Abstract

Aquatic environments around the world have become mixtures of different types of pollutants, including pharmaceuticals. The presence of pharmaceuticals in aquatic environments has raised concerns regarding the possibility of unintended effects on aquatic animals. South Africa is currently the largest consumer of HIV antiretroviral drugs (ARVs) worldwide. Nevirapine (NVP), a first-line ARV, has been associated with serious liver toxicity in humans and has been repeatedly detected in South African surface water. We investigated the potential effect of NVP on the growth of larvae and juveniles of the Mozambique tilapia (Oreochromis mossambicus) through a chronic laboratory exposure. Larval and early juvenile stages were exposed to the highest reported environmental relevant concentration of NVP in South African surface water (1.48 μg/L) for 60 days in a static renewal system. Body mass and total length measurements were recorded and analysed for individuals aged 1, 5, 30 and 60 days. In total, 455 fish were assessed. The growth parameters of larvae exposed to NVP were not statistically significantly different (p>0.05) from those of control larvae. However, the juveniles exposed to NVP showed a slightly lower mean growth rate between the 30th and 60th day compared with the control fish. These results suggest that the concentration of NVP in South African surface water has no significant detrimental effects on fish growth during the first 2 months of their life. Further studies to investigate the effects on all life stages of fish are needed as it is evident that the growth rate of exposed fish could be affected after this stage.
 Significance:
 
 This study was the first to investigate the effect of an antiretroviral drug in surface water on fish growth.
 Chronic exposure to the highest environmentally relevant concentration of nevirapine in South African waters did not affect the growth of early life stages of Mozambique tilapia.
 The levels of antiretrovirals in aquatic systems should be monitored closely as their consumption is likely to increase in the future.

Highlights

  • We investigated the potential effect of NVP on the growth of larvae and juveniles of the Mozambique tilapia (Oreochromis mossambicus) through a chronic laboratory exposure

  • Case studies include the collapse of a fish population exposed to a synthetic oestrogen in Canada[5]; reduced hatching success of zebrafish (Danio rerio) embryos exposed to sulfonamides[6]; histological changes in the organs of rainbow trout (Oncorhynchus mykiss) and common carp (Cyprinus caprio) exposed to diclofenac[7]; and liver damage and altered health in Mozambique tilapia (Oreochromis mossambicus) exposed to efavirenz, an antiretroviral (ARV)[8]

  • The length and mass measurements of larvae in all exposure containers and groups were very similar for 1- and 5-day-old fish, but 30- and 60-day-old fish showed variations in growth rate in the same container and in all groups

Read more

Summary

Introduction

The presence of human pharmaceuticals in aquatic environments around the world is considered to be one of the pollution problems of emerging concern as the effect of these pharmaceuticals on aquatic animals is still largely unknown.[1,2] There are growing concerns that pharmaceuticals in water may have unintended effects on fish.[3,4] Case studies include the collapse of a fish population exposed to a synthetic oestrogen in Canada[5]; reduced hatching success of zebrafish (Danio rerio) embryos exposed to sulfonamides[6]; histological changes in the organs of rainbow trout (Oncorhynchus mykiss) and common carp (Cyprinus caprio) exposed to diclofenac[7]; and liver damage and altered health in Mozambique tilapia (Oreochromis mossambicus) exposed to efavirenz, an antiretroviral (ARV)[8]. It is not a surprise that South African surface water contains all types of ARVs used in the country, and that these ARVs have been detected in tissues of fish.[16,17] Currently, little information is available on the effects ARVs may have on fish health

Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call