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. Author manuscript; available in PMC: 2017 Oct 1.
Published in final edited form as: Diagn Microbiol Infect Dis. 2016 Jul 12;86(2):136–140. doi: 10.1016/j.diagmicrobio.2016.07.009

Table 4.

Genetic characterization of H.pylori strains isolated from gastritis patients

Patien
t
Biopsy
location
Intergenic
region*
cagA Empty site** hspA vacA s/m Culture
conditions
1 A/C + + s1/m2 Anaerobic
3 A/C + + s1/m1/m2 Micro/Ana
4 A + + s1/m1 Anaerobic
5 A/C + + m1/m2 Anaerobic
7 A/C + + s1/m2 Anaerobic
8 C + s1/m2 Micro/Ana
17 A + + s1/m2 Anaerobic
19 C + + s1/m1/m2 Micro/Ana
21 A + s1/m2 Anaerobic
23 A + + s1/m2 Micro/Ana
24 A/C + + s1/m2 Micro/Ana
25 A + + s1/m2 Anaerobic
26 A/C + + s1/m1 Anaerobic
27 A + + s1/m1 Anaerobic

A= antrum

C= corpus

s= signal sequence

m=middle region

Micro=micro-aerobic conditions

Ana=anaerobic conditions

*

Negative for the 180bp insert

**

Empty-site PCR was performed only on cagA negative strains in order to determine presence or absence of the cag pathogenicity island. The presence of a band in the empty site PCR represents the lack of Pathogenicity Island.