Background: This study was conducted to investigate the presence of Bacillus cereus in meat, meat products, and some seafood in Libya. Materials and Methods: One hundred and thirty‑one samples were collected from different geographic localities in Libya. The samples were subjected to microbiological analysis for enumeration and isolation of B. cereus by conventional cultural, biochemical, and molecular identification using polymerase chain reaction (PCR) and partial sequencing of 16S rDNA techniques. Results: Of 131 samples, only 38 (29%) isolates were found to be B. cereus based on their cultural characteristics on Mannitol Egg‑Yolk Polymyxin (MYP) medium that included 30% beef, 38.2% beef products (minced, burger, kabab, and sausage), 31.8% camel meat, and 48% chicken products (burger, sausage, kabab, and liver). However, B. cereus was not detected from mutton and seafood samples. Seventeen isolates were subjected to molecular identification using PCR and partial sequencing of 16S rDNA technique and confirmed to be B. cereus. The confirmed B. cereus strains were tested for their antibiotic sensitivity profiles and showed a high percentage of multiresistance phenotype. Conclusions: The results provide a better understanding of B. cereus isolated from food of animal origin in Libya and suggest that meat and meat products might play an important role in the spreading of B. cereus through the food chain with antimicrobial resistance characteristics.
Hesham Taher Naas(6-2018)

The study presents results obtained by examination of cloacal swabs from poultry for the presence of verotoxigenic stains of E.coli O157:H7. Twenty samples (9.2%0 of 216 samples examined were positive for E.coli O157. Out of the twenty E.coli O157, 19 strains were positive for the production of both verotoxins (V1 and V2). However, none of them was positive for the presence of H7 antigen.
Hesham Taher Naas(1-2022)

Seventy five random samples were collected (25 raw milk, 50 local different made soft cheeses) from different supermarkets in Tripoli- Libya. The Objectives of this study were: (i)- to clear the incidence rate and count of coliforms as an indicator microorganisms for fecal contamination in raw milk and locally made soft cheese samples manufactured by traditional methods and (ii)- to make comparison between the most famous two conventional methods used for counting of such group of microorganisms. Coliforms were recovered from all the raw milk samples using the two methods (most probable number using liquid lauryl sulphate broth and sold plating method using violet red bile agar). The mean count for the former media was 28x106 while for the later one was 15x106 cfu/ml. For cheese samples (locally made Ricotta and Maasora), positive samples were 78% (39 samples) using MPN method, while 76% (38 samples) using sold plating media VRBA. The mean coliform count for positive samples using MPN was 18x107 cfu/g, while for VRBA plates the mean count for positive samples was 21x106 cfu/g. all counts were higher using MPN than VRBA for the same sample in both raw milk and cheese samples, although, clear difference in count between the two methods was recorded in cheese than that in raw milk, conditions that may affect the count in both raw milk and cheese were discussed. Factors that may limit
Hesham Taher Naas(1-2007)