Skip to main content
  • Loading metrics

Postharvest Disease of Banana Caused by Fusarium musae: A Public Health Concern?

  • David Triest ,

    Affiliation BCCM/IHEM Collection of Biomedical Fungi, Service of Mycology and Aerobiology, Scientific Institute of Public Health, Brussels, Belgium

  • Marijke Hendrickx

    Affiliation BCCM/IHEM Collection of Biomedical Fungi, Service of Mycology and Aerobiology, Scientific Institute of Public Health, Brussels, Belgium

Banana Crown Rot Postharvest Disease

Banana is one of the most important tropical crops and is affected by several fungal diseases, such as crown rot postharvest disease [1]. Crown rot is responsible for significant losses in banana fruits [1, 2]. Predominantly, Colletotrichum musae and Fusarium spp. are its causative agents [1, 2]. Inoculum sources include mainly infected flowers but also decaying leaves, and fungal transfer can occur from banana stalks onto the crown surface during the cutting of banana bunches (knife-induced) as well as when the bunches are cleaned in contaminated water (Fig 1) [1]. Fungal infection starts at harvest, and the first symptoms of crown rot appear only after packaging and shipping from producing countries to consuming countries [1, 2]. Crown rot begins with a mycelium development on the crown surface, followed by an internal development [2]. This internal development can, subsequently, affect the peduncle and the whole fruit, leading to softening and blackening of the fruit tissue [2]. Postharvest fungicidal treatments are applied to control crown rot disease, though severely affected banana fruits are still found in consumer markets [3]. Moreover, onset and spreading of the disease is unpredictable and can also induce early ripening of banana fruits during transport [2].

Fig 1. Development of banana crown rot postharvest disease and suggested modes of transfer to cause an opportunistic human pathogenic infection with F. musae.

F. musae as Etiological Agent of Banana Crown Rot

Recent studies showed that the fungal species F. musae is frequently found associated with banana crown rot [1, 3]. The species was installed in 2011 (according to multilocus phylogeny and mating experiments) as a separate, sister species from F. verticillioides sensu stricto, which is also frequently found associated with banana crown rot [1, 3, 4]. Originally, F. musae was known as a distinct, banana-infecting population within F. verticillioides, and both species are practically impossible to distinguish morphologically [4]. Whereas F. verticillioides has a broad plant host specificity (maize, rice, banana, etc.), F. musae seems restricted in its plant pathogenicity and has, until now, only been recovered from banana fruits [4, 5]. To date, F. musae has been isolated from banana fruits coming from several producing countries in Latin America (Mexico, Panama, Ecuador, etc.), the Canary Islands, and the Philippines, but not from banana-producing countries in Africa [1, 4, 5]. Moreover, it has been observed that F. musae strains have a significantly greater ability to cause infection on banana fruits than F. verticillioides strains [6]. Another difference with typical F. verticillioides strains (i.e., isolated from maize) is that F. musae strains are unable to produce the mycotoxin fumonisin because of the absence of the fumonisin biosynthesis gene cluster [4].

F. musae as a Human Pathogen

Because of the recent installment of F. musae as a separate species (in 2011) and, consequently, the fact that several strains previously identified as F. verticillioides were actually shown to be F. musae, its epidemiology is not yet fully elucidated. The latter justifies the need for retrospective studies that reidentify F. verticillioides strains. One such retrospective study showed that five strains collected in the period 2001–2008 and morphologically identified as F. verticillioides appeared to be F. musae, according to multilocus phylogeny [7]. Of interest is that all five strains were clinical isolates, and four were isolated from immune-suppressed patients [7].

In addition, further screening by performing sequence similarity searches in public databases revealed several other cases of human infection associated with F. musae [7]. These were keratitis cases (i.e., eye infections) from the multistate, contact lens–associated outbreak in the United States as well as superficial infections such as sinusitis [79]. Whereas F. verticillioides is a well-established opportunistic human pathogen, F. musae was not until this study, which implied its first report as a human pathogen [7]. Another retrospective study reidentifying F. verticillioides strains showed that human pathogenic F. musae infections, both deep-invasive and superficial, are probably not as uncommon as previously expected [10], and this is also shown in a one-year survey assessing the identity of Fusarium isolates coming from two hospitals in Belgium [11, 12]. It is estimated that approximately 20% of human pathogenic F. verticillioides infections are in fact infections caused by F. musae [5]. Important to take into consideration with the latter is that human infections associated with F. verticillioides account for approximately 10% of the total amount of Fusarium infections, and a Fusarium infection is considered to be the second most occurring mold infection in humans [13].

Fusarium Virulence Determinants

At least 70 species of the soil-borne fungal genus Fusarium are known to be associated with opportunistic human disease, and most of them are members of a species complex [13]. The species complex most frequently found associated with human infection is the F. solani species complex (between 40% and 60% of the reported cases), followed by the F. oxysporum species complex and the F. fujikuroi species complex (each accounting for approximately 20% of the cases) [13]. Both F. musae and F. verticillioides are members of the F. fujikuroi species complex. Fusarium spp. are also well-known plant pathogens that are able to infect a diverse range of plant hosts, and several formae speciales have been defined. Increasing evidence indicates the presence of host-specific virulence determinants [14]. Despite the availability of whole genome sequences of some important plant pathogenic Fusarium spp., knowledge about Fusarium virulence determinants remains fragmentary and largely undefined, except for the secreted in xylem (SIX) effectors in F. oxysporum (i.e., virulence factors secreted by F. oxysporum in the plant vascular system) and several Fusarium mycotoxin encoding regions [14]. Gene expression data from F. oxysporum f. sp. cubense causing banana wilt disease has highlighted an important role for proteins putatively involved in root attachment, cell degradation, detoxification, transport, secondary metabolite biosynthesis, signal transduction, and conidial germination, which is crucial for spreading of the disease in plants as well as for transfer to humans [15, 16]. In addition, comparative genome analyses have revealed that F. solani f. sp. pisi and F. oxysporum f. sp. lycopersici have, in addition to their core genome, an adaptive genome with dispensable chromosomes that are enriched in host-specific genes towards pathogenicity of pea and tomato, respectively. [14, 17, 18]. Also, F. verticillioides appears to exhibit chromosomes with rapidly evolving genes encoding potential virulence determinants [14]. Moreover, Ma et al. [17] showed that horizontal gene transfer of the pathogenicity chromosomes can convert a non–plant pathogenic F. oxysporum strain (initially having only a core genome) into a tomato pathogen. Whether Fusarium spp. require an adaptive genome to cause a human infection or whether a core genome is already sufficient remains to be elucidated.

Acquisition of a Human Pathogenic F. musae Infection

Since F. musae has only been found on banana fruits, unlike F. verticillioides, its mode of transfer to cause an opportunistic human infection seems clear and involves an important role for banana crown rot postharvest disease. Although a direct link between a human pathogenic F. musae infection and a F. musae-infected banana fruit as the source has not yet been established, two important observations are made: (i) The only known environmental habitat of F. musae is the banana fruit; (ii) All currently known cases of human infection with F. musae as the causative agent involve patients hospitalized in non–banana-producing countries (the US and European countries). As such, it is hypothesized that marketed banana fruits contaminated with F. musae but not yet visibly affected by crown rot postharvest disease most likely lead to an opportunistic human pathogenic F. musae infection after the susceptible human host is brought into contact with it (Fig 1). However, two alternative hypotheses can be proposed. A first is that the currently known cases of F. musae-infected patients acquired their infection after travelling to a banana-producing country, where they came into contact with F. musae-contaminated banana material or cleaning water. The second alternative hypothesis assumes that the habitat and distribution of F. musae is not as limited as currently described, and F. musae is also present on currently unknown plant or environmental substrates other than banana.

The F. musae “banana crown rot” route of infection (i.e., the main hypothesis) deviates from the commonly proposed routes of infection of Fusarium species. Because of their efficient mechanisms for dispersal, an opportunistic human pathogenic Fusarium infection in the immune-suppressed patient population is often thought to be acquired after inhalation of contaminated (environmental or hospital) air, and their recovery from hospital water–related systems—which act as Fusarium reservoirs—also suggests a nosocomial origin [1921]. Superficial infections in immune-competent individuals, on the other hand, are often acquired after trauma involving tissue breakdowns at the skin and exposure to Fusarium-contaminated materials (wood, plant leaves, etc.) [22].

Future Perspectives

The occurrence of F. musae as a human pathogen in non–banana-producing countries and its plant host specificity for banana suggests that banana crown rot postharvest disease may be a potential public health concern of importance. The establishment of a direct link between a human infection and a F. musae-infected banana fruit as the source is one of the major future perspectives. Difficulties for future studies, however, will be the fact that transfer to humans can occur at multiple points (the travel history of the patient will need to be evaluated) and that the potential banana fruit source will often no longer be available for analysis at the time a patient is diagnosed with a F. musae infection. However, when a potential banana fruit source is still available, F. musae may be isolated and compared with the clinical isolate by molecular typing methods or whole genome sequencing. Also, it needs to be investigated whether other Fusarium spp. associated with banana crown rot postharvest disease, such as F. verticillioides, are transferred in the same way to cause a human pathogenic infection. Further (retrospective) analyses and clinical surveys, using multilocus sequencing for identification, will need to be performed to fully elucidate the epidemiology of F. musae infections in banana fruits as well as in humans. Moreover, it needs to be investigated whether F. musae can be isolated from other plant or environmental substrates, such as hospital water–related systems or air samples. Nevertheless, improvement of postharvest fungicidal treatments to prevent banana crown rot postharvest disease, better control measurements, and better process hygiene criteria for the processing of banana fruits are recommended. In addition, resistant banana cultivars may need to be searched.


  1. 1. Kamel MAM, Cortesi P, Saracchi M (2016) Etiological agents of crown rot of organic bananas in Dominican Republic. Postharvest Biol Technol 120: 112–120.
  2. 2. Lassois L, Jijakli MH, Chillet M, de Lapeyre de Bellaire L (2010) Crown rot of bananas: preharvest factors involved in postharvest disease development and integrated control methods. Plant Dis 94: 648–658.
  3. 3. Molnár O, Bartók T, Szécsi Á (2015) Occurrence of Fusarium verticillioides and Fusarium musae on banana fruits marketed in Hungary. Acta Microbiol Immunol Hung 62: 109–119. pmid:26132832
  4. 4. Van Hove F, Waalwijk C, Logrieco A, Munaut F, Moretti A (2011) Gibberella musae (Fusarium musae) sp. nov., a recently discovered species from banana is sister to F. verticillioides. Mycologia 103: 570–585. pmid:21177490
  5. 5. Triest D, Piérard D, De Cremer K, Hendrickx M (2016) Fusarium musae infected banana fruits as potential source of human fusariosis: may occur more frequently than we might think and hypotheses about infection. Commun Integr Biol 9: e1162934. pmid:27195070
  6. 6. Moretti A, Mulè G, Susca A, González-Jaén MT, Logrieco A (2004) Toxin profile, fertility and AFLP analysis of Fusarium verticillioides from banana fruits. Eur J Plant Pathol 110: 601–609.
  7. 7. Triest D, Stubbe D, De Cremer K, Piérard D, Detandt M, Hendrickx M (2015) Banana infecting fungus, Fusarium musae, is also an opportunistic human pathogen: are bananas potential carriers and source of fusariosis? Mycologia 107: 46–53. pmid:25361833
  8. 8. Chang DC, Grant GB, O’Donnell K, Wannemuehler KA, Noble-Wang J, Rao CY, et al. (2006) Multistate outbreak of Fusarium keratitis associated with use of a contact lens solution. JAMA 296: 953–963. pmid:16926355
  9. 9. O’Donnell K, Sarver BA, Brandt M, Chang DC, Noble-Wang J, Park BJ, et al. (2007) Phylogenetic diversity and microsphere array-based genotyping of human pathogenic Fusaria, including isolates from the multistate contact lens-associated U.S. keratitis outbreak of 2005 and 2006. J Clin Microbiol 45: 2235–2248. pmid:17507522
  10. 10. Esposto MC, Prigitano A, Tortorano AM (2016) Fusarium musae as cause of superficial and deep-seated human infections. J Mycol Med 2016 Apr 15. pii: S1156-5233(16)00049-4. pmid:27091579
  11. 11. Becker PT, de Bel A, Martiny D, Ranque S, Piarroux R, Cassagne C, et al. (2014) Identification of filamentous fungi isolates by MALDI-TOF mass spectrometry: clinical evaluation of an extended reference spectra library. Med Mycol 52: 826–834. pmid:25349253
  12. 12. Triest D, Stubbe D, De Cremer K, Piérard D, Normand AC, Piarroux R, et al. (2015) Use of matrix-assisted laser desorption ionization-time of flight mass spectrometry for identification of molds of the Fusarium genus. J Clin Microbiol 53: 465–476. pmid:25411180
  13. 13. Guarro J (2013) Fusariosis, a complex infection caused by a high diversity of fungal species refractory to treatment. Eur J Clin Microbiol Infect Dis 32: 1491–1500. pmid:23934595
  14. 14. Sperschneider J, Gardiner DM, Thatcher LF, Lyons R, Singh KB, Manners JM, et al. (2015) Genome-wide analysis in three Fusarium pathogens identifies rapidly evolving chromosomes and genes associated with pathogenicity. Genome Biol Evol 7: 1613–1627. pmid:25994930
  15. 15. Guo L, Han L, Yang L, Zeng H, Fan D, Zhu Y, et al. (2014) Genome and transcriptome analysis of the fungal pathogen Fusarium oxysporum f. sp. cubense causing banana vascular wilt disease. PLoS One 9: e95543. pmid:24743270
  16. 16. Deng GM, Yang QS, He WD, Li CY, Yang J, Zuo CW, et al. (2015) Proteomic analysis of conidia germination in Fusarium oxysporum f. sp. cubense tropical race 4 reveals new targets in ergosterol biosynthesis pathway for controlling Fusarium wilt of banana. Appl Microbiol Biotechnol 99: 7189–7207. pmid:26129952
  17. 17. Ma LJ, van der Does HC, Borkovich KA, Coleman JJ, Daboussi MJ, Di Pietro A, et al. (2010) Comparative genomics reveals mobile pathogenicity chromosomes in Fusarium. Nature 464:367–373. pmid:20237561
  18. 18. Coleman JJ, Rounsley SD, Rodriguez-Carres M, Kuo A, Wasmann CC, Grimwood J, et al. (2009) The genome of Nectria haematococca: contribution of supernumerary chromosomes to gene expansion. PLoS Genet 5:e1000618. pmid:19714214
  19. 19. Nucci M, Anaissie E (2007) Fusarium infections in immunocompromised patients. Clin Microbiol Rev 20: 695–704. pmid:17934079
  20. 20. Short DPG, O’Donnell K, Zhang N, Juba JH, Geiser DM (2011) Widespread occurrence of diverse pathogenic types of the fungus Fusarium in bathroom plumbing drains. J Clin Microbiol 49: 4264–4272. pmid:21976755
  21. 21. O’Donnell K, Sutton DA, Rinaldi MG, Magnon KC, Cox PA, Revankar SG, et al. (2004) Genetic diversity of human pathogenic members of the Fusarium oxysporum complex inferred from multilocus DNA sequence data and amplified fragment length polymorphism analyses: evidence for the recent dispersion of a geographically widespread clonal lineage and nosocomial origin. J Clin Microbiol 42: 5109–5120. pmid:15528703
  22. 22. Al-Hatmi AM, Meis JF, de Hoog GS (2016) Fusarium: molecular diversity and intrinsic drug resistance. PLoS Pathog 12: e1005464. pmid:27054821