Abstract:
Diarrhoeal disease is a worldwide public health problem mostly affecting children,
the immunocompromised and elderly in developing countries. Among children in
developing countries, Enterotoxigenic Escherichia coli (ETEC) alone is responsible
for more than 650 million diarrhoeal episodes and 2,000,000 deaths annually.
However, in most developing countries including Kenya, there is a paucity of data on
prevalence and characterictics of specific bacterial etiologies of diarrhoeal illness.
Diarrhoea outbreaks have been common on yearly basis in Kenya. This study was
carried out from September 2006 to March 2008 in Machakos District Hospital, a
referral hospital serving most of the lower part of the former Eastern Province. Its
catchment includes the neighbouring divisional and distict hospitals in Kitui, Mwingi
and Mbooni. It has a bed capacity of 250. During the study, a total of 301
participants were enrolled following specific inclusion criteria. The participants
ranged in age from 4 months to 85 years with a median age of 14 years and 7
months. The study was designed to detect bacterial pathogens associated with
diarrhoea and in particular ETEC. Feacal specimens were collected and cultured in
selective and differential media and E. coli phenoptypes identified using standard
biochemical methods. A mixture of eight specific primers were used in a single PCR
(Multiplex Polymerase Chain Reaction; mPCR) to detect diarrhoeagenic E. coli
pathogotypes. Ninety eight isolates from thirty three out of 300 participants (11%)
identified as ETEC positive were subcultured on Colonising Factor Antigen Agar
(CFA) and analysed for hydrophobicity as presumptive indication of CFA presence.
This gave a presumptive confirmation for CFA and Coli Surface Antigens (CS)
which were then analysed using another set of mPCR with specific primers. Other bacterial agents were biochemically identified. They included S. dysenteriae (8/300;
2.7%), S. flexneri (13/300; 4.3%), S. sonnei (1/300; 0.3%), S. boydii (1/300; 0.3%),
Untypable Shigella (44/300;14.7%) Salmonella spp (1/300;0.3%), Serratia spp
(1/300; 0.3%), Pseudomonas spp (1/300; 0.3%), and Klebsiella spp (37/300; 12.3%).
Shigella and Salmonella were then serotyped using specific polyvalent and
monovalent antisera from Denka Seiken, Japan. Antibiotic susceptibility tests were
performed on all isolates using the disc diffusion and minimum inhibitory
concentration methods. ETECs as well as other Enteric bacteria were resistant to
more than four antibiotics (Chloramphenical (28%), Cotrimoxazole (78%), Co amoxilav (70%) Erythromycin (98%) Ciprofloxacin (5%), Cefotoxime (18%) and
Tetracyclin (56%). Those found resiatant to third generation cephalosporins were
tested for Extended Spectrum Beta Lactamases (ESBL) while those resistant to
quinolones were tested for Gyrase resistance genes (Gyrase A, B and
Topoisomerases). Sequencing was done on all Gyrase and topoisomerase positive
isolates for detection of mutations. From the study, ETEC was detected significantly
more often in children less than five years old (25/300) than in those aged above six
years (8/300) (X
2 = 4.2; P<0.05). Among the ETECs isolated, CFAI, CS1, CS2, CS3,
CS5, CS6, CS14 and CS19 were detected. Other than ETEC which was the main
focus of the study, Atypical enteropathogenic E. coli (EPEC), enteroinvasive E. coli
(EIEC) and enteroraggregative E. coli (EAEC) were also detected though with
slightly lower frequencies in both children and adults (16.0%, 8% and 36.4%,
respectively). Enterohaemorrhagic E. coli (EHEC) was only isolated in children and
adults with bloody diarrhoea (2.1%). Enteroaggregative E. coli was the most
prevalent pathotype (83/228 ;36.4%). Shigella spp (67/300; 22.3%) were isolated in atients of all age groups. The drug susceptibility results revealed multidrug
resistance in these isolates. ETECs were resistant to Chloramphenical (28%),
Cotrimoxazole (78%), Augmentin (70%) Erythromycin (98%) Ciprofloxacin (5%)
and Tetracycline (56%). The quinolone resistance gene (gyrA) was detected in 10%
of quinolone resistant isolates. Sequence analysis of strains with decreased
susceptibilities or total resistance to fluoroquinolones showed a single mutation at
either Ser-83 or Asp-87 codon. No mutations were detected in the gyrB, and
topoisomerase genes. Extended – Spectrum Beta Lactamase (ESBL) was detected in
(18/300; 6%). ETEC, other E. coli pathotypes and Shigella spp were shown to be
heterogenous by Pulsed Field Gel Eletrophoresis. The main etiologies of diarrhoea
found were ETEC and other E. coli pathotypes, Shigella spp and Salmonella spp
while the main CFs detected were CFAI (25/98), CS3 (1/98), CS6 (13/98), CS7
(2/98), CS14(12/98) and CS19 (12/98). The establishment of the existence of ETECs
carrying varied CFA / CSs and multidrug resistance (MDR) phenotypes in this study
is of great public health concern. There is a possibility of a reservoir in the
population in the study area and the possibility of the reservoir spreading is real. This
may lead to difficulties in the management of diarrhoeal disease. It is possible CS19
was detected for the first time in this country. The CS19 together with CS6 which are
persistent adhesins can be utilised in the formulation of a novel vaccine for the
prevention of diarrhoea due to ETEC.