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. 2023 Dec 22:16:7775-7795.
doi: 10.2147/IDR.S429990. eCollection 2023.

Emerging and Fastidious Uropathogens Were Detected by M-PCR with Similar Prevalence and Cell Density in Catheter and Midstream Voided Urine Indicating the Importance of These Microbes in Causing UTIs

Affiliations

Emerging and Fastidious Uropathogens Were Detected by M-PCR with Similar Prevalence and Cell Density in Catheter and Midstream Voided Urine Indicating the Importance of These Microbes in Causing UTIs

Dakun Wang et al. Infect Drug Resist. .

Abstract

Introduction: This study compared microbial compositions of midstream and catheter urine specimens from patients with suspected complicated urinary tract infections to determine if emerging and fastidious uropathogens are infecting the bladder or are contaminants.

Methods: Urine was collected by in-and-out catheter (n = 1000) or midstream voiding (n = 1000) from 2000 adult patients (≥60 years of age) at 17 DispatchHealth sites across 11 states. The two groups were matched by age (mean 81 years), sex (62.1% female, 37.9% male), and ICD-10-CM codes. Microbial detection was performed with multiplex polymerase chain reaction (M-PCR) with a threshold for "positive detection" ≥ 10,000 cells/mL for bacteria or any detection for yeast. Results were divided by sex.

Results: In females, 28 of 30 microorganisms/groups were found by both collection methods, while in males 26 of 30 were found by both. There were significant overlaps in the detection and densities of classical uropathogens including Escherichia coli, Enterococcus faecalis, and Klebsiella pneumoniae, as well as emerging uropathogens including Actinotignum schaalii and Aerococcus urinae. In females, detection rates were slightly higher in midstream voided compared to catheter-collected (p = 0.0005) urine samples, while males showed the opposite trend (p < 0.0001). More polymicrobial infections were detected in midstream voided compared to catheter-collected samples (64.4% vs 45.7%, p < 0.0001) in females but the opposite in males (35.6% vs 47.0%, p = 0.002).

Discussion: In-and-out catheter-collected and midstream voided urine specimens shared significant similarities in microbial detections by M-PCR, with some differences found for a small subset of organisms and between sexes.

Conclusion: Non-invasive midstream voided collection of urine specimens for microbial detection and identification in cases of presumed UTI does not result in significantly more contamination compared to in-and-out catheter-collected specimens. Additionally, organisms long regarded as contaminants should be reconsidered as potential uropathogens.

Keywords: catheter; diagnostic testing; midstream voided; multiplex polymerase chain reaction; standard urine culture; urinary tract infection.

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Conflict of interest statement

D.B., N.L., E.H., R.A.F., and M.M. are employees of Pathnostics, and D.W. and X.Z. are paid consultants of Pathnostics. L.A.A. reports personal fees from Pathnostics, outside the submitted work. In addition, N.L. has patents (10,160,991, 11,053,532, 17/335,767, 63/493,416, AU2018254514 B2, BR112019021943-9 B1 and NZ 759292) issued to Pathnostics; pending patents (17/178,091 17/880,227 63/503,939) to Pathnostics. D.B. reports patents (US10160991, US11053532, US17178091, US17335767, AU2018254514B2, BR1120190219439B1, NZ759292) issued to PATHNOSTICS; pending patents (US17830227, US18351385, US18351286, US63493416, US63503393, US63514785, PCTUS2216816, PCTUS2277477, EP3612638, JP2022042545, CA3175879, CA3176586, CA3061015, HK620200143373, CN2018800399569, IL294577) to PATHNOSTICS. The authors report no other conflicts of interest in this work.

Figures

Figure 1
Figure 1
Study design. A flow chart of subject selection for analysis.
Figure 2
Figure 2
Microbial densities of the top 6 detected classical uropathogenic bacteria for female (A) and male (B) subjects. Each dot represents the non-zero microbial density (plotted along the y-axis) for a single microorganism detected by either collection method (arranged along the x-axis) in a single specimen. Blue and red lines indicate the median values for the midstream voided and catheter-collected specimens, respectively. *p < 0.05.
Figure 3
Figure 3
Microbial densities of the top detected emerging uropathogenic bacteria for both female (A) and male (B) subjects. Each dot represents the non-zero microbial density (plotted along the y-axis) for a single microorganism detected by either collection method (arranged along the x-axis) in a single specimen. Blue and red lines indicate the median values for the midstream voided and catheter-collected specimens, respectively. *p < 0.05.
Figure 4
Figure 4
Microbial densities of the top detected uropathogenic CoNS and VGS for both female (A) and male (B) subjects. Each dot represents the non-zero microbial density (plotted along the y-axis) for a single microorganism detected by either collection method (arranged along the x-axis) in a single specimen. Blue and red lines indicate the median values for the midstream voided and catheter-collected specimens, respectively. *p < 0.05.
Figure 5
Figure 5
Microbial densities of yeast for both female (A) and male (B) subjects. Each dot represents the non-zero microbial density (plotted along the y-axis) for a single microorganism detected by either collection method (arranged along the x-axis) in a single specimen. Blue and red lines indicate the median values for the midstream voided and catheter-collected specimens, respectively. *p < 0.05.

References

    1. Schmiemann G, Kniehl E, Gebhardt K, Matejczyk MM, Hummers-Pradier E. The diagnosis of urinary tract infection: a systematic review. Dtsch Arztebl Int. 2010;107(21):361–367. doi: 10.3238/arztebl.2010.0361 - DOI - PMC - PubMed
    1. Price TK, Dune T, Hilt EE, et al. The clinical urine culture: enhanced techniques improve detection of clinically relevant microorganisms. J Clin Microbiol. 2016;54(5):1216–1222. doi: 10.1128/jcm.00044-16 - DOI - PMC - PubMed
    1. Brubaker L, Wolfe AJ. The female urinary microbiota, urinary health and common urinary disorders. Ann Transl Med. 2017;5(2):. doi: 10.21037/13209 - DOI - PMC - PubMed
    1. Wolfe AJ, Toh E, Shibata N, et al. Evidence of uncultivated bacteria in the adult female bladder. J Clin Microbiol. 2012;50(4):1376–1383. doi: 10.1128/jcm.05852-11 - DOI - PMC - PubMed
    1. Lotte R, Lotte L, Ruimy R. Actinotignum schaalii (formerly Actinobaculum schaalii): a newly recognized pathogen—review of the literature. Clin Microbiol Infect. 2016;22(1):28–36. doi: 10.1016/j.cmi.2015.10.038 - DOI - PubMed