An insight into the salivary gland content of the human body louse, Pediculus humanus

Abstract Human body lice, Pediculus humanus humanus, are blood-feeding parasites that live in clothing and feed several times per day. Saliva injected during louse feeding induces pruritis and local inflammation in the skin. If untreated, chronic Pediculosis can cause systemic negative health effect...

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Main Authors: David M. Bland, Stephen Lu, Sazzad Mahmood, José M. C. Ribeiro
Format: Article
Language:English
Published: Nature Portfolio 2025-05-01
Series:Scientific Reports
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Online Access:https://doi.org/10.1038/s41598-025-01412-5
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author David M. Bland
Stephen Lu
Sazzad Mahmood
José M. C. Ribeiro
author_facet David M. Bland
Stephen Lu
Sazzad Mahmood
José M. C. Ribeiro
author_sort David M. Bland
collection DOAJ
description Abstract Human body lice, Pediculus humanus humanus, are blood-feeding parasites that live in clothing and feed several times per day. Saliva injected during louse feeding induces pruritis and local inflammation in the skin. If untreated, chronic Pediculosis can cause systemic negative health effects. Despite the medical importance of body lice and their longstanding association with humans, characterization of their saliva has been limited. To address this, we extracted RNA and protein from two of the body louse’s morphologically distinct sets of salivary glands (Bean-shaped and U-shaped) and generated transcript and protein profiles for each. Additionally, we performed fluorescent staining and confocal microscopy on each gland type to enhance descriptions of their structure and gross cellular architecture. Analysis of body louse salivary gene products and proteins revealed that the overwhelming majority were not closely related to biomolecules of known function, highlighting the organism’s unique and understudied saliva composition. Despite the contrasting morphology of the two gland types, there was a high degree of overlap in the salivary products produced. This finding suggests strong Darwinian selection pressure to maintain both salivary gland types, given that it would be simpler to have a single morphologically identical set of glands. Here we present the first next-generation sequencing and proteomic characterization of the human body louse sialome, discuss the potential physiological importance of louse salivary proteins, and consider possible explanations for why lice have a complex salivary gland system despite inordinate redundancy in the protein repertoire of the Bean- and U-shaped salivary glands.
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spelling doaj-art-aa5e4927e0a945b59e3e01b2b1bae4d42025-08-20T03:22:09ZengNature PortfolioScientific Reports2045-23222025-05-0115111210.1038/s41598-025-01412-5An insight into the salivary gland content of the human body louse, Pediculus humanusDavid M. Bland0Stephen Lu1Sazzad Mahmood2José M. C. Ribeiro3Laboratory of Bacteriology, National Institute of Allergy and Infectious DiseasesVector Biology Section, Laboratory of Malaria and Vector Research, National Institute of Allergy and Infectious DiseasesTick-Pathogen Transmission Unit, Laboratory of Bacteriology, National Institute of Allergy and Infectious DiseasesVector Biology Section, Laboratory of Malaria and Vector Research, National Institute of Allergy and Infectious DiseasesAbstract Human body lice, Pediculus humanus humanus, are blood-feeding parasites that live in clothing and feed several times per day. Saliva injected during louse feeding induces pruritis and local inflammation in the skin. If untreated, chronic Pediculosis can cause systemic negative health effects. Despite the medical importance of body lice and their longstanding association with humans, characterization of their saliva has been limited. To address this, we extracted RNA and protein from two of the body louse’s morphologically distinct sets of salivary glands (Bean-shaped and U-shaped) and generated transcript and protein profiles for each. Additionally, we performed fluorescent staining and confocal microscopy on each gland type to enhance descriptions of their structure and gross cellular architecture. Analysis of body louse salivary gene products and proteins revealed that the overwhelming majority were not closely related to biomolecules of known function, highlighting the organism’s unique and understudied saliva composition. Despite the contrasting morphology of the two gland types, there was a high degree of overlap in the salivary products produced. This finding suggests strong Darwinian selection pressure to maintain both salivary gland types, given that it would be simpler to have a single morphologically identical set of glands. Here we present the first next-generation sequencing and proteomic characterization of the human body louse sialome, discuss the potential physiological importance of louse salivary proteins, and consider possible explanations for why lice have a complex salivary gland system despite inordinate redundancy in the protein repertoire of the Bean- and U-shaped salivary glands.https://doi.org/10.1038/s41598-025-01412-5RNA sequencingSialomeTranscriptomeHematophagous arthropodsVectorSalivary gland
spellingShingle David M. Bland
Stephen Lu
Sazzad Mahmood
José M. C. Ribeiro
An insight into the salivary gland content of the human body louse, Pediculus humanus
Scientific Reports
RNA sequencing
Sialome
Transcriptome
Hematophagous arthropods
Vector
Salivary gland
title An insight into the salivary gland content of the human body louse, Pediculus humanus
title_full An insight into the salivary gland content of the human body louse, Pediculus humanus
title_fullStr An insight into the salivary gland content of the human body louse, Pediculus humanus
title_full_unstemmed An insight into the salivary gland content of the human body louse, Pediculus humanus
title_short An insight into the salivary gland content of the human body louse, Pediculus humanus
title_sort insight into the salivary gland content of the human body louse pediculus humanus
topic RNA sequencing
Sialome
Transcriptome
Hematophagous arthropods
Vector
Salivary gland
url https://doi.org/10.1038/s41598-025-01412-5
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