Mycoflora Associated with the Goat's Hair and Sheep Wool in Taif, Saudi
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Vol. 11(11), pp. 458-465, 21 March, 2017 DOI: 10.5897/AJMR2017-8462 Article Number: 9E112A863291 ISSN 1996-0808 African Journal of Microbiology Research Copyright © 2017 Author(s) retain the copyright of this article http://www.academicjournals.org/AJMR Full Length Research Paper Mycoflora associated with the goat’s hair and sheep wool in Taif, Saudi Arabia Mohamed Fadl Awad1,2 1Botany and Microbiology Department, Faculty of Science, Al-azhar University, Assuit Branch, Egypt. 2Biology Department, Faculty of Science, Taif University, Kingdom of Saudi Arabia. Received 24 January, 2017; Accepted 14 February, 2017 The objective of this study was to evaluate the occurrence of mycoflora in 30 samples of healthy goat’s hair and sheep wool collected from different localities in Taif, Saudi Arabia, and the ability of some fungal isolates for keratinase activities. Sixty four species belonging to 28 genera were collected from the two substrates. The wool of sheep was polluted with fungi than goat hairs, and contained high total counts and number of fungal genera and species. Nine species of true dermatophytes isolated belonged to Microsporum (3 species) and Trichophyton (6 species). Several keratinophilic species were isolated of which, Chrysosporium indicum, Chrysosporium keratinophilum and Chrysosporium tropicum were the most prevalent. The commonest saprophytes in order of frequency were members of the genera, Aspergillus, Penicillium, Alternaria and Cochliobolus. In addition, the other genera found included Acremonium, Chaetomum, Cladosporium, Cochliobolus, Fusarium, Mucor, Paecilomyces, Phoma, Rhizopus, Scopulariopsis, Stachybotrys, Trichoderma and others. Five species from 20 tested isolates (Aspergillus niger, C. keratinophilum, C. tropicum, Microsporum gypseum and Trichoderma viride) had high keratinase activity. The results of this study indicate that both goat hair and sheep wool provide a suitable habitat for dermatophytes and other keratinophilic fungi. Most of these fungi play an important role in the degradation of keratin substrates, so that they can help preserve the environment and reduce pollution. Key words: Mycoflora, goat’s hair, sheep wool, keratinase activities, Saudi Arabia. INTRODUCTION Keratinophilic fungi are natural colonizers of keratinous groups. Hyphomycetes include dermatophytes and a substrates. Some are keratolytic and play an important great variety of non dermatophyte filamentous fungi. ecological role in decomposing α-keratins, insoluble They occur on cornfield debris in the soil and degrade fibrous proteins (Filipello Marchisio, 2000). Keratinophilic hard keratin and keratinous material. Therefore, they play fungi include a variety of filamentous fungi mainly an important ecological role in decomposing such residue comprising of hyphomycetes and several other taxonomic (Filipello Marchisio, 2000; Sharma and Rajak, 2003). *Corresponding author. E-mail: [email protected]. Tel: +966561326724. Author(s) agree that this article remains permanently open access under the terms of the Creative Commons Attribution License 4.0 International License Awad 459 Animals are known to carry dermatophytes and other penicillin as bacteriostatic agents. The plates were incubated at keratinophilic fungi on their hairs. These animals may act 25°C for 2-4 weeks and the developing fungal colonies were as a source of human and animal infections by direct counted, identified (based on morphological and microscopic characters) and calculated per 10 hair fragments for each sample. contact or by contaminating working areas and dwelling The relative importance value (RN) was calculated (Ali-Shtayeh and places (Ripon, 1982). Therefore, the studies on Asad AI Sheikh, 1988; Shearer and Webster, 1985). dermatophytes and keratinophilic fungi present on the hair of domestic animals are of considerable significance. Keratinophilic fungi along with dermatophytes are The dilution-plate method responsible for various cutaneous mycoses. The dilution-plate method described by Johnson and Curl (1972) Dermatophytes require keratin for growth. These fungi was used for estimation of saprophytic fungi associated with the can cause different types of tinea in humans and animals. hair and wool. Czapek Dox Agar medium from Sigma (sucrose The majority of the fungi responsible for diseases in 30.0, sodium nitrate 3.0, potassium chloride 0.5, magnesium sulfate human beings and animals exist freely in nature as soil heptahydrate 0.5 iron(ii) sulfate heptahydrate 0.01, di-potassium saprophytes (Kumari et al., 2005). hydrogen phosphate 1.0, Agar 15.0) was used in which rose-bengal (1/15000) and chloramphenicol (25 µg/ml) was added as The presence of keratinophilic fungi on hairs of various bacteriostatic agents. Three plates were used for each sample and animals has been briefly reviewed by numerous the plates were incubated at 25°C for 2-3 weeks. The developing researchers in many parts of the world (Ali-Shtayeh et al., fungi were counted, identified and calculated per g hair. 2000; Dobrowolska et al., 2006; Al-Duboon and Farhan, 2007; Nichita and Marcu, 2010; Sallam and ALKolaibe, 2010; Jain and Sharma, 2012; Emenuga and Oyeka, Screening of fungi for keratinase activity 2013; Enany et al., 2013). Twenty fungal isolates were screened by using solid medium Keratin is the major component of poultry feathers method (Wawrzkiewiez et al., 1991). Chicken feather was cut into waste. Distribution of keratinolytic microbes in the nature small fragments, washed extensively with water and detergent and is widespread. Some fungal strains can produce keratin dried in a ventilated oven at 40°C for 72 h to prepare feather proteases which have keratolytic activity and can powder. The feather powder which was the only source of carbon, was added to the sterile agar medium. The diameter of the clear keratinolyse feather. These enzymes have been zone was measured after 7 days at room temperature to quantify produced by fungi, including the species of Aspergillus activity. Keratinase activity of fungus was detected as a clear zone spp., Cochliobolus spp., Mucor spp. and Penicillium spp. around the colony. (Friedrich et al., 1999; Soomro et al., 2012; Ramakrishnaiah et al., 2013; Singh, 2014; Singh et al., 2016). RESULTS AND DISCUSSION The aim of this investigation was to study the occurrence, distribution and prevalence of mycoflora Dermatophytic and keratinophilic fungi (using hair associated with goat’s hair and sheep wool in Taif, Saudi baiting technique) Arabia and the ability of some fungal isolates for keratolytic activity. Sixteen species belonging to 3 genera of dermatophytes and closely related fungi were isolated from goat (13 species and 3 genera) and sheep hairs (14 species and 3 MATERIALS AND METHODS genera). The most contaminated hairs were that of sheep Thirty samples of each of healthy goat’s hair and sheep wool were with the higher total counts (226 isolates/300 fragments) collected from different localities in Taif, Saudi Arabia. The samples and a wide spectrum of species (14 species) than that of were placed in sterile polyethylene bags, transferred immediately to goat (174 isolates and 13 species) as shown in Table 1. the laboratory, and stored in a refrigerator (3-5°C) until examination. Similar observations were obtained from goats and sheep For isolation of mycobiota associated with hair or wool samples, two in many parts of the world (Nasser and Abdel-Sater, methods were used: 1997; El-Said et al., 2009; Sallam and ALKolaibe, 2010). Chrysosporium was the most frequent genus and Hair-baiting technique emerged in 90 and 96.6% of the samples comprising 83.3 and 80.5% of total isolates and have relative For isolation of dermatophytes and other keratinophilic fungi, the importance value RIV of 173.3 and 177.1 of goat and hair-baiting technique (Vanbreuseghem, 1952) was employed. Five fragments from each sample were scattered on the surface of sheep, respectively. This genus was also isolated from moistened sterile soil (20 to 25% moisture content) in sterile plates goat and sheep hairs in Yemen as reported by Sallam (3 plates for each sample). The plates were incubated at 25°C for and ALKolaibe (2010), indicating that Chrysosporium was 10-12 weeks and the soil in plates was remoistened with sterile recorded in 73 and 68% of the goat hairs and sheep wool distilled water whenever necessary. The molds which appear on the samples constituting 57.1 and 47.1% of total fungi, hair fragments were transferred to the surface of Sabouraud's respectively. Also, in Libya, El-Said et al. (2009) dextrose agar medium from Sigma (mycological peptone 10.00, dextrose 40.00, agar 15.00) in 1000 ml of distilled water (Moss and observed that Chrysosporium was the most frequent McQuown, 1969). The medium was supplemented with 0.5 g genus and emerged in 92 and 96% of the samples cycloheximide (actidione), 40 μg/ml streptomycin and 20 units/ml comprising 91.2 and 87.8% of the total isolates and have 460 Afr. J. Microbiol. Res. Table 1. Total isolates (TI, calculated per 300 hair fragments), number of cases of isolation (NCI, out of 30 samples), occurrence remarks (OR) and relative importance values (RIV) of dermatophytic and keratinophilic fungi recovered from hairs of 30 animals of each goats and sheep at 25°C. Goats hair Sheep wool TI NCI & OR RIV TI NCI & OR RIV Chrysosporium 145 27H 173.3 182 29H 177.1 C. asperatium Carmichael 13 5L 24.1 - - C dermatitidis Carmichael 13 8L 34.1 15 8M 33.3 C. indicum (Randhawa and Sandhau) Garg 15 8M 35.2 17 6L 27.5 C. keratinophilum D. Frey ex J.W. Carmich. 45 12M 65.9 73 19H 95.6 C. pannorum (Link) Hughes - - - 3 2R 8.0 C. tropicum Carmichael 49 10M 61.5 62 14M 74.0 C. xerophilum Pitt 10 6L 25.8 12 4L 18.6 Microsporum 5 3R 12.9 9 7L 27.3 M. canis Bodin - - - 1 1R 3.8 M. ferrugineum M. Ota - - - 2 2R 7.5 M. gypseum (E. Bodin) Guiart & Grigoraki 5 3R 12.9 6 5L 19.3 Trichophyton 24 16H 67.1 35 18H 75.48 T.ajelloi (Vanbreus.) Ajello 2 2R 7.8 - - - T.