scholarly journals Molecular based prevalence of shigatoxigenic Escherichia coli in rectal swab of apparently healthy cattle in Mymensingh district, Bangladesh

2017 ◽  
Vol 4 (2) ◽  
pp. 1 ◽  
Author(s):  
Jayedul Hassan ◽  
K Nazir ◽  
Md Parvej ◽  
Tazrin Kamal ◽  
Md Rahman
2017 ◽  
Vol 24 (2) ◽  
pp. 1-7 ◽  
Author(s):  
Md-Montasir Mamun ◽  
Jayedul Hassan ◽  
K Nazir ◽  
Md-Alimul Islam ◽  
Khalada Zesmin ◽  
...  

PLoS ONE ◽  
2016 ◽  
Vol 11 (12) ◽  
pp. e0168160 ◽  
Author(s):  
Balichene P. Madoshi ◽  
Egle Kudirkiene ◽  
Madundo M. A. Mtambo ◽  
Amandus P. Muhairwa ◽  
Athumani M. Lupindu ◽  
...  

2014 ◽  
Vol 3 (1) ◽  
pp. 12-14 ◽  
Author(s):  
Jayedul Hassan ◽  
Md Shafiullah Parvej ◽  
Md Bahanur Rahman ◽  
Md Shahidur Rahman Khan ◽  
Md Tanvir Rahman ◽  
...  

Cattle are considered as one of the sources of pathogenic E. coli worldwide. The present study was designed to determine the prevalence and identification of the E. coli isolated from rectal swab of apparently healthy cattle in Mymensingh, Bangladesh. A total of 128 rectal swab samples were assessed by cultural, morphological and biochemical examination followed by Polymerase Chain Reaction (PCR) using primers ECO-1 and ECO-2 that are specific for E. coli 16S rRNA gene. Data obtained from this study were analyzed based on the age, sex, breed and management systems of cattle. This study revealed a 75% prevalence of E. coli in the rectal swab of cattle. Higher prevalence was found in female cattle of unorganized farming systems, and in cattle ?3 years of age. From this study, it may be concluded that, irrespective of age, sex, breed and management system, E. coli is prevailing in the rectal swab of apparently healthy cattle. DOI: http://dx.doi.org/10.3329/mh.v3i1.19775 Microbes and Health, June 2014. 3(1): 12-14


1996 ◽  
Vol 116 (1) ◽  
pp. 1-7 ◽  
Author(s):  
K. S. Sandhu ◽  
R. C. Clarke ◽  
K. McFadden ◽  
A. Brouwer ◽  
M. Louie ◽  
...  

SummaryThis study determined the prevalence of theeaeA gene and its relationship to serotype and type of verotoxin produced in a collection of 432 verotoxigenicEscherichia coli(VTEC) obtained from the faeces of healthy cows and calves in a systematic random survey involving 80 dairy farms in Southwest Ontario. A PCR amplification procedure involving primer pairs which target the conserved central region of the O157:H7eaeA. gene showed that 151 (35·2%) strains were positive for the eaeA gene. All isolates (9–21 for each O group) of O groups 5, 26, 69, 84, 103, 111, 145 and 157 were positive, whereas all isolates (7–34 for each O group) of O groups 113, 132, and 153 and serotype O156:NM (38 isolates) were negative foreaeA. Seventy-three percent of 130 isolates ofeaeA-positive serotypes produced VT1 only compared with 20% of 253 isolates ofeaeA-negative serotypes. We conclude that there is a strong association between certain O groups and theeaeA gene, that serotypes ofeaeA-positive and eaeA-negative VTEC implicated in human and cattle disease are present at high frequency in the faeces of healthy cattle, that VT1 is more frequently associated witheaeA-positive than witheaeA-negative serogroups, and that the eaeA gene is more frequently found in VTEC from calves compared with VTEC from adult cattle.


2012 ◽  
Vol 60 (1) ◽  
pp. 1-15 ◽  
Author(s):  
Domonkos Sváb ◽  
István Tóth

Long polar fimbriae (Lpf) are recently discovered adhesins and increasingly important genetic markers of pathogenicEscherichia colistrains. The presence and genotype diversity of Lpf operons was screened in a collection of 97Escherichia coliO157 strains representing different pathotypes, isolated from healthy cattle (n = 43) and human patients (n = 54) in several countries. Individual structural genes of Lpf were scanned by PCR, and allelic variants were detected with a recently developed typing scheme. Ninety-five strains carried at least one whole Lpf operon (geneslpfABCDand/orlpfABCDE). The 64 enterohaemorrhagic (EHEC) and 24 enteropathogenic (EPEC) strains all carried two Lpf operons, allele 3 oflpfA1and allele 2 oflpfA2, a combination characteristic of the O157:H7/NM serotype. Out of the 9 bovine atypical (AT;stx-, eae-) strains, 7 carried one complete Lpf operon, allele 1 oflpfA2. The atypical strains belonged to main phylogenetic groups A and B1, while the EHEC and EPEC strains were from group D. Lpf variants carried by the 72 strains of theEscherichia coliReference Collection (ECOR) were determined with the same typing scheme. Alleles were detected in 25 strains, of which 6 were found negative for the respective Lpf operons in earlier studies. The marker value of the Lpf allelic combination for the O157:H7/NM serotype was confirmed, and further evidence was given for the presence of at least two different genetic lineages of atypical bovineE. coliO157 strains.


2011 ◽  
Vol 77 (23) ◽  
pp. 8259-8264 ◽  
Author(s):  
José A. Orden ◽  
Pilar Horcajo ◽  
Ricardo de la Fuente ◽  
José A. Ruiz-Santa-Quiteria ◽  
Gustavo Domínguez-Bernal ◽  
...  

ABSTRACTSubtilase cytotoxin (SubAB) from verotoxin (VT)-producingEscherichia coli(VTEC) strains was first described in the 98NK2 strain and has been associated with human disease. However, SubAB has recently been found in two VT-negativeE. colistrains (ED 591 and ED 32). SubAB is encoded by two closely linked, cotranscribed genes (subAandsubB). In this study, we investigated the presence ofsubABgenes in 52 VTEC strains isolated from cattle and 209 strains from small ruminants, using PCR. Most (91.9%) VTEC strains from sheep and goats and 25% of the strains from healthy cattle possessedsubABgenes. The presence ofsubABin a high percentage of the VTEC strains from small ruminants might increase the pathogenicity of these strains for human beings. Some differences in the results of PCRs and in the association with some virulence genes suggested the existence of different variants ofsubAB. We therefore sequenced thesubAgene in 12 strains and showed that thesubAgene in most of thesubAB-positive VTEC strains from cattle was almost identical (about 99%) to that in the 98NK2 strain, while thesubAgene in most of thesubAB-positive VTEC strains from small ruminants was almost identical to that in the ED 591 strain. We propose the termssubAB1to describe the SubAB-coding genes resembling that in the 98NK2 strain andsubAB2to describe those resembling that in the ED 591 strain.


Author(s):  
Samiran Bandyopadhyay ◽  
Debaraj Bhattacharyya ◽  
Indranil Samanta ◽  
Jaydeep Banerjee ◽  
Md Habib ◽  
...  

PEDIATRICS ◽  
1955 ◽  
Vol 16 (2) ◽  
pp. 215-227
Author(s):  
Merlin L. Cooper ◽  
Edward W. Walters ◽  
Helen M. Keller ◽  
James M. Sutherland ◽  
Hollis J. Wiseman

During an outbreak of epidemic diarrhea a new serotype of Escherichia coli: E. coli 0127:B8, was isolated from 44 of 145 infants and from 1 nurse among 82 adult personnel in attendance. Among the 44 infants whose rectal swab cultures were positive, 20 were in the first month of life, 16 were 2 to 6 months of age, and 6 were 7 to 12 months of age, a total of 42 being in the first year of life. Severe epidemic diarrhea associated with the presence of E. coli 0127:B8 was characterized by the sudden development of extreme abdominal distention among some of the infants; explosive onset of diarrhea and the presence of a pungent, musty, objectionable odor not noticed around other patients with diarrhea. E. coli 0127: B8 was isolated more frequently while the patients were having diarrhea. Neomycin® was used orally for the specific treatment of patients with diarrhea. The early dosage was small due to our caution in using a new antibiotic. Over the 4 months period of this study the dosage was gradually increased. The average dose was 40 mg./kg./day for the patients with positive cultures and 46 mg./kg./day for those with negative cultures. Of 22 patients with positive cultures, 12 who were treated with Neomycin® alone or in addition to other antibiotics continued to show the presence of E. coli 0127:B8 after Neomycin® therapy had been terminated; however, only 2 of these patients had recurrence of diarrhea, both having had negative cultures while receiving Neomycin®. The administration of Neomycin® to every infant on the 2 wards, regardless of clinical condition, was followed by a decreasing incidence of diarrhea and decreasing detection of E. coli 0127:B8. The dose of Neomycin® was 40 to 50 mg./kg./day. It is our feeling that Neomycin® administered orally was of definite clinical value therapeutically and prophylactically but in the dosage used was inadequate bacteriologically. Four deaths occurred among the 44 infants whose rectal swab cultures were positive for E. coli 0127:B8 and necropsy studies were made on each. A hemorrhagic enteritis was present in 3 infants and in the fourth infant the cause of death was a congenital heart condition. Death of 1 patient with negative rectal swab cultures may very likely be attributed to severe diarrhea. Sera from patients and personnel failed to show the presence of agglutinins for E. coli 0127:B8. in vitro sensitivity tests showed that the order of decreasing bactericidal effectiveness of 5 antibiotics for E. coli 027:B8 was polymyxin, Neomycin®, chloramphenicol, Achromycin®, and Terramycin®. All strains were resistant to dihydrostreptomycin and sodium sulfadiazine. Only the last strains isolated from 2 patients showed increased resistance to Neomycin®, four-and sixteenfold when compared with the first strains isolated from the same patients.


2018 ◽  
pp. 1720-1724 ◽  
Author(s):  
Shahin Mahmud ◽  
K. H. M. Nazmul Hussain Nazir ◽  
Md. Tanvir Rahman

Aim: The present study was carried out to determine the prevalence and molecular detection of fluoroquinolone-resistant Escherichia coli carrying qnrA and qnrS genes in healthy broiler chickens in Mymensingh, Bangladesh, and also to identify the genes responsible for such resistance. Materials and Methods: A total of 65 cloacal swabs were collected from apparently healthy chickens of 0-14 days (n=23) and 15-35 days (n=42) old. The samples were cultured onto Eosin Methylene Blue Agar, and the isolation and identification of the E. coli were performed based on morphology, cultural, staining, and biochemical properties followed by polymerase chain reaction (PCR) targeting E. coli 16S rRNA genes. The isolates were subjected to antimicrobial susceptibility test against five commonly used antibiotics under fluoroquinolone (quinolone) group, namely gatifloxacin, levofloxacin, moxifloxacin, ofloxacin, and pefloxacin by disk diffusion method. Detection of qnrA and qnrS genes was performed by PCR. Results: Among the 65 cloacal samples, 54 (83.08%) were found to be positive for E. coli. Antibiotic sensitivity test revealed that, of these 54 isolates, 18 (33.33%) were found to be resistant to at least one fluoroquinolone antibiotic. The highest resistance was observed against pefloxacin (61.11%). By PCR, of 18 E. coli resistant to fluoroquinolone, 13 (72.22%) were found to be positive for the presence of qnrS. None of the isolates were found positive for qnrA. Conclusion: Fluoroquinolone-resistant E. coli harboring qnrS genes is highly prevalent in apparently healthy broiler chickens and possesses a potential threat to human health.


2013 ◽  
Vol 79 (17) ◽  
pp. 5411-5413 ◽  
Author(s):  
Claudio Zweifel ◽  
Nicole Cernela ◽  
Roger Stephan

ABSTRACTShiga toxin-producingEscherichia coliO26:H11/H−strains showing the characteristics of the emerging human-pathogenic ST29 clone (stx2a+only,eae+, plasmid gene profilehlyA+etpD+) were detected from human patients and healthy cattle, indicating a possible reservoir. Sheep also appear to shed strains related to the new pathogenic clone O26:H11/H−(ST29,stx1a+only,eae+, plasmid gene profilehlyA+etpD+).


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