太平洋白虾副溶血性弧菌的鉴定及致病性和耐药基因的分子检测

Muhammad Arif Mulya, Fachriyan Hasmi Pasaribu, Usamah Afiff, Munti Yuhana
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引用次数: 1

摘要

摘要本研究旨在对太平洋白对虾弧菌病病原副溶血性弧菌的致病性和耐药基因进行鉴定和分子检测。从对虾肝胰脏中采集副溶血性弧菌分离株,进行生化检测和16S rRNA基因测序确认。采用溶血试验和PCR检测毒力基因toxR、耐热直接溶血素(tdh)和tdh相关溶血素(trh)的存在。采用Kirby-Bauer法鉴定菌株对氨苄西林(AMP)、四环素(TET)、环丙沙星(CIP)、恩诺沙星(ENR)和氯霉素(CHL)的耐药模式。生化试验和PCR-16SrRNA基因测序证实12株分离株为副溶血性弧菌,并扩增382 bp(100%)毒株的toxR基因。所有分离株的α溶血活性扩增量均为199 bp。所有副溶血性弧菌分离株均对AMP耐药,42%的分离株对tet耐药。然而,对CIP、ENR和CHL没有显示出耐药性。基于pcr的分析结果检测到ampC(42%)和tetB(83%)的耐药基因。【关键词】抗生素,对虾,耐药性,毒力,副溶血性弧菌分离株副溶血性弧菌双孔氏肝胰腺、双孔氏弧菌生物克隆、双孔氏弧菌登根聚合酶链反应(PCR)-双孔氏弧菌16S rRNA。溶血方法PCR检测了溶血酶、毒杆菌、抗热直接溶血素(tdh)和tdh相关溶血素(trh)。方法Kirby Bauer digunakan untuk karakterisasi耐药的抗菌药物有:抗菌氨苄西林(AMP)、四环素(TET)、氯氨苯尼科尔(CHL)、siprofloksasin (CIP)和enrofloksasin (ENR)。Uji biokimia dan sekuensing gen PCR-16SrRNA memastikan bahwa 12 isolat adalah V.副溶血性V. yang selanjutnya diverfikasi dengan amplifikasi gen toxR berukuran 382 bp(100%分离)。α活血菌(Aktivitas alfa hemisjuga dikonfirmasi dengan扩增子PCR (199 bp))中Seluruh isolat相关拮抗menunjukkan resistansinya terhadap AMP, 42%阻力春节,有些ada resistansi杨ditunjukkan篇CIP, ENR丹的背影。基于PCR分析,分离得到蒙哈西坎根耐药菌ampC(42%)和根tetB(83%)。Kata kunci:抗生素,udang,耐药,病毒,副溶血性弧菌
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Characterization and molecular detection of pathogenicity and antibioticresistance genes in Vibrio parahaemolyticus isolated from pacific white shrimp
ABSTRACT   This study aimed to conduct the characterization and molecular detection of the pathogenicity and antibiotic-resistance genes in Vibrio parahaemolyticus, as the causative agent of vibriosis in Pacific white shrimp. The V. parahaemolyticus isolates were collected from the shrimp’s hepatopancreas, before biochemical test and polymerase chain reaction (PCR) sequencing of the 16S rRNA gene confirmation. The hemolysis test and PCR were applied to detect the presence of virulence genes, namely toxR, thermostable direct haemolysin (tdh), and tdh-related haemolysin (trh). The Kirby-Bauer method was used for characterizing the resistance patterns against ampicillin (AMP), tetracycline (TET), cyprofloxacin (CIP), enrofloxacin (ENR), and chloramphenicol (CHL). The biochemical tests and PCR-16SrRNA gene sequencing confirmed that 12 isolates belonged to V. parahaemolyticus that were further verified by amplification of the toxR gene in 382 bp (100% of the isolates). The alpha hemolysis activity was also confirmed by the amplicon of 199 bp in all isolates. All V. parahaemolyticus isolates showed their resistance to AMP and 42% of the isolates were TET-resistant. However, no resistance was shown to CIP, ENR, and CHL. The PCR-based analysis resulted a detectable resistance gene of ampC (42% of the isolates) and tetB (83% of the isolates). Keywords: antibiotics, shrimp, resistance, virulency, Vibrio parahaemolyticus   ABSTRAK   Penelitian ini bertujuan untuk melakukan karakterisasi dan deteksi molekular dari gen patogenisitas dan resistansi antibiotik pada Vibrio parahaemolyticus, agen penyebab vibriosis pada udang vaname. Isolat V. parahaemolyticus dikoleksi dari hepatopankreas, diuji secara biokimiawi dan selanjutnya dikonfirmasi dengan polymerase chain reaction (PCR)-sekuensing dari gen 16S rRNA. Tes hemolisis dan metode PCR diterapkan untuk mendeteksi keberadaan gen virulensi toxR, thermostable direct haemolysin (tdh) and tdh-related haemolysin (trh). Metode Kirby Bauer digunakan untuk karakterisasi pola resistansi terhadap ampisilin (AMP), tetrasiklin (TET), kloramfenikol (CHL), siprofloksasin (CIP) dan enrofloksasin (ENR). Uji biokimia dan sekuensing gen PCR-16SrRNA memastikan bahwa 12 isolat adalah V. parahaemolyticus yang selanjutnya diverifikasi dengan amplifikasi gen toxR berukuran 382 bp (100% isolat). Aktivitas alfa hemolisis juga dikonfirmasi dengan amplikon PCR (199 bp) di semua isolat. Seluruh isolat V. parahaemolyticus menunjukkan resistansinya terhadap AMP, 42% resistan TET, tidak ada resistansi yang ditunjukkan pada CIP, ENR dan CHL. Analisis berbasis PCR menghasilkan gen resistan yang terdeteksi dari gen ampC (42% isolat) dan gen tetB (83% isolat). Kata kunci: Antibiotik, udang, resistansi, virulensi, Vibrio parahaemolyticus
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