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S114

Abstracts / Journal of Clinical Virology 82S (2016) S1–S142

participants reporting the correct virus for specimen 3646, 3647

and 3650. A new pilot is due to be sent out in June 2016 and it will

contain 6 freeze–dried samples with the same matrix as previously

used.

Conclusion:

This study established that there is a need in offer-

ing a scheme for the molecular detection of the most important

Respiratory Viruses. The new scheme is expected to be available

from April 2017 and is available for laboratories that performing

molecular testing for respiratory pathogens.

http://dx.doi.org/10.1016/j.jcv.2016.08.228

Abstract no: 198

Presentation at ESCV 2016: Poster 189

Genotyping and epidemiology analysis of

human rhinovirus among children with severe

acute respiratory infection in Shanghai, China

2013–2014

R.J. Lu

, N. Zhu, W.J. Tan

National Institute for Viral Disease Control and

Prevention, Chinese Center for Disease Control and

Prevention, Beijing, China

Background:

Human rhinovirus (HRV) belongs to the

Enterovirus genus and Picornaviridae family, which has been

classified into three species, HRV-A to HRV-C. HRV is a common

cause of mild acute respiratory infection (ARI) in children. How-

ever, in recent years, HRV has been identified as an etiological agent

of severe acute respiratory infection (SARI) C such as pneumonia,

bronchiolitis and asthma, especially HRV-C discovered in 2006. In

China, HRV species, epidemiological data and clinical profiles are

limited on HRV infection in children with SARI.

Objectives:

To investigate the epidemiological characteristics,

clinical features and genotype diversity of human rhinoviruses

from children with severe acute respiratory infections.

Study design:

441 nasopharyngeal aspirates were collected

from children with SARI in Shanghai from 2013 to 2014. Nested

RT-PCR was employed for preliminary HRV detection and phyloge-

netic analysis on VP4/VP2 region was used to further characterize

the viruses. The clinical and epidemiological characteristics of the

patients with HRV infection were analyzed.

Results:

HRV was detected in 132 (29.9%) of the 441 specimens:

HRV-A in 70 (56%), HRV-B in 10 (7.6%), HRV-C in 31 (23.5%) and

HRV untyped in 21 (18.9%). HRV-A to HRV-C detections peaked

in September, August and October, corresponding with autumn,

respectively. A higher detection frequency of HRV-A and HRV-C

occurred in the <5 years age groups. Cough, fever and wheezing

were the most common symptoms and pneumonia was the most

common diagnosis in patients with HRV infection. Overall there

were no significant differences in the clinical symptom and diag-

nosis between the patients infected with HRV-A and HRV-C. HRV-C

is recently discovered species and may be associated with SARI,

asthma and wheezing. Phylogenetic analysis showed that HRV-C

strains in present study belonged to C3, C6, C13, C15, C16, C18, C24,

C27, C30, C37 and C39 genotypes especially, and C6, C16 and C24

were themost frequently genotypes, whichwere different from the

reports from Japan, Paraguay and Hong Kong China. In addition, 53

(40.2%) HRV positive patients were co-infected with other respira-

tory viruses, among which the most HRV-associated co-infections

involved human bocavirus (HBoV), adenovirus (ADV) and human

parainfluenza virus (PIV).

Conclusion:

Our study showed that HRVwas frequently present

in children with SARI in Shanghai, China. The clinical symptom and

diagnosis of patients infected with HRV-A were similar with HRV-C

species. 11genotypes for HRV-C were found and C6, C16 and C24

genotypes were the most common.

http://dx.doi.org/10.1016/j.jcv.2016.08.229

Abstract no: 204

Presentation at ESCV 2016: Poster 190

RSV surveillance in Sweden – How can we

improve it?

Heli Harvala

1 ,

, AnnaSara Carnahan

2

,

Mia Brytting

2

1

Public Health Agency of Sweden and ECDC, Sweden

2

Public Health Agency of Sweden, Sweden

Introduction:

National RSV surveillance in Sweden aims to

guide clinicians through the RSV season and help them to opti-

mize the timing of RSV immunoprophylaxis, in order to prevent

serious cases of RSV among infants. Estimating the burden of RSV

infection will likely become an important aim of surveillance as

vaccines approach the commercial market. We evaluated how RSV

diagnostics is currently performed in Sweden and the usefulness of

RSV surveillance to clinicians.

Methods:

Clinical microbiology laboratories (

n

= 24) and clinics

(

n

= 5) are invited to report all laboratory-confirmed RSV infections

to the Public Health Agency of Sweden. These data are analysed

and results published weekly. The first questionnaire on methods

was sent to all reporting units, and the second on usefulness of

RSV surveillance to readers of the weekly report. Swedish Quality

Control Program (EQUALIS) data on the performance of laboratory

testing were also analysed.

Results:

23 laboratories and four clinics responded to the first

questionnaire, and 77 readers to the second. All except two labora-

tories use commercial and/or in-house PCR (15 and 7 laboratories,

respectively). RSV PCR is also performed in seven clinical chem-

istry laboratories; none participate in EQUALIS or RSV surveillance.

Chromatographic antigen detection (referred as near-patient test,

NPT)was reported to be used by three laboratories and eight clinics;

three of these clinics do not currently participate RSV surveillance.

NPT-results obtained only in two laboratories and one clinic are

confirmed by another assay. RSV-NPT sensitivity was 0.23 based

EQUALIS panel 2015. Reporting took 15min/week (4–60min); nine

laboratories found it time-consuming. Most clinical readers use the

published RSV data (38/45), either to guide timing of RSV immuno-

prophylaxis (

n

= 14), as staff information (

n

= 10) or for hospital

preparedness (

n

= 14).

Discussion:

RSV surveillance data is widely used by clinicians,

but a need for a faster reporting platform was identified. Further-

more, the importance of confirming RSV-NPT results should be

highlighted. Clinical chemistry laboratories and clinics perform-

ing RSV-NPT will be encouraged to participate in EQUALIS and RSV

surveillance. These measures will improve Swedish RSV surveil-

lance and awareness of RSV in the pre-vaccination era.

http://dx.doi.org/10.1016/j.jcv.2016.08.230