Detection performance of PCR for Legionella pneumophila in environmental samples: a systematic review and meta-analysis

被引:4
作者
Yin, Xin [1 ,2 ]
Chen, Ying-Zhou [1 ,3 ]
Ye, Qi-Qing [1 ,2 ]
Liao, Li-Juan [3 ]
Cai, Zhuo-Rui [4 ]
Lin, Min [5 ]
Li, Jia-Na [6 ]
Zhang, Geng-Biao [6 ]
Peng, Xiao-Li [5 ]
Shi, Wen-Fang [7 ]
Guo, Xu-Guang [1 ,7 ,8 ,9 ]
机构
[1] Guangzhou Med Univ, Affiliated Hosp 3, Dept Clin Lab Med, Guangzhou 510150, Peoples R China
[2] Guangzhou Med Univ, Dept Pediat, Pediat Sch, Guangzhou 510182, Peoples R China
[3] Guangzhou Med Univ, Dept Clin Med, Sch Clin 1, Guangzhou 511436, Peoples R China
[4] Guangzhou Med Univ, Dept Prevent Med, Sch Publ Hlth, Guangzhou 511436, Peoples R China
[5] Guangzhou Med Univ, Clin Sch Tradit Chinese & Western Med, Dept Tradit Chinese & Western Med Clin Med, Guangzhou 511436, Peoples R China
[6] Guangzhou Med Univ, Sch Clin 2, Dept Med Imaging, Guangzhou 511436, Peoples R China
[7] Guangzhou Med Univ, Sch Clin 3, Dept Clin Med, Guangzhou 511436, Peoples R China
[8] Guangzhou Med Univ, Affiliated Hosp 3, Key Lab Major Obstetr Dis Guangdong Prov, Guangzhou 510150, Peoples R China
[9] Guangzhou Med Univ, Affiliated Hosp 3, Guangdong Higher Educ Inst, Key Lab Reprod & Genet, Guangzhou 510150, Peoples R China
关键词
Legionella pneumophila; L; pneumophila; PCR; Diagnosis; REAL-TIME PCR; POLYMERASE-CHAIN-REACTION; WATER SAMPLES; QUANTITATIVE PCR; CULTURE; SPP; QUANTIFICATION; QPCR;
D O I
10.1186/s12941-022-00503-9
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Background Legionellosis remains a public health problem. The most common diagnostic method to detect Legionella pneumophila (L. pneumophila) is culture. Polymerase chain reaction (PCR) is a fast and accurate method for this detection in environmental samples. Methods Four databases were searched for studies that evaluated the detection efficiency of PCR in L. pneumophila. The quality evaluation was conducted using Review Manager 5.3. We used Meta-DiSc 1.4 software and the Stata 15.0 software to create forest plots, a meta-regression, a bivariate boxplot and a Deeks' funnel plot. Results A total of 18 four-fold tables from 16 studies were analysed. The overall pooled sensitivity and specificity of PCR was 94% and 72%, respectively. The positive likelihood ratio (RLR) and negative likelihood ratio (NLR) was 2.73 and 0.12, respectively. The result of the diagnostic odds ratio (DOR) was 22.85 and the area under the curve (AUC) was 0.7884. Conclusion Establishing a laboratory diagnostic tool for L. pneumophila detection is important for epidemiological studies. In this work, PCR demonstrated a promising diagnostic accuracy for L. pneumophila.
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页数:12
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