African Journal of Biotechnology

HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH

 

Afr. J. Biotechnol.


Vol. 2 No. 9


Viewing options:


 • Abstract
 • Full text
 •Reprint (PDF) (236K)

Search Pubmed for articles by:


Smith SI

Odunukwe NN



Other links:


PubMed Citation


Related articles in PubMed


 

African Journal of Biotechnology Vol. 2 (9), pp. 322-324, September 2003

ISSN 1684-5315  © 2003 Academic Journals

 

 

Short Communication

 

Plasmid profile of Escherichia coli 0157:H7 from apparently healthy animals

 

Smith SI1*, Aboaba OO2, Odeigha P3, Shodipo K2, Adeyeye JA3, Ibrahim A3, Adebiyi T1, Onibokun H1 and Odunukwe NN1

 

1Molecular Biology and Biotechnology Division, Nigerian Institute of Medical Research, P.M.B. 2013, Yaba, Lagos, Nigeria.

2Department of Microbiology, University of Lagos, Nigeria.

3Department of Cell Genetics, University of Lagos, Nigeria.

 

*Corresponding author; E-mail: stellaismith@yahoo.com, Fax: 00 2341 862 865.

 

Accepted 22 August 2003

 

 
   

Abstract

 
Abstract
Introduction

Materials and Methods

Results and Discussion
References
 

 

 

One hundred samples from healthy animals were screened for the presence of enterohaemorrhagic Escherichia coli 0157: H7 and 17 were positive for EHEC 0157:H7 after confirmation using serology kits. Antibiotic susceptibility patterns showed the isolates to be highly susceptible to the various antibiotics screened with a few showing multiple antibiotic resistance. The plasmid profiles revealed that 8/17 (47%) of the animal isolates harboured detectable plasmids ranging in size from 0.564 kb to >23 kb.

 

Key words: Escherichia coli, EHEC, animals, plasmid profile.

 
   

Introduction

 
Abstract
Introduction

Materials and Methods

Results and Discussion
References

 

 

 

Infection caused by Escherichia coli 0157:H7 has become a significant public health problem world-wide (Armstrong et al., 1996). The forms of transmission are animal-to-person, waterborne and person to person (Armstrong et al., 1996; Coia, 1998). Cattle faeces has been recognised as the principal reservoir of the microorganism in waterborne and food-borne E. coli 0157:H7 outbreaks and sporadic infections (Armstrong et al., 1996; Coia, 1998). Enterohaemorrhagic E. coli (EHEC) 0157:H7 is the dorminant shiga toxin producing strain that is known to be associated with both outbreak and sporadic cases of human diseases ranging from uncomplicated diarrhoea to haemorrhagic colitis and haemolytic uraemic syndrome (HUS). Their ability to cause severe diseases is related to their capacity to secrete shiga toxins also called verotoxins.

 

The prevalence of EHEC in animals has not been studied in Nigeria to the best of our knowledge. In this report, the commonly consumed animals in Nigeria were investigated for the prevalence of EHEC 0157:H7.

 

 
   

Materials and Methods

 

 
Abstract
Introduction

Materials and Methods

Results and Discussion
References

 

 

 

Faeces from cattle, pigs, rams and goats observed defaecating were collected from Ventata farms, Gbagada Cattle Ranch, and Ajayi Farms in Lagos State and Pakoto farm in Ifo, Ogun State in universal sterile container and immediately transported to the laboratory for processing and culture. Briefly, 1 g suspension of faeces was placed in 9 ml of peptone water and vortexed. After which, 0.1 ml of the same buffer was equally spread onto the surface of sorbitol MacConkey agar and incubated for 24 h at 370C. 

 

Non-sorbitol fermenting colonies were picked and characterized using biochemical systems. The sorbitol negative colonies were serologically typed for 0157:H7 antigens by slide agglutination with polyvalent and monovalent anti-E. coli O and H sera (Biogenetics Diagnostics, Padua, Italy). Haemolytic activity of the isolates were tested by culturing the isolates in BHI containing 7% human blood and incubating at 370C for 24 h.

 

Susceptibility of the organisms to antibiotics was tested by the disk diffusion method on BHI according to Bauer et al. (1966). The following antibiotics were used: ampicillin, colistin, gentamicin, nitrofurantoin, cotrimoxazole, streptomycin and tetracycline. The method of Birnboim and Doly (1979) was employed for plasmid screening. The DNA were electrophoresed on 0.8% agarose gel, stained with ethidium bromide, visualized by UV transillumination and photographed. Molecular weights were calculated based on molecular weight standard.

 
   

Results and Discussion

 
Abstract
Introduction

Materials and Methods

Results and Discussion
References

 

 

 

Table 1. Distribution of serologically confirmed E. coli isolates and their sources.

 

Animal type

No. of samples

Non-sorbitol fermenters

Serologically confirmed

Cow

40

27

7

Ram

30

13

2

Pig

17

12

5

Goat

13

6

3

Total

100

58

17

 

 

 

EHEC 0157:H7 was isolated from 17% of animals in this study (Table 1). The E. coli isolates showed haemolytic activity on blood agar plates. Our results show that 18% of the animal isolates showed multiple antibiotic resistance while when tetracycline resistance was taken alone it was 35% (Table 2). There has been increasing concern of the possible development of resistance to antimicrobial agents in the Enterobacteriaceae, especially E. coli as a result of the use of such agents in animal feed (Willis, 2000). This resistance is quite high and it could be as a result of the widespread use of such agent in animal feed in Nigeria. Plasmid profile analyses revealed that there are detectable plasmids in 47% of the isolates. Plasmids were detected from eight (47%) animal isolates, three from cows (>23.13 and 4.361 kb; 0.564 kb), one from goat (>23.13 kb), two from pigs (>23.13, 2.322 and 2 kb; >23.13 kb. The last two from ram had sizes of >23.13 kb each (Figure 1).

 

 

Table 2. Antibiotic susceptibility patterns of the E. coli isolates.

 

Code

Antibiotic susceptibility patterns

    no.

Ap

Col

Gen

Nal

Nit
Cot

Str

Tet

P1

R

R

S

S

S

S

S

R

P2

S

R

S

S

S

S

S

R

P3

S

R

S

S

S

S

R

S

P4

S

S

S

S

S

S

S

R

G1

S

S

S

S

S

R

S

R

G2

S

R

S

S

S

S

S

S

P5

S

R

S

  S

S

S

S

S

G3

S

R

S

S

S

S

S

S

R1

S

R

R

R

R

R

R

R

R2

S

R

S

S

S

S

S

S

C1

R

R

S

R

R

R

R

R

C2

R

R

S

R

R

R

R

S

C3

R

S

S

S

S

S

S

S

C4

S

S

S

S

S

S

S

S

C5

S

R

S

S

S

S

S

S

C6

S

R

S

S

S

R

S

S

C7

S

R

S

S

S

S

S

S

 

Ap, ampicillin; Col, colistin; Gen, gentamicin; Nal, nalidixic acid; Nit,

nitrofurantoin; Cot, cotrimoxazole; Str, streptomycin; Tet, tetracycline.

R, resistant; S, sensitive.

P, pig; G, goat; R, ram; C, cow.

 

 

 

 

Figure 1. Agarose gel electrophoresis showing plasmid profile of EHEC from the isolates. (a) Lanes: M, molecular weight marker (l, HindIII digest); 1, ram isolate; 2, pig isolate; 3, pig isolate; 4, cow isolate (>23.13 kb); 5, cow isolate  (9.416 kb). (b) Lanes: M, molecular weight marker (l, HindIII digest), 1, cow isolate (no plasmid); 2, cow isolate (0.564 kb); 3, cow isolate (no plasmid); 4, goat isolate (no plasmid); 5, goat isolate (>23.13 kb); 6, ram isolate (>23.13 kb); 7, goat isolate (no plasmid).

 

All the isolates had large molecular weight plasmids >23.130 kb. Large molecular weight plasmids (90 kb) have commonly been associated with toxigenic strains (Bopp et al., 2003). Further virulence tests on these isolates are required as these animals are commonly consumed animals in Nigeria. The goat and ram isolates shared the same plasmid size (>23.13 kb) and were from the same farm, showing that the EHEC isolates may be epidemiologica