final seminar

49

Upload: raed-najeeb-alkhursan

Post on 14-Apr-2017

142 views

Category:

Self Improvement


0 download

TRANSCRIPT

Page 1: Final seminar
Page 2: Final seminar

Occurrence of fungi in poultry feed with cultural and molecular detection of their aflatoxigenic

activityM.Sc. Student

Raed Najeeb Kadhim

SupervisorsProf.Dr. Mohammed H.Khudor Prof.Dr.Basil A.Abbas

Page 3: Final seminar

Mycotoxins

• Low-molecular-weight natural products produced as secondary metabolites by fungi.

• Lack of visible appearance of fungus does not negate presence of mycotoxins. Toxins can remain in the organism after fungus has been removed.

• Mycotoxins greatly resist decomposition and even temperature treatments, such as cooking and freezing.

• Resistant to breakdown in an animal’s digestive system.

Page 4: Final seminar

Some important toxigenic fungi

Aspergillus

Penicillium

Alternaria

Fusarium

Toxigenic fungi

Page 5: Final seminar

Aspergillus

• Found in soil, plant debris, and indoor air environment•Aspergillus flavus is The most important species which cause aspergillosis in animals as well as in man and in birds. •Aspergillus flavus causes mycotic abortion in cattle and sheep.Ingestion of high amounts of aflatoxin may induce lethal effects, also cause sinusitis, cerebral aspergillosis, meningitis, pulmonary aspergillosis, cutaneous aspergillosis and hepatosplenic aspergillosis.•Produces many toxins as aflatoxins (B1, B2, ,G1,G2, M1, M2) Gliotoxin, Sterigmatocystin, and Methoxy Sterigmatocystin.

Page 6: Final seminar

Some important mycotoxins

Today 300 - 400 mycotoxins are known

Common mycotoxins

Aflatoxin Deoxynivalenol ZearalenoneFumonisinOchratoxin

Page 7: Final seminar

Aflatoxins

• Produced by Aspergillus. flavus, A.parasiticus and A. oryzae.• There are types: aflatoxins B1 (AFB1) and B2(AFB2),G1(AFG1),G2(AFG2),M1(AFM1) andM2(AFM2). •Aflatoxin B1 occurs most frequently and is most toxic and carcinogenic.

Page 8: Final seminar

Method

Page 9: Final seminar

Collection of samples of poultry feed

Culturing on PDA,MEA& SDA

Isolation

Identification

Morphological by culture Microscopically Molecular

Cultural method (on

CAM medium

PCR UV NH4 Sol.Light Microscope

A. flavus

Sequences analysis

Page 10: Final seminar

The Aim of Study

1 Study the occurrence of mycoflora in poultry feed.

Determination of aflatoxigenic A.flavus. Compatible homology aflatoxigenic A.flavus strains with other strains in the gene bank.

Page 11: Final seminar

Results1- Morphological and microscopic

identification

Page 12: Final seminar

Aspergillus

PenicilliumFigure(1)

Page 13: Final seminar

Rhizopus

Chladosporium Figure(2)

Page 14: Final seminar

Mucor

Alternaria Figure(3)

Page 15: Final seminar

Fusarium

Figure(4)

Page 16: Final seminar

A.flavus

A.niger Figure(5)

Page 17: Final seminar

A.fumigatus

A.terreus Figure(6)

Page 18: Final seminar

A.flavipes

A.carbonarius Figure(7)

Page 19: Final seminar

A.ochraceus

A.candidus Figure(8)

Page 20: Final seminar

A.parasiticus

Figure(9)

Page 21: Final seminar

Calculation of frequency and relative density of genera and Aspergillus spp .

Page 22: Final seminar

Table(1):Range and average count cfu/g of recovered molds genera from poultry feed samples

Page 23: Final seminar

Table(2):Frequency and relative density of recovered mold genera from poultry feed samples .

Page 24: Final seminar

Table(3):Range and average count cfu/g of recovered Aspergillus spp. from poultry feed samples

Page 25: Final seminar

Table(4):Frequency and relative density of recovered Aspergillus spp. from poultry feed samples

Page 26: Final seminar

2 -Cultural detectiona-UV light

Page 27: Final seminar

Control

Figure(10)

Control Non aflatoxigenic

Aflatoxigenic

Page 28: Final seminar

b-Ammonia vapor

Page 29: Final seminar

Figure(11)

Control

Page 30: Final seminar

3-Molecular by PCR

Page 31: Final seminar

Figure(12): Agarose gel electrophoretic of PCR products obtained from DNA of fungal isolates showing amplicons for aflR primer. Lanes: M-

100bp standard, Lanes1–7: A. flavus (aflatoxin producer) amplicon corresponding to 798 bp .

Page 32: Final seminar

Table(5):Detection of aflatoxigenic and nonaflatoxigenic A.flavus isolates from poultry feed by three methods

16

Page 33: Final seminar

Sequencing analysis of PCR product

Page 34: Final seminar
Page 35: Final seminar

Conclusions1-There were contamination with aflatoxin in poultry feed in farms and local markets in Basrah governorate.

2- There are several fungi in collected poultry feed .

3-Several identification and detection methods o aflatoxigenic Aspergillus flavus were used , the most specific , powerful and accurate methods were molecular methods (PCR and sequences analysis) .These two methods detect the specific gene and genetic sequences which produce the aflatoxin.

Page 36: Final seminar

4- The sequences analysis revealed that the

poultry feed were contaminated with

aflatoxigenic A.flavus isolates , and these

isolates were compatible(100% and 99%) with

other A.flavus strains in gene bank.

Conclusions

Page 37: Final seminar

Recommendations

1- Deep study should be done on mycotoxigenic fungi and the amount of mycotoxin in several farms storage and local markets in Basrah governorate.2- Control and prevent factors such as moister and temperature which play important role in fungal growth and mycotoxin production by make them unsuitable .

Page 38: Final seminar

3- Bioassay is very important measurement in this type of studies, so it is recommended to held more deep studies to estimate the effect of degradation residues on domestic animals especially blood parameters and status.

4- Application of biocontrol agent as a powerful control factor for aflatoxins especially the aflatoxin B1( AFB1).

Recommendations

Page 39: Final seminar

CATCTATTCACACCCACACGGCTCTGCCCACCCCGAATGGTAGCAGTAGCGTCTCCGCCATCTTTTCTCATCAGAGTCCGCCGCCACCCGTGGAGACCCAGGGCCTTGGAGGAGATCTGGCTGGTCAGGAGCAAAGCACCCTGTCTTCCCTAACAGTCGATTCGGAATTCGGGGGCTCGTTGCAGTCAATGGAACACGGAAACCATGCCGATTTCTTGGCCGAGTCGACGGGGAGTCTTTTCGACGCGTTTTTGGAAGTAGGGACCCCCATGATCGACCCGTTCCTCGAGTCGGCCCCACTACCACCGTTTCAGGCGCGCTATTGCTGCTTTTCGCTAGCACTACAAACACTGACCCACCTCTTCCCCCACGCCCCGCTGGGCTGTCAACTACGGCTGACGGACGGTGAGGACAGTTCGTACAACCTGATGACGACTGATATGGTCATCTCGGGGAACAAGAGGGCTACCGATGCGGTCCGGAAGATCCTCGGGTGTTCGTGCGCGCAGGATGGCTACTTGCTGAGCATGGTCGTCCTTATCGTTCTCAAGGTGCTGGCATGGTATGCTGCGGCAGCAGGCACCCAGTGTACCTCAACGGCGGCGAGTGGAGAAACCAACAGTGGCAGCTGTAGCAACAGTCCCGCCACCGTGTCCAGTGGCTGTCTGACGGAAGAGCGCGTGCTGCACCTCCCTAGTATGGTGGGCGAGGATTGTGTGGATGAGGAAGACCAGCCGCGAGTGGCGGCACAGCTTGTTCTGAGCGAACTGCACTATTATGTTCTTTTATTTTTGTTGTTGCTCTTAGTCTGCGTTCTCTGTGTCTCTTATCTGTGGAGTGTATTATT

Page 40: Final seminar
Page 41: Final seminar

ACGCCGTCATCGCGGCTGGTCTTCTCATCCACACAATCCTCGCCCACCATACTAGGGAGGTGCAGCACGCGCTCTTCCGTCAGACAGCCACTGGACACGGTGGCGGGACTGTTGCTACAGCTGCCACTGTTGGTTTCTCCACTCGCCGCCGTTGAGGTACACTGGGTGCCTGCTGCCGCAGCATACCATGCCAGCACCTTGAGAACGATAAGGACGACCATGCTCAGCAAGTAGCCATCCTGCGCGCACGAACACCCGAGGATCTTCCGGACCGCATCGGTAGCCCTCTTGTTCCCCGAGATGACCATATCAGTCGTCATCAGGTTGTACGAACTGTCCTCACCGTCCGTCAGCCGTAGTTGACAGCCCAGCGGGGCGTGGGGGAAGAGGTGGGTCAGTGTTTGTAGTGCTAGCGAAAAGCAGCAATAGCGCGCCTGAAACGGTGGTAGTGGGGCCGACTCGAGGAACGGGTCGATCATGGGGGTCCCTACTTCCAAAAACGCGTCGAAAAGACTCCCCGTCGACTCGGCCAAGAAATCGGCATGGTTTCCGTGTTCCATTGACTGCAACGAGCCCCCGAATTCCGAATCGACTGTTAGGGAAGACAGGGTGCTTTGCTCCTGACCAGCCAGATCTCCTCCAAGGCCCTGGGTCTCCACGGGTGGCGGCGGACTCTGATGAGAAAAGATGGCGGAGACGCTACTGCTACCATTCAGGGTGGGCAGAGCGTGTGGTGGTTGATTCGATTGACGATGAGATTGTGGATGCGGTTATATAACCCTCCCCTTCTCGGGCCGGGCGTTCTCGCTTCTGTCACATATTAATTTTCCGTTCTAACTAGCCTTC

Page 42: Final seminar
Page 43: Final seminar

CACTATCCACACACGCTCTGCCCACCCCCATGGTAGCAGTAGCGTCTCCGCCATCTTTTCTCATCAGAGTCCGCCGCCACCCGTGGAGACCCAGGGCCTTGGAGGAGATCTGGCTGGTCAGGAGCAAAGCACCCTGTCTTCCCTAACAGTCGATTCGGAATTCGGGGGCTCTTTGCAGTCAATGGAACACGGAAACCATGCCGATTTCTTGGCCGAGTCGACGGGGAGTCTTTTCGACGCGTTTTTGGAAGTAGGGACCCCCATGATCGACCCGTTCCTCGAGTCGGCCCCACTACCACCGTTTCAGGCGCGCTATTGCTGCTTTTCGCTAGCACTACAAACACTGACCCACCTCTTCCCCCACGCCCCGCTGGGCTGTCAACTACGGCTGACGGACGGTGAGGACAGTTCGTACAACCTGATGACGACTGATATGGTCATCTCGGGGAACAAGAGGGCTACCGATGCGGTCCGGAAGATCCTCGGGTGTTCGTGCGCGCAGGATGGCTACTTGCTGAGCATGGTCGTCCTTATCGTTCTCAAGGTGCTGGCATGGTATGCTGCGGCAGCAGGCACCCAGTGTACCTCAACGGCGGCGAGTGGAGAAACCAACAGTGGCAGCTGTAGCAACAGTCCCGCCACCGTGTCCAGTGGCTGTCTGACGGAAGAGCGCGTGCTGCACCTCCCTAGTATGATGGGCGAGGATTGTGTGGATGAGGAAGACCAGCCGCGAGTGGCGGCACAGCTTGTTCTGAGCGAACTGCACTAAAAACCCGTGCACCAAGCTAACTTTACT

Page 44: Final seminar
Page 45: Final seminar

GGAGGGTTCCCTCGCGGGCTGGTCTTCTCATCCACACAATCCTCGCCCACCATACTAGGGAGGTGCAGCACGCGCTCTTCCGTCAGACAGCCACTGGACACGGTGGCGGGACTGTTGCTACAGCTGCCACTGTTGGTTTCTCCACTCGCCGCCGTTGAGGTACACTGGGTGCCTGCTGCCGCAGCATACCATGCCAGCACCTTGAGAACGATAAGGACGACCATGCTCAGCAAGTAGCCATCCTGCGCGCACGAACACCCGAGGATCTTCCGGACCGCATCGGTAGCCCTCTTGTTCCCCGAGATGACCATATCAGTCGTCATCAGGTTGTACGAACTGTCCTCACCGTCCGTCAGCCGTAGTTGACAGCCCAGCGGGGCGTGGGGGAAGAGGTGGGTCAGTGTTTGTAGTTCTATATAATCTTTATTTATATATTCTTTTATTTGTCTATATTGTAGATTTTTTTTATTTTTTATTCTTTCTTTTTTATAATATACTTTTTTTT

Page 46: Final seminar
Page 47: Final seminar

AGGGGGGGGGGGAATTGATCGCGGCTGGTCTTCTCATCCACACAATCCTCGCCCACTCATACTAGGGAGGTGCAGCACGCGCTCTTCCGTCAGACAGCCACTGGACACGGTGGCGGGACTGTTGCTACAGCTGCCACTGTTGGTTTCTCCACTCGCCGCCGTTGAGGTACACTGGGTGCCTGCTGCCGCAGCATACCATGCCAGCACCTTGAGAACGATAAGGACGACCATGCTCAGCAAGTAGCCATCCTGCGCGCACGAACACCCGAGGATCTTCCGGACCGCATCGGTAGCCCTCTTGTTCCCCGAGATGACCATATCAGTCGTCATCAGGTTGTACGAACTGTCCTCACCGTCCGTCAGCCGTAGTTGACAGCCCAGCGGGGCGTGGGGGAAGAGGTGGGTCATTTTTTGTTTTATTTGCGAATTTCTGTAATTTCGTTCCTGTTAAGGTCGTTTATTTTTTGTTGTACTATTTCTTTTCTTTTATTCTGATTTGTTTTTT

Page 48: Final seminar
Page 49: Final seminar