{"title":"咀嚼烟草或无烟烟草中产生黄曲霉毒素的曲霉的分子和荧光检测和分离方法","authors":"Adeena Siddiqui, Saira Yahya, Shaista Fatima, Misbah Khadim","doi":"10.1016/j.toxicon.2025.108377","DOIUrl":null,"url":null,"abstract":"<div><div>Tobacco contains many harmful chemicals, toxins, and carcinogens that can cause serious health hazards. Mycotoxins are present in all forms of tobacco, including smokeless tobacco (SLT) which are harmful for human health and associated with different types of cancer. Using microbial and molecular techniques, we identified aflatoxigenic <em>Aspergillus</em> species in SLT. Fifty samples of chewing tobacco were collected randomly from different locations of Karachi. Fungi were grown on Sabouraud Dextrose agar (SDA) by spread plate method and <em>A. flavus</em> was identified macroscopically, microscopically and by amplifying the ITS region. Confirmed isolates of <em>A. flavus</em> were analyzed for aflatoxin production by Ammonia vapor test and by UV on coconut agar medium (CAM). The regulatory genes (<em>aflR and aflS</em>) associated with aflatoxins in <em>A. flavus</em> were also amplified. Different fungal species were identified from SLT samples in which <em>A. flavus</em> was the most dominant. Aflatoxin production analysis by ammonia vapor test revealed that 64 % isolates were aflatoxigenic while on Coconut agar medium (CAM) 43 % isolates were aflatoxigenic. Aflatoxins were quantified in only <em>A. flavus</em> positive samples which were in the range of 10–47 μg/kg. Aflatoxin concentration detected in SLT was above the recommended level of FDA standard in majority of the samples.</div></div>","PeriodicalId":23289,"journal":{"name":"Toxicon","volume":"261 ","pages":"Article 108377"},"PeriodicalIF":2.6000,"publicationDate":"2025-04-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Molecular and fluorometric based approach for the detection and isolation of aflatoxin producing Aspergillus sp. in chewing or smokeless tobacco\",\"authors\":\"Adeena Siddiqui, Saira Yahya, Shaista Fatima, Misbah Khadim\",\"doi\":\"10.1016/j.toxicon.2025.108377\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Tobacco contains many harmful chemicals, toxins, and carcinogens that can cause serious health hazards. Mycotoxins are present in all forms of tobacco, including smokeless tobacco (SLT) which are harmful for human health and associated with different types of cancer. Using microbial and molecular techniques, we identified aflatoxigenic <em>Aspergillus</em> species in SLT. Fifty samples of chewing tobacco were collected randomly from different locations of Karachi. Fungi were grown on Sabouraud Dextrose agar (SDA) by spread plate method and <em>A. flavus</em> was identified macroscopically, microscopically and by amplifying the ITS region. Confirmed isolates of <em>A. flavus</em> were analyzed for aflatoxin production by Ammonia vapor test and by UV on coconut agar medium (CAM). The regulatory genes (<em>aflR and aflS</em>) associated with aflatoxins in <em>A. flavus</em> were also amplified. Different fungal species were identified from SLT samples in which <em>A. flavus</em> was the most dominant. Aflatoxin production analysis by ammonia vapor test revealed that 64 % isolates were aflatoxigenic while on Coconut agar medium (CAM) 43 % isolates were aflatoxigenic. Aflatoxins were quantified in only <em>A. flavus</em> positive samples which were in the range of 10–47 μg/kg. Aflatoxin concentration detected in SLT was above the recommended level of FDA standard in majority of the samples.</div></div>\",\"PeriodicalId\":23289,\"journal\":{\"name\":\"Toxicon\",\"volume\":\"261 \",\"pages\":\"Article 108377\"},\"PeriodicalIF\":2.6000,\"publicationDate\":\"2025-04-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Toxicon\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0041010125001515\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"PHARMACOLOGY & PHARMACY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Toxicon","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0041010125001515","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
Molecular and fluorometric based approach for the detection and isolation of aflatoxin producing Aspergillus sp. in chewing or smokeless tobacco
Tobacco contains many harmful chemicals, toxins, and carcinogens that can cause serious health hazards. Mycotoxins are present in all forms of tobacco, including smokeless tobacco (SLT) which are harmful for human health and associated with different types of cancer. Using microbial and molecular techniques, we identified aflatoxigenic Aspergillus species in SLT. Fifty samples of chewing tobacco were collected randomly from different locations of Karachi. Fungi were grown on Sabouraud Dextrose agar (SDA) by spread plate method and A. flavus was identified macroscopically, microscopically and by amplifying the ITS region. Confirmed isolates of A. flavus were analyzed for aflatoxin production by Ammonia vapor test and by UV on coconut agar medium (CAM). The regulatory genes (aflR and aflS) associated with aflatoxins in A. flavus were also amplified. Different fungal species were identified from SLT samples in which A. flavus was the most dominant. Aflatoxin production analysis by ammonia vapor test revealed that 64 % isolates were aflatoxigenic while on Coconut agar medium (CAM) 43 % isolates were aflatoxigenic. Aflatoxins were quantified in only A. flavus positive samples which were in the range of 10–47 μg/kg. Aflatoxin concentration detected in SLT was above the recommended level of FDA standard in majority of the samples.
期刊介绍:
Toxicon has an open access mirror Toxicon: X, sharing the same aims and scope, editorial team, submission system and rigorous peer review. An introductory offer Toxicon: X - full waiver of the Open Access fee.
Toxicon''s "aims and scope" are to publish:
-articles containing the results of original research on problems related to toxins derived from animals, plants and microorganisms
-papers on novel findings related to the chemical, pharmacological, toxicological, and immunological properties of natural toxins
-molecular biological studies of toxins and other genes from poisonous and venomous organisms that advance understanding of the role or function of toxins
-clinical observations on poisoning and envenoming where a new therapeutic principle has been proposed or a decidedly superior clinical result has been obtained.
-material on the use of toxins as tools in studying biological processes and material on subjects related to venom and antivenom problems.
-articles on the translational application of toxins, for example as drugs and insecticides
-epidemiological studies on envenoming or poisoning, so long as they highlight a previously unrecognised medical problem or provide insight into the prevention or medical treatment of envenoming or poisoning. Retrospective surveys of hospital records, especially those lacking species identification, will not be considered for publication. Properly designed prospective community-based surveys are strongly encouraged.
-articles describing well-known activities of venoms, such as antibacterial, anticancer, and analgesic activities of arachnid venoms, without any attempt to define the mechanism of action or purify the active component, will not be considered for publication in Toxicon.
-review articles on problems related to toxinology.
To encourage the exchange of ideas, sections of the journal may be devoted to Short Communications, Letters to the Editor and activities of the affiliated societies.