Hilary C. Kelly, MPH

According to conventional wisdom, invasive fungal infections affect limited populations. These diseases tend to be cast as medical zebras even among people at greatest risk, including immunosuppressed patients and those residing in specific geographic areas of the United States. However, fungal disease epidemiology is changing. New risk groups have been identified, zoonotic epidemics with human spillover have taken hold, antifungal resistance has emerged, and previously defined endemic zones are expanding. Here we describe 4 of the most clinically consequential examples of emerging fungal infections. This overview does not cover the multidrug-resistant Candida auris because it has been covered extensively elsewhere.

 Infectious disease specialists have and will continue to act on the front lines as fungal diseases continue to appear in new and curious places. 

1. AZOLE-RESISTANT ASPERGILLUS FUMIGATUS 

 is a mold common in the environment, and most people breathe in Aspergillus spores every day without getting sick. It is the most common cause of invasive mold infections in people who are immunocompromised and have lung diseases,

 and mortality from invasive aspergillosis is high (>25%).

 The development of azole antifungal medications such as voriconazole, itraconazole, and posaconazole has greatly improved survival since the late 1990s

; however, infections caused by azole-resistant 

 This resistance was first detected in Europe but has now been found across the globe, including recently in the United States.

 is associated with treatment failure and mortality rates greater than 88%.

strains associated with the use of azole agricultural fungicides.

 can develop resistance during incidental exposure to azole fungicides applied to treat and prevent fungal disease in crops. When these resistant strains cause invasive infections in humans, the efficacy of azole antifungal drugs is reduced. Agricultural azole use has increased in recent decades; in the United States, usage has increased by more than 500% from 2000 (579 metric tons) to 2015 (2940 metric tons).

 has been found in patients without a history of taking azole medications, supporting the idea that these resistant strains originated in the environment and not during prolonged azole therapy.

The US Centers for Disease Control and Prevention is collecting clinical isolates of 

 to monitor for azole resistance. More information on this program and isolate submission can be found at 

cdc.gov/fungal/aspergillus-resistance.html

. Clinicians should consider azole- resistant aspergillosis in patients who do not respond to antifungal treatment, even in patients who are azole naïve, although other causes of treatment failure exist.

2. INVASIVE PULMONARY ASPERGILLOSIS AND SEVERE INFLUENZA

Invasive pulmonary aspergillosis (IPA) affects primarily patients immunocompromised by stem cell or organ transplantation, chemotherapy, or immunosuppressive medications. However, in the past decade, 

 has emerged as a complication among patients with severe influenza requiring intensive care unit (ICU) admission. Since 2010, several US cases of IPA following severe influenza have been reported.

 However, findings from a recent multicenter study in Belgium and the Netherlands suggest that this condition may be more common than anticipated in some regions. The study found that about 20% of 432 ICU patients with severe influenza developed IPA within 3 days of ICU admission.

 About half of those who developed IPA were not immunocompromised. Patients with IPA in severe influenza have developed a rapidly progressive tracheobronchitis, with mortality rates of 46% to 61%.

 may invade lung tissue in the absence of a compromised immune system through disruption of the respiratory epithelium from severe influenza.

The geographic extent of IPA in patients with severe influenza is unknown outside the Netherlands and Belgium; it may be a novel phenomenon or previously present but unrecognized. Until more definitive research and surveillance can answer this question, it is important for clinicians to consider diagnosis and treatment of invasive aspergillosis in patients with severe influenza who are not getting better with treatment, even in those who are not immunocompromised. Fungal culture or galactomannan antigen testing of bronchoalveolar lavage fluid can aid in diagnosis.

behaves quite differently from sporotrichosis caused by the better-known 

 infection in humans often resemble those of 

 infection, classically a localized skin ulceration with spreading lymphangitis, 

 infections appear more virulent, with up to 20% of cases progressing to disseminated disease.

 Additionally, these infections may fail to respond to antifungal therapy.

 However, the major difference between these 

 species is in how these infections are acquired. Sporotrichosis from 

 is also known as rose gardener’s disease because it is frequently caused by traumatic inoculation from plants, whereas cats are the main reservoir and source of transmission of 

, making this an emerging zoonotic disease.

), typically after the cat is scratched or bitten by an infected or colonized cat.

Feline-to-human transmission similarly occurs through scratches, bites, or contact with lesions of infected cats.

 was found only in the southeast region of Brazil, around São Paulo and Rio de Janeiro. Since then, it has spread throughout much of southern Brazil, with thousands of cases in humans and cats reported at a single center in Rio de Janeiro since 1998.

Given the close contact cats often have with people, and the tens of millions of stray cats in the United States and elsewhere,

 there is concern that this outbreak could spread to other areas as it has within Brazil.

 Clinicians, particularly infectious disease physicians, dermatologists, and veterinarians, should be aware of this emerging disease, as early identification will be key in minimizing spread of this fungus.

4. US ENDEMIC MYCOSES: COCCIDIOIDOMYCOSIS AND HISTOPLASMOSIS

Many physicians have been trained to associate endemic fungal diseases with specific geographic areas. However, a growing body of evidence suggests that for the fungi that cause these diseases, classical endemic ranges have expanded.

In the United States, coccidioidomycosis (commonly called valley fever), caused by 

, occurs mainly in Arizona and Southern California (

 Histoplasmosis is normally thought to exist in areas around the Mississippi and Ohio river valleys.

 However, these observations are based on half-century-old studies.

 Outside these ranges, physicians may not consider these illnesses in the differential diagnosis for many patients. For example, both fungal infections may be clinically indistinguishable from bacterial community acquired pneumonia,

 and both can cause lung nodules that mimic lung cancer,

 leading to unnecessary treatments and delays in appropriate therapy.

Locally acquired coccidioidomycosis cases have been recorded as far north as Washington State,

 and soil samples linked to these cases tested positive for 

 Similarly, histoplasmosis can cause infections far outside its classical range, as suggested by animal cases as far away as Alaska

 and human cases reported to public health departments north of the endemic areas identified in the 1950s, specifically in Michigan, Minnesota, and Wisconsin.

Some have hypothesized that climate change and human activities are contributing to expanding geographic ranges, although increased detection capacity or other factors may be involved.

 Increasing periods of drought and higher temperatures in the West interspersed with high rainfall are thought to be conducive to 

 growth in the soil and airborne dispersal under the “grow and blow” hypothesis.

 Likewise, climate and land-use changes could be contributing to a widening of the regions with soils that are well suited for 

 Whatever the reason for the apparent spread of these endemic fungi, practitioners outside these regions should consider these infections as possible causes of illness.

Fungi grow in vastly diverse environments, which occasionally include the bodies of humans and animals. Although the ecological factors associated with fungal disease are complex and poorly understood, the 4 examples described here highlight the need for vigilance as new fungal diseases emerge and familiar ones morph in range and risk groups. As epidemiologists aim to quantify the burden and longitudinal trends in fungal disease, our surveillance systems need to keep pace with the changing fungal world. Among the 4 fungal diseases discussed, only 1 (coccidioidomycosis) is nationally notifiable.

 Improved public health surveillance for these diseases could serve clinical and public health practices alike, by informing patient care and public health policy.

Kelly is an Oak Ridge Institute for Science and Education fellow in the Mycotic Diseases Branch at the US Centers for Disease Control and Prevention (CDC) in Atlanta, Georgia, working on invasive mold infection surveillance.

Henry is a fourth-year medical student at Columbia University who plans on specializing in emergency medicine. He recently completed the CDC Epidemiology Elective Program with the Mycotic Diseases Branch.

Jackson is the lead of the CDC’s Fungal Epidemiology Team, which is devoted to tracking and preventing a wide range of invasive fungal diseases, both established and emerging.

Beer is an epidemiologist in the Mycotic Diseases Branch at the CDC, with special interests in invasive mold infections.

The findings and conclusions in this report are those of the authors and do not necessarily represent the official position of the US Centers for Disease Control and Prevention.

1.        Contagion Live Editorial Staff. Top 5 Infectious Disease Concerns to Watch in 2019. Contagion Live website. www.contagionlive.com/news/top-5-infectious-disease-concerns-to-watch-in-2019. Published 2019. Accessed February 27, 2019.

2.        Kontoyiannis DP, Marr KA, Park BJ, et al. Prospective surveillance for invasive fungal infections in hematopoietic stem cell transplant recipients, 2001—2006: overview of the transplant&#8208;associated infection surveillance network (TRANSNET) database. 

. 2010 Apr 15;50(8):1091-100. doi: 10.1086/651263.

3.        Stevens RW, Kammers K. Exploring primary prophylaxis for invasive pulmonary aspergillosis. Contagion Live website. www.contagionlive.com/publications/contagion/2018/december/exploring-primary-prophylaxis-for-invasive-pulmonary-aspergillosis. Published 2018. Accessed February 27, 2019.

4.        Webb BJ, Ferraro JP, Rea S, Kaufusi S, Goodman BE, Spalding J. Epidemiology and clinical features of invasive fungal infection in a US health care network. 

. 2018 Jul 31;5(8):ofy187. doi: 10.1093/ofid/ofy187.

5.        Beer KD, Farnon EC, Jain S, et al. Multidrug-resistant 

 carrying mutations linked to environmental fungicide exposure — three states, 2010—2017. 

. 2018 Sep 28;67(38):1064-1067. doi: 10.15585/mmwr.mm6738a5.

6.        Pappas PG, Alexander BD, Andes DR, et al. Invasive fungal infections among organ transplant recipients: results of the transplant&#8208;associated infection surveillance network (TRANSNET). 

. 2010 Apr 15;50(8):1101-11. doi: 10.1086/651262.

7.        Patterson TF, Thompson GRI, Denning DW, et al. Practice guidelines for the diagnosis and management of Aspergillosis: 2016 update by the Infectious Diseases Society of America. 

. 2016 Aug 15;63(4):e1-e60. doi: 10.1093/cid/ciw326.

8.        Verweij PE, Chowdhary A, Melchers WJG, Meis JF. Azole resistance in 

: can we retain the clinical use of mold-active antifungal azoles? 

. 2016 Feb 1;62(3):362-8. doi: 10.1093/cid/civ885.

9.        Vermeulen E, Lagrou K, Verweij PE. Azole resistance in 

. 2013 Dec;26(6):493-500. doi: 10.1097/QCO.0000000000000005.

10.      Van der Linden JWM, Arendrup MC, Warris A, et al. Prospective multicenter international surveillance of azole resistance in Aspergillus fumigatus. 

. 2015 Jun;21(6):1041-4. doi: 10.3201/eid2106.140717.

11.      Steinmann J, Hamprecht A, Vehreschild MJGT, et al. Emergence of azole-resistant invasive aspergillosis in HSCT recipients in Germany. 

. 2015 May;70(5):1522-6. doi: 10.1093/jac/dku566.

12.      Van Der Linden JWM, Snelders E, Kampinga GA, et al. Clinical implications of azole resistance in 

. 2011 Oct;17(10):1846-54. doi: 10.3201/eid1710.110226.

13.      Snelders E, Huis In ’t Veld RA, Rijs AJ, Kema GH, Melchers WJ, Verweij PE. Possible environmental origin of resistance of Aspergillus fumigatus to medical triazoles. 

. 2009 Jun;75(12):4053-7. doi: 10.1128/AEM.00231-09.

14.      Snelders E, van der Lee HAL, Kuijpers J, et al. Emergence of azole resistance in 

 and spread of a single resistance mechanism. 

. 2008 Nov 11;5(11):e219. doi: 10.1371/journal.pmed.0050219.

15.      Verweij PE, Kema GH, Zwaan B, Melchers WJ. Triazole fungicides and the selection of resistance to medical triazoles in the opportunistic mould 

. 2013 Feb;69(2):165-70. doi: 10.1002/ps.3390.

16.      International Environmental AMR Forum. 

Initiatives for Addressing Antimicrobial Resistance in the Environment: Current Situation and Challenges

.; 2018. https://wellcome.ac.uk/sites/default/files/antimicrobial-resistance-environment-report.pdf. Accessed February 27, 2019.

17.      Battaglin WA, Sandstrom MW, Kuivila KM, Kolpin DW, Meyer MT. Occurrence of azoxystrobin, propiconazole, and selected other fungicides in US streams, 2005—2006. 

. 2011 Jun;218(1-4):307-322. doi:10.1007/s11270-010-0643-2.

18.      Lamoth F, Calandra T. Let’s add invasive aspergillosis to the list of influenza complications. 

. 2018 Oct;6(10):733-735. doi: 10.1016/S2213-2600(18)30332-1.

19.      Schauwvlieghe AFAD, Rijnders BJA, Philips N, et al. Invasive aspergillosis in patients admitted to the intensive care unit with severe influenza: a retrospective cohort study. 

. 2018 Oct;6(10):782-792. doi: 10.1016/S2213-2600(18)30274-1.

20.      Crum-Cianflone NF. Invasive aspergillosis associated with severe influenza infections. 

. 2016 Aug 10;3(3):ofw171. doi: 10.1093/ofid/ofw171.

21.      Shah MM, Hsiao EI, Kirsch CM, Gohil A, Narasimhan S, Stevens DA. Invasive pulmonary aspergillosis and influenza co-infection in immunocompetent hosts: case reports and review of the literature. 

. 2018 Jun;91(2):147-152. doi: 10.1016/j.diagmicrobio.2018.01.014.

22.      Ajmal S, Mahmood M, Abu Saleh O, Larson J, Sohail MR. Invasive fungal infections associated with prior respiratory viral infections in immunocompromised hosts. 

. 2018 Aug;46(4):555-558. doi: 10.1007/s15010-018-1138-0.

23.      Vanderbeke L, Spriet I, Breynaert C, Rijnders BJA, Verweij PE, Wauters J. Invasive pulmonary aspergillosis complicating severe influenza: epidemiology, diagnosis and treatment. 

. 2018 Dec;31(6):471-480. doi: 10.1097/QCO.0000000000000504.

24.      Bonifaz A, Tirado-Sánchez A. Cutaneous disseminated and extracutaneous sporotrichosis: current status of a complex disease. 

. 2017 Feb 10;3(1). pii: E6. doi: 10.3390/jof3010006.

25.      Gremião IDF, Miranda LHM, Reis EG, Rodrigues AM, Pereira SA. Zoonotic epidemic of sporotrichosis: cat to human transmission. 

. 2017 Jan 19;13(1):e1006077. doi: 10.1371/journal.ppat.1006077.

26.      Brandolt TM, Madrid IM, Poester VR, et al. Human sporotrichosis: A zoonotic outbreak in southern Brazil, 2012-2017. 

27.      Macêdo-Sales PA, Souto SRLS, Destefani CA, et al. Domestic feline contribution in the transmission of Sporothrix in Rio de Janeiro State, Brazil: a comparison between infected and non-infected populations. 

. 2018 Jan 18;14(1):19. doi: 10.1186/s12917-018-1340-4.

28.      Gremiao IDFG, Menezes RC, Schubach TMP, Figueiredo ABF, Cavalcanti MCH, Pereira SA. Feline sporotrichosis: epidemiological and clinical aspects. 

. 2015 Jan;53(1):15-21. doi: 10.1093/mmy/myu061.

29.      Gremião IDF, Miranda LHM, Reis EG, Rodrigues AM, Pereira SA. Zoonotic epidemic of sporotrichosis: cat to human transmission. 

30.      De Farias MR. Image of cat with 

31.      Williams G. US is overrun with more than 50 million feral cats. 

. http://america.aljazeera.com/articles/2013/11/6/us-is-overrun-withmorethan50millionferalcats.html. Published 2013.

32.      Edwards PQ, Palmer CE. Prevalence of sensitivity to coccidioidin, with special Reference to specific and nonspecific reactions to coccidioidin and to histoplasmin. 

. 1957 Jan;31(1):35-60. doi:10.1378/chest.31.1.35.

33.      Brown J, Benedict K, Park BJ, Thompson GR, III. Coccidioidomycosis: epidemiology. 

. 2013 Jun 25;5:185-97. doi: 10.2147/CLEP.S34434.

34.      Edwards LB, Acquaviva FA, Livesay VT, Cross FW, Palmer CE. An atlas of sensitivity to tuberculin, PPD-B, and histoplasmin in the United States. 

35.      Maiga AW, Deppen S, Scaffidi BK, et al. Mapping histoplasma capsulatum exposure, United States. 

. 2018 Oct;24(10):1835-1839. doi: 10.3201/eid2410.180032.

36.      Hage CA, Knox KS, Wheat LJ. Endemic mycoses: overlooked causes of community acquired pneumonia. 

. 2012 Jun;106(6):769-76. doi: 10.1016/j.rmed.2012.02.004.

37.      Deppen SA, Blume JD, Kensinger CD, et al. Accuracy of FDG-PET to diagnose lung cancer in areas with infectious lung disease: a meta-analysis. 

. 2014 Sep 24;312(12):1227-36. doi: 10.1001/jama.2014.11488.

38.      Marsden-Haug N, Goldoft M, Ralston C, et al. Coccidioidomycosis acquired in Washington state. 

. 2013 Mar;56(6):847-50. doi: 10.1093/cid/cis1028.

39.      Litvintseva AP, Marsden-Haug N, Hurst S, et al. Valley fever: finding new places for an old disease: coccidioides immitis found in Washington state soil associated with recent human infection. 

. 2015 Jan 1;60(1):e1-3. doi: 10.1093/cid/ciu681.

40.      Benedict K, Thompson GR, Deresinski S, Chiller T. Mycotic infections acquired outside areas of known endemicity, United States. 

. 2015 Nov;21(11):1935-41. doi: 10.3201/eid2111.

41.      Armstrong PA, Jackson BR, Haselow D, et al. Multistate epidemiology of histoplasmosis, United States, 2011—2014. 

. 2018 Mar;24(3):425-431. doi: 10.3201/eid2403.

42.      Chiller T. Valley fever: timely diagnosis, early assessment, and proper management. Medscape website. www.medscape.org/viewarticle/853791_2. Published 2016. Accessed March 8, 2019.

43.      Greer A, Ng V, Fisman D. Climate change and infectious diseases in North America: the road ahead. 

. 2008 Mar 11;178(6):715-22. doi: 10.1503/cmaj.081325.

44.      Kolivras KN, Comrie AC. Climate and infectious disease in the southwestern United States. 

. 2004 Sep;28(3):387-398. doi:10.1191/0309133304pp417ra.

45.      Tamerius JD, Comrie AC. Coccidioidomycosis incidence in Arizona predicted by seasonal precipitation. 

. 2011;6(6):e21009. doi: 10.1371/journal.pone.0021009.

46.      Centers for Disease Control and Prevention. Coccidioidomycosis/Valley Fever (Coccidioides spp). National Notifiable Diseases Surveillance System. wwwn.cdc.gov/nndss/conditions/coccidioidomycosis/. Accessed February 28, 2019.

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New public health perspectives on aspergillosis, sporotrichosis, histoplasmosis, and coccidioidomycosis.

Hilary C. Kelly, MPH

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