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Table 1 Summary of HMPV molecular diagnostic approaches and their characteristics

From: Epidemiology and diagnosis technologies of human metapneumovirus in China: a mini review

Methods

Operation time

Limit of detection

Experimental cost

Characteristics

RT-PCR [24, 25]

3–5 h

1000 copies/reaction

Low

RT-PCR has been widely used for performing epidemiological investigation of HMPV, while which requires complex instruments and trained workers

RT-qPCR [27, 28]

1–3 h

10 ~ 100 copies/reaction

Low

RT-qPCR has been widely amplified in HMPV monitoring in clinical samples

LAMP [34, 35]

 ~ 1.5 h

 < 10 copies/reaction

High

Advantages: High sensitivity and specificity, rapid diagnosis with simple reaction procedure, and constant temperature

Disadvantages: High requirements of primers, high false positive rate, and high cost

RAA [38]

15 ~ 30 min

100 copies/reaction

High

Advantages: High sensitivity and specificity, and rapid diagnosis of virus infection

Disadvantages: High cost and high positive rate

RT-RPA combined with CRISPR-Cas12a [45]

 < 30 min

 < 700 copies/reaction

High

Advantages: High sensitivity and specificity, and rapid diagnosis of virus infection

Disadvantages: High cost and high positive rate

mNGS [48]

5 ~ 10 days

Not determined

High

Advantages: High sensitivity and specificity, and rapid diagnosis of unknown pathogens

Disadvantages: High cost and time-consuming

Virus isolation [51]

3 ~ 4 days or more time

Not determined

High

Advantages: The “gold standard” for pathogen detection

Disadvantages: High cost and time-consuming, and low isolation rate, and requires complex instruments and trained workers