Ra. Oberhelman et al., EVALUATION OF ALKALINE PHOSPHATASE-LABELED IPAH PROBE FOR DIAGNOSIS OF SHIGELLA INFECTIONS, Journal of clinical microbiology, 31(8), 1993, pp. 2101-2104
The presence of many enteropathogens which are not easily detectable b
y routine stool culture has led to the development of alternative diag
nostic methods. One of these techniques, nucleic acid probe hybridizat
ion, has been used to identify Shigella spp. and enteroinvasive Escher
ichia coli (EIEC) in stool specimens through the detection of genetic
material encoded by a specific large almost-equal-to 200-kbp virulence
-related plasmid. In the present study, an alkaline phosphatase-labell
ed oligonucleotide probe developed to detect the gene for ipaH, a repe
titive genetic sequence thought to be present on both the virulence-re
lated plasmid and the chromosomes of all strains of Shigella and EIEC,
was tested in a developing-country setting through a prospective clin
ical trial. In a group of 219 Peruvian adults and children with acute
gastroenteritis, the ipaH probe detected 85% of cases of shigellosis a
nd demonstrated a specificity of 95% when compared with simultaneous d
etection by several stool culture techniques. Additionally, three case
s of EIEC infection which could not be diagnosed by culture methods al
one were detected with the ipaH probe and were confirmed by plasmid an
alysis and Sereny testing. These preliminary results suggest that, wit
h further research, the ipaH probe should prove to be a useful and rap
id adjunct in the diagnosis of acute gastroenteritis in developing cou
ntries.