ISSN: 3105-7888 mse.journal@ksph.kz

Возбудители острых респираторных инфекций, выявленные методом мультиплексной ПЦР в режиме реального времени в эпидемический сезон 2023 года в Казахстане

Original Research Клиническая медицина

Возбудители острых респираторных инфекций, выявленные методом мультиплексной ПЦР в режиме реального времени в эпидемический сезон 2023 года в Казахстане

УДК: 616.9 DOI: 10.24412/1609-8692-2025-2-136-150 Страница(-ы): 45-61 2

Аннотация

Введение. Острые респираторные инфекции остаются значимой проблемой общественного здравоохранения, при этом комплексные данные о спектре одновременно циркулирующих вирусных и бактериальных респираторных возбудителей в Казахстане ограничены. Мультиплексная ПЦР в режиме реального времени позволяет одновременно выявлять широкий спектр респираторных мишеней и расширяет возможности эпидемиологической оценки в период сезонного подъёма заболеваемости.
Цель. Изучить распределение вирусных и бактериальных респираторных возбудителей среди пациентов с острыми респираторными инфекциями в Алматы в эпидемический сезон 2023–2024 гг. с использованием мультиплексной ПЦР в режиме реального времени, а также оценить возрастные особенности выявляемости и частоту множественных положительных результатов.
Материалы и методы. Респираторные образцы от 374 пациентов с клинически диагностированными острыми респираторными инфекциями, обследованных с ноября 2023 г. по январь 2024 г., анализировали с использованием мультиплексных ПЦР-тестов в режиме реального времени, включавших 30 респираторных мишеней — 19 вирусных и 11 бактериальных. Описательно оценивали частоту выявления возбудителей, возрастные особенности положительных результатов и комбинации одновременно выявленных ПЦР-мишеней.
Результаты. Вирусные мишени были выявлены у 195 из 374 пациентов (52,1%). Наиболее часто определялись риновирус (24,3%) и вирус гриппа A (14,7%). Бактериальные мишени выявлены у 240 пациентов (64,2%); наиболее часто обнаруживались Haemophilus influenzae, Streptococcus pneumoniae и Moraxella catarrhalis. Множественные положительные ПЦР-мишени зарегистрированы у 202 пациентов (54,0%): у 94 выявлены две, у 67 — три, у 41 — четыре и более мишени. Установлены также возрастные особенности выявляемости отдельных вирусных и бактериальных возбудителей.
Обсуждение. Полученные результаты свидетельствуют о гетерогенной структуре респираторных возбудителей в эпидемический сезон и высокой частоте одновременного выявления нескольких молекулярных мишеней. Вместе с тем выявление бактериальной ДНК методом ПЦР не позволяет однозначно отличить колонизацию от активной инфекции. Кроме того, одновременный положительный результат на общую мишень вируса гриппа A и его подтип не следует автоматически трактовать как наличие двух самостоятельных вирусных инфекций. Поэтому множественные положительные результаты корректнее интерпретировать как молекулярное совместное выявление возбудителей, а не как подтверждённую клиническую коинфекцию без дополнительных клинических и микробиологических данных.
Заключение. Мультиплексная ПЦР в режиме реального времени позволила комплексно охарактеризовать спектр респираторных возбудителей у пациентов с ОРИ в Алматы в сезон 2023–2024 гг. Среди вирусных мишеней преобладали риновирус и вирус гриппа A, среди бактериальных — H. influenzae, S. pneumoniae и M. catarrhalis. Результаты подтверждают потенциальную значимость мультиплексной молекулярной диагностики для эпидемиологического надзора и поддержки клинических решений при условии осторожной интерпретации бактериальных и множественных ПЦР-положительных результатов.

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Полный текст

Introduction

Acute respiratory infections (ARIs) remain one of the leading causes of morbidity and mortality worldwide, particularly affecting vulnerable populations such as children, older adults, and individuals with chronic illnesses [1]. According to the World Health Organization (WHO), ARIs account for a substantial proportion of healthcare visits and hospitalizations during seasonal peaks, especially in winter [2]. Viral pathogens such as rhinoviruses, influenza viruses, and respiratory syncytial virus (RSV) are frequently detected in ARIs. Bacterial pathogens, including Streptococcus pneumoniae and Staphylococcus aureus, may also be identified as primary pathogens or in mixed detections [3]. Rapid and accurate identification of respiratory pathogens is important for clinical management and infection-control strategies [4].

In Kazakhstan, ARIs represent a persistent public health burden, with seasonal outbreaks placing considerable strain on healthcare systems [5]. Although ARIs are known to impose a substantial disease burden, regional epidemiological surveillance studies characterizing both viral and bacterial detections remain limited. The prevalence and clinical implications of simultaneous detection of multiple respiratory pathogens are also insufficiently characterized in the local context, despite evidence that clinically confirmed co-infections may be associated with increased disease severity and prolonged hospitalization [6, 7].

Conventional diagnostic approaches, including culture-based methods and serology, can be time-consuming and may have limited sensitivity for some pathogens [8]. Multiplex real-time polymerase chain reaction (PCR), in contrast, enables simultaneous detection of multiple respiratory targets within a short time frame. This technology has been widely used for clinical diagnostics and epidemiological monitoring of respiratory pathogens, particularly during influenza and COVID-19 epidemics [9-15].

The 2023–2024 respiratory season in Kazakhstan was marked by increased ARI activity [5]. Despite the growing use of multiplex PCR in surveillance systems, regional data comprehensively describing circulating viral and bacterial respiratory targets and multi-pathogen detections during epidemic periods remain limited. Such data can support diagnostic strategies, antimicrobial stewardship, and public health responses [7].

This study aimed to analyze the distribution of viral and bacterial respiratory pathogens among patients with ARIs in Almaty during the 2023–2024 epidemic season using a multiplex real-time PCR panel capable of detecting 30 respiratory pathogens. Age-specific detection patterns and the frequency of simultaneous detection of multiple pathogens were also assessed.

Materials and Methods

Study design and setting. This descriptive laboratory-based study included patients with clinically diagnosed ARIs tested in Almaty, Kazakhstan, between November 2023 and January 2024. A total of 374 patients were included.

Laboratory testing. Respiratory specimens were tested at the OHKZ laboratory using Allplex™ Respiratory Panel 1–4 kits (Seegene, Republic of Korea) together with an OHKZ-developed assay for four additional bacterial targets. The combined testing scheme comprised 30 respiratory targets, described in the source manuscript as 19 viral and 11 bacterial targets (Table 1).

Variables and definitions. Outcomes included detection of at least one viral target, detection of at least one bacterial target, age-specific pathogen detection rates, and simultaneous detection of multiple targets. Multi-pathogen detections were categorized as two, three, or four or more detected targets per patient. Age categories were 0–1, 2–5, 6–10, 11–20, 21–30, 31–40, 41–50, 51–60, and ≥61 years, consistent with Figures 3 and 4.

Statistical analysis. Data were summarized descriptively using absolute counts and percentages. No inferential statistical testing is reported; therefore, between-month and between-age comparisons are interpreted descriptively rather than as statistically significant differences.

Reporting completeness. The source manuscript does not specify the respiratory specimen type(s), sampling and transport procedures, nucleic acid extraction method, PCR instrument, Ct cut-off/interpretation criteria, positive, negative and internal controls, or detailed quality-control procedures. These parameters were not reconstructed and should be supplied from the laboratory protocol by the authors before submission to ensure reproducibility.



 

Table 1 - Respiratory pathogens targeted by Allplex™ Respiratory Panel Kits (Seegene, Republic of Korea)

Reagents

Target category

Target pathogen

Abbreviations

AllplexTM Respiratory

Panel 1

(Seegene, South Korea)

7 Viruses, including variants of Influenza A

Respiratory Syncytial Virus A

Respiratory Syncytial Virus B

Influenza A virus

Influenza A (H1)

Influenza A (H1N1 pdm09)

Influenza A (H3)

Influenza B virus

RSV A

RSV B

Flu A

Flu A (H1)

Flu A (H1N1)

Flu A (H3)

Flu B

AllplexTM Respiratory

Panel 2

(Seegene, South Korea)

7 Viruses

Human Adenovirus

Human Enterovirus

Parainfluenza virus 1

Parainfluenza virus 2

Parainfluenza virus 3

Parainfluenza virus 4

Metapneumovirus

HADV

HEV

PIV 1

PIV 2

PIV 3

PIV 4

MNV

AllplexTM Respiratory

Panel 3

(Seegene, South Korea)

5 Viruses Including 3 Variants of Coronavirus

Bocavirus

Rhinovirus

Coronavirus NL63

Coronavirus 229E

Coronavirus OC43

BoV

RhV

CoV NL63

CoV 229E

CoV OC43

AllplexTM Respiratory

Panel 4

(Seegene, South Korea)

7 Bacteria

Streptococcus pneumoniae

Mycoplasma pneumoniae

Haemophilus influenzae

Legionella pneumophila

Chlamydophila pneumoniae

Bordetella pertussis

Bordetella parapertussis

S. pneumoniae

M. pneumoniae

H. influenzae

L. pneumophila

C. pneumoniae

B. pertussis

B. parapertussis

Respiratory Bacteria, 4 types (The test was developed in the OHKZ Laboratory)

4 Bacteria

Klebsiella pneumoniae

Pseudomonas aeruginosa

Staphylococcus aureus

Moraxella catarrhalis

K. pneumoniae

P. aeruginosa

S. aureus

M. catarrhalis

 


Results

I. Respiratory viral detections

Among 374 examined patients, at least one viral pathogen was detected in 195 (52.1%). The most frequently detected viruses were rhinovirus (24.3%), influenza A virus (14.7%), and adenovirus (5.9%). In December 2023, relatively high detection rates were observed for influenza A virus and respiratory syncytial virus A (RSV A), whereas in January 2024 the detection rates of rhinovirus, adenovirus, and RSV A increased (Figure 1).


 

Figure 1 - Detection rates of respiratory viruses among ARI patients in Almaty, Kazakhstan,

from November 2023 to January 2024 using multiplex real-time PCR


II. Respiratory bacterial detections

Respiratory bacterial targets were detected in 240 of 374 patients (64.2%). The most common bacterial detections were Haemophilus influenzae (32.9%), Streptococcus pneumoniae (24.9%), Moraxella catarrhalis (23.8%), Staphylococcus aureus (12.8%), Klebsiella pneumoniae (3.5%), and Pseudomonas aeruginosa (1.6%). Mycoplasma pneumoniae was not detected. Bordetella pertussis was detected in 2.4% of cases (Figure 2).


 

Figure 2 - Detection rates of respiratory bacterial pathogens among ARI patients in Almaty, Kazakhstan,

from November 2023 to January 2024.


III. Positivity rates of respiratory pathogens by age

Positivity rates of respiratory viruses by age

Age-specific viral detection rates were evaluated descriptively. Most viral targets were detected more frequently in children younger than 5 years than in adults, with the exception of influenza A virus. In the 0–1-year age category, adenovirus (14.3%), RSV A (11.4%), and RSV B (14.3%) showed higher positivity rates than in several older age categories (Figure 3). The overall positivity rate for influenza A virus was 14.7%, with the highest observed rate in the 31–40-year age group; among patients aged ≥61 years, the rate was 15.9%. In children aged ≤10 years, the average positivity rate for rhinovirus was 35.2%, the highest among the reported viral detections (Figure 3).


 

   

Figure 3 - Positivity rates of respiratory viruses by age

 


Positivity rates of respiratory bacteria by age

In children younger than 10 years, H. influenzae, S. pneumoniae, and M. catarrhalis were among the most frequently detected bacterial targets, whereas H. influenzae and S. aureus predominated among adults. B. pertussis was detected across several age categories (Figure 4).


 

  

Figure 4 - Positivity rates of respiratory bacteria by age


IV. Multiple respiratory pathogen detections

Among the 374 patients tested, a single viral target was detected in 33 patients (8.8%), a single bacterial target in 63 patients (16.8%), and no investigated target was detected in 76 patients (20.3%). Multiple positive assay targets were recorded in 202 patients (54.0%). Among the 202 patients with multiple positive targets, two targets were detected in 94 patients (46.5%), three in 67 patients (33.2%), and four or more in 41 patients (20.3%) (Figure 5).

Among the bacterial targets represented in the multiple-detection profiles, Streptococcus pneumoniae, Staphylococcus aureus, Haemophilus influenzae, Moraxella catarrhalis, and Klebsiella pneumoniae were among the most frequently detected (Table 2).


Figure 5 - Distribution of single and multiple respiratory pathogen detections among ARI patients


Table 2 - Combinations of multiple respiratory pathogen targets detected by multiplex real-time PCR

Multiple detection (2 targets)

Multiple detection (3 targets)

Category

Pathogens

N. of case

Category

Pathogens

N. of case

Bacteria
+Bacteria

H.influenzae+S.pneumoniae

8

Bacteria
only

H.influenzae+M.catarrhalis+S.pneumoniae

6

H.influenzae+M.catarrhalis

6

H.influenzae+K.pneumoniae+S.aureus

2

M.catarrhalis+S.pneumoniae

5

M.catarrhalis+S.aureus+S.pneumoniae

1

K.pneumoniae+S.aureus

3

Mixed

(Virus
+Bacteria)

H.influenzae+S.pneumoniae+Rhinovirus

8

H.influenzae+S.aureus

2

M.catarrhalis+Influenza A virus+Influenza A virus H3

7

S.aureus+S.pneumoniae

2

H.influenzae+Influenza A virus+Influenza A virus H3

5

B.pertussis+H.influenzae

1

H.influenzae+M.catarrhalis+Adenovirus

3

B.pertussis+S.aureus

1

H.influenzae+M.catarrhalis+Rhinovirus

3

H.influenzae+K.pneumoniae

1

S.pneumoniae+Influenza A virus+Influenza A virus H3

3

H.influenzae+P.aeruginosa

1

H.influenzae+M.catarrhalis+Respiratory syncytial virus A

2

K.pneumoniae+M.catarrhalis

1

H.influenzae+S.pneumoniae+Respiratory syncytial virus B

2

Virus
+Bacteria

M.catarrhalis+Rhinovirus

8

H.influenzae+Adenovirus+Rhinovirus

2

H.influenzae+Rhinovirus

6

M.catarrhalis+S.pneumoniae+Rhinovirus

2

S.pneumoniae+Rhinovirus

4

S.aureus+S.pneumoniae+Rhinovirus

2

M.catarrhalis+Respiratory syncytial virus B

3

S.aureus+Influenza A virus+Influenza A virus H3

2

H.influenzae+Respiratory syncytial virus A

2

H.influenzae+S.aureus+Respiratory syncytial virus B

1

H.influenzae+Respiratory syncytial virus B

2

H.influenzae+S.aureus+Rhinovirus

1

M.catarrhalis+Adenovirus

2

H.influenzae+S.pneumoniae+Adenovirus

1

S.pneumoniae+Respiratory syncytial virus A

2

H.influenzae+S.pneumoniae+Parainfluenza virus 4

1

S.pneumoniae+Respiratory syncytial virus B

2

H.influenzae+S.pneumoniae+Respiratory syncytial virus A

1

B.pertussis+Adenovirus

1

H.influenzae+Bocavirus+Rhinovirus

1

B.pertussis+Coronavirus 229E

1

M.catarrhalis+S.aureus+Rhinovirus

1

B.pertussis+Rhinovirus

1

M.catarrhalis+S.pneumoniae+Coronavirus NL63

1

C.pneumoniae+Adenovirus

1

M.catarrhalis+S.pneumoniae+Respiratory syncytial virus A

1

H.influenzae+Adenovirus

1

S.aureus+S.pneumoniae+Parainfluenza virus 4

1

H.influenzae+Parainfluenza virus 2

1

S.aureus+S.pneumoniae+Respiratory syncytial virus B

1

H.influenzae+Parainfluenza virus 3

1

S.aureus+Enterovirus+Parainfluenza virus 4

1

K.pneumoniae+Respiratory syncytial virus B

1

S.pneumoniae+Enterovirus+Rhinovirus

1

M.catarrhalis+Bocavirus

1

Virus

only

Influenza A virus+Influenza A virus H3+Rhinovirus

3

M.catarrhalis+Enterovirus

1

Influenza A virus+Influenza A virus H3 virus 3

+Parainfluenza

1

P.aeruginosa+Rhinovirus

1

S.aureus+Parainfluenza virus 1

1

S.aureus+Rhinovirus

1

Virus+Virus

Influenza A virus+Influenza A virus H3

18

Coronavirus NL63+Parainfluenza virus 4

1

Total

94

Total

67

Multiple detection (4 or more targets)

Pathogens

N. of case

H.influenzae+M.catarrhalis+S.pneumoniae+Rhinovirus

4

M.catarrhalis+S.pneumoniae+Influenza A virus+Influenza A virus H3

2

B. pertussis+H.influenzae+M. catarrhalis+S.pneumoniae+Adenovirus+Rhinovirus

1

B.pertussis+H.influenzae+M.catarrhalis+S.pneumoniae+Respiratory syncytial virus B

1

B.pertussis+H.influenzae+M.catarrhalis+S.pneumoniae+Rhinovirus

1

B.pertussis+H.influenzae+S.pneumoniae+Adenovirus

1

C.pneumoniae+H.influenzae+M. catarrhalis+S.pneumoniae+Adenovirus+Respiratory syncytial virus A+Rhinovirus

1

H.influenzae+K.pneumoniae+S.aureus+Influenza A virus+Influenza A virus H3

1

H.influenzae+M.catarrhalis+P.aeruginosa+Adenovirus+Rhinovirus

1

H.influenzae+M.catarrhalis+S.aureus+S.pneumoniae+Influenza A virus+Influenza A virus H3

1

H.influenzae+M.catarrhalis+S.aureus+S.pneumoniae+Rhinovirus

1

H.influenzae+M.catarrhalis+S.aureus+Influenza A virus+Influenza A virus H3+Rhinovirus

1

H.influenzae+M.catarrhalis+S.pneumoniae+Adenovirus+Respiratory syncytial virus A

1

H.influenzae+M.catarrhalis+S.pneumoniae+Bocavirus

1

H.influenzae+M.catarrhalis+S.pneumoniae+Enterovirus

1

H.influenzae+M.catarrhalis+S.pneumoniae+Parainfluenza virus 3+Rhinovirus

1

H.influenzae+M.catarrhalis+S.pneumoniae+Parainfluenza virus 4

1

H.influenzae+M.catarrhalis+S.pneumoniae+Respiratory syncytial virus B

1

H.influenzae+M.catarrhalis+S.pneumoniae+Respiratory syncytial virus B+Rhinovirus

1

H.influenzae+M.catarrhalis+Enterovirus+Influenza A virus+Influenza A virus H3+Rhinovirus

1

H.influenzae+M.catarrhalis+Enterovirus+Parainfluenza virus 3+Rhinovirus

1

H.influenzae+M.catarrhalis+Influenza A virus+Influenza A virus H3

1

H.influenzae+P.aeruginosa+S.pneumoniae+Influenza A virus+Influenza A virus H3

1

H.influenzae+S.aureus+Influenza A virus+Influenza A virus H3

1

H.influenzae+S.pneumoniae+Adenovirus+Respiratory syncytial virus A+Rhinovirus

1

H.influenzae+S.pneumoniae+Influenza A virus+Influenza A virus H3

1

H.influenzae+S.pneumoniae+Influenza A virus+Influenza A virus H3+Parainfluenza virus 3

1

H.influenzae+S.pneumoniae+Influenza A virus+Influenza A virus H3+Rhinovirus

1

H.influenzae+Adenovirus+Bocavirus+Respiratory syncytial virus B+Rhinovirus

1

H.influenzae+Influenza A virus+Influenza A virus H3+Rhinovirus

1

K.pneumoniae+S.aureus+Influenza A virus+Influenza A virus H3

1

M.catarrhalis+S.pneumoniae+Adenovirus+Respiratory syncytial virus B

1

M.catarrhalis+S.pneumoniae+Influenza A virus+Influenza A virus H3+Rhinovirus

1

M.catarrhalis+Adenovirus+Respiratory syncytial virus A+Rhinovirus

1

S.aureus+S.pneumoniae+Enterovirus+Respiratory syncytial virus A+Rhinovirus

1

S.pneumoniae+Adenovirus+Coronavirus NL63+Rhinovirus

1

Adenovirus+Bocavirus+Influenza A virus+Influenza A virus H3+Respiratory syncytial virus A

1

Total

41

 


Discussion

This study describes the distribution of respiratory pathogen detections during the 2023–2024 epidemic season in Almaty, Kazakhstan, using multiplex real-time PCR. Among 374 patients with ARIs, viral targets were detected in 52.1%, with rhinovirus (24.3%) and influenza A virus (14.7%) the most common. Bacterial targets were detected in 64.2%, most often H. influenzae, S. pneumoniae, and M. catarrhalis. Multiple targets were reported in 54.0% of patients, indicating a high frequency of mixed molecular detections in the study sample.

These findings are broadly consistent with international evidence showing that rhinovirus, RSV, influenza viruses, and major bacterial respiratory pathogens contribute substantially to the burden of acute and lower respiratory infections [1]. The relative frequency of individual pathogens, however, varies by age, clinical setting, geography, season, sampling strategy, and diagnostic platform.

In a multicenter study of adults hospitalized with community-acquired pneumonia in the United States, rhinovirus, influenza virus, and RSV were among the most common viral detections, while S. pneumoniae and H. influenzae were also identified [3]. Jiang et al. demonstrated the feasibility of a three-tube multiplex real-time PCR assay for simultaneous detection of nine microorganisms causing ARIs, supporting the broader diagnostic principle of multiplex molecular testing [15]. In an Italian hospital series, rhinovirus/enterovirus, RSV, and influenza viruses were among the leading respiratory viral detections, with age-related differences and co-detections particularly relevant in pediatric samples [16]. Longitudinal surveillance in Moscow likewise documented persistent seasonal circulation of influenza viruses, RSV, rhinovirus, and other respiratory viruses [17].

In Kazakhstan, the present findings are broadly aligned with previous observations. A metagenomic study of adult ARI patients identified human rhinovirus (16.3%), betaherpesvirus 7 (14.3%), and Epstein-Barr virus (8.2%) among prevalent viral agents, with Streptococcus spp., Pseudomonas aeruginosa, and Burkholderia spp. among bacterial contributors [18]. A media report citing national sanitary-epidemiological surveillance data for the same epidemic season indicated that rhinovirus accounted for the largest proportion of non-influenza respiratory virus detections, followed by RSV, adenovirus, coronavirus, parainfluenza virus, bocavirus, and metapneumovirus [5]. These observations are directionally consistent with the prominence of rhinovirus and RSV in the present dataset, although differences in population, sampling, and testing methods limit direct comparison.

Taken together, the results underscore the complexity of respiratory pathogen detection in ARIs and the presence of age-specific patterns. Multiplex PCR provides rapid, broad detection and may support diagnostic decision-making and antimicrobial stewardship when interpreted together with clinical findings. Prior studies have associated clinically confirmed viral-bacterial co-infections with greater disease severity and worse outcomes in selected pediatric and adult hospitalized populations [19, 20]. However, the present study did not collect clinical outcome data and therefore cannot establish an association between multi-target detection and disease severity. In addition, bacterial PCR positivity may reflect colonization rather than active infection; detection alone should not be used as a stand-alone indication for antibiotic therapy [21].

Evidence from interventional studies also supports cautious interpretation of molecular diagnostics. In a randomized trial of hospitalized patients with community-acquired pneumonia, adding multiplex real-time PCR to conventional microbiological testing increased etiological detection but did not produce a statistically significant reduction in total antibiotic days; the authors did not support routine implementation of the strategy as an initial test for all hospitalized CAP patients [21]. Thus, the value of multiplex PCR is greatest when results are integrated with clinical assessment, sample quality, and antimicrobial stewardship rather than interpreted in isolation.

Limitations of the study

This study has several limitations. First, it was conducted in a single city over a three-month epidemic-season period, which limits the generalizability of the findings to other regions of Kazakhstan and to other respiratory seasons. Second, clinical outcome data were not available; therefore, associations between detected pathogens, multiple detections, and disease severity could not be assessed. Third, detection of bacterial DNA by PCR does not distinguish colonization from active bacterial infection, particularly for organisms that may colonize the upper respiratory tract. Fourth, the multiplex panel contains both generic influenza A and subtype-specific targets. Consequently, simultaneous positivity for these assay targets may represent a single influenza A infection rather than infection with two independent viruses, and target-level counting may overestimate the number of distinct pathogens in some multi-positive profiles. Finally, the analysis was descriptive and did not include inferential or multivariable statistical testing. These limitations should be considered when interpreting the reported positivity and multiple-detection rates.

Conclusion

Multiplex real-time PCR provided broad characterization of respiratory pathogens detected among patients with acute respiratory infections in Almaty during the 2023–2024 season. Rhinovirus and influenza A virus predominated among viral detections, whereas H. influenzae, S. pneumoniae, and M. catarrhalis were the most frequently detected bacterial targets. Multiple assay targets were reported in more than half of patients, but these findings should be interpreted as molecular co-detection rather than confirmed clinical co-infection without additional clinical and microbiological evidence. The results support the potential value of multiplex molecular diagnostics for respiratory surveillance and clinical decision support, while emphasizing cautious interpretation of bacterial and multiple-target PCR positivity.

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Заявления

Этическое одобрение
Исследование основывалось на анализе данных, полученных в рамках рутинной лабораторной диагностики, и не предусматривало изменения стандартного объема медицинской помощи или дополнительных вмешательств в отношении пациентов. В соответствии с применимыми локальными требованиями отдельное одобрение этического комитета и получение дополнительного информированного согласия для данного вида анализа не требовались.
Вклад авторов
Концептуализация - Heesuk Min; методология - Yongha Kim; валидация - Yoonkyung Choi; формальный анализ - Seiick Joo, Умирбекова Лаззат Жаксылыковна; проведение исследования - Yongha Kim, Yoonkyung Choi, Абирова Жазира Мейрамовна, Утаганов Бахыт Кустаевич; ресурсы - Seehyen Ham; курирование данных - Seiick Joo, Амина Мурадалиева; написание первоначального варианта рукописи - Салима Мамутбаева, Minjoong Jang; рецензирование и редактирование рукописи - Mincheol Lee, Minjoong Jang; визуализация - Амина Мурадалиева, Seehyen Ham; научное руководство - Mincheol Lee; администрирование проекта - Geonsang Park. Все авторы ознакомились с окончательной версией рукописи и одобрили ее.
Конфликт интересов
Авторы заявляют об отсутствии конфликта интересов.
Финансирование
Внешнее финансирование исследования не заявлено.
Доступность данных
В рукописи представлены агрегированные результаты исследования. Условия доступа к исходному обезличенному набору индивидуальных данных в исходной версии не указаны и должны быть уточнены автором для корреспонденции до подачи статьи.

Как цитировать

Mamutbayeva S., Mincheol Lee, Geonsang Park, Heesuk Min, Minjoong Jang, Seiick Joo, Yongha Kim, Seehyen Ham, Yoonkyung Choi, Muradalieva A., Abiyrova Zh.M., Utaganov B.K., Umirbekova L.Zh.. Respiratory pathogens detected by multiplex real-time PCR in patients with acute respiratory infections in Almaty, Kazakhstan, during the 2023–2024 epidemic season. Scientific and Practical Journal «Medicine, Science and Education». 2025;(2):45-61. DOI: 10.24412/1609-8692-2025-2-136-150.

CC BY Статья доступна на условиях лицензии CC BY 4.0.