | San Joaquin Valley | KCPH | UA |
| RMSCC2279 c | C. immitis | SRR3468080 | San Joaquin Valley | KCPH | UA |
| RMSCC2280 c | C. immitis | SRR3468081 | San Joaquin Valley | KCPH | UA |
| RMSCC2281 c | C. immitis | SRR3468017 | San Joaquin Valley | KCPH | UA |
| RMSCC3480 c | C. posadasii | SRR3468051 | Sonora, Mexico | I. Gutierrez | UA |
| RMSCC3487 c | C. posadasii | SRR3468052 | Sonora, Mexico | I. Gutierrez | UA |
| RMSCC3488 | C. posadasii | GCA_000150055.1 | Sonora, Mexico | I. Gutierrez | UA |
| RMSCC1040 | C. posadasii | NA | Tucson, Arizona | UA | UA |
| RMSCC1043 | C. posadasii | NA | Tucson, Arizona | UA | UA |
| RMSCC1044 | C. posadasii | NA | Tucson, Arizona | UA | UA |
| RMSCC1045 | C. posadasii | NA | Tucson, Arizona | UA | UA |
| RMSCC3796 | C. posadasii | NA | Venezuela | G. San-Blas |
a Often patient diagnosis location. b Northern Arizona University (NAU) University of Arizona (UA) c Isolate IDs were changed in Bioproject PRJNA274372 [7].
Table 2.
Temperature Specific Linear Model Slope Estimates for Radial Growth Rate at 28 °C or 37 °C.
Table 2.
Temperature Specific Linear Model Slope Estimates for Radial Growth Rate at 28 °C or 37 °C.
| Colony Diameter at 28 °C | Colony Diameter at 37 °C | |||||
|---|---|---|---|---|---|---|
| Species | mm/Day | 95% CI | P a | mm/day | 95% CI | P a |
| C. immitis × Day | 3.73 | 3.53–3.92 | 0.072 | 0.64 | 0.51–0.78 | <0.001 |
| C. posadasii × Day | 3.47 | 0.55–0.02 | 1.82 | 0.98–1.38 | ||
| N b | 85 | 85 | ||||
a difference between estimated slope, b number of isolates.
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Mead, H.L.; Hamm, P.S.; Shaffer, I.N.; Teixeira, M.d.M.; Wendel, C.S.; Wiederhold, N.P.; Thompson, G.R., III; Muñiz-Salazar, R.; Castañón-Olivares, L.R.; Keim, P.; et al. Differential Thermotolerance Adaptation between Species of Coccidioides. J. Fungi 2020, 6, 366. https://doi.org/10.3390/jof6040366
AMA Style
Mead HL, Hamm PS, Shaffer IN, Teixeira MdM, Wendel CS, Wiederhold NP, Thompson GR III, Muñiz-Salazar R, Castañón-Olivares LR, Keim P, et al. Differential Thermotolerance Adaptation between Species of Coccidioides. Journal of Fungi. 2020; 6(4):366. https://doi.org/10.3390/jof6040366
Chicago/Turabian StyleMead, Heather L., Paris S. Hamm, Isaac N. Shaffer, Marcus de Melo Teixeira, Christopher S. Wendel, Nathan P. Wiederhold, George R. Thompson, III, Raquel Muñiz-Salazar, Laura Rosio Castañón-Olivares, Paul Keim, and et al. 2020. "Differential Thermotolerance Adaptation between Species of Coccidioides" Journal of Fungi 6, no. 4: 366. https://doi.org/10.3390/jof6040366
APA StyleMead, H. L., Hamm, P. S., Shaffer, I. N., Teixeira, M. d. M., Wendel, C. S., Wiederhold, N. P., Thompson, G. R., III, Muñiz-Salazar, R., Castañón-Olivares, L. R., Keim, P., Plude, C., Terriquez, J., Galgiani, J. N., Orbach, M. J., & Barker, B. M. (2020). Differential Thermotolerance Adaptation between Species of Coccidioides. Journal of Fungi, 6(4), 366. https://doi.org/10.3390/jof6040366
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