Research Article: Filamentous Fungi in Respiratory Infections. What Lies Beyond Aspergillosis and Mucormycosis?

Date Published: April 28, 2016

Publisher: Public Library of Science

Author(s): Anuradha Chowdhary, Kshitij Agarwal, Jacques F. Meis, Donald C Sheppard.


Partial Text

Respiratory tract infections are globally responsible for one-third of infectious disease–associated mortality, accounting for 4.3 million annual deaths. Among these, fungal infections of the respiratory tract are largely unrecognized, and the true burden is elusive [1]. Despite treatment, most invasive fungal infections are associated with high mortality rates of >50% [2]. In general, fungal infections of the respiratory tract are considered synonymous with invasive pulmonary infections caused by Aspergillus spp. and in some centers by Mucorales. However, over the last decade, a number of uncommon filamentous fungi, such as Scedosporium, Fusarium, Penicillium, melanized moulds, and basidiomycetes, have emerged as etiological agents of well-characterized respiratory disorders. It is therefore that the term “respiratory mycosis” has now broadened to include not just invasive disease but also lesser-recognized entities such as fungal ball, severe asthma with fungal sensitization (SAFS), fungus-associated chronic cough (FACC), allergic bronchopulmonary mycosis (ABPM), and allergic fungal rhinosinusitis (AFRS) [3–6]. Notably, both FACC and SAFS have recently been recognized as distinct clinical entities [7,8]. The former manifests as chronic intractable cough in response to pharyngeal colonization by filamentous basidiomycetes, which has been associated with allergic sensitization [7]. The latter, on the other hand, is a reference to poorly controlled asthma, despite optimal management, with evidence of fungal sensitization (short of being labelled ABPM) [6]. Aspergillus spp. are considered to be the major culprit of SAFS, although a range of other fungi, such as Alternaria and Cladosporium spp., are also involved [8]. Both conditions respond favourably to oral antifungal agents, thereby proving a definite role of fungi [9,10]. Moreover, new pathophysiological associations hitherto unknown, such as fungal sensitization and ABPM in patients with chronic obstructive pulmonary disease (COPD), are unfolding [11,12]. Further, emergence of resistance in filamentous fungi to azole antifungal drugs used as mainstay of therapy is another challenging scenario witnessed in the last two decades. This emerging problem is primarily attributed to the widespread usage of azole fungicides in the environment for agricultural and material preservation practices [13]. Here, we aim to provide an overview of the ever-expanding spectrum of human respiratory mycoses and the fungi involved, excluding Aspergillus and Mucorales.

Several soil-inhabiting genera of the ascomycete order Onygenales, such as Histoplasma, Coccidioides, Blastomyces, and Penicillium (Talaromyces) marnefeii, are thermally dimorphic pathogens, primarily inflicting lungs, while other ascomycetes are at best considered as opportunistic pathogens on a background of underlying local and/or systemic risk factors. The latter group includes most fungi encountered frequently in clinical practice. With the exception of aspergilli, which are the commonest respiratory fungal pathogens, other filamentous fungi causing respiratory diseases include Mucorales, black fungi, and species of Fusarium, Scedosporium, and Penicillium. Fusarium spp., conventionally regarded as agents of onychomycosis, are now well known to cause fatal respiratory mycosis. Pulmonary infections are most commonly seen with the Fusarium solani species complex, which mimics aspergillosis and is associated with a worse outcome given the resistance to common antifungal agents [14], while F. vasinfectum is associated with ABPM and hypersensitivity pneumonitis [15,16]. Similarly, species of Scedosporium apiospermum complex and Lomentospora prolificans (previously Scedosporium prolificans) are considered “emerging” human pathogens. Clinically, all organ systems can be infected, although pulmonary infections are the most common [17]. L. prolificans typically causes infections in immunocompromised patients, which are associated with high mortality. The spectrum of respiratory diseases due to S. apiospermum ranges from sinusitis, pulmonary fungal ball, ABPM, and pneumonia [17]. Scedosporium bears a curious association with cystic fibrosis, in which it is seen as a frequently isolated filamentous mould, second only to Aspergillus [17]. S. aurantiacum (a member of the S. apiospermum complex) is mainly isolated from patients with cystic fibrosis and other chronic lung diseases. Treatment outcomes with Scedosporium spp. are usually poor, with L. prolificans being resistant to almost all antifungal agents [17].

The FBM, colloquially called white moulds, have begun to gain importance lately, with systemic studies demonstrating the pathogenic potential of this group of fungi as agents of respiratory and systemic diseases. FBM are usually sterile in culture and appear as cottony white colonies that make routine laboratory identification difficult (Fig 1A). Occasionally, specific characteristics such as spicules, hyphal pegs, clamp connections, arthroconidia, and/or chlamydoconidia may be seen, but they best serve to distinguish FBM fungi from other hyaline ascomycetes (Fig 1B) [3,4,21]. In the past, isolation of these moulds from clinical samples was labelled as contamination; however, lately, several reports incriminating many genera of the phylum Basidiomycota as agents of human disease have been published [4,21]. Notably, FBM such as Schizophyllum commune, Bjerkandera adusta, Hormographiella aspergillata, Ceriporia lacerata, Perennniporia spp., Tyromyces fissilis, and Irpex lacteus are described as agents of respiratory diseases [4,5,22–24]. Substantial numbers of white moulds isolated from clinical samples continue to be unidentified, perhaps because of the unavailability of GenBank sequence data for identification [4]. Among the FBM, S. commune (Fig 1) is probably the best studied, and in a review of 71 infections with S. commune, 94% were respiratory cases (Fig 1C) [22]. Another FBM, H. aspergillata, has been reported from Europe and North America as a cause of invasive, predominantly pulmonary disease in patients with haematological malignancies and haematopoietic stem cell recipients and is associated with a high case fatality [4,25]. Sporotrichum (Phanaerochaete) pruinosum is best known for causing chronic lung disease and allergic sensitization in patients with chronic respiratory diseases [4,26]. Lately, a number of newer FBM have been reported as human pathogens. Perenniporia spp. and Ceriporia lacerata have been incriminated in intracavitary pulmonary fungal ball and fungal pneumonia [23,24]. The list of medically relevant FBM moulds is therefore by no means exhaustive, and with growing awareness among microbiologists and pulmonologists, it will expand in the future.

FBM are better known as allergens than agents of invasive disease, and their noninvasive respiratory manifestations include colonization, allergen sensitization, and allergic sinopulmonary mycoses. Allergic phenomena involving the lower respiratory tract can manifest as bronchial asthma in atopic individuals, which has been attributed to S. commune and Bjerkandera adusta [27–28] or ABPM due to S. commune (Fig 1D) [22], while that of the upper respiratory tract manifests as allergic fungal sinusitis [4,22]. Also, sensitization against S. commune has been reported in patients with COPD, but the clinical implication of this needs to be established [11]. Further, FACC is mainly reported from Japan [5]. The FBM B. adusta has been shown to colonize the pharynx of susceptible individuals and produce a chronic uneasiness that produces the cough [11]. In FACC patients, FBM have been found in induced sputum cultures [5]. It is pertinent to emphasize here that FBM are slow growers and require prolonged incubation of culture plates for up to 10 days. This is in strong contrast to other filamentous moulds such as Mucorales and Aspergillus, which grow within 2 to 3 days of incubation. Thus, the detection of FBM is hampered in microbiology laboratories that discard culture plates of respiratory specimens within 2 days. Furthermore, it has been proposed that a subset of patients with FACC exhibit sensitization to B. adusta, thereby displaying allergic fungal cough (AFC) that is more severe and difficult to control than the nonsensitized patients with FACC [7]. Low-dose itraconazole has been proposed as therapy for FACC, but the efficacy of this intervention is not unequivocally proven yet [10]. Another unique bronchopulmonary colonization syndrome attributable to S. commune has been reported exclusively from Japan and involves bronchial impaction of mucus loaded with fungal hyphae [29].

Most melanized fungi that cause infections are free-living plant saprobes implanted into human tissue as a result of trauma, but respiratory mycoses occur secondary to inhalation of fungal spores. The moulds implicated in respiratory infections belong to the orders Chaetothyriales (Exophiala), Pleosporales (Alternaria, Bipolaris, Curvularia, and Exserohilum), Sordiales (Chaetomium), and Venturiales (Verruconis) of Ascomycota [30]. Among the Pleosporales, Alternaria alternata and species of Bipolaris, Curvularia, and Exserohilum are associated with AFRS, bronchial asthma, hypersensitivity pneumonitis, ABPM, and invasive lung disease [15,31–34]. AFRS is a form of polypoid chronic rhinosinusitis caused by type 1 hypersensitivity to fungal antigens. In addition, the disease is characterized by elevated total serum immunoglobulin E, accumulation of thick, eosinophil-laden mucin with noninvasive fungal hyphae within the paranasal sinuses, and nasal polyposis. Although Aspergillus species are the most common cause of fungal sinus disease worldwide, allergic fungal rhinosinusitis is more commonly caused by black fungi [35]. Additionally, A. alternata is known to produce a severe form of asthma through outdoor allergen sensitization [31]. Chaetomium spp. are rarely reported as agents of human disease, although Chaetomium globosum has been characterized as a cause of fatal pneumonia in patients with haematological malignancies or organ transplants [32,34]. Other respiratory infections attributable to Chaetomium spp. include sinusitis and empyema [33]. Also, Verruconis gallopava and Ochroconis spp. have been isolated from lower respiratory tract secretions and are responsible for invasive and probably allergic lower respiratory tract disease [33,34].

The majority of clinical experience with the above-mentioned diverse fungi represents isolated cases or small series of infections. Therefore, evidence-based algorithms for specific treatment are not available and therapy remains a challenge. Corticosteroids, administered systemically or locally, remain the mainstay of treatment for allergic sinopulmonary manifestations. The management of these disorders focuses on three facets. Firstly, as environmental modification is usually impractical, the main focus is to suppress the inflammation with steroids. Alternatively, systemic antifungal agents have been used successfully with the aim of reducing the fungal load albeit best as adjuncts to steroids. Oral itraconazole has proven to be of benefit in disorders such as FACC, SAFS, and ABPM [5,9,15]. Notably, FBM are resistant to echinocandins, and the empirical use of these agents in patients had been associated with breakthrough infections [25]. Also, polyene antifungals like amphotericin B show modest activity against melanized fungi, though some species of Curvularia and Exophiala could be resistant [30].




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