棘气孔与志贺氏单胞菌共感染的形态和分子特征:Bagrus bajad的免疫学和组织病理学鉴定

IF 3.5 3区 医学 Q3 IMMUNOLOGY Microbial pathogenesis Pub Date : 2025-03-01 Epub Date: 2025-02-07 DOI:10.1016/j.micpath.2025.107365
Marwa M. Attia , Abdullah Albaqami , Rania I. Mohamed , Hanim S. Heikal , Asmaa W. Soliman , Mohamed Abdelsalam
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引用次数: 0

摘要

野生鱼类种群中寄生虫和细菌感染之间复杂的相互作用对水生健康管理提出了重大挑战。本研究调查了埃及野生采食Bagrus bajad的棘口吸虫(abanthostomum abconcondium)和棘口吸虫(Acanthostomum spiniceps)与志贺氏单胞菌(Plesiomonas shigelides)的共感染情况。利用形态学、分子学、免疫学和组织病理学方法的结合,我们检查了200个鱼标本的寄生虫感染和随后的细菌定植。寄生虫学检查显示,潜存棘棘棘螨的患病率为22.5%和30%,光镜下形态特征明显。通过16S rRNA测序,鉴定出66.7%的感染鱼中有志贺氏杆菌。10株分离菌株与已知志贺氏单胞杆菌具有较高的遗传相似性(98.06 ~ 99.85%)和系统发育聚类性。抗生素敏感性试验显示多重耐药模式,所有分离株均对甲氧苄啶和青霉素耐药。基于pcr的筛选分别在80%、90%和70%的分离株中检测到毒力基因astA、actP和ahpA。免疫评价结果显示,与单纯寄生虫感染组(200-260±27.00 μg/mL)和未感染组(85-120 μg/mL)相比,共感染组血清溶菌酶活性显著升高(430-450±25.00 μg/mL)。组织病理学检查显示广泛的肠道损伤,包括绒毛破坏和寄生虫侵入粘膜下层。这些发现强调了bbajad中复杂的宿主-寄生虫-细菌相互作用,并强调了与志贺氏单胞杆菌共同感染相关的潜在健康风险,强调了对野生鱼类种群进行综合监测和管理策略的必要性。
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Morphological and molecular characterization of Acanthostomum species with Plesiomonas shigelloides coinfection: Immunological and histopathological appraisal in Bagrus bajad
The complex interactions between parasitic and bacterial infections in wild fish populations present significant challenges for aquatic health management. This study investigated the coinfection of acanthostomid trematodes (Acanthostomum absconditum and Acanthostomum spiniceps) and the bacterium Plesiomonas shigelloides in wild caught Bagrus bajad from Egypt. Using a combination of morphological, molecular, immunological, and histopathological approaches, we examined 200 fish specimens for parasitic infection and subsequent bacterial colonization. Parasitological examination revealed prevalence rates of 22.5 % for A. absconditum and 30 % for A. spiniceps, with distinct morphological features characterized through light microscopy. Bacterial isolation and molecular identification through 16S rRNA sequencing identified P. shigelloides in 66.7 % of parasite-infected fish. Ten bacterial isolates showed high genetic similarity (98.06–99.85 %) and phylogenetic clustering with known P. shigelloides strains. Antibiotic susceptibility testing revealed multidrug resistance patterns, with all isolates resistant to trimethoprim, and penicillin. PCR-based screening detected virulence gene astA, actP, and ahpA in 80 %, 90 %, and 70 % of isolates, respectively. Immunological assessment showed significantly elevated serum lysozyme activity in coinfected fish (430–450 ± 25.00 μg/mL) compared to those with parasitic infection alone (200–260 ± 27.00 μg/mL) and uninfected controls (85–120 μg/mL). Histopathological examination revealed extensive intestinal damage, including villous destruction and parasitic penetration into the submucosa. These findings highlight the complex host-parasite-bacteria interactions in B. bajad and underscore potential health risks associated with P. shigelloides coinfection, emphasizing the need for comprehensive monitoring and management strategies in wild fish populations.
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来源期刊
Microbial pathogenesis
Microbial pathogenesis 医学-免疫学
CiteScore
7.40
自引率
2.60%
发文量
472
审稿时长
56 days
期刊介绍: Microbial Pathogenesis publishes original contributions and reviews about the molecular and cellular mechanisms of infectious diseases. It covers microbiology, host-pathogen interaction and immunology related to infectious agents, including bacteria, fungi, viruses and protozoa. It also accepts papers in the field of clinical microbiology, with the exception of case reports. Research Areas Include: -Pathogenesis -Virulence factors -Host susceptibility or resistance -Immune mechanisms -Identification, cloning and sequencing of relevant genes -Genetic studies -Viruses, prokaryotic organisms and protozoa -Microbiota -Systems biology related to infectious diseases -Targets for vaccine design (pre-clinical studies)
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