OPCE-STR.vp Acta Bot. Croat. 71 (1), 147–157, 2012 CODEN: ABCRA 25 ISSN 0365-0588 eISSN 1847-8476 Incidence of post-harvest disease and airborne fungal spores in a vegetable market UMESH B. KAKDE1*, HEMALATA U. KAKDE2 1 Department of Botany, Government of Maharashtra’s Ismail Yusuf College, Jogeshwari (E), Mumbai, 400 060 India 2 Shree Gauri Dutt Mittal College, Sion, Mumbai-22 India Abstract – The sampling of bioaerosols has been carried out using a Rotorod sampler as well as by exposing culture plates. The screening of some common vegetables was also done for the isolation of fungi as market pathogens to study post-harvest diseases. Alto- gether, fifty nine fungal spore types and 78 species of 33 genera belonging to different groups were recorded respectively on the rotorod strips and on exposed Petri dishes. Many saprophytic and pathogenic fungi were found to be associated with sampled vegeta- bles from the market. In all forty-six fungal species belonging to 26 genera were recov- ered from five varieties of vegetables collected from the same market. The most dominant forms of fungi were of Aspergillus followed by Cladosporium, Penicillium, Alternaria, Fusarium, Curvularia, Trichoderma, and Rhizopus. Aspergillus niger, A. flavus, A. fumigatus, Penicillium spp. and Cladosporium herbarum, found to be dominant during the period of investigation. Important mycotoxin-producing fungi such as A. flavus, A. fumigatus and Fusarium moniliforme were isolated from the vegetables collected from the market. Keywords: Bioaerosols, vegetable, saprophyte, pathogen, mycotoxin, post-harvest dis- ease Introduction In many market places, spoiled material, dumped plant material and debris are often present and are likely to act as reservoirs of plant pathogens due to the constant build up of the spore population from fungi growing on them. The activity of nearly all fungi is to carry out biodegradation and deterioration because of their requirements for prime sources of carbon, nitrogen and other nutrients (PITT and HOCKING 1985). The deterioration of raw vegetables may also be caused by physical damage, the action of their own enzymes, microbial action or a combination of these factors. ACTA BOT. CROAT. 71 (1), 2012 147 * Corresponding address: B-12, Gagan Mahal, Sir Pochkhanwala Road, Worli, Mumbai, 400025, India, e-mail: drumeshkakde@gmail.com Copyright® 2012 by Acta Botanica Croatica, the Faculty of Science, University of Zagreb. All rights reserved. U:\ACTA BOTANICA\Acta-Botan 1-12\474 Kakde and Kakde.vp 26. o ujak 2012 13:42:00 Color profile: Disabled Composite 150 lpi at 45 degrees The spoilage occurring during the processing, distribution, and sale of fresh vegetables is often referred to as post-harvest spoilage or marketing disease. As a general rule, vege- tables become more susceptible to infection by post-harvest pathogens as they ripen. Vege- table and fruits are perishable products with active metabolisms during the postharvest pe- riod (ECKERT 1975). Therefore, proper handling and environmental conditions after har- vesting are essential in maintaining product quality. Mechanical damage has dual importance because it not only reduces the value of vegetables but an also increases the chance for microbial spoilage. Post-harvest diseases are responsible for significant loss of vegetable and fruit production (FRAZIER 1967). A study of bio-aerosols in a market environment showed that most of the fungi found on vegetables and fruits originated in the field or developed during transportation (PANDU- RANJAN and SURYANARAYANAN 1985). Airborne spores can cause infection to salable arti- cles. Although many types of microbial spoilage result from invasion by parasitic microor- ganism, much spoilage also results when normally saprophytic microorganisms behave as opportunistic parasites. For example tomatoes can be spoiled by members of the Fusarium and Geotrichum families (BRACKETT 1987). The spraying of water to give a fresh appear- ance to vegetables and fruits in the market also provides a moist surface that encourages the growth of molds in storages. Bioaerosols in market environments may have some implications for the health of the people working in there. Most of the fungi present in high concentrations in market envi- ronments have been suspected of being causative agents of respiratory diseases in humans and infections of produce. The adverse effects of inhaled fungal propagules on the immune system have been well documented by various workers (DAY 1986; BURGE 1985, 1989; LACEY 1991). Fungal infection can also increase the chances of contamination by mycotoxins, which can cause neurological disorders, liver cancers, lung cancers and other diseases. Many molds capable of producing mycotoxins are also frequent contaminants of food and agri- cultural commodities. Molds, which are of importance in food because of potential myco- toxin production, include members of the genera Aspergillus, Trichothecium, Fusarium. The mycotoxins that are currently receiving the most attention as potential hazards to hu- man and animal health include aflatoxin, ochratoxin A, sterigmatocystin, patulin, penicillic acid, citrinin, zearalenone and the toxic trichothecenes. All these compounds cause some degree of acute toxicity when received in high amounts (KRAMER et al. 1960; HUDSON 1969; WILLIE and MOREHOUSE 1978; BULLERMAN 1979; WICKLOW and SHOTTWELL 1983; MILLER 1990, 1992). No systematic studies on the incidence of post-harvest disease and airborne fungal spores in a vegetable market have been published. However, such information is needed to evaluate the relationship between the prevalence of fungal spores and post-harvest diseases of vegetables due to airborne fungi in markets, and to understand the type of mold exposure that can cause health effects. Hence, the present study was undertaken in one of the major vegetable markets of Nagpur city to investigate post-harvest disease due to the prevalence of airborne fungi in the market. In this paper we describe the measurement of airborne fun- gal spores and post-harvest diseases made in a vegetable market in Nagpur. 148 ACTA BOT. CROAT. 71 (1), 2012 KAKDE U. B., KAKDE H. U. U:\ACTA BOTANICA\Acta-Botan 1-12\474 Kakde and Kakde.vp 26. o ujak 2012 13:42:01 Color profile: Disabled Composite 150 lpi at 45 degrees Material and methods The geographical location of Nagpur is 79 degrees 8 minutes east and 21 degrees 8 min- ute north. Thus it can be said that Nagpur falls in the Deccan plateau region. The city is lo- cated in Maharashtra State and lies in the center of India; the zero milestone of India is situ- ated within this city. An aero-mycological survey was carried out in a vegetable market at Fule market (21° 8’ 45” N/79° 5’ 26”E) in Nagpur city. It is one of the main outdoor vegeta- ble markets of Nagpur City (M.S.), from which a number of vegetables are marketed and transported to different local and outstation markets. This market is situated in the heart of the city and surrounded on all sides by schools, quarters, gardens, railway station etc. The study was undertaken at different seasonal climatic conditions i.e., monsoon (June– Sep- tember), winter (October–February) and summer (March–May) for the period of two years. Bioaerosols were sampled using a rotorod air sampler and settle plates (9 cm diameter Perti dishes) to provide quantitative and qualitative measurements of fungal spores respec- tively. The rotorod air sampler with a sampling rate of 100 L min–1 (Tilak Air Sampler, 1982) was used to analyze the total spore counts. The sampler was operated for 15 min. at the height of one meter above the ground level at fifteen day intervals. The sampling was done during morning (07 am to 10 am) when the market was most active. Exposed cello- phane tapes were mounted with glycerin jelly and examined under a microscope. The trapped spores were identified with the help of reference slides and available standard liter- ature (AINSWORTH et al. 1972; TILAK 1982, 1989; NAIR et al. 1986). For the qualitative analysis of fungi three different media were used: Czapek’s Dox Agar (CZ), Potato Dextrose Agar (PDA) and Martin’s Rose Bengal Agar (MRBA). Two Petri dishes of each medium were exposed for 3 minutes at intervals of 15 days during morning when market activities like loading unloading, agitation, weighing of vegetables were at their peak. All the Petri dishes were kept at different heights (0.5–1 m) above the ground. After exposure to the air the Petri dishes were brought to the laboratory in pre-ster- ilized polythene bags and incubated at 25 °C for 5–7 days. Colonies were counted and iden- tified. The identification of colonies was based on their color, size, shape and other mor- phological features (GILMAN 1957, BARNETT 1960, RAPER and FENELL 1965, RAPER and THOM 1968, SMITH 1969, AINSWORTH et al. 1972, ELLIS 1971). The temperature and relative humidity of the air during the experiments were also recorded. Samples of fresh as well as previously infected or rotten vegetables (cabbage, beans, onion, potato, tomato) were collected in pre-sterilized polythene bags from the same mar- ket to examine post-harvest fungi. For the growth of fungi, these vegetables were incubated using a sterile moist blotter method for 5 to 7 days. Fungi were isolated from these vegeta- ble samples and observed directly by preparing lacto-phenol cotton blue mounts. Fungi isolated by this technique were sub-cultured to Sabouraud’s agar and CZ medium and colo- nies grown for further identification up to species level. Results and discussion Quantitative and qualitative analysis of air samples showed that the market environ- ment was contaminated by some major fungal spore types such as Aspergillus, Penicillium, Cladosporium, Alternaria. The spore population of fungi followed a definite seasonal ACTA BOT. CROAT. 71 (1), 2012 149 INCIDENCE OF POST-HARVEST DISEASE AND AIRBORNE FUNGAL SPORES U:\ACTA BOTANICA\Acta-Botan 1-12\474 Kakde and Kakde.vp 26. o ujak 2012 13:42:01 Color profile: Disabled Composite 150 lpi at 45 degrees variation in the weather prevailing over the market environment. The highest incidence of spores was observed during August to January (monsoon and winter) while March-May (summer) was the lean period. Quantitative and qualitative analysis of bioaerosols: Altogether 59 spore types and 78 fungal species were identified from the air of vegeta- ble market by the rotorod sampler and settle plate method respectively. These belonged to 33 genera. Three spore types from the Zygomycotina, 13 from the Ascomycotina, 3 from the Basiodiomycotina and 30 from the Deuteromycotina were recovered by rotorod sam- pling. Unidentified, less frequent spore types, pollen grains and other bioerosols were clas- sified as other types. Sixty-six species belonging to the class Deuteromycotina were identi- fied from the settle plates, 10 from the Zygomycotina and 2 from the Ascomycotina. Unidentified colonies including yeasts and less frequent taxa were grouped as unidentified colonies (Tab. 1, 2). More spore types and fungal species were found in the months of August, November and January than in April and May (summer). During the monsoon and winter seasons more varieties of vegetables and fruits are available in the market than at other time. The greater concentration of fungal spores during the winter and rainy seasons may be due to the greater availability of dead and decaying material in the market yard acting as sources 150 ACTA BOT. CROAT. 71 (1), 2012 KAKDE U. B., KAKDE H. U. Tab. 1. Incidence of the dominant spore types collected in air samples in a vegetable market. Spore Types Average spores/m3 Per cent contribution Range (spores/m3) ASCOMYCOTINA Chaetomium 24 0.7 0–85 BASIDIOMYCOTINA Smuts 46 1.3 0–120 Uredospores 32 0.9 0–95 DEUTEROMYCOTINA Alternaria 464 13.2 120–800 Aspergillus/Penicillium* 1260 35.9 985–5200 Cercospora 41 1.2 0–100 Cladosporium 623 17.8 425–2000 Curvularia 202 5.8 85–520 Drechslera 40 1.1 0–95 Fusarium 53 1.5 0–120 Helminthosporium 126 3.6 10–300 Nigrospora 65 1.9 0–150 Pithomyces 24 0.7 0–95 Hyphal fragments 54 1.5 20–150 Other Types# 456 13.0 125–900 * Small, spherical and similar type of spores, Aspergillus, Penicillium, Trichoderma, Mucor, Rhizopus. # – less frequent, unidentified spores, pollen grains and other bioaerosols. U:\ACTA BOTANICA\Acta-Botan 1-12\474 Kakde and Kakde.vp 26. o ujak 2012 13:42:01 Color profile: Disabled Composite 150 lpi at 45 degrees of inoculum. This coupled with moisture caused by dew in winter and rain in the monsoon, may promote profuse growth of fungi and subsequent sporulation and discharge of spores into the atmosphere. In the two-year study Aspergillus-Penicillium type spores (small rounded) were the major spore type found, contributing 35.9% for the first year and 34.8% for the second year of the investigation to the total bioaerosols. Rest of the bioaerosols were made up of Clado- sporium, Alternaria, Curvularia and Helminthosporium (Tab. 1). Among the total counts of viable fungi identified, we recognized Aspergillus, Penicil- lium, Cladosporium, Alternaria and Curvularia as the most abundant genera. Aspergillus ACTA BOT. CROAT. 71 (1), 2012 151 INCIDENCE OF POST-HARVEST DISEASE AND AIRBORNE FUNGAL SPORES Tab. 2. Incidence of the most common (contribution > 5%) fungal species identified from settle plate samples in a vegetable market Fungal species Total colonies Per cent contri- bution ZYGOMYCOTINA Cunninghamella echinulata 25 0.5 C. elegans 33 0.7 Mucor globosus 27 0.5 Rhizomucor pusillus 28 0.6 Rhizopus oryzae 25 0.5 R. stolonifer 76 1.5 ASCOMYCOTINA Chaetomium globosum 26 0.5 DEUTEROMYCOTINA Alternaria brassicae 81 1.6 A. solani 112 2.2 A. tenuis 140 2.8 Aspergillus candidus 129 2.6 A. flavipes 38 0.8 A. flavus 258 5.1 A. fumigates 126 2.5 A. niger 321 6.4 A. ochraceous 44 0.9 A. sydowi 42 0.8 A. terreus 46 0.9 A. versicolor 25 0.5 Botrytis cinerea 25 0.5 Candida albicans 33 0.7 Cladosporium epiphyllum 215 4.3 C. herbarum 242 4.8 Fungal species Total colonies Per cent contri- bution C. lignicola 160 3.2 Colletotrichum sp. 61 1.2 Curvularia geniculata 39 0.8 C. lunata 117 2.3 C. oryzae 55 1.1 C. tetramera 45 0.9 Drechslera australiensis 42 0.8 Fusarium chlamydosporum 29 0.6 F. moniliforme 140 2.8 F. oxysporum 47 0.9 F. solani 136 2.7 Helminthosporium nodulosum 45 0.9 H. oryzae 80 1.6 Nigrospora sphaerica 40 0.8 Penicillium citrinum 131 2.6 P. chrysogenum 169 3.4 P. italicum 104 2.1 P. nigricans 124 2.5 P. oxalic 40 0.8 Phoma lingam 93 1.9 Sporotrichum roseum 36 0.7 Trichoderma harzianum 76 1.5 T. viride 86 1.7 Trichothecium roseum 25 0.5 Verticillium glaucum 25 0.5 Sterile Colonies 25 0.5 Unidentified colonies* 943 18.7 (* Less frequent (<.5%), unidentified colony forming units) U:\ACTA BOTANICA\Acta-Botan 1-12\474 Kakde and Kakde.vp 26. o ujak 2012 13:42:01 Color profile: Disabled Composite 150 lpi at 45 degrees species were the most prevalent throughout the seasons. The most dominant species iso- lated were Aspergillus niger, A. flavus, A. fumigatus, Alternaria solani, Cladosporium her- barum, Curvularia lunata, Rhizopus stolonifer, Penicillium chrysogenum, P. italicum. The majority of these fungal species were present throughout the year. Aspergillus species fol- lowed a seasonal trend. Meteorological conditions such as high temperature and low humi- dity during the summer contribute fewer fungi while in the rainy season the concentration of fungi is significantly increased in the atmosphere of market. High concentrations of these fungal spores have been reported in different working environments (SUMBALI and BADYAL 1991, SULIA and KHAN 1980, ROSAS et al. 1992, KAKDE et al. 2001). Spores of some fungi (Aspergillus, Penicillium, Cladosporium etc.) become airborne as a consequence of active liberation mechanism or more often in working environments by agitation of their substrates (INGOLD 1971). Handling of unwashed vegetables was respons- ible for the increase of the spore load concentration in the air especially of Cladosporium and Penicillium (LEHTONEN et al. 1993). These genera were also isolated from the surface samples of vegetables. The seasonal pattern of Aspergillus, Cladosporium, Penicillium, Alternaria and other dominant fungi are governed by the availability of dead and decaying organic matter and their prevalence throughout the year was because of abundant substrata available for their growth in all the seasons in the market. In the present investigation variation in the spore concentrations was recorded in the different months (Fig. 1). The difference in the spore concentration and types could be due to the prevailing environmental conditions and pres- ence of agricultural waste, plant debris and infected vegetables and fruits in the market en- vironments. The release of fungal spores and consequently their concentrations in the at- mosphere are the result of the action of many biological and environmental factors. The occurrence of fungal spores in the air is markedly seasonal because of these organisms’ sensitivity to weather changes (HJELMROOS 1993, CRAIG and LEVETIN 2000, STEPALSKA and WOLEK 2005). 152 ACTA BOT. CROAT. 71 (1), 2012 KAKDE U. B., KAKDE H. U. 0 2 4 6 8 10 12 July Aug Sept Oct Nov Dec Jan Feb Mar April May June Months P e r c e n t c o n tr ib u ti o n Spore Types Fungal Species Fig. 1. Seasonal distribution of fungal spores and species during the sampling period in a vegetable market yard. U:\ACTA BOTANICA\Acta-Botan 1-12\474 Kakde and Kakde.vp 26. o ujak 2012 13:42:01 Color profile: Disabled Composite 150 lpi at 45 degrees Altogether forty-six fungi from 26 genera were isolated from selected common vegeta- bles collected. There were 5 Zygomycotina species; one Ascomycotina and the rest of the species were Deuteromycotina. The largest number of species (46) was found on cabbage and cauliflower, 27 on tomato, 26 on bean, 24 on potato, and 15 on onion (Tab. 3). Some of the species found are presented in figure 2. In the present investigation a few more fungal species were isolated from the air during August, November, December and January (Fig. 1). The incidence of post-harvest diseases in the vegetables was also higher than in other months. As the concentration of fungal spores in the air decreases, the frequency of occurrence of fungi on the vegetables also de- creases, and vice-versa. Aspergillus species were found to be the chief contaminant from the total species isolated. The most frequently isolated fungal species from vegetables were Aspergillus niger, A. flavus, Penicillium crysogenum, Curvularia spp., Cladosporiun herbarum, Rhizopus stolonifer, Alternaria spp., Fusarium spp. Aspergillus has been re- ported as the dominant spore type in markets and other environments by many researchers (SULLIA and KHAN 1980, PANDURAJAN and SURRYANARAYANAN 1985, SANTRA and CHANDA 1989, ABDEL-HAFEZ et al. 1989, SUMBALI and BADYAL 1991, DUCHAINE et al. 2001, KAKDE et al. 2001). In the last few years it has been reported that the spores and sclerotia of toxic fungi con- tain very large concentrations of mycotoxins. The spores of Aspergillus flavus and A. parasiticus have been reported to contain 1100 mg g–1 of aflatoxin, which is carcinogenic to human beings (WICKLOW and SHOTWELL 1983). ACTA BOT. CROAT. 71 (1), 2012 153 INCIDENCE OF POST-HARVEST DISEASE AND AIRBORNE FUNGAL SPORES Tab. 3. Fungi isolated from different vegetables collected from a vegetable market Vegetables Major fungal species associated Cabbage (Brassica oleracia) Aspergillus niger, A. fumigatus, A. versicolor, A. flavus, Alternaria brassicae, A. alternata, A. solani, Botrytis cinerea, Cercospora brassicae, Cladosporium herbarum, Curvularia lunata, Fusarium brassicae, F. moniliforme, Penicillium chrysogenum, Phoma brassicae, Phoma lingam, Rhizopus sp., Trichoderma herzianum, T. viride Bean (Dolichos lablab) Aspergillus niger, A. flavus, A. fumigatus, Alternaria solani, A. brassicae, Botrytis cinerea, Cladosporium species, Fusarium spp., Rhizopus sp., Penicillium crysogenum, Penicillium species, Onion (Allium cepa) Alternaria tenuis, A. solani, Aspergillus niger, A. flavus, Botrytis cinerea, Cladosporium herbarum, Colletotrichum sp., Fusarium moniliforme, Rhizopus sp., Penicillium digitatum, Trichoderma spp. Potato (Solanum tuberosum) Aspergillus niger, A. flavus, Alternaria brassicae, A. solani, A alternata, Botrytis cinera, Cercospora brassicae, Cladosporium herbarum, Curvularia lunata, Fusarium spp., F. moniliforme, Rhizopus stolonifer, Penicillium chrysogenum, Phoma lingam, Rhizoctonia solani, Trichoderma herzianum Tomato (Lycopersicon esculentum) Aspergillus niger, A. flavus, Alternaria alternata, A. solani, Botrytis cinera, Cladosporium herbarum, Cladosporium sp., Colletotrichum sp., Fusarium moniliforme, Fusarium solani, Rhizopus stolonifer, Penicillium chrysogenum, Saccharomyces sp. U:\ACTA BOTANICA\Acta-Botan 1-12\474 Kakde and Kakde.vp 26. o ujak 2012 13:42:01 Color profile: Disabled Composite 150 lpi at 45 degrees A series of experiments on fungal species isolated both from vegetables and air were carried out. One such experiment reported the correlation coefficient (r) between percent occurrence of 15 fungal species on selected vegetables (x) and percent occurrence in air (y) as 0.7595. This indicates a strong positive linear dependence between x and y. 154 ACTA BOT. CROAT. 71 (1), 2012 KAKDE U. B., KAKDE H. U. Fig. 2. Some common fungi isolated from the vegetables collected from the market: a – Alternaria solani, b – Aspergillus niger, c – Aspergillus flavus, d – Aspergillus fumigatus, e – Clado- sporium herbarum, f – Curvularia lunata, g – Chaetomium gobosum, h – Fusarium moniliforme, i – Helminthosporium orza, j – Rhizopus sp, k – Penicillium citrinum, l – Penicillium chrysogenum U:\ACTA BOTANICA\Acta-Botan 1-12\474 Kakde and Kakde.vp 26. o ujak 2012 13:42:06 Color profile: Disabled Composite 150 lpi at 45 degrees Can it be concluded that, in the population of these fungal species, the population correlation coefficient, r = 0.50 is significant? The problem in this situation is to test the null hypothesis H0: r = 0.50 against the alternative hypothesis H0: r ¹ 0.50. We are given n = 15, r = 0.7595 and r0 = 0.50. Z r r e e � � � � �� � � � � � � �� � � � 1 2 1 1 1 2 1 0 795 1 0 795 0log log . . .9950 W e e � � � � � � � � � � � � �� � � � 1 2 1 1 1 2 1 0 50 1 0 50 00 0 log log . . . 5493 T Z W n� � � � � � � �( ) ( . . ) .3 0 9950 0 5493 12 15440 The table value at 5% level of significance is 1.96. Since, T �196. , we accept H0 at the 5% level of significance and conclude that the data support the hypothesis. Hence, using information on the percentage isolation of fungal species on vegetables, the percentage isolation in air can be predicted. Conclusion The most frequent associated fungi isolated from the vegetable and fruits were Asper- gillus niger, A. flavus, Penicillium crysogenum, Curvularia spp., Alternaria spp., Fusarium spp. Aspergillus, Penicillium, Cladosporium, Fusarium, Alternaria etc. These fungi were most prevalent in the air of market environment and also found to be responsible for most of the decay of the vegetables during storage. Hence, there is probably a cyclic relationship existing between the prevalence of fungal bioaerosols and spoilage diseases in market environments. That may be due to the growth of fungi on dumped plant materials, packing leaves, infected vegetables and fruits, where fungi grow saprophytically and produce spores profusely, consequently contaminating the environment. There was a good corre- lation between the number of visible mold growths on collected vegetables from the market and the concentration of airborne molds in the market environment. Although there were fewer fungal species in the air, all the dominant fungal spores recovered from the air were also isolated from the samples of vegetables collected. Hence, both air and surface sampling are necessary to evaluate mold problems in such environments. The number of mold growths on salable articles is a good predictor of airborne mold concentration. References ABDEL-HAFEZ, S. I. I., EL-SAID, A. H. 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