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1.
J Microbiol Biotechnol ; 34(8): 1705-1710, 2024 Aug 28.
Article in English | MEDLINE | ID: mdl-39081252

ABSTRACT

Plastic waste has emerged as a major environmental concern in recent years. As plastic waste discharged into the marine environment, it undergoes a breakdown process, eventually accumulating in aquatic organisms in the form of microplastics (MPs). To date, reduced food intake, nutritional absorption, and impaired immune system are known adverse effects of MPs-exposed aquatic organisms. This study aims to investigate whether MP exposure accelerated white spot syndrome virus (WSSV) infection in Pacific white shrimp (Penaeus vannamei) via laboratory tests. Briefly, experimental shrimp were divided into four groups; WSSV (group 1); MP (group 2); WSSV + MP (group 3); and Control (group 4). No mortality was observed in group 2, group 4, and even in group 1. However, group 3 showed a cumulative mortality of 50% during the experimental period. The PCR assay results showed no WSSV in the other three groups (groups 1, 2, and 4), but the dead and alive shrimp collected from group 3 were confirmed to be infected with the virus. Histopathological examination revealed normal structures in the hepatopancreas, gill, and muscle tissues of group 4, whereas numerous abnormally shaped nuclei were detected in the gill tissue of group 2. Moreover, group 1 showed minor WSSV-related lesions with few basophilic inclusion bodies in the gills, interestingly, group 3 exhibited severe lesions with numerous basophilic inclusion bodies in the gills. In conclusion, this study confirmed the correlation between the viral disease of shrimp and MPs, which can cause significant economic losses to the shrimp aquaculture industry.


Subject(s)
Gills , Microplastics , Penaeidae , White spot syndrome virus 1 , Animals , Penaeidae/virology , Microplastics/toxicity , Gills/virology , Gills/pathology , Aquaculture , Water Pollutants, Chemical/toxicity , Hepatopancreas/virology , Hepatopancreas/pathology
2.
J Microbiol Biotechnol ; 34(5): 1146-1153, 2024 May 28.
Article in English | MEDLINE | ID: mdl-38563108

ABSTRACT

The increasing economic losses associated with growth retardation caused by Enterocytozoon hepatopenaei (EHP), a microsporidian parasite infecting penaeid shrimp, require effective monitoring. The internal transcribed spacer (ITS)-1 region, the non-coding region of ribosomal clusters between 18S and 5.8S rRNA genes, is widely used in phylogenetic studies due to its high variability. In this study, the ITS-1 region sequence (~600-bp) of EHP was first identified, and primers for a polymerase chain reaction (PCR) assay targeting that sequence were designed. A newly developed nested-PCR method successfully detected the EHP in various shrimp (Penaeus vannamei and P. monodon) and related samples, including water and feces collected from Indonesia, Thailand, South Korea, India, and Malaysia. The primers did not cross-react with other hosts and pathogens, and this PCR assay is more sensitive than existing PCR detection methods targeting the small subunit ribosomal RNA (SSU rRNA) and spore wall protein (SWP) genes. Phylogenetic analysis based on the ITS-1 sequences indicated that the Indonesian strain was distinct (86.2% nucleotide sequence identity) from other strains collected from Thailand and South Korea, and also showed the internal diversity among Thailand (N = 7, divided into four branches) and South Korean (N = 5, divided into two branches) samples. The results revealed the ability of the ITS-1 region to determine the genetic diversity of EHP from different geographical origins.


Subject(s)
DNA, Ribosomal Spacer , Enterocytozoon , Microsporidiosis , Penaeidae , Phylogeny , Polymerase Chain Reaction , Enterocytozoon/genetics , Enterocytozoon/isolation & purification , Enterocytozoon/classification , Penaeidae/microbiology , Penaeidae/parasitology , Animals , DNA, Ribosomal Spacer/genetics , Polymerase Chain Reaction/methods , Microsporidiosis/microbiology , Microsporidiosis/diagnosis , DNA, Fungal/genetics , DNA Primers/genetics , Feces/microbiology , Feces/parasitology , Sequence Analysis, DNA , Thailand
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