Assessing the performance of trūRapid™ FOUR heartworm antigen test for early detection in experimentally infected dogs in comparison to other point-of-care tests.

IF 3.7 2区 医学 Q1 PARASITOLOGY
Pabasara Weerarathne, Tiana L Sanders, Alexa Starnes, Maureen A Kelly, Pablo D Jimenez Castro, Frances M Moore, Demitria M Vasilatis, Christian M Leutenegger, Chinta Lamichhane, Haichen Song, Guilherme G Verocai
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引用次数: 0

Abstract

Background: The American Heartworm Society (AHS) recommends diagnosing canine heartworm (HW) infection using both antigen and microfilaria detection tests. Antigen-antibody immune complexes may block antigen detection. Therefore, the AHS recommends immune complex dissociation (ICD) via heat treatment for discordant cases. The trūRapid™ FOUR antigen test kit (Antech Diagnostics) is a novel commercially available point-of-care (POC) device. This study evaluated the performance of trūRapid™ FOUR compared to other commercially available POC tests, namely SNAP® 4Dx® Plus (IDEXX), VETSCAN® Flex4 (Zoetis), and a plate-based assay, DiroCHEK® (Zoetis), for early detection of HW infection in experimentally infected dogs.

Methods: Archival frozen serum samples from six purpose-bred beagles experimentally infected with Dirofilaria immitis were collected weekly for 5.5 months, from week 1 to week 22 post-infection. Sera were tested for the detection of HW antigen, pre- and post-ICD, via heat treatment (103 °C for 10 min in a heat block) using each of the commercial antigen tests. DiroCHEK® results were interpreted using optical density readings.

Results: HW antigen was not detected in samples collected from week 1 through week 19. In week 20, the trūRapid™ FOUR, SNAP® 4Dx® Plus, and VETSCAN® Flex4 detected HW antigen in one out of six samples (16.7%) post-ICD, while DiroCHEK® detected two (33.3%) post-ICD. In week 21, the trūRapid™ FOUR, SNAP® 4Dx® Plus, and DiroCHEK® detected HW antigen in four out of the five (80%) post-ICD samples, whereas the VETSCAN® Flex4 detected three out of the four (75%) post-ICD samples. In week 22, HW antigen was detected in one of six (16.7%) pre-ICD by all tests; trūRapid™ FOUR, SNAP® 4Dx® Plus, and DiroCHEK® detected HW antigen on all six (100%) samples post-ICD, while VETSCAN® Flex4 detected four of six samples (66.7%).

Conclusions: Our findings indicate that trūRapid™ FOUR and other commercially available antigen detection tests can detect HW antigen as early as 5 months post-infection when serum is subjected to heat treatment. The performance of trūRapid™ FOUR is comparable to other widely used commercial antigen kits. Its ease of use and ability to detect HW infection earlier in the course of antigenemia makes it an excellent POC diagnostic tool, allowing for prompt clinical intervention, and increasing patient quality of life.

与其他护理点检测相比,评估trūRapid™FOUR心丝虫抗原检测在实验感染犬的早期检测中的性能。
背景:美国心丝虫协会(AHS)建议诊断犬心丝虫(HW)感染同时使用抗原和微丝检测试验。抗原-抗体免疫复合物可阻断抗原检测。因此,美国AHS建议通过热处理免疫复合物解离(ICD)治疗不一致的病例。trūRapid™FOUR抗原检测试剂盒(Antech Diagnostics)是一种新型的市售护理点(POC)设备。本研究评估了trūRapid™FOUR与其他市售POC检测的性能,即SNAP®4Dx®Plus (IDEXX)、VETSCAN®Flex4 (Zoetis)和基于板的DiroCHEK®(Zoetis),用于早期检测实验感染犬的HW感染。方法:对6只实验感染免疫双丝虫的专用饲养小猎犬,从感染后第1周至第22周,每周采集存档冷冻血清标本,为期5.5个月。使用每种商业抗原测试,通过热处理(103°C,在热块中加热10分钟),检测血清中HW抗原的检测,icd前后。使用光密度读数解释DiroCHEK®结果。结果:第1周至第19周标本中未检出HW抗原。在第20周,trūRapid™FOUR, SNAP®4Dx®Plus和VETSCAN®Flex4在icd后的6个样本中检测到1个(16.7%)HW抗原,而DiroCHEK®检测到2个(33.3%)icd后。在第21周,trūRapid™FOUR、SNAP®4Dx®Plus和DiroCHEK®在5个icd后样本中检测到4个(80%)HW抗原,而VETSCAN®Flex4在4个icd后样本中检测到3个(75%)HW抗原。第22周,6例预icd中有1例(16.7%)检测到HW抗原;trūRapid™FOUR, SNAP®4Dx®Plus和DiroCHEK®在icd后的所有六个样品中检测到HW抗原(100%),而VETSCAN®Flex4在六个样品中检测到四个(66.7%)。结论:我们的研究结果表明trūRapid™FOUR和其他市售抗原检测方法可以在感染后5个月对血清进行热处理时检测出HW抗原。trūRapid™FOUR的性能可与其他广泛使用的商用抗原试剂盒相媲美。它的易用性和在抗原血症过程中早期检测HW感染的能力使其成为一种优秀的POC诊断工具,允许及时的临床干预,并提高患者的生活质量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Parasites & Vectors
Parasites & Vectors 医学-寄生虫学
CiteScore
6.30
自引率
9.40%
发文量
433
审稿时长
1.4 months
期刊介绍: Parasites & Vectors is an open access, peer-reviewed online journal dealing with the biology of parasites, parasitic diseases, intermediate hosts, vectors and vector-borne pathogens. Manuscripts published in this journal will be available to all worldwide, with no barriers to access, immediately following acceptance. However, authors retain the copyright of their material and may use it, or distribute it, as they wish. Manuscripts on all aspects of the basic and applied biology of parasites, intermediate hosts, vectors and vector-borne pathogens will be considered. In addition to the traditional and well-established areas of science in these fields, we also aim to provide a vehicle for publication of the rapidly developing resources and technology in parasite, intermediate host and vector genomics and their impacts on biological research. We are able to publish large datasets and extensive results, frequently associated with genomic and post-genomic technologies, which are not readily accommodated in traditional journals. Manuscripts addressing broader issues, for example economics, social sciences and global climate change in relation to parasites, vectors and disease control, are also welcomed.
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