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. 2020 Dec 17;59(1):e01986-20. doi: 10.1128/JCM.01986-20

TABLE 4.

Performance of tetraplex real-time PCRa

Source
of
DNA
No. of
samples
Previous
detectionb
No. detected by:
Duplex real-time PCRc
Tetraplex real-time PCR
E. histolytica E. dispar Negative E. histolytica E. dispar E. moshkovskii E. bangladeshi Negative
Culture (n = 27) 11 E. histolytica 11 0 0 11 0 0 0 0
9 E. dispar 0 9 0 0 9 0 0 0
3 E. moshkovskii 0 0 0 0 0 3 0 0
1 E. bangladeshi 0 0 0 0 0 0 1 0
3 Negative 0 0 3 0 0 0 0 3
Stool (n = 46) 12 E. histolytica 12 0 0 12 0 0 0 0
16 E. dispar 0 16 0 0 16 3d 0 0
1 E. moshkovskii 0 0 0 0 0 1 0 0
17 Negative 0 0 17 3 0 0 0 14
LA (n = 41) 38 E. histolytica 38 0 0 38 0 0 0 0
3 Negative 0 0 3 0 0 0 0 3
a

The performance of the tetraplex real-time PCR was compared with that of an existing duplex real-time PCR for E. histolytica and E. dispar in clinical samples. LA, liver abscess (aspirate).

b

Previous diagnosis was based on a combination of different tests such as culture (and zymodeme), conventional and nested PCR, antigen detection E. histolytica II ELISA (TechLab), and duplex real-time PCR. “0” indicates a negative test result. Negative, previously negative for E. histolytica and E. dispar species.

c

Data were determined by the use of a previously described existing duplex real-time PCR (46).

d

Tetraplex real-time PCR detected these as mixed infections of E. dispar and E. moshkovskii.