Detection of bacterial load in drinking water samples by 16s rRNA ribotyping and RAPD analysis

被引:0
|
作者
Zameer, Mariyam [1 ]
Mahmood, Saleha [1 ]
Mushtaq, Zubaria [1 ]
Tabasum, Bushra [2 ]
Ali, Qurban [2 ]
Mahmood, Nasir [3 ]
Jamil, Nadia [1 ]
Munir, Soniya [1 ]
机构
[1] Univ Punjab, Coll Earth & Environm Sci, Lahore, Pakistan
[2] Univ Punjab, Ctr Excellence Mol Biol, Lahore, Pakistan
[3] Univ Hlth Sci, Dept Allied Hlth Sci & Chem Pathol, Lahore, Pakistan
来源
ADVANCEMENTS IN LIFE SCIENCES | 2015年 / 2卷 / 03期
关键词
Drinking water; Bacteriological contamination; RAPD analysis; 16S rRNA gene amplification;
D O I
暂无
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Safe and healthy drinking water is inaccessible to more than 20% of the world population. Among some major risks to safety of potable water, contamination with pathogenic microorganisms is the most alarming and harmful Therefore, it is needed to develop and implement fast and accurate methods for the detection of bacterial contamination in water. Methods: Biological analysis of drinking water samples obtained from nine different collection points of Lahore city was carried out and total of six different bacterial strains were isolated. Biochemical characterization was done under standard laboratory conditions. Molecular identification of these isolates was done by using random amplified polymorphic DNA (RAPD) analysis. Results: The drinking water sample collected from Punjab University showed highest bacterial count 1066/0.5 ml of drinking water while residential area of University of the Punjab contained least number of bacterial counts i.e., 38/0.5 ml of drinking water. Amplification patterns of isolates SZ1, SZ3, SZ4 and SZ6 obtained by RAPD were found similar to genus Bacillus. While, SZ2 and SZ5 had unique amplification patterns identical to Bacillus megaterium. All the six bacterial strains were tested for the presence of protease, lipase, cellulase, and amylase. Strain SZ2 gave positive result for all of them except amylase. Conclusion: Tube well water of Punjab University area of Lahore is safe for drinking purpose except admin block tube. It is recommended to monitor the bacteriological load of drinking water at regular intervals in order to control water borne bacterial diseases.
引用
收藏
页码:135 / 141
页数:7
相关论文
共 50 条
  • [21] Studying Bacterial Diversity of Verhniy Kaban Lake by 16S rRNA Analysis
    Kharchenko, Anastasia
    Sverdrup, Anthony Elias
    Frolova, Ludmila
    HELIX, 2019, 9 (05): : 5545 - 5555
  • [22] 16S rRNA metagenomic analysis of bacterial flora in patients with chronic dacryocystitis
    Uematsu, Masafumi
    Kosai, Kosuke
    Kusano, Mao
    Sasaki, Daisuke
    Inoue, Daisuke
    Mohamed, Yasser Helmy
    Tang, Diya
    Mohamed, Mohamed Talaat
    Yanagihara, Katsunori
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2024, 65 (07)
  • [23] Polymerase chain reaction detection of bacterial 16S rRNA gene in human blood
    Moriyama, Kosei
    Ando, Chie
    Tashiro, Kosuke
    Kuhara, Satoru
    Okamura, Seiichi
    Nakano, Shuji
    Takagi, Yasumitsu
    Miki, Takeyoshi
    Nakashima, Yoshiyuki
    Hirakawa, Hideki
    MICROBIOLOGY AND IMMUNOLOGY, 2008, 52 (07) : 375 - 382
  • [24] Parallel Detection of Bacterial Pathogens in Cerebrospinal Fluid with 16S rRNA Probe Microarray
    刘毅
    韩金祥
    朱波
    黄海燕
    JournalofMicrobiologyandImmunology, 2004, (03) : 210 - 217
  • [25] Ribotyping of Indian isolates of Pasteurella multocida based on 16S and 23S rRNA genes
    Saxena, MK
    Kumar, AA
    Chaudhari, P
    Shivachandra, SB
    Singh, VP
    Sharma, B
    VETERINARY RESEARCH COMMUNICATIONS, 2005, 29 (06) : 527 - 535
  • [26] Ribotyping of Indian Isolates of Pasteurella multocida Based on 16S and 23S rRNA Genes
    M. K. Saxena
    A. A. Kumar
    P. Chaudhari
    S. B. Shivachandra
    V. P. Singh
    B. Sharma
    Veterinary Research Communications, 2005, 29 : 527 - 535
  • [27] Comparative phylobiomic analysis of the bacterial community of water kefir by 16S rRNA gene amplicon sequencing and ARDRA analysis
    Gulitz, A.
    Stadie, J.
    Ehrmann, M. A.
    Ludwig, W.
    Vogel, R. F.
    JOURNAL OF APPLIED MICROBIOLOGY, 2013, 114 (04) : 1082 - 1091
  • [28] Clinical Utility of Bacterial Identification by 16S rRNA Sequencing
    Uhrmacher, J. A.
    Pasculle, A. W.
    Kant, J. A.
    JOURNAL OF MOLECULAR DIAGNOSTICS, 2008, 10 (06): : 597 - 597
  • [29] Isolation of new bacterial species from drinking water biofilms and proof of their in situ dominance with highly specific 16S rRNA probes
    Kalmbach, S
    Manz, W
    Szewzyk, U
    APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1997, 63 (11) : 4164 - 4170
  • [30] Identification of active bacterial communities in a model drinking water biofilm system using 16S rRNA-based clone libraries
    Keinänen-Toivola, MM
    Revetta, RP
    Santo Domingo, JW
    FEMS MICROBIOLOGY LETTERS, 2006, 257 (02) : 182 - 188