Abstract
In the past few years, fungal diseases caused estimated over 1.6 million deaths annually and over one billion people suffer from severe fungal diseases (Brown et al., 2012; Anonymous, 2017b). Public health surveillance of fungal diseases is generally not compulsory, suggesting that most estimates are conservative (Casadevall, 2017; Anonymous, 2017a). Fungal disease can also damage plants and crops, causing major losses in agricultural activities and food production (Savary et al., 2012). Animal pathogenic fungi are threatening bats, amphibians and reptiles with extinction (Casadevall, 2017). It is estimated that fungi are the highest threat for animal-host and plant-host species, representing the major cause (approximately 65%) of pathogen-driven host loss (Fisher et al., 2012). In this complex scenario, it is now clear that the global warming and accompanying climate changes have resulted in increased incidence of many fungal diseases (Garcia-Solache and Casadevall, 2010). On the basis of all these factors, concerns on the occurrence of a pandemic of fungal origin in a near future have been raised (Casadevall, 2017). In this context, to stop forgetting and underestimating fungal diseases is mandatory.
Keywords: fungal diseases, fungal infection, public health, fungal pathogen, fungi
The Burden of Human Fungal Infections
Currently, there are few antifungal drugs approved for use in humans (Pianalto and Alspaugh, 2016). The last antifungals approved for human use were characterized in 2002. This scenario may be linked to an imbalance between funding and mortality rates in the field of fungal diseases (Rodrigues, 2016). For instance, cryptococcal meningitis results in approximately 180 000 deaths annually globally (Rajasingham et al., 2017), as compared to 429 000 deaths caused by malaria or 1.6 million tuberculosis-deaths (as estimated by WHO in 2015 and 2017, respectively). However, cryptococcosis received less than 0.5% of the global research and development funding, while malaria and tuberculosis received together 35.5% of the total investment in research and development in infectious diseases (Moran et al., 2015). Current therapeutic to treat fungal diseases remain unsatisfactory, and to develop novel therapeutic alternatives a significant investment in dedicated research is required (Coelho and Casadevall, 2016). Novel antifungal are in different clinical development stages, and these new compounds such as AR-12 (Baxter et al., 2011), BHBM (Mor et al., 2015), CD101 (Zhao et al., 2016), E1210/11 (Pfaller et al., 2011), F901318 (Wiederhold et al., 2017), Ilicicolin H (Singh et al., 2012), Nikkomycin Z (Hector et al., 1990), Sampangine (Agarwal et al., 2008), Scy-078 (Lepak et al., 2015), Sertraline (Zhai et al., 2012), T-2307 (Mitsuyama et al., 2008), Tamoxifen (Dolan et al., 2009), and VT-1129 (Douglas et al., 1994). Some of these (VT-119 and Nikkomycin Z, for example) belong to new classes of drugs, i.e., they act through different mechanisms and molecular targets than the already approved drugs, and may provide a much-needed extension to the limited therapies currently available. Programs specifically offering funding to mycological research are necessary to potentiate further development of effective antifungal therapy and ultimately reduce mortality from fungal diseases.
The Impact of Fungal Infections on Food Crops and Disproportionate Impact in Developing Countries
Fungal diseases in developing countries demand special attention. Many of the fungal diseases in Latin America are often overlooked, although they clearly fulfill the criteria to be classified as neglected human diseases (Rodrigues, 2016, 2018). The general impact of fungal pathogens on human health goes beyond the ability of fungi to infect humans, since they destroy a third of all food crops annually (Fisher et al., 2012), causing economical loss and impacting global poverty. Statistics from the 2009–2010 world harvest (www.fao.org or FAOSTAT1) suggest fungi-induced losses in five of the most important crops globally (rice, wheat, maize, potatoes, and soybean). If those losses were mitigated, these crops would have been enough to feed 8.5% of the seven billion populations in 2011 (Fisher et al., 2012). Furthermore, in a hypothetical event where these five crops were affected simultaneously, approximately 61% of the world’s population would not have food (Fisher et al., 2012). The most economically devastating fungi are Magnaporthe oryzae, affecting rice and wheat, followed by Botrytis cinerea, which has a broad host range and Puccinia spp., affecting wheat (Dean et al., 2012). Several high-value crops produced in the tropics, such as bananas, coffee, cacao, spices, mangos, and several nuts, are currently affected by fungal infections and these crops are not produced colder climates (Drenth and Guest, 2016). Therefore dependence of crop produced in tropical regions aggravated with a lack of biodefense and preparedness might result in disastrous economical consequences worldwide.
Fungal infections of invertebrate hosts may also impact agricultural crises due to ecological imbalance. For instance, bee broods are susceptible to fungal infections caused by genera of Ascosphaera and Aspergillus (Jensen et al., 2013), and the agricultural production worldwide is highly dependent on pollination mediated by bees (Aizen et al., 2009; Stein et al., 2017). Fungal infection of bees may precipitate a disaster (Bromenshenk et al., 2010), with unpreceded impact on agriculture and various plant species.
The Impact of Fungal Infections on Animal Species
When fungi cause animal disease the outcomes are quite dramatic and scientists have been trying to raise attention to the effects of fungal infections in decreasing biodiversity, an effect aggravated (if not triggered) by global warming (Fisher et al., 2012; Seyedmousavi et al., 2018). Bat decimation caused by Geomyces destructans and several frog species by Batrachochytrium dendrobatidis are well known events. In invertebrates we already mentioned the case of bees, and further species may be affected but further research is needed. For example, there is a debate regarding if a marine Aspergillus spp. is associated with the decline of coral reefs (Kim and Harvell, 2004; Soler-Hurtado et al., 2016). Overall, the examples of species decimation in mammals, plants, and bees by fungal pathogens should prompt investigation of similar phenomenon in a wider scale, for example, other insects and in aquatic life.
Critical Interactions of Fungi With the Environment
It is important to highlight that most of the plant-fungal interactions are beneficial to both plants and fungi, with this symbiotic interaction improving plant growth, development, foraging, acquisition of soil resources, and tolerance to stress (Zeilinger et al., 2016). For instance, Trichoderma induces biofertilization of crops. The addition of Trichoderma hamatum or Trichoderma koningii to the production fields can increase crop productivity up to 300% (Benitez et al., 2004). Trichoderma spp. also acts in the mycoparasitism, the direct attack of one fungal species on another (Harman et al., 2004; Almeida et al., 2007), being described as potential biological control agent against important phytopathogenic fungi such as Fusarium spp., Rhizoctonia solani, Sclerotium rolfsii, Sclerotinia sclerotiorum, B. cinerea, and Pythium spp. (Zeilinger and Omann, 2007). Thus, mycoparasitism-based strategies could decrease the use of agrochemicals and antifungals in crop cultivation. In this sense, a better understanding of the fungal diversity and its impact on plant-fungal interactions would be highly beneficial to improve phytopathogen control.
The Urgency of Combatting Fungal Infections
The reduced number of antifungals impact human health not only due to lack of therapy to cure human patients. Medically approved antifungal drugs have been used for agricultural purposes for decades (Azevedo et al., 2015). Most human pathogens have environmental niches, implying that the agricultural use of medically-approved drugs imposes the concrete risk of fostering drug resistance (Verweij et al., 2009; Zavrel and White, 2015). Emergence of antifungal resistance can endanger the already limited treatments options, with calamitous effects for treatment outcomes (Perlin et al., 2017). The development of new antifungal drugs is urgent to improve both human health and agricultural production.
The worsening of global warming opens a Pandora box for fungal diseases. Some thermally intolerant fungi with current pathogenic potential should acquire the ability to survive at mammalian temperatures (Garcia-Solache and Casadevall, 2010). This threat is heightened since some fungi can take advantage of a natural selection-adaptation strategy, and consequently to adapt to higher temperature by thermal selection (de Crecy et al., 2009; Panackal, 2011).
The collaboration between all these affected disciplines would be critical in facilitating at detecting epidemics early on and preventing further spread. The concept of One Health (King et al., 2008), with integration and communication between medical doctors, veterinarians, and food safety officials has been implemented with remarkable success and should become a standard for transmissible diseases (Ghosh et al., 2018). We have included a table summarizing basic information regarding distribution and etiological agent of important human mycoses (Table 1).
Table 1.
Fungal diseases | Distribution and etiological agent | Reference |
---|---|---|
Aspergillosis | Worldwide mycosis, caused by Aspergillus spp. Wide spectrum of infections in humans, but mainly in immunocompromised individuals. There are more than 250 species of Aspergillus, of these fewer than 40 are reported to cause infections in humans. Aspergillus fumigatus and Aspergillus flavus are the most common human pathogens. | Latge, 1999; Sugui et al., 2014 |
Blastomycosis | Endemic mycosis located to the south central and north central United States, caused by Blastomyces dermatitidis and Blastomyces gilchristii that can affects immunocompetent and immunocompromised individuals. | Castillo et al., 2016; McBride et al., 2017 |
Candidiasis | Worldwide mycosis, caused by Candida spp, a major cause of morbidity and mortality worldwide, and the main causative agent in systemic fungal infections. Among the Candida species, Candida albicans is the most common to cause infections in humans. | Pfaller and Diekema, 2007; Yapar, 2014 |
Coccidioidomycosis | Endemic to Southwestern United States and Central and South America, caused by Coccidioides immitis and Coccidioides posadasii. | Twarog and Thompson, 2015; Stockamp and Thompson, 2016 |
Cryptococcosis | Wordlwide distribution, caused by Cryptococcus neoformans. Affects immunocompromised hosts, and is a major cause of HIV-related deaths. One noticeable outbreak in Vancouver Islands of C. gattii in immunocompetent patients. | Casadevall and Perfect, 1998; Heitman et al., 2011; Almeida et al., 2015 |
Dermatophytosis | Worldwide, Trichophyton rubrum and Trychophyton interdigitale have been described as the most common to cause dermatophytosis, but many other species contribute. The most frequent type of superficial mycosis in humans, attacking skin and nails. | Weitzman and Summerbell, 1995; Bitencourt et al., 2018; Persinoti et al., 2018 |
Histoplasmosis | Worldwide?, Histoplasma capsulatum is the etiologic agent, mostly immunocompromised individuals, it is one of the most common invasive fungal pulmonary diseases. | Cano and Hajjeh, 2001; Guimaraes et al., 2006 |
Paracoccidiodomycosis | Endemic to Latin America, caused by thermodimorphic fungi of the Paracoccidioides species, is the most prevalent systemic mycosis in Latin America. | Colombo et al., 2011; Theodoro et al., 2012 |
Pneumocystis pneumonia | Worldwide, caused by Pneumocystis jiroveci, affects patients that were immunosuppressed, such as cancer patients receiving chemotherapy or HIV patients. | Thomas and Limper, 2004; Morris and Norris, 2012 |
Sporotrichosis | Worldwide, subcutaneous and subacute/chronic disease caused by dimorphic fungus of the genus Sporothrix that affects humans and other mammals. | Chakrabarti et al., 2015; Conceicao-Silva and Morgado, 2018 |
The negative impact of any infectious disease is usually higher in neglected populations. Lack of access to healthcare, underfunded healthcare, and delayed diagnosis lead to higher burden of fungal diseases. The economy of countries in developing countries strongly relies on agricultural production. Another fungal blight, if not managed properly, can still have disastrous economical and societal consequences.
The old adage “know your enemy” illustrates the major point of this essay: significant investment in fungal research, including fungal biology, human and plant pathogenicity, therapeutic agents, diagnostic tools, and vaccines, has the potential to avoid a global catastrophe. This call has been made by most, if not all, prominent fungal researchers (Molloy et al., 2017; Casadevall, 2018). We urge more attention to fungal biology and pathogenesis globally with special attention to diseases affecting developing countries, as a safeguard for prevention of losses in agriculture, environmental losses, and damage to human health.
Author Contributions
All authors listed have made a substantial, direct and intellectual contribution to the work, and approved it for publication.
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Footnotes
Funding. FA acknowledged support from Fundação de Amparo a Pesquisa do Estado de São Paulo (2016/03322-7) and CNPq (Conselho Nacional de Desenvolvimento Científico e Tecnológico). MR is supported by the Brazilian agencies CAPES Coordenação de Aperfeiçoamento de Pessoal de Nível Superior, Finance Code 001, CNPq and the Instituto Nacional de Ciência e Tecnologia de Inovação em Doenças de Populações Negligenciadas (INCT-IDPN). MR is currently on a leave from a position of Associate Professor at Institute of Microbiology, Federal University of Rio de Janeiro, Brazil.
References
- Agarwal A. K., Xu T., Jacob M. R., Feng Q., Lorenz M. C., Walker L. A., et al. (2008). Role of heme in the antifungal activity of the azaoxoaporphine alkaloid sampangine. Eukaryot. Cell 7 387–400. 10.1128/EC.00323-07 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Aizen M. A., Garibaldi L. A., Cunningham S. A., Klein A. M. (2009). How much does agriculture depend on pollinators? Lessons from long-term trends in crop production. Ann. Bot. 103 1579–1588. 10.1093/aob/mcp076 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Almeida F., Wolf J. M., Casadevall A. (2015). Virulence-associated enzymes of Cryptococcus neoformans. Eukaryot. Cell 14 1173–1185. 10.1128/EC.00103-15 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Almeida F. B., Cerqueira F. M., Silva Rdo N., Ulhoa C. J., Lima A. L. (2007). Mycoparasitism studies of Trichoderma harzianum strains against Rhizoctonia solani: evaluation of coiling and hydrolytic enzyme production. Biotechnol. Lett. 29 1189–1193. 10.1007/s10529-007-9372-z [DOI] [PubMed] [Google Scholar]
- Anonymous (2017a). Stop neglecting fungi. Nat. Microbiol. 2:17120. 10.1038/nmicrobiol.2017.120 [DOI] [PubMed] [Google Scholar]
- Anonymous (2017b). The Burden of Fungal Disease, on LIFE. Available at: http://go.nature.com/2sMKpuN [Google Scholar]
- Azevedo M. M., Faria-Ramos I., Cruz L. C., Pina-Vaz C., Rodrigues A. G. (2015). Genesis of azole antifungal resistance from agriculture to clinical settings. J. Agric. Food Chem. 63 7463–7468. 10.1021/acs.jafc.5b02728 [DOI] [PubMed] [Google Scholar]
- Baxter B. K., DiDone L., Ogu D., Schor S., Krysan D. J. (2011). Identification, in vitro activity and mode of action of phosphoinositide-dependent-1 kinase inhibitors as antifungal molecules. ACS Chem. Biol. 6 502–510. 10.1021/cb100399x [DOI] [PMC free article] [PubMed] [Google Scholar]
- Benitez T., Rincon A. M., Limon M. C., Codon A. C. (2004). Biocontrol mechanisms of Trichoderma strains. Int. Microbiol. 7 249–260. [PubMed] [Google Scholar]
- Bitencourt T. A., Rezende C. P., Quaresemin N. R., Moreno P., Hatanaka O., Rossi A., et al. (2018). Extracellular vesicles from the dermatophyte trichophyton interdigitale modulate macrophage and keratinocyte Functions. Front. Immunol. 9:2343. 10.3389/fimmu.2018.02343 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bromenshenk J. J., Henderson C. B., Wick C. H., Stanford M. F., Zulich A. W., Jabbour R. E., et al. (2010). Iridovirus and microsporidian linked to honey bee colony decline. PLoS One 5:e13181. 10.1371/journal.pone.0013181 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Brown G. D., Denning D. W., Gow N. A. R., Levitz S. M., Netea M. G., White T. C. (2012). Hidden killers: human fungal infections. Sci. Transl. Med. 4:165rv13. 10.1126/scitranslmed.3004404 [DOI] [PubMed] [Google Scholar]
- Cano M. V., Hajjeh R. A. (2001). The epidemiology of histoplasmosis: a review. Semin. Respir. Infect. 16 109–118. 10.1053/srin.2001.24241 [DOI] [PubMed] [Google Scholar]
- Casadevall A. (2017). Don’t forget the fungi when considering global catastrophic biorisks. Health Secur. 15 341–342. 10.1089/hs.2017.0048 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Casadevall A. (2018). Fungal diseases in the 21st century: the near and far horizons. Pathog. Immun. 3 183–196. 10.20411/pai.v3i2.249 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Casadevall A., Perfect J. R. (1998). Cryptococcus Neoformans. Washington, DC: ASM Press; 10.1128/9781555818241 [DOI] [Google Scholar]
- Castillo C. G., Kauffman C. A., Miceli M. H. (2016). Blastomycosis. Infect. Dis. Clin. North Am. 30 247–264. 10.1016/j.idc.2015.10.002 [DOI] [PubMed] [Google Scholar]
- Chakrabarti A., Bonifaz A., Gutierrez-Galhardo M. C., Mochizuki T., Li S. (2015). Global epidemiology of sporotrichosis. Med. Mycol. 53 3–14. 10.1093/mmy/myu062 [DOI] [PubMed] [Google Scholar]
- Coelho C., Casadevall A. (2016). Cryptococcal therapies and drug targets: the old, the new and the promising. Cell Microbiol. 18 792–799. 10.1111/cmi.12590 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Colombo A. L., Tobon A., Restrepo A., Queiroz-Telles F., Nucci M. (2011). Epidemiology of endemic systemic fungal infections in Latin America. Med. Mycol. 49 785–798. 10.3109/13693786.2011.577821 [DOI] [PubMed] [Google Scholar]
- Conceicao-Silva F., Morgado F. N. (2018). Immunopathogenesis of human sporotrichosis: what we already know. J. Fungi 4:E89. 10.3390/jof4030089 [DOI] [PMC free article] [PubMed] [Google Scholar]
- de Crecy E., Jaronski S., Lyons B., Lyons T. J., Keyhani N. O. (2009). Directed evolution of a filamentous fungus for thermotolerance. BMC Biotechnol. 9:74. 10.1186/1472-6750-9-74 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dean R., Van Kan J. A., Pretorius Z. A., Hammond-Kosack K. E., Di Pietro A., Spanu P. D., et al. (2012). The Top 10 fungal pathogens in molecular plant pathology. Mol. Plant Pathol. 13 414–430. 10.1111/j.1364-3703.2011.00783.x [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dolan K., Montgomery S., Buchheit B., Didone L., Wellington M., Krysan D. J. (2009). Antifungal activity of tamoxifen: in vitro and in vivo activities and mechanistic characterization. Antimicrob. Agents Chemother. 53 3337–3346. 10.1128/AAC.01564-08 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Douglas C. M., Foor F., Marrinan J. A., Morin N., Nielsen J. B., Dahl A. M., et al. (1994). The saccharomyces-cerevisiae Fks1 (Etg1) gene encodes an integral membrane-protein which is a subunit of 1,3-beta-D-glucan synthase. Proc. Natl. Acad. Sci. U.S.A. 91 12907–12911. 10.1073/pnas.91.26.12907 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Drenth A., Guest D. I. (2016). Fungal and oomycete diseases of tropical tree fruit crops. Annu. Rev. Phytopathol. 54 373–395. 10.1146/annurev-phyto-080615-095944 [DOI] [PubMed] [Google Scholar]
- Fisher M. C., Henk D. A., Briggs C. J., Brownstein J. S., Madoff L. C., McCraw S. L., et al. (2012). Emerging fungal threats to animal, plant and ecosystem health. Nature 484 186–194. 10.1038/nature10947 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Garcia-Solache M. A., Casadevall A. (2010). Global warming will bring new fungal diseases for mammals. MBio 1:e00061-10. 10.1128/mBio.00061-10 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ghosh P. N., Fisher M. C., Bates K. A. (2018). Diagnosing emerging fungal threats: a one health perspective. Front. Genet. 9:376. 10.3389/fgene.2018.00376 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Guimaraes A. J., Nosanchuk J. D., Zancope-Oliveira R. M. (2006). Diagnosis of histoplasmosis. Braz. J. Microbiol. 37 1–13. 10.1590/S1517-83822006000100001 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Harman G. E., Howell C. R., Viterbo A., Chet I., Lorito M. (2004). Trichoderma species - opportunistic, avirulent plant symbionts. Nat. Rev. Microbiol. 2 43–56. 10.1038/nrmicro797 [DOI] [PubMed] [Google Scholar]
- Hector R. F., Zimmer B. L., Pappagianis D. (1990). Evaluation of nikkomycins X and Z in murine models of coccidioidomycosis, histoplasmosis, and blastomycosis. Antimicrob. Agents Chemother. 34 587–593. 10.1128/AAC.34.4.587 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Heitman J., Kozel T. R., Kwon-Chung J., Perfect J. R., Casadevall A. (2011). Cryptococcus: From Human Pathogen to Model Yeast. Washington, DC: ASM Press. [Google Scholar]
- Jensen A. B., Aronstein K., Flores J. M., Vojvodic S., Palacio M. A., Spivak M. (2013). Standardmethods for fungal brood disease research. J. Apic. Res. 52 1–39. 10.3896/IBRA.1.52.1.13 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kim K., Harvell C. D. (2004). The rise and fall of a six-year coral-fungal epizootic. Am. Nat. 164(Suppl. 5), S52–S63. 10.1086/424609 [DOI] [PubMed] [Google Scholar]
- King L. J., Anderson L. R., Blackmore C. G., Blackwell M. J., Lautner E. A., Marcus L. C., et al. (2008). Executive summary of the AVMA One health initiative task force report. J. Am. Vet. Med. Assoc. 233 259–261. 10.2460/javma.233.2.259 [DOI] [PubMed] [Google Scholar]
- Latge J. P. (1999). Aspergillus fumigatus and aspergillosis. Clin. Microbiol. Rev. 12 310–350. 10.1128/CMR.12.2.310 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lepak A. J., Marchillo K., Andes D. R. (2015). Pharmacodynamic target evaluation of a novel oral glucan synthase inhibitor, SCY-078 (MK-3118), using an in vivo murine invasive candidiasis model. Antimicrob. Agents Chemother. 59 1265–1272. 10.1128/AAC.04445-14 [DOI] [PMC free article] [PubMed] [Google Scholar]
- McBride J. A., Gauthier G. M., Klein B. S. (2017). Clinical manifestations and treatment of blastomycosis. Clin. Chest. Med. 38 435–449. 10.1016/j.ccm.2017.04.006 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mitsuyama J., Nomura N., Hashimoto K., Yamada E., Nishikawa H., Kaeriyama M., et al. (2008). In vitro and in vivo antifungal activities of T-2307, a novel arylamidine. Antimicrob. Agents Chemother. 52 1318–1324. 10.1128/AAC.01159-07 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Molloy S. F., Chiller T., Greene G. S., Burry J., Govender N. P., Kanyama C., et al. (2017). Cryptococcal meningitis: a neglected NTD? PLoS Negl. Trop. Dis. 11:e0005575. 10.1371/journal.pntd.0005575 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mor V., Rella A., Farnoud A. M., Singh A., Munshi M., Bryan A., et al. (2015). Identification of a new class of antifungals targeting the synthesis of fungal sphingolipids. MBio 6:e00647. 10.1128/mBio.00647-15 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Moran M. C., Chapman N., Abela-Oversteegen L., Chowdhary V., Doubell A., Whittall C., et al. (2015). G-FINDER: neglected disease research and developent: the ebola effect. Policy Cures 8 13–85. [Google Scholar]
- Morris A., Norris K. A. (2012). Colonization by Pneumocystis jirovecii and its role in disease. Clin. Microbiol. Rev. 25 297–317. 10.1128/CMR.00013-12 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Panackal A. A. (2011). Global climate change and infectious diseases: invasive mycoses. J. Earth Sci. Clim. Chang. 2:108 10.4172/2157-7617.1000108 [DOI] [Google Scholar]
- Perlin D. S., Rautemaa-Richardson R., Alastruey-Izquierdo A. (2017). The global problem of antifungal resistance: prevalence, mechanisms, and management. Lancet Infect. Dis. 17 e383–e392. 10.1016/S1473-3099(17)30316-X [DOI] [PubMed] [Google Scholar]
- Persinoti G. F., Martinez D. A., Li W., Dogen A., Billmyre R. B., Averette A., et al. (2018). Whole-genome analysis illustrates global clonal population structure of the ubiquitous dermatophyte pathogen Trichophyton rubrum. Genetics 208 1657–1669. 10.1534/genetics.117.300573 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pfaller M. A., Diekema D. J. (2007). Epidemiology of invasive candidiasis: a persistent public health problem. Clin. Microbiol. Rev. 20 133–163. 10.1128/CMR.00029-06 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pfaller M. A., Duncanson F., Messer S. A., Moet G. J., Jones R. N., Castanheira M. (2011). In vitro activity of a novel broad-spectrum antifungal, E1210, tested against Aspergillus spp. determined by CLSI and EUCAST broth microdilution methods. Antimicrob. Agents Chemother. 55 5155–5158. 10.1128/AAC.00570-11 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pianalto K. M., Alspaugh J. A. (2016). New horizons in antifungal therapy. J. Fungi 2:E26. 10.3390/jof2040026 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rajasingham R., Smith R. M., Park B. J., Jarvis J. N., Govender N. P., Chiller T. M., et al. (2017). Global burden of disease of HIV-associated cryptococcal meningitis: an updated analysis. Lancet Infect. Dis. 17 873–881. 10.1016/S1473-3099(17)30243-8 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rodrigues M. L. (2016). Funding and innovation in diseases of neglected populations: the paradox of cryptococcal meningitis. PLoS Negl. Trop. Dis. 10:e0004429. 10.1371/journal.pntd.0004429 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rodrigues M. L. (2018). Neglected disease, neglected populations: the fight against Cryptococcus and cryptococcosis. Mem. Inst. Oswaldo Cruz 113:e180111. 10.1590/0074-02760180111 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Savary S., Ficke A., Aubertot J. N., Hollier C. (2012). Crop losses due to diseases and their implications for global food production losses and food security. Food Secur. 4 519–537. 10.1007/s00203-017-1426-6 [DOI] [PubMed] [Google Scholar]
- Seyedmousavi S., Bosco S. M. G., de Hoog S., Ebel F., Elad D., Gomes R. R., et al. (2018). Fungal infections in animals: a patchwork of different situations. Med. Mycol. 56 165–187. 10.1093/mmy/myx104 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Singh S. B., Liu W., Li X., Chen T., Shafiee A., Card D., et al. (2012). Antifungal spectrum, in vivo efficacy, and structure-activity relationship of ilicicolin h. ACS Med. Chem. Lett. 3 814–817. 10.1021/ml300173e [DOI] [PMC free article] [PubMed] [Google Scholar]
- Soler-Hurtado M. M., Sandoval-Sierra J. V., Machordom A., Dieguez-Uribeondo J. (2016). Aspergillus sydowii and other potential fungal pathogens in gorgonian octocorals of the ecuadorian pacific. PLoS One 11:e0165992. 10.1371/journal.pone.0165992 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Stein K., Coulibaly D., Stenchly K., Goetze D., Porembski S., Lindner A., et al. (2017). Bee pollination increases yield quantity and quality of cash crops in Burkina Faso, West Africa. Sci. Rep. 7:17691. 10.1038/s41598-017-17970-2 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Stockamp N. W., Thompson G. R., III (2016). Coccidioidomycosis. Infect. Dis. Clin. North Am. 30 229–246. 10.1016/j.idc.2015.10.008 [DOI] [PubMed] [Google Scholar]
- Sugui J. A., Kwon-Chung K. J., Juvvadi P. R., Latge J. P., Steinbach W. J. (2014). Aspergillus fumigatus and related species. Cold Spring Harb. Perspect. Med. 5 a019786. 10.1101/cshperspect.a019786 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Theodoro R. C., Teixeira M. D., Felipe M. S. S., Paduan K. D., Ribolla P. M., San-Blas G., et al. (2012). Genus paracoccidioides: species recognition and biogeographic aspects. PLoS One 7:e37694. 10.1371/journal.pone.0037694 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Thomas C. F., Jr., Limper A. H. (2004). Pneumocystis pneumonia. N. Engl. J. Med. 350 2487–2498. 10.1056/NEJMra032588 [DOI] [PubMed] [Google Scholar]
- Twarog M., Thompson G. R., III (2015). Coccidioidomycosis: recent updates. Semin. Respir. Crit. Care Med. 36 746–755. 10.1055/s-0035-1562900 [DOI] [PubMed] [Google Scholar]
- Verweij P. E., Snelders E., Kema G. H., Mellado E., Melchers W. J. (2009). Azole resistance in Aspergillus fumigatus: a side-effect of environmental fungicide use? Lancet Infect. Dis. 9 789–795. 10.1016/S1473-3099(09)70265-8 [DOI] [PubMed] [Google Scholar]
- Weitzman I., Summerbell R. C. (1995). The dermatophytes. Clin. Microbiol. Rev. 8 240–259. 10.1128/CMR.8.2.240 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wiederhold N. P., Law D., Birch M. (2017). Dihydroorotate dehydrogenase inhibitor F901318 has potent in vitro activity against Scedosporium species and Lomentospora prolificans. J. Antimicrob. Chemother. 72 1977–1980. 10.1093/jac/dkx065 [DOI] [PubMed] [Google Scholar]
- Yapar N. (2014). Epidemiology and risk factors for invasive candidiasis. Ther. Clin. Risk Manag. 10 95–105. 10.2147/TCRM.S40160 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Zavrel M., White T. C. (2015). Medically important fungi respond to azole drugs: an update. Future Microbiol. 10 1355–1373. 10.2217/FMB.15.47 [DOI] [PubMed] [Google Scholar]
- Zeilinger S., Gupta V. K., Dahms T. E., Silva R. N., Singh H. B., Upadhyay R. S., et al. (2016). Friends or foes? Emerging insights from fungal interactions with plants. FEMS Microbiol. Rev. 40 182–207. 10.1093/femsre/fuv045 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Zeilinger S., Omann M. (2007). Trichoderma biocontrol: signal transduction pathways involved in host sensing and mycoparasitism. Gene Regul. Syst. Bio. 1 227–234. 10.4137/GRSB.S397 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Zhai B., Wu C., Wang L., Sachs M. S., Lin X. (2012). The antidepressant sertraline provides a promising therapeutic option for neurotropic cryptococcal infections. Antimicrob. Agents Chemother. 56 3758–3766. 10.1128/AAC.00212-12 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Zhao Y., Perez W. B., Jimenez-Ortigosa C., Hough G., Locke J. B., Ong V., et al. (2016). CD101: a novel long-acting echinocandin. Cell Microbiol. 18 1308–1316. 10.1111/cmi.12640 [DOI] [PMC free article] [PubMed] [Google Scholar]